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Showing metabocard for Deoxypyridinoline (HMDB0000569)

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Record Information
Version5.0
StatusDetected and Quantified
Creation Date2005-11-16 15:48:42 UTC
Update Date2021-09-14 15:37:02 UTC
HMDB IDHMDB0000569
Secondary Accession Numbers
  • HMDB00569
Metabolite Identification
Common NameDeoxypyridinoline
DescriptionDeoxypyridinoline (DPD) is a breakdown product of type I fibrillar collagen, it occurs mainly in Type I collagen of bone. DPD shows a high specificity for bone, and the measurement of urinary DPD is not influenced by newly collagens and dietary intake. DPD cross-links of type 1 collagen are excreted in urine either as free or peptide-bound moieties. It is the peptide-bound cross-links that decrease by the greatest amount in response to bisphosphonate therapy. DPD is one of the most extensively characterized biochemical bone markers, but the interpretation of results is hampered by biologic and other preanalytical variability. Biochemical bone markers can provide a valuable tool in the management of metabolic bone diseases. Their most recognized application in clinical practice is for monitoring treatment for osteoporosis as an adjunct to bone mineral density measurements. Other applications that have been investigated include their use as a diagnostic tool for bone diseases other than osteoporosis and as predictive markers for bone loss and the risk of bone fracture. DPD measured in urine follow a circadian or diurnal cycle with a peak in the early morning and nadir in the late afternoon to early evening. The magnitude of the diurnal change, i.e., nadir concentration divided by peak concentration, expressed as a percentage is around 70% (range, 53-75%). (PMID: 11805003 , 17229003 , 16751696 ).
Structure
Data?1582752140
MOLSDFPDBSMILESInChI

MOL for HMDB0000569 (Deoxypyridinoline)

Not Available

3D MOL for HMDB0000569 (Deoxypyridinoline)

Not Available

3D SDF for HMDB0000569 (Deoxypyridinoline)

Not Available

3D-SDF for HMDB0000569 (Deoxypyridinoline)

Not Available

PDB for HMDB0000569 (Deoxypyridinoline)

Not Available

3D PDB for HMDB0000569 (Deoxypyridinoline)

Not Available

SMILES for HMDB0000569 (Deoxypyridinoline)

Not Available

INCHI for HMDB0000569 (Deoxypyridinoline)

Not Available
View in JSmolView NMR AssignmentsView Stereo Labels
SynonymsNot Available
Chemical FormulaC18H28N4O7
Average Molecular Weight412.4375
Monoisotopic Molecular Weight412.19579927
IUPAC NameNot Available
Traditional NameNot Available
CAS Registry Number83462-55-9
SMILESNot Available
InChI Identifier
InChI=1S/C18H28N4O7/c19-12(16(24)25)3-1-2-6-22-8-10(4-5-13(20)17(26)27)11(15(23)9-22)7-14(21)18(28)29/h8-9,12-14H,1-7,19-21H2,(H3-,23,24,25,26,27,28,29)/t12-,13-,14-/m0/s1
InChI KeyZAHDXEIQWWLQQL-IHRRRGAJSA-N
Chemical Taxonomy
ClassificationNot classified
Ontology
Physiological effectNot Available
Disposition
Biological locationSource
ProcessNot Available
Role
Industrial application
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic Properties
Predicted Molecular PropertiesNot Available
Predicted Chromatographic Properties

Predicted Retention Times

Underivatized

Chromatographic MethodRetention TimeReference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.0.88 minutes32390414
Predicted by Siyang on May 30, 202210.728 minutes33406817
Predicted by Siyang using ReTip algorithm on June 8, 20229.39 minutes32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid609.4 seconds40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid414.2 seconds40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid199.8 seconds40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid55.2 seconds40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid166.5 seconds40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid56.7 seconds40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid326.2 seconds40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid282.5 seconds40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)1283.9 seconds40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid608.4 seconds40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid58.8 seconds40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid629.6 seconds40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid165.7 seconds40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid252.9 seconds40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate950.7 seconds40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA913.2 seconds40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water658.4 seconds40023050

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
DeoxypyridinolineN[C@@H](CCCC[N+]1=CC(CC[C@H](N)C([O-])=O)=C(C[C@H](N)C(O)=O)C(O)=C1)C(O)=O5132.4Standard polar33892256
DeoxypyridinolineN[C@@H](CCCC[N+]1=CC(CC[C@H](N)C([O-])=O)=C(C[C@H](N)C(O)=O)C(O)=C1)C(O)=O3495.8Standard non polar33892256
DeoxypyridinolineN[C@@H](CCCC[N+]1=CC(CC[C@H](N)C([O-])=O)=C(C[C@H](N)C(O)=O)C(O)=C1)C(O)=O3901.3Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Deoxypyridinoline,1TMS,isomer #1C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@H](N)C(=O)[O-]3613.5Semi standard non polar33892256
Deoxypyridinoline,1TMS,isomer #2C[Si](C)(C)OC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(CC[C@H](N)C(=O)[O-])=C1C[C@H](N)C(=O)O3673.8Semi standard non polar33892256
Deoxypyridinoline,1TMS,isomer #3C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C13599.2Semi standard non polar33892256
Deoxypyridinoline,1TMS,isomer #4C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O3729.9Semi standard non polar33892256
Deoxypyridinoline,1TMS,isomer #5C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]3734.8Semi standard non polar33892256
Deoxypyridinoline,1TMS,isomer #6C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@H](N)C(=O)[O-])C(=O)O3724.9Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #1C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C3555.1Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #10C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C3554.9Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #11C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O3563.0Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #12C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]3553.8Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #13C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O3693.5Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #14C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]3700.4Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #15C[Si](C)(C)N([C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O)[Si](C)(C)C3829.8Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #16C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3697.6Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #17C[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-])[Si](C)(C)C3876.8Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #18C[Si](C)(C)N([C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@H](N)C(=O)[O-])C(=O)O)[Si](C)(C)C3831.7Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #2C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C13470.7Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #3C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C3556.1Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #4C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O3574.3Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #5C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3565.0Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #6C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C13537.1Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #7C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O3649.9Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #8C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]3651.6Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #9C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)C(=O)O3652.2Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #1C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C13473.6Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #10C[Si](C)(C)OC(=O)[C@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@H](N)C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C3689.4Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #11C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3573.6Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #12C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-]3696.4Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #13C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C3722.9Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #14C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3528.3Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #15C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]3529.8Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #16C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3549.4Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #17C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]3662.5Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #18C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O3656.7Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #19C[Si](C)(C)OC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(CC[C@H](N)C(=O)[O-])=C1C[C@H](N)C(=O)O3762.2Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #2C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3538.7Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #20C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3658.9Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #21C[Si](C)(C)OC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1C[C@H](N)C(=O)O3799.2Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #22C[Si](C)(C)OC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(CC[C@H](N)C(=O)[O-])=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3767.8Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #23C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O3571.1Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #24C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]3560.5Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #25C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C1)N([Si](C)(C)C)[Si](C)(C)C3693.6Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #26C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3568.6Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #27C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C13688.2Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #28C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C13712.8Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #29C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3713.8Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #3C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3536.7Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #30C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O3788.5Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #31C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O3795.2Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #32C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3846.2Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #33C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]3790.2Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #34C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O3844.4Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #35C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3792.3Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #4C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3551.9Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #5C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C3457.8Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #6C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C3453.6Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #7C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3461.4Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #8C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O3571.3Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #9C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3556.1Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #1C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3476.9Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #1C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3516.6Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #1C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C5406.9Standard polar33892256
Deoxypyridinoline,4TMS,isomer #10C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C3479.0Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #10C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C3663.4Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #10C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C5025.4Standard polar33892256
Deoxypyridinoline,4TMS,isomer #11C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3487.5Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #11C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3635.0Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #11C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]4877.2Standard polar33892256
Deoxypyridinoline,4TMS,isomer #12C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-]3610.6Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #12C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-]3674.9Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #12C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-]5452.3Standard polar33892256
Deoxypyridinoline,4TMS,isomer #13C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3482.9Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #13C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3648.1Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #13C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]4964.2Standard polar33892256
Deoxypyridinoline,4TMS,isomer #14C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C13605.2Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #14C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C13692.8Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #14C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C15526.1Standard polar33892256
Deoxypyridinoline,4TMS,isomer #15C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C13617.1Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #15C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C13636.5Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #15C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C15392.5Standard polar33892256
Deoxypyridinoline,4TMS,isomer #16C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3617.2Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #16C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3731.6Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #16C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]4668.5Standard polar33892256
Deoxypyridinoline,4TMS,isomer #17C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C3685.5Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #17C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C3757.3Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #17C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C5108.6Standard polar33892256
Deoxypyridinoline,4TMS,isomer #18C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O3693.3Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #18C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O3760.4Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #18C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O5144.0Standard polar33892256
Deoxypyridinoline,4TMS,isomer #19C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C3721.4Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #19C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C3732.0Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #19C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C5170.5Standard polar33892256
Deoxypyridinoline,4TMS,isomer #2C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3478.0Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #2C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3492.3Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #2C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]5379.5Standard polar33892256
Deoxypyridinoline,4TMS,isomer #20C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3689.6Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #20C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3754.2Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #20C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]5194.5Standard polar33892256
Deoxypyridinoline,4TMS,isomer #21C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3735.3Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #21C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3709.2Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #21C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O4972.2Standard polar33892256
Deoxypyridinoline,4TMS,isomer #22C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3694.5Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #22C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3729.0Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #22C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]4960.6Standard polar33892256
Deoxypyridinoline,4TMS,isomer #23C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]3563.4Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #23C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]3600.6Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #23C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]5047.8Standard polar33892256
Deoxypyridinoline,4TMS,isomer #24C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3574.5Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #24C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3636.7Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #24C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O5065.6Standard polar33892256
Deoxypyridinoline,4TMS,isomer #25C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C3671.8Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #25C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C3650.3Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #25C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C5566.1Standard polar33892256
Deoxypyridinoline,4TMS,isomer #26C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3582.6Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #26C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3613.6Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #26C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]5008.3Standard polar33892256
Deoxypyridinoline,4TMS,isomer #27C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C13693.8Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #27C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C13603.3Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #27C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C15508.1Standard polar33892256
Deoxypyridinoline,4TMS,isomer #28C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C13672.0Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #28C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C13654.0Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #28C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C15507.5Standard polar33892256
Deoxypyridinoline,4TMS,isomer #29C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3711.5Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #29C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3711.5Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #29C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]4740.1Standard polar33892256
Deoxypyridinoline,4TMS,isomer #3C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3478.8Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #3C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3527.3Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #3C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C5470.3Standard polar33892256
Deoxypyridinoline,4TMS,isomer #30C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O3802.9Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #30C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O3690.9Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #30C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O5138.1Standard polar33892256
Deoxypyridinoline,4TMS,isomer #31C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]3752.7Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #31C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]3712.7Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #31C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]5127.6Standard polar33892256
Deoxypyridinoline,4TMS,isomer #32C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3747.9Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #32C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3738.4Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #32C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O5149.0Standard polar33892256
Deoxypyridinoline,4TMS,isomer #33C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3754.3Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #33C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3743.1Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #33C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O5148.4Standard polar33892256
Deoxypyridinoline,4TMS,isomer #34C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)C(=O)O3800.8Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #34C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)C(=O)O3705.0Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #34C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)C(=O)O5210.2Standard polar33892256
Deoxypyridinoline,4TMS,isomer #35C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3754.0Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #35C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3731.2Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #35C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]5198.4Standard polar33892256
Deoxypyridinoline,4TMS,isomer #36C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3616.7Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #36C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3732.9Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #36C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]4651.5Standard polar33892256
Deoxypyridinoline,4TMS,isomer #37C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C3691.9Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #37C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C3763.5Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #37C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C5102.0Standard polar33892256
Deoxypyridinoline,4TMS,isomer #38C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O3686.3Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #38C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O3754.5Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #38C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O5138.9Standard polar33892256
Deoxypyridinoline,4TMS,isomer #39C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3725.6Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #39C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3715.7Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #39C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C5088.3Standard polar33892256
Deoxypyridinoline,4TMS,isomer #4C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3560.5Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #4C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3618.1Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #4C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]5118.0Standard polar33892256
Deoxypyridinoline,4TMS,isomer #40C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]3688.5Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #40C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]3732.3Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #40C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]5113.0Standard polar33892256
Deoxypyridinoline,4TMS,isomer #41C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O3721.4Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #41C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O3721.8Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #41C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O5053.4Standard polar33892256
Deoxypyridinoline,4TMS,isomer #42C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3686.0Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #42C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3746.7Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #42C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]5040.9Standard polar33892256
Deoxypyridinoline,4TMS,isomer #43C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3862.4Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #43C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3773.6Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #43C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O4801.8Standard polar33892256
Deoxypyridinoline,4TMS,isomer #44C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3796.3Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #44C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3802.4Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #44C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]4796.9Standard polar33892256
Deoxypyridinoline,4TMS,isomer #45C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3802.0Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #45C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3806.1Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #45C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4797.3Standard polar33892256
Deoxypyridinoline,4TMS,isomer #46C[Si](C)(C)N([C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O)[Si](C)(C)C3880.5Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #46C[Si](C)(C)N([C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O)[Si](C)(C)C3860.2Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #46C[Si](C)(C)N([C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O)[Si](C)(C)C5200.7Standard polar33892256
Deoxypyridinoline,4TMS,isomer #47C[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-])[Si](C)(C)C3953.8Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #47C[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-])[Si](C)(C)C3813.9Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #47C[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-])[Si](C)(C)C5186.0Standard polar33892256
Deoxypyridinoline,4TMS,isomer #48C[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-])[Si](C)(C)C3958.4Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #48C[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-])[Si](C)(C)C3827.2Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #48C[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-])[Si](C)(C)C5265.5Standard polar33892256
Deoxypyridinoline,4TMS,isomer #5C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3575.2Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #5C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3634.6Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #5C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O5066.9Standard polar33892256
Deoxypyridinoline,4TMS,isomer #6C[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3671.0Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #6C[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3669.1Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #6C[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C5629.1Standard polar33892256
Deoxypyridinoline,4TMS,isomer #7C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3587.3Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #7C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3599.1Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #7C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]4931.2Standard polar33892256
Deoxypyridinoline,4TMS,isomer #8C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C3697.6Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #8C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C3604.6Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #8C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C5504.2Standard polar33892256
Deoxypyridinoline,4TMS,isomer #9C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C3677.6Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #9C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C3637.5Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #9C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C5438.0Standard polar33892256
Deoxypyridinoline,5TMS,isomer #1C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3519.3Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #1C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3600.8Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #1C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]4669.0Standard polar33892256
Deoxypyridinoline,5TMS,isomer #10C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3678.2Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #10C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3724.3Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #10C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C4880.3Standard polar33892256
Deoxypyridinoline,5TMS,isomer #11C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3697.9Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #11C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3727.1Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #11C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O4912.4Standard polar33892256
Deoxypyridinoline,5TMS,isomer #12C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3726.0Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #12C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3671.0Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #12C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O4754.5Standard polar33892256
Deoxypyridinoline,5TMS,isomer #13C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3683.0Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #13C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3695.6Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #13C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]4744.9Standard polar33892256
Deoxypyridinoline,5TMS,isomer #14C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3542.1Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #14C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3749.9Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #14C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]4312.1Standard polar33892256
Deoxypyridinoline,5TMS,isomer #15C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C3639.4Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #15C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C3754.0Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #15C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C4858.6Standard polar33892256
Deoxypyridinoline,5TMS,isomer #16C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C3633.5Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #16C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C3760.3Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #16C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C4859.4Standard polar33892256
Deoxypyridinoline,5TMS,isomer #17C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3652.6Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #17C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3707.0Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #17C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C4690.4Standard polar33892256
Deoxypyridinoline,5TMS,isomer #18C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3632.3Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #18C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3724.2Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #18C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]4709.9Standard polar33892256
Deoxypyridinoline,5TMS,isomer #19C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C3647.3Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #19C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C3720.1Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #19C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C4772.6Standard polar33892256
Deoxypyridinoline,5TMS,isomer #2C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3515.9Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #2C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3630.8Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #2C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C4800.9Standard polar33892256
Deoxypyridinoline,5TMS,isomer #20C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3624.8Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #20C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3743.3Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #20C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4793.9Standard polar33892256
Deoxypyridinoline,5TMS,isomer #21C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3771.5Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #21C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3798.4Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #21C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O4461.4Standard polar33892256
Deoxypyridinoline,5TMS,isomer #22C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3729.8Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #22C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3821.8Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #22C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]4463.0Standard polar33892256
Deoxypyridinoline,5TMS,isomer #23C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3735.9Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #23C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3818.2Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #23C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4492.2Standard polar33892256
Deoxypyridinoline,5TMS,isomer #24C[Si](C)(C)OC(=O)[C@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C3842.2Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #24C[Si](C)(C)OC(=O)[C@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C3863.3Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #24C[Si](C)(C)OC(=O)[C@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C4943.9Standard polar33892256
Deoxypyridinoline,5TMS,isomer #25C[Si](C)(C)OC(=O)[C@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3895.4Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #25C[Si](C)(C)OC(=O)[C@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3837.4Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #25C[Si](C)(C)OC(=O)[C@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C4992.2Standard polar33892256
Deoxypyridinoline,5TMS,isomer #26C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C3882.2Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #26C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C3806.1Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #26C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C4781.4Standard polar33892256
Deoxypyridinoline,5TMS,isomer #27C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3639.4Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #27C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3720.0Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #27C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]4402.8Standard polar33892256
Deoxypyridinoline,5TMS,isomer #28C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3717.6Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #28C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3673.9Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #28C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C4863.0Standard polar33892256
Deoxypyridinoline,5TMS,isomer #29C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]3696.4Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #29C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]3692.5Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #29C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]4882.9Standard polar33892256
Deoxypyridinoline,5TMS,isomer #3C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C3644.2Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #3C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C3625.6Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #3C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C5258.7Standard polar33892256
Deoxypyridinoline,5TMS,isomer #30C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3678.2Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #30C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3729.7Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #30C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C4880.1Standard polar33892256
Deoxypyridinoline,5TMS,isomer #31C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3689.7Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #31C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3722.2Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #31C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O4909.5Standard polar33892256
Deoxypyridinoline,5TMS,isomer #32C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3711.3Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #32C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3683.6Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #32C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O4827.0Standard polar33892256
Deoxypyridinoline,5TMS,isomer #33C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3673.1Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #33C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3710.5Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #33C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4818.2Standard polar33892256
Deoxypyridinoline,5TMS,isomer #34C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N[Si](C)(C)C)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O3842.1Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #34C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N[Si](C)(C)C)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O3768.3Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #34C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N[Si](C)(C)C)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O4538.3Standard polar33892256
Deoxypyridinoline,5TMS,isomer #35C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3780.0Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #35C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3795.0Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #35C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]4539.1Standard polar33892256
Deoxypyridinoline,5TMS,isomer #36C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3787.6Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #36C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3798.2Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #36C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4540.4Standard polar33892256
Deoxypyridinoline,5TMS,isomer #37C[Si](C)(C)OC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1C[C@H](N)C(=O)O3932.7Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #37C[Si](C)(C)OC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1C[C@H](N)C(=O)O3783.4Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #37C[Si](C)(C)OC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1C[C@H](N)C(=O)O4944.7Standard polar33892256
Deoxypyridinoline,5TMS,isomer #38C[Si](C)(C)OC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(CC[C@H](N)C(=O)[O-])=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3867.6Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #38C[Si](C)(C)OC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(CC[C@H](N)C(=O)[O-])=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3837.6Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #38C[Si](C)(C)OC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(CC[C@H](N)C(=O)[O-])=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C4960.1Standard polar33892256
Deoxypyridinoline,5TMS,isomer #39C[Si](C)(C)OC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3946.3Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #39C[Si](C)(C)OC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3801.8Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #39C[Si](C)(C)OC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C5008.3Standard polar33892256
Deoxypyridinoline,5TMS,isomer #4C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3518.6Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #4C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3611.4Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #4C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]4741.4Standard polar33892256
Deoxypyridinoline,5TMS,isomer #40C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O3773.7Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #40C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O3798.4Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #40C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O4443.3Standard polar33892256
Deoxypyridinoline,5TMS,isomer #41C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3727.9Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #41C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3811.8Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #41C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]4474.1Standard polar33892256
Deoxypyridinoline,5TMS,isomer #42C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3726.6Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #42C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3826.9Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #42C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4446.1Standard polar33892256
Deoxypyridinoline,5TMS,isomer #43C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)N([Si](C)(C)C)[Si](C)(C)C3835.1Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #43C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)N([Si](C)(C)C)[Si](C)(C)C3861.5Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #43C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)N([Si](C)(C)C)[Si](C)(C)C4937.0Standard polar33892256
Deoxypyridinoline,5TMS,isomer #44C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C3885.3Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #44C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C3813.1Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #44C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C4917.8Standard polar33892256
Deoxypyridinoline,5TMS,isomer #45C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C13880.0Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #45C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C13826.3Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #45C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C14857.9Standard polar33892256
Deoxypyridinoline,5TMS,isomer #46C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O3980.1Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #46C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O3879.6Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #46C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O4592.2Standard polar33892256
Deoxypyridinoline,5TMS,isomer #47C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3985.3Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #47C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3885.5Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #47C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O4592.7Standard polar33892256
Deoxypyridinoline,5TMS,isomer #48C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3919.8Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #48C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3910.9Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #48C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4590.4Standard polar33892256
Deoxypyridinoline,5TMS,isomer #5C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C13641.7Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #5C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C13583.3Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #5C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C15198.6Standard polar33892256
Deoxypyridinoline,5TMS,isomer #6C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C13634.1Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #6C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C13641.1Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #6C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C15318.9Standard polar33892256
Deoxypyridinoline,5TMS,isomer #7C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3639.2Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #7C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3717.1Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #7C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]4413.6Standard polar33892256
Deoxypyridinoline,5TMS,isomer #8C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3719.3Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #8C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3688.8Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #8C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C4930.0Standard polar33892256
Deoxypyridinoline,5TMS,isomer #9C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3698.7Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #9C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3714.1Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #9C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4951.9Standard polar33892256
Deoxypyridinoline,6TMS,isomer #1C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3583.7Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #1C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3721.9Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #1C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]4077.4Standard polar33892256
Deoxypyridinoline,6TMS,isomer #10C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3766.7Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #10C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3794.8Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #10C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4244.1Standard polar33892256
Deoxypyridinoline,6TMS,isomer #11C[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3917.6Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #11C[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3792.6Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #11C[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C4791.9Standard polar33892256
Deoxypyridinoline,6TMS,isomer #12C[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3852.3Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #12C[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3826.0Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #12C[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C4757.7Standard polar33892256
Deoxypyridinoline,6TMS,isomer #13C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C3896.9Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #13C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C3773.1Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #13C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C4616.2Standard polar33892256
Deoxypyridinoline,6TMS,isomer #14C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3716.8Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #14C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3811.7Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #14C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C4107.7Standard polar33892256
Deoxypyridinoline,6TMS,isomer #15C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3696.9Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #15C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3827.2Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #15C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]4140.0Standard polar33892256
Deoxypyridinoline,6TMS,isomer #16C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3698.5Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #16C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3834.7Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #16C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4140.0Standard polar33892256
Deoxypyridinoline,6TMS,isomer #17C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)N([Si](C)(C)C)[Si](C)(C)C3815.7Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #17C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)N([Si](C)(C)C)[Si](C)(C)C3855.0Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #17C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)N([Si](C)(C)C)[Si](C)(C)C4724.8Standard polar33892256
Deoxypyridinoline,6TMS,isomer #18C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C3851.1Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #18C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C3801.1Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #18C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C4567.2Standard polar33892256
Deoxypyridinoline,6TMS,isomer #19C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C13851.5Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #19C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C13821.5Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #19C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C14645.7Standard polar33892256
Deoxypyridinoline,6TMS,isomer #2C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3682.7Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #2C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3677.9Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #2C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C4526.0Standard polar33892256
Deoxypyridinoline,6TMS,isomer #20C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C3943.7Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #20C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C3888.6Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #20C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C4266.6Standard polar33892256
Deoxypyridinoline,6TMS,isomer #21C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3948.9Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #21C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3887.7Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #21C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O4290.3Standard polar33892256
Deoxypyridinoline,6TMS,isomer #22C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3902.2Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #22C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3910.7Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #22C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4292.2Standard polar33892256
Deoxypyridinoline,6TMS,isomer #23C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3780.6Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #23C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3773.9Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #23C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O4198.7Standard polar33892256
Deoxypyridinoline,6TMS,isomer #24C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3756.5Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #24C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3790.5Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #24C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]4229.7Standard polar33892256
Deoxypyridinoline,6TMS,isomer #25C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3737.8Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #25C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3804.5Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #25C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4209.2Standard polar33892256
Deoxypyridinoline,6TMS,isomer #26C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C3907.7Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #26C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C3774.0Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #26C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C4730.6Standard polar33892256
Deoxypyridinoline,6TMS,isomer #27C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C3847.8Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #27C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C3826.3Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #27C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C4755.1Standard polar33892256
Deoxypyridinoline,6TMS,isomer #28C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C13895.2Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #28C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C13789.4Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #28C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C14680.6Standard polar33892256
Deoxypyridinoline,6TMS,isomer #29C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3984.5Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #29C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3854.9Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #29C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O4347.5Standard polar33892256
Deoxypyridinoline,6TMS,isomer #3C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3675.8Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #3C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3693.7Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #3C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]4538.7Standard polar33892256
Deoxypyridinoline,6TMS,isomer #30C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3994.1Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #30C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3860.0Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #30C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O4350.3Standard polar33892256
Deoxypyridinoline,6TMS,isomer #31C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3930.0Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #31C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3886.1Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #31C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4351.9Standard polar33892256
Deoxypyridinoline,6TMS,isomer #32C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3941.1Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #32C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3895.3Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #32C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C4248.4Standard polar33892256
Deoxypyridinoline,6TMS,isomer #33C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O3946.2Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #33C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O3881.5Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #33C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O4269.6Standard polar33892256
Deoxypyridinoline,6TMS,isomer #34C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3894.4Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #34C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3910.2Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #34C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4273.6Standard polar33892256
Deoxypyridinoline,6TMS,isomer #35C[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-])[Si](C)(C)C4150.6Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #35C[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-])[Si](C)(C)C3982.4Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #35C[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-])[Si](C)(C)C4400.0Standard polar33892256
Deoxypyridinoline,6TMS,isomer #4C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3676.9Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #4C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3724.7Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #4C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C4673.3Standard polar33892256
Deoxypyridinoline,6TMS,isomer #5C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3667.0Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #5C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3731.2Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #5C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C4676.3Standard polar33892256
Deoxypyridinoline,6TMS,isomer #6C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3684.6Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #6C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3688.8Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #6C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C4592.5Standard polar33892256
Deoxypyridinoline,6TMS,isomer #7C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3667.0Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #7C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3712.1Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #7C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4608.8Standard polar33892256
Deoxypyridinoline,6TMS,isomer #8C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3786.9Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #8C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3771.5Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #8C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O4211.6Standard polar33892256
Deoxypyridinoline,6TMS,isomer #9C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3743.9Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #9C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3797.1Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #9C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]4219.5Standard polar33892256
Deoxypyridinoline,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@H](N)C(=O)[O-]3884.3Semi standard non polar33892256
Deoxypyridinoline,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(CC[C@H](N)C(=O)[O-])=C1C[C@H](N)C(=O)O3927.8Semi standard non polar33892256
Deoxypyridinoline,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C13869.1Semi standard non polar33892256
Deoxypyridinoline,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O3989.1Semi standard non polar33892256
Deoxypyridinoline,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]4008.1Semi standard non polar33892256
Deoxypyridinoline,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@H](N)C(=O)[O-])C(=O)O3995.6Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C4061.2Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C(C)(C)C4057.7Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O4056.0Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]4055.1Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O4170.4Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]4187.1Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)N([C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O)[Si](C)(C)C(C)(C)C4262.7Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4193.7Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #17CC(C)(C)[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-])[Si](C)(C)C(C)(C)C4309.2Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #18CC(C)(C)[Si](C)(C)N([C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@H](N)C(=O)[O-])C(=O)O)[Si](C)(C)C(C)(C)C4275.0Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C13996.5Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C(C)(C)C4064.7Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O4075.9Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4079.3Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C14043.8Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O4123.0Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]4140.2Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O4132.9Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C14181.3Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@H](N)C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4395.3Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4269.9Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-]4379.6Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4423.6Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C4223.0Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]4231.3Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O4223.0Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]4343.9Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O4331.5Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(CC[C@H](N)C(=O)[O-])=C1C[C@H](N)C(=O)O4438.1Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4236.1Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4347.2Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)OC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O4489.7Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(CC[C@H](N)C(=O)[O-])=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4453.7Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O4239.9Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]4246.0Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4382.7Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #26CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4251.7Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C14369.4Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C14402.1Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #29CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4394.1Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4244.6Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #30CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O4467.4Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O4481.6Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #32CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1)C(=O)O4516.3Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #33CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]4473.8Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #34CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O4519.5Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #35CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]4490.6Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O4239.6Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C(C)(C)C4158.9Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C(C)(C)C4159.0Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4163.3Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O4249.4Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4255.5Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C4339.8Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C4196.0Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C5357.6Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C(C)(C)C4334.1Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C(C)(C)C4344.8Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C(C)(C)C5029.3Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4353.8Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4312.3Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4921.0Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-]4504.4Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-]4328.8Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-]5348.0Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #13CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4344.6Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #13CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4327.9Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #13CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4989.3Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C14510.0Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C14351.4Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C15406.3Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C14546.9Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C14287.1Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C15308.7Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #16CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4479.8Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #16CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4394.9Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #16CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4762.3Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #17CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C(C)(C)C4571.1Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #17CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C(C)(C)C4406.6Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #17CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C(C)(C)C5077.3Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #18CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O4599.7Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #18CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O4420.0Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #18CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O5099.3Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #19CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4635.0Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #19CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4375.0Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #19CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C5118.8Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4352.6Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4177.7Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]5333.0Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #20CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]4614.2Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #20CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]4405.1Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #20CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]5131.3Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #21CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1)C(=O)O4639.5Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #21CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1)C(=O)O4353.4Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #21CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1)C(=O)O4979.4Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #22CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4588.2Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #22CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4370.9Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #22CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4969.4Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #23CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]4421.8Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #23CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]4260.1Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #23CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]5062.9Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #24CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O4413.0Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #24CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O4290.4Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #24CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O5086.2Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4566.6Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4281.7Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C5464.8Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #26CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4432.8Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #26CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4268.1Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #26CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]5046.1Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C14610.8Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C14236.0Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C15424.2Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C14561.1Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C14286.1Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C15427.1Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #29CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4580.2Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #29CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4336.7Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #29CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4833.8Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4340.1Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4208.4Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C5406.6Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #30CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O4703.4Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #30CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O4304.5Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #30CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O5119.3Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #31CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]4651.8Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #31CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]4321.5Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #31CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]5109.8Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #32CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O4636.8Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #32CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O4351.4Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #32CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O5131.2Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #33CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O4656.6Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #33CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O4356.7Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #33CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O5132.0Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #34CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O4709.7Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #34CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O4316.0Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #34CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O5173.5Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #35CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]4676.8Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #35CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]4339.4Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #35CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]5164.5Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #36CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4464.2Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #36CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4396.2Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #36CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4746.0Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #37CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C(C)(C)C4573.8Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #37CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C(C)(C)C4412.9Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #37CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C(C)(C)C5070.7Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #38CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O4576.0Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #38CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O4414.5Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #38CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O5090.5Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #39CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C4620.0Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #39CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C4361.6Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #39CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C5055.2Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4438.4Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4271.7Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]5118.9Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #40CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]4589.0Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #40CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]4384.9Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #40CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]5065.8Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #41CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O4617.7Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #41CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O4370.4Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #41CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O5038.8Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #42CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]4586.1Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #42CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]4393.9Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #42CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]5029.6Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #43CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1)C(=O)O4739.7Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #43CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1)C(=O)O4428.9Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #43CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1)C(=O)O4828.7Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #44CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4687.9Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #44CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4450.4Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #44CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4825.4Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #45CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]4706.2Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #45CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]4454.6Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #45CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]4826.3Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #46CC(C)(C)[Si](C)(C)N([C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O)[Si](C)(C)C(C)(C)C4776.3Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #46CC(C)(C)[Si](C)(C)N([C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O)[Si](C)(C)C(C)(C)C4470.1Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #46CC(C)(C)[Si](C)(C)N([C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O)[Si](C)(C)C(C)(C)C5118.9Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #47CC(C)(C)[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-])[Si](C)(C)C(C)(C)C4824.4Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #47CC(C)(C)[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-])[Si](C)(C)C(C)(C)C4425.9Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #47CC(C)(C)[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-])[Si](C)(C)C(C)(C)C5105.2Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #48CC(C)(C)[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-])[Si](C)(C)C(C)(C)C4842.7Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #48CC(C)(C)[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-])[Si](C)(C)C(C)(C)C4441.8Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #48CC(C)(C)[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-])[Si](C)(C)C(C)(C)C5162.4Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O4428.3Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O4289.8Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O5087.4Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4588.3Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4304.0Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C5515.2Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4451.9Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4254.9Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4987.2Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C4629.2Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C4237.9Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C5421.3Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C4557.5Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C4266.4Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C5373.5Standard polar33892256
Spectra
Biological Properties
Cellular Locations
  • Cytoplasm
Biospecimen Locations
  • Blood
  • Urine
Tissue Locations
  • Kidney
  • Platelet
  • Skeletal Muscle
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected and Quantified0.0007 +/- 0.00018 uMAdult (>18 years old)BothNormal details
UrineDetected and Quantified0.005 (0.001 - 0.015) umol/mmol creatinineAdult (>18 years old)Not SpecifiedNormal details
UrineDetected and Quantified0.0086 (0.0004-0.016) umol/mmol creatinineAdult (>18 years old)BothNormal details
UrineDetected and Quantified0.0047 +/- 0.0004 umol/mmol creatinineAdult (>18 years old)BothNormal details
Abnormal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected and Quantified0.0006 +/- 0.0001 uMAdult (>18 years old)BothGrowth hormone deficiency details
UrineDetected and Quantified0.015 (0.001 - 0.03) umol/mmol creatinineAdult (>18 years old)Not SpecifiedMultiple myeloma details
UrineDetected and Quantified0.019 +/- 0.0026 umol/mmol creatinineAdult (>18 years old)BothCongestive heart failure details
UrineDetected and Quantified0.0066 +/- 0.0006 umol/mmol creatinineAdult (>18 years old)BothLiver fibrosis details
Associated Disorders and Diseases
Disease References
Growth hormone deficiency
  1. Rodriguez-Arnao J, James I, Jabbar A, Trainer PJ, Perrett D, Besser GM, Ross RJ: Serum collagen crosslinks as markers of bone turn-over during GH replacement therapy in growth hormone deficient adults. Clin Endocrinol (Oxf). 1998 Apr;48(4):455-62. [PubMed:9640412 ]
Multiple myeloma
  1. Dizdar O, Barista I, Kalyoncu U, Karadag O, Hascelik G, Cila A, Pinar A, Celik I, Kars A, Tekuzman G: Biochemical markers of bone turnover in diagnosis of myeloma bone disease. Am J Hematol. 2007 Mar;82(3):185-91. [PubMed:17022050 ]
Congestive heart failure
  1. Shane E, Mancini D, Aaronson K, Silverberg SJ, Seibel MJ, Addesso V, McMahon DJ: Bone mass, vitamin D deficiency, and hyperparathyroidism in congestive heart failure. Am J Med. 1997 Sep;103(3):197-207. [PubMed:9316552 ]
Cirrhosis
  1. Afdhal NH, Keaveny AP, Cohen SB, Nunes DP, Maldonado N, O'Brien M, Stone PJ: Urinary assays for desmosine and hydroxylysylpyridinoline in the detection of cirrhosis. J Hepatol. 1997 Dec;27(6):993-1002. [PubMed:9453424 ]
Associated OMIM IDs
External LinksNot Available
References
Synthesis ReferenceHatch, Robert P. Method for the synthesis of deoxypyridinoline. U.S. (1998), 7 pp.
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Haderslev KV, Tjellesen L, Sorensen HA, Staun M: Alendronate increases lumbar spine bone mineral density in patients with Crohn's disease. Gastroenterology. 2000 Sep;119(3):639-46. [PubMed:10982756 ]
  2. Tanaka K, Inaba M, Goto H, Nagata-Sakurai M, Sakai S, Yamada S, Ueda M, Ishimura E, Nishizawa Y: Paraarticular trabecular bone loss at the ultradistal radius and increased arterial stiffening in postmenopausal patients with rheumatoid arthritis. J Rheumatol. 2006 Apr;33(4):652-8. [PubMed:16583470 ]
  3. Romanello M, Noris Suarez K, Bettica P, Moro L: Detection of pyridinium cross-links in human bile. Calcif Tissue Int. 1995 Dec;57(6):415-8. [PubMed:8581871 ]
  4. Hoff AO, Catala-Lehnen P, Thomas PM, Priemel M, Rueger JM, Nasonkin I, Bradley A, Hughes MR, Ordonez N, Cote GJ, Amling M, Gagel RF: Increased bone mass is an unexpected phenotype associated with deletion of the calcitonin gene. J Clin Invest. 2002 Dec;110(12):1849-57. [PubMed:12488435 ]
  5. Hodsman AB, Fraher LJ, Ostbye T, Adachi JD, Steer BM: An evaluation of several biochemical markers for bone formation and resorption in a protocol utilizing cyclical parathyroid hormone and calcitonin therapy for osteoporosis. J Clin Invest. 1993 Mar;91(3):1138-48. [PubMed:8450043 ]
  6. Kaufmann J, Mueller A, Voigt A, Carl HD, Gursche A, Zacher J, Stein G, Hein G: Hydroxypyridinium collagen crosslinks in serum, urine, synovial fluid and synovial tissue in patients with rheumatoid arthritis compared with osteoarthritis. Rheumatology (Oxford). 2003 Feb;42(2):314-20. [PubMed:12595629 ]
  7. Giangregorio LM, Hicks AL, Webber CE, Phillips SM, Craven BC, Bugaresti JM, McCartney N: Body weight supported treadmill training in acute spinal cord injury: impact on muscle and bone. Spinal Cord. 2005 Nov;43(11):649-57. [PubMed:15968302 ]
  8. Pronchenko IA, Buzulina VP, Tomolina NA, Vedernikova RN, Ermakova IP: [Biochemical markers of bone metabolism and bone tissue losses after allotransplantation of the cadaveric kidney: a cross-sectional]. Klin Lab Diagn. 2005 Nov;(11):3-8. [PubMed:16404967 ]
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