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Record Information

Version

5.0

Status

Detected and Quantified

Creation Date

2019-02-15 22:30:46 UTC

Update Date

2022-03-07 03:18:15 UTC

HMDB ID

HMDB0240295

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Succinylaminoimidazole carboxamide riboside

Description

Succinylaminoimidazole carboxamide riboside, also known as SAICAr, is the riboside form of the better known compound SAICAR (the ribotide). Ribosides chemically resemble ribotides except they do not contain a phosphate group. The appearance of succinylaminoimidazolecarboxamide riboside (SAICAriboside) and succinyladenosine (S-Ado) in cerebrospinal fluid, in urine, and, to a lesser extent, in plasma is characteristic of a heritable deficiency known as adenylosuccinate lyase deficiency (ADSL). Adenylosuccinate lyase deficiency is responsible for a range of symptoms that involve psychomotor retardation, often accompanied by epileptic seizures, and autistic features. In adenylosuccinate lyase deficiency it is believed that the buildup of SAICAr causes neurotoxic effects. In the severely affected individuals, the concentration levels of SAICAr and S-Ado are comparable, whereas in people with milder forms of the disease, the concentration of S-Ado is more than double that of those more severely affected, while SAICAr concentration levels remain comparable. Therefore, when present in sufficiently high levels, SAICAr can act as a metabotoxin and an acidogen. An acidogen is an acidic compound that induces acidosis, which has multiple adverse effects on many organ systems. A metabotoxin is an endogenously produced metabolite that causes adverse health effects at chronically high levels. Acidosis typically occurs when arterial pH falls below 7.35. In infants with acidosis the initial symptoms include poor feeding, vomiting, loss of appetite, weak muscle tone (hypotonia), and lack of energy (lethargy). These can progress to heart, liver, and kidney abnormalities, seizures, coma, and possibly death. These are also the characteristic symptoms of untreated adenylosuccinate lyase deficiency. Many affected children with organic acidemias experience intellectual disability or delayed development.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv1652305231917452D          

 26 27  0  0  0  0            999 V2000
10000.2775 9999.2142    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10001.678610000.1320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.392610000.5447    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10003.108710000.1320    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10003.822710000.5447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10004.538710000.1320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10005.252710000.5447    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10004.5387 9999.3064    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10003.1087 9999.3064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.8227 9998.8925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10002.3926 9998.8925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10001.6786 9999.3064    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9999.1147 9998.6834    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9997.3238 9998.6917    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.856610000.5447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.141610000.1320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9998.237310000.6260    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9997.569910000.1410    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9997.8248 9999.3564    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9998.6498 9999.3564    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9998.904710000.1410    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10000.295910000.0505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.628510000.5355    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9999.883410001.3201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.708410001.3201    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10000.963310000.5355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  3  1  0  0  0  0
  2 12  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  9  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 15 16  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 17 18  1  0  0  0  0
 17 21  1  0  0  0  0
 22 26  2  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 26  2  1  0  0  0  0
  1 22  1  0  0  0  0
 20 13  1  6  0  0  0
 19 14  1  6  0  0  0
 18 15  1  1  0  0  0
 21 23  1  1  0  0  0
M  END

HMDB0240295
     RDKit          3D
Succinylaminoimidazole carboxamide riboside
 44 45  0  0  0  0  0  0  0  0999 V2000
   -0.1078   -0.8160    1.9561 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1857   -0.2202    0.7176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7242    0.4037   -0.1336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1581    0.5417    0.1326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6517    0.0874    1.1834 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9552    1.1935   -0.8182 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3772    1.3676   -0.5893 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1224    0.2282   -1.1493 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5827    0.3528   -0.9831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0913    1.3888   -0.4913 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4211   -0.7031   -1.3812 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5619    1.5412    0.9004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7833    2.2510    1.5837 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6073    0.9044    1.5250 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0098    0.8164   -1.1797 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2801    0.4694   -0.9941 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4158   -0.1725    0.1752 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6591   -0.6902    0.6995 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4892    0.3186    1.1048 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7715    0.0544    0.7173 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1339    0.9660   -0.4578 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4217    0.7382   -0.8907 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8229   -1.3632    0.1834 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9298   -2.2803    1.2303 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4000   -1.4900   -0.3729 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0424   -2.8298   -0.3573 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8183   -1.5748    2.0290 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3685   -0.5251    2.8350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5259    1.5632   -1.7101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6329    2.3771   -1.0520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8701    0.1290   -2.2316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7886   -0.7536   -0.7101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1032   -1.0347   -0.6913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4716    0.3045    2.3317 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0591    0.7029   -1.7222 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5045   -1.3961    1.5394 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4871    0.2170    1.5413 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4454    0.7245   -1.3102 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0306    2.0307   -0.1788 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0147    1.5072   -0.6404 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5805   -1.5029   -0.5879 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8363   -1.8636    2.1191 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3137   -1.0135   -1.3638 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1721   -2.9500   -0.8046 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
  7 12  1  0
 12 13  2  0
 12 14  1  0
  3 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 20 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 17  2  1  0
 25 18  1  0
  1 27  1  0
  1 28  1  0
  6 29  1  0
  7 30  1  6
  8 31  1  0
  8 32  1  0
 11 33  1  0
 14 34  1  0
 16 35  1  0
 18 36  1  1
 20 37  1  1
 21 38  1  0
 21 39  1  0
 22 40  1  0
 23 41  1  6
 24 42  1  0
 25 43  1  6
 26 44  1  0
M  END


  Mrv1652305231917452D          

 26 27  0  0  0  0            999 V2000
10000.2775 9999.2142    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10001.678610000.1320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.392610000.5447    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10003.108710000.1320    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10003.822710000.5447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10004.538710000.1320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10005.252710000.5447    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10004.5387 9999.3064    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10003.1087 9999.3064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.8227 9998.8925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10002.3926 9998.8925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10001.6786 9999.3064    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9999.1147 9998.6834    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9997.3238 9998.6917    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.856610000.5447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.141610000.1320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9998.237310000.6260    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9997.569910000.1410    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9997.8248 9999.3564    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9998.6498 9999.3564    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9998.904710000.1410    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10000.295910000.0505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.628510000.5355    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9999.883410001.3201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.708410001.3201    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10000.963310000.5355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  3  1  0  0  0  0
  2 12  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  9  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 15 16  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 17 18  1  0  0  0  0
 17 21  1  0  0  0  0
 22 26  2  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 26  2  1  0  0  0  0
  1 22  1  0  0  0  0
 20 13  1  6  0  0  0
 19 14  1  6  0  0  0
 18 15  1  1  0  0  0
 21 23  1  1  0  0  0
M  END
> <DATABASE_ID>
HMDB0240295

> <DATABASE_NAME>
hmdb

> <SMILES>
NC1=C(N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O)C(=O)N[C@@H](CC(O)=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C13H18N4O9/c14-10-7(11(23)16-4(13(24)25)1-6(19)20)15-3-17(10)12-9(22)8(21)5(2-18)26-12/h3-5,8-9,12,18,21-22H,1-2,14H2,(H,16,23)(H,19,20)(H,24,25)/t4-,5+,8+,9+,12+/m0/s1

> <INCHI_KEY>
XNKLTOHYNRQCLJ-ZZZDFHIKSA-N

> <FORMULA>
C13H18N4O9

> <MOLECULAR_WEIGHT>
374.306

> <EXACT_MASS>
374.107378176

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
34.040602622446364

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-({5-amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1H-imidazol-4-yl}formamido)butanedioic acid

> <ALOGPS_LOGP>
-2.02

> <JCHEM_LOGP>
-4.201329705566113

> <ALOGPS_LOGS>
-1.60

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
5.150009542463305

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.9902277252424114

> <JCHEM_PKA_STRONGEST_BASIC>
4.551507547451454

> <JCHEM_POLAR_SURFACE_AREA>
217.45999999999998

> <JCHEM_REFRACTIVITY>
79.7798

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.50e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-({5-amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]imidazol-4-yl}formamido)butanedioic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0240295
     RDKit          3D
Succinylaminoimidazole carboxamide riboside
 44 45  0  0  0  0  0  0  0  0999 V2000
   -0.1078   -0.8160    1.9561 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1857   -0.2202    0.7176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7242    0.4037   -0.1336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1581    0.5417    0.1326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6517    0.0874    1.1834 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9552    1.1935   -0.8182 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3772    1.3676   -0.5893 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1224    0.2282   -1.1493 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5827    0.3528   -0.9831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0913    1.3888   -0.4913 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4211   -0.7031   -1.3812 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5619    1.5412    0.9004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7833    2.2510    1.5837 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6073    0.9044    1.5250 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0098    0.8164   -1.1797 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2801    0.4694   -0.9941 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4158   -0.1725    0.1752 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6591   -0.6902    0.6995 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4892    0.3186    1.1048 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7715    0.0544    0.7173 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1339    0.9660   -0.4578 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4217    0.7382   -0.8907 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8229   -1.3632    0.1834 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9298   -2.2803    1.2303 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4000   -1.4900   -0.3729 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0424   -2.8298   -0.3573 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8183   -1.5748    2.0290 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3685   -0.5251    2.8350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5259    1.5632   -1.7101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6329    2.3771   -1.0520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8701    0.1290   -2.2316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7886   -0.7536   -0.7101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1032   -1.0347   -0.6913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4716    0.3045    2.3317 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0591    0.7029   -1.7222 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5045   -1.3961    1.5394 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4871    0.2170    1.5413 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4454    0.7245   -1.3102 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0306    2.0307   -0.1788 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0147    1.5072   -0.6404 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5805   -1.5029   -0.5879 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8363   -1.8636    2.1191 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3137   -1.0135   -1.3638 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1721   -2.9500   -0.8046 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
  7 12  1  0
 12 13  2  0
 12 14  1  0
  3 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 20 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 17  2  1  0
 25 18  1  0
  1 27  1  0
  1 28  1  0
  6 29  1  0
  7 30  1  6
  8 31  1  0
  8 32  1  0
 11 33  1  0
 14 34  1  0
 16 35  1  0
 18 36  1  1
 20 37  1  1
 21 38  1  0
 21 39  1  0
 22 40  1  0
 23 41  1  6
 24 42  1  0
 25 43  1  6
 26 44  1  0
M  END

HEADER    PROTEIN                                 23-MAY-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-MAY-19         0                                  
HETATM    1  N   UNK     0    8667.1858665.200   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0    8669.8008666.913   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0    8671.1338667.683   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0    8672.4708666.913   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0    8673.8028667.683   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0    8675.1398666.913   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0    8676.4728667.683   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0    8675.1398665.372   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0    8672.4708665.372   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0    8673.8028664.599   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0    8671.1338664.599   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0    8669.8008665.372   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0    8665.0148664.209   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0    8661.6718664.225   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0    8660.7998667.683   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0    8659.4648666.913   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0    8663.3768667.835   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0    8662.1308666.930   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0    8662.6068665.465   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0    8664.1468665.465   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0    8664.6228666.930   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0    8667.2198666.761   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0    8665.9738667.666   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0    8666.4498669.131   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0    8667.9898669.131   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0    8668.4658667.666   0.000  0.00  0.00           C+0
CONECT    1   22                                                            
CONECT    2    3   12   26                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    4   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    2                                                            
CONECT   13   20                                                            
CONECT   14   19                                                            
CONECT   15   16   18                                                       
CONECT   16   15                                                            
CONECT   17   18   21                                                       
CONECT   18   19   17   15                                                  
CONECT   19   18   20   14                                                  
CONECT   20   19   21   13                                                  
CONECT   21   20   17   23                                                  
CONECT   22   26   23    1                                                  
CONECT   23   22   24   21                                                  
CONECT   24   25   23                                                       
CONECT   25   24   26                                                       
CONECT   26   22   25    2                                                  
MASTER        0    0    0    0    0    0    0    0   26    0   54    0
END

COMPND    HMDB0240295
HETATM    1  N1  UNL     1      -0.108  -0.816   1.956  1.00  0.00           N  
HETATM    2  C1  UNL     1       0.186  -0.220   0.718  1.00  0.00           C  
HETATM    3  C2  UNL     1      -0.724   0.404  -0.134  1.00  0.00           C  
HETATM    4  C3  UNL     1      -2.158   0.542   0.133  1.00  0.00           C  
HETATM    5  O1  UNL     1      -2.652   0.087   1.183  1.00  0.00           O  
HETATM    6  N2  UNL     1      -2.955   1.193  -0.818  1.00  0.00           N  
HETATM    7  C4  UNL     1      -4.377   1.368  -0.589  1.00  0.00           C  
HETATM    8  C5  UNL     1      -5.122   0.228  -1.149  1.00  0.00           C  
HETATM    9  C6  UNL     1      -6.583   0.353  -0.983  1.00  0.00           C  
HETATM   10  O2  UNL     1      -7.091   1.389  -0.491  1.00  0.00           O  
HETATM   11  O3  UNL     1      -7.421  -0.703  -1.381  1.00  0.00           O  
HETATM   12  C7  UNL     1      -4.562   1.541   0.900  1.00  0.00           C  
HETATM   13  O4  UNL     1      -3.783   2.251   1.584  1.00  0.00           O  
HETATM   14  O5  UNL     1      -5.607   0.904   1.525  1.00  0.00           O  
HETATM   15  N3  UNL     1      -0.010   0.816  -1.180  1.00  0.00           N  
HETATM   16  C8  UNL     1       1.280   0.469  -0.994  1.00  0.00           C  
HETATM   17  N4  UNL     1       1.416  -0.173   0.175  1.00  0.00           N  
HETATM   18  C9  UNL     1       2.659  -0.690   0.699  1.00  0.00           C  
HETATM   19  O6  UNL     1       3.489   0.319   1.105  1.00  0.00           O  
HETATM   20  C10 UNL     1       4.771   0.054   0.717  1.00  0.00           C  
HETATM   21  C11 UNL     1       5.134   0.966  -0.458  1.00  0.00           C  
HETATM   22  O7  UNL     1       6.422   0.738  -0.891  1.00  0.00           O  
HETATM   23  C12 UNL     1       4.823  -1.363   0.183  1.00  0.00           C  
HETATM   24  O8  UNL     1       4.930  -2.280   1.230  1.00  0.00           O  
HETATM   25  C13 UNL     1       3.400  -1.490  -0.373  1.00  0.00           C  
HETATM   26  O9  UNL     1       3.042  -2.830  -0.357  1.00  0.00           O  
HETATM   27  H1  UNL     1      -0.818  -1.575   2.029  1.00  0.00           H  
HETATM   28  H2  UNL     1       0.369  -0.525   2.835  1.00  0.00           H  
HETATM   29  H3  UNL     1      -2.526   1.563  -1.710  1.00  0.00           H  
HETATM   30  H4  UNL     1      -4.633   2.377  -1.052  1.00  0.00           H  
HETATM   31  H5  UNL     1      -4.870   0.129  -2.232  1.00  0.00           H  
HETATM   32  H6  UNL     1      -4.789  -0.754  -0.710  1.00  0.00           H  
HETATM   33  H7  UNL     1      -8.103  -1.035  -0.691  1.00  0.00           H  
HETATM   34  H8  UNL     1      -5.472   0.305   2.332  1.00  0.00           H  
HETATM   35  H9  UNL     1       2.059   0.703  -1.722  1.00  0.00           H  
HETATM   36  H10 UNL     1       2.504  -1.396   1.539  1.00  0.00           H  
HETATM   37  H11 UNL     1       5.487   0.217   1.541  1.00  0.00           H  
HETATM   38  H12 UNL     1       4.445   0.725  -1.310  1.00  0.00           H  
HETATM   39  H13 UNL     1       5.031   2.031  -0.179  1.00  0.00           H  
HETATM   40  H14 UNL     1       7.015   1.507  -0.640  1.00  0.00           H  
HETATM   41  H15 UNL     1       5.580  -1.503  -0.588  1.00  0.00           H  
HETATM   42  H16 UNL     1       4.836  -1.864   2.119  1.00  0.00           H  
HETATM   43  H17 UNL     1       3.314  -1.013  -1.364  1.00  0.00           H  
HETATM   44  H18 UNL     1       2.172  -2.950  -0.805  1.00  0.00           H  
CONECT    1    2   27   28
CONECT    2    3    3   17
CONECT    3    4   15
CONECT    4    5    5    6
CONECT    6    7   29
CONECT    7    8   12   30
CONECT    8    9   31   32
CONECT    9   10   10   11
CONECT   11   33
CONECT   12   13   13   14
CONECT   14   34
CONECT   15   16   16
CONECT   16   17   35
CONECT   17   18
CONECT   18   19   25   36
CONECT   19   20
CONECT   20   21   23   37
CONECT   21   22   38   39
CONECT   22   40
CONECT   23   24   25   41
CONECT   24   42
CONECT   25   26   43
CONECT   26   44
END

HMDB0240295
     RDKit          3D
Succinylaminoimidazole carboxamide riboside
 44 45  0  0  0  0  0  0  0  0999 V2000
   -0.1078   -0.8160    1.9561 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1857   -0.2202    0.7176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7242    0.4037   -0.1336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1581    0.5417    0.1326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6517    0.0874    1.1834 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9552    1.1935   -0.8182 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3772    1.3676   -0.5893 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1224    0.2282   -1.1493 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5827    0.3528   -0.9831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0913    1.3888   -0.4913 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4211   -0.7031   -1.3812 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5619    1.5412    0.9004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7833    2.2510    1.5837 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6073    0.9044    1.5250 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0098    0.8164   -1.1797 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2801    0.4694   -0.9941 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4158   -0.1725    0.1752 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6591   -0.6902    0.6995 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4892    0.3186    1.1048 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7715    0.0544    0.7173 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1339    0.9660   -0.4578 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4217    0.7382   -0.8907 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8229   -1.3632    0.1834 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9298   -2.2803    1.2303 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4000   -1.4900   -0.3729 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0424   -2.8298   -0.3573 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8183   -1.5748    2.0290 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3685   -0.5251    2.8350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5259    1.5632   -1.7101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6329    2.3771   -1.0520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8701    0.1290   -2.2316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7886   -0.7536   -0.7101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1032   -1.0347   -0.6913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4716    0.3045    2.3317 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0591    0.7029   -1.7222 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5045   -1.3961    1.5394 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4871    0.2170    1.5413 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4454    0.7245   -1.3102 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0306    2.0307   -0.1788 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0147    1.5072   -0.6404 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5805   -1.5029   -0.5879 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8363   -1.8636    2.1191 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3137   -1.0135   -1.3638 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1721   -2.9500   -0.8046 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
  7 12  1  0
 12 13  2  0
 12 14  1  0
  3 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 20 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 17  2  1  0
 25 18  1  0
  1 27  1  0
  1 28  1  0
  6 29  1  0
  7 30  1  6
  8 31  1  0
  8 32  1  0
 11 33  1  0
 14 34  1  0
 16 35  1  0
 18 36  1  1
 20 37  1  1
 21 38  1  0
 21 39  1  0
 22 40  1  0
 23 41  1  6
 24 42  1  0
 25 43  1  6
 26 44  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
SAICAr	HMDB
SAICAriboside	HMDB
SAICA riboside	HMDB
(2S)-2-[5-Amino-1-(beta-D-ribosyl)imidazole-4-carboxamido]succinic acid	HMDB
(S)-2-[5-Amino-1-(D-ribosyl)imidazole-4-carboxamido]succinate	HMDB
1-(Ribosyl)-4-(N-succinocarboxamide)-5-aminoimidazole	HMDB
1-(Ribosyl)-5-amino-4-(N-succinocarboxamide)-imidazole	HMDB
Ribosyl-4-(N-succinocarboxamide)-5-aminoimidazole	HMDB
Succinyl-5-aminoimidazole-4-carboxamide-1-ribose	HMDB
Succinylaminoimidazolecarboxamide ribose	HMDB
(2S)-2-[5-Amino-1-(b-D-ribosyl)imidazole-4-carboxamido]succinate	HMDB
(2S)-2-[5-Amino-1-(b-D-ribosyl)imidazole-4-carboxamido]succinic acid	HMDB
(2S)-2-[5-Amino-1-(beta-D-ribosyl)imidazole-4-carboxamido]succinate	HMDB
(2S)-2-[5-Amino-1-(β-D-ribosyl)imidazole-4-carboxamido]succinate	HMDB
(2S)-2-[5-Amino-1-(β-D-ribosyl)imidazole-4-carboxamido]succinic acid	HMDB
(S)-2-[5-Amino-1-(D-ribosyl)imidazole-4-carboxamido]succinic acid	HMDB
Succinylaminoimidazole carboxamide riboside	HMDB

Chemical Formula

C₁₃H₁₈N₄O₉

Average Molecular Weight

374.306

Monoisotopic Molecular Weight

374.107378176

IUPAC Name

(2S)-2-({5-amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1H-imidazol-4-yl}formamido)butanedioic acid

Traditional Name

(2S)-2-({5-amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]imidazol-4-yl}formamido)butanedioic acid

CAS Registry Number

17388-80-6

SMILES

NC1=C(N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O)C(=O)N[C@@H](CC(O)=O)C(O)=O

InChI Identifier

InChI=1S/C13H18N4O9/c14-10-7(11(23)16-4(13(24)25)1-6(19)20)15-3-17(10)12-9(22)8(21)5(2-18)26-12/h3-5,8-9,12,18,21-22H,1-2,14H2,(H,16,23)(H,19,20)(H,24,25)/t4-,5+,8+,9+,12+/m0/s1

InChI Key

XNKLTOHYNRQCLJ-ZZZDFHIKSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1-ribosyl-imidazolecarboxamides. These are organic compounds containing the imidazole ring linked to a ribose ring through a 1-2 bond.

Kingdom

Organic compounds

Super Class

Nucleosides, nucleotides, and analogues

Class

Imidazole ribonucleosides and ribonucleotides

Sub Class

1-ribosyl-imidazolecarboxamides

Direct Parent

1-ribosyl-imidazolecarboxamides

Alternative Parents

Substituents

1-ribosyl-imidazolecarboxamide
Aspartic acid or derivatives
N-acyl-alpha amino acid or derivatives
N-acyl-alpha-amino acid
N-glycosyl compound
Glycosyl compound
Pentose monosaccharide
Alpha-amino acid or derivatives
2-heteroaryl carboxamide
Imidazolyl carboxylic acid derivative
Imidazole-4-carbonyl group
N-substituted imidazole
Monosaccharide
Aminoimidazole
Dicarboxylic acid or derivatives
Imidazole
Vinylogous amide
Tetrahydrofuran
Azole
Heteroaromatic compound
Amino acid or derivatives
Amino acid
Carboxamide group
Secondary carboxylic acid amide
Secondary alcohol
Carboxylic acid derivative
Organoheterocyclic compound
Azacycle
Oxacycle
Carboxylic acid
Organonitrogen compound
Hydrocarbon derivative
Amine
Organic oxygen compound
Alcohol
Carbonyl group
Organic oxide
Organopnictogen compound
Organic nitrogen compound
Primary amine
Primary alcohol
Organooxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Urine (PMID: 10102915)

Source

Exogenous

Exogenous (HMDB: HMDB0240295)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	-2	ALOGPS
logP	-4.2	ChemAxon
logS	-1.6	ALOGPS
pKa (Strongest Acidic)	2.99	ChemAxon
pKa (Strongest Basic)	4.55	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	217.46 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	79.78 m³·mol⁻¹	ChemAxon
Polarizability	34.04 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	174.655	30932474
DeepCCS	[M-H]-	172.26	30932474
DeepCCS	[M-2H]-	205.193	30932474
DeepCCS	[M+Na]+	180.568	30932474
AllCCS	[M+H]+	180.2	32859911
AllCCS	[M+H-H2O]+	177.7	32859911
AllCCS	[M+NH4]+	182.5	32859911
AllCCS	[M+Na]+	183.1	32859911
AllCCS	[M-H]-	180.7	32859911
AllCCS	[M+Na-2H]-	180.5	32859911
AllCCS	[M+HCOO]-	180.3	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
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.	2.15 minutes	32390414
Predicted by Siyang on May 30, 2022	10.7226 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	9.23 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	516.9 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	241.7 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	38.1 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	162.5 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	71.9 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	336.4 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	269.2 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	861.0 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	569.2 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	80.5 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	967.4 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	191.1 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	264.8 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	697.9 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	473.2 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	476.7 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Succinylaminoimidazole carboxamide riboside	NC1=C(N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O)C(=O)N[C@@H](CC(O)=O)C(O)=O	4688.1	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside	NC1=C(N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O)C(=O)N[C@@H](CC(O)=O)C(O)=O	2937.2	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside	NC1=C(N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O)C(=O)N[C@@H](CC(O)=O)C(O)=O	3499.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Succinylaminoimidazole carboxamide riboside,1TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N)[C@H](O)[C@@H]1O	3335.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,1TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N)[C@@H]1O	3345.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,1TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C1N	3319.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,1TMS,isomer #4	C[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)C(=O)O	3298.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,1TMS,isomer #5	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1	3286.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,1TMS,isomer #6	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O	3367.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,1TMS,isomer #7	C[Si](C)(C)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)[C@@H](CC(=O)O)C(=O)O	3318.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)=C2N)[C@H](O)[C@@H]1O	3246.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #10	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]1O	3341.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #11	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)=C2N)[C@@H]1O	3280.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #12	C[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C)C=N1)C(=O)O	3251.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #13	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C)C=N1	3252.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #14	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O[Si](C)(C)C	3337.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #15	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)=C1N	3269.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #16	C[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)C(=O)O[Si](C)(C)C	3213.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #17	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O	3287.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #18	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)[Si](C)(C)C	3226.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #19	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O	3287.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)=C2N)[C@H](O)[C@@H]1O	3245.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #20	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)[Si](C)(C)C	3221.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #21	C[Si](C)(C)N(C1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O)[Si](C)(C)C	3351.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #22	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O	3378.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N)[C@H](O[Si](C)(C)C)[C@@H]1O	3282.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N)[C@H](O)[C@@H]1O[Si](C)(C)C	3289.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #5	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H]1O	3351.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)=C2N)[C@H](O)[C@@H]1O	3284.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #7	C[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O)C=N1)C(=O)O	3264.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #8	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O)C=N1	3269.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TMS,isomer #9	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N)[C@@H]1O[Si](C)(C)C	3290.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)=C2N)[C@H](O)[C@@H]1O	3173.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #10	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3223.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #11	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	3298.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)=C2N)[C@H](O[Si](C)(C)C)[C@@H]1O	3203.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #13	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	3294.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)=C2N)[C@H](O)[C@@H]1O[Si](C)(C)C	3211.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O	3283.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #16	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H]1O	3326.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #17	C[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=N1)C(=O)O	3184.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #18	C[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O)C=N1)C(=O)O[Si](C)(C)C	3195.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #19	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]1O	3256.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)=C2N)[C@H](O[Si](C)(C)C)[C@@H]1O	3183.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #20	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O)C=N1)[Si](C)(C)C	3182.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #21	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=N1	3184.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #22	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]1O	3259.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #23	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O)C=N1)[Si](C)(C)C	3189.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #24	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3295.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #25	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)=C2N)[C@@H]1O[Si](C)(C)C	3207.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #26	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	3286.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #27	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]1O	3325.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #28	C[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C)C=N1)C(=O)O[Si](C)(C)C	3177.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #29	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O[Si](C)(C)C	3249.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)=C2N)[C@H](O)[C@@H]1O[Si](C)(C)C	3182.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #30	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C)C=N1)[Si](C)(C)C	3167.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #31	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O[Si](C)(C)C	3250.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #32	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C)C=N1)[Si](C)(C)C	3173.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #33	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C1N([Si](C)(C)C)[Si](C)(C)C	3282.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #34	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O[Si](C)(C)C	3327.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #35	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O	3241.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #36	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)[Si](C)(C)C	3153.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #37	C[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)C(=O)O	3234.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #38	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O	3273.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #39	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1	3224.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #4	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H]1O	3250.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #40	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O	3269.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #41	C[Si](C)(C)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)[C@@H](CC(=O)O)C(=O)O	3295.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)=C2N)[C@H](O)[C@@H]1O	3165.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)=C2N)[C@H](O[Si](C)(C)C)[C@@H]1O	3178.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)=C2N)[C@H](O)[C@@H]1O[Si](C)(C)C	3184.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #8	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H]1O	3254.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TMS,isomer #9	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N)[C@H](O)[C@@H]1O	3167.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)=C2N)[C@H](O[Si](C)(C)C)[C@@H]1O	3149.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #10	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O	3218.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #11	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H]1O	3235.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)=C2N)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3144.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #13	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	3232.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N)[C@H](O[Si](C)(C)C)[C@@H]1O	3138.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #15	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	3232.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #16	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N)[C@H](O)[C@@H]1O[Si](C)(C)C	3137.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #17	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O	3219.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #18	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H]1O	3237.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #19	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3272.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)=C2N)[C@H](O)[C@@H]1O[Si](C)(C)C	3144.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #20	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)=C2N)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3162.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #21	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	3265.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #22	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	3267.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #23	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C	3270.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #24	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	3269.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #25	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O	3260.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #26	C[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=N1)C(=O)O[Si](C)(C)C	3151.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #27	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3236.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #28	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=N1)[Si](C)(C)C	3131.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #29	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]1O	3246.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #3	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H]1O	3234.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #30	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O)C=N1)[Si](C)(C)C	3156.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #31	C[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O)C=N1)C(=O)O	3242.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #32	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]1O	3242.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #33	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3235.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #34	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=N1)[Si](C)(C)C	3144.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #35	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O)C=N1	3248.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #36	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]1O	3247.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #37	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3267.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #38	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3273.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #39	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	3269.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N)[C@H](O)[C@@H]1O	3137.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #40	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O[Si](C)(C)C	3236.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #41	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C)C=N1)[Si](C)(C)C	3149.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #42	C[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C)C=N1)C(=O)O	3232.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #43	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O[Si](C)(C)C	3233.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #44	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C)C=N1	3235.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #45	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O[Si](C)(C)C	3238.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #46	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)=C1N([Si](C)(C)C)[Si](C)(C)C	3265.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #47	C[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)C(=O)O[Si](C)(C)C	3218.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #48	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O	3249.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #49	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)[Si](C)(C)C	3235.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)=C2N)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3147.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #50	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)[Si](C)(C)C	3230.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #6	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	3235.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)=C2N)[C@H](O[Si](C)(C)C)[C@@H]1O	3129.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #8	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	3232.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TMS,isomer #9	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)=C2N)[C@H](O)[C@@H]1O[Si](C)(C)C	3130.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)=C2N)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3146.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #10	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	3231.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #11	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	3213.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C	3231.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #13	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	3217.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O	3240.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #15	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3218.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #16	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3137.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #17	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	3232.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #18	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	3219.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #19	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C	3235.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #2	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	3227.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #20	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	3222.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #21	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O	3244.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #22	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3265.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #23	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3250.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #24	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	3260.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #25	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C	3264.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #26	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3230.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #27	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=N1)[Si](C)(C)C	3150.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #28	C[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=N1)C(=O)O	3226.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #29	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3222.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N)[C@H](O[Si](C)(C)C)[C@@H]1O	3136.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #30	C[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O)C=N1)C(=O)O[Si](C)(C)C	3243.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #31	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]1O	3244.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #32	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O)C=N1)[Si](C)(C)C	3242.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #33	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=N1	3230.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #34	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3232.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #35	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O)C=N1)[Si](C)(C)C	3244.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #36	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3261.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #37	C[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C)C=N1)C(=O)O[Si](C)(C)C	3241.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #38	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O[Si](C)(C)C	3243.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #39	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C)C=N1)[Si](C)(C)C	3235.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #4	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	3223.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #40	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C)C=N1)[Si](C)(C)C	3238.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #41	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)[Si](C)(C)C	3238.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N)[C@H](O)[C@@H]1O[Si](C)(C)C	3134.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O	3233.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #7	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H]1O	3220.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #8	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3229.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,5TMS,isomer #9	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)=C2N)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3131.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #1	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3210.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #1	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3005.5	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #1	C[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4467.7	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #10	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	3236.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #10	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	3042.6	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #10	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	4115.5	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #11	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C	3239.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #11	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C	3037.4	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #11	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C	4078.4	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3241.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3001.4	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4245.6	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #13	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3227.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #13	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3022.9	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #13	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4319.8	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	3237.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	3032.5	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	4052.7	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C	3241.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C	3026.4	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C	4016.0	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #16	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3269.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #16	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3041.5	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #16	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4045.2	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #17	C[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=N1)C(=O)O[Si](C)(C)C	3242.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #17	C[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=N1)C(=O)O[Si](C)(C)C	3006.5	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #17	C[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=N1)C(=O)O[Si](C)(C)C	4244.1	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #18	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3228.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #18	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3032.6	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #18	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4312.7	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #19	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=N1)[Si](C)(C)C	3234.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #19	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=N1)[Si](C)(C)C	3051.6	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #19	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=N1)[Si](C)(C)C	4052.0	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3157.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2943.8	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4750.1	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #20	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O)C=N1)[Si](C)(C)C	3239.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #20	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O)C=N1)[Si](C)(C)C	3027.1	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #20	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O)C=N1)[Si](C)(C)C	3996.6	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #21	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=N1)[Si](C)(C)C	3241.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #21	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=N1)[Si](C)(C)C	3043.5	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #21	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=N1)[Si](C)(C)C	3989.5	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #22	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C)C=N1)[Si](C)(C)C	3240.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #22	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C)C=N1)[Si](C)(C)C	3029.6	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #22	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C)C=N1)[Si](C)(C)C	4034.1	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	3244.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	2992.6	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	4310.4	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #4	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	3219.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #4	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	3018.8	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #4	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	4376.8	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C	3243.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C	2988.1	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C	4272.2	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #6	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	3219.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #6	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	3010.3	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #6	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	4325.3	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O	3235.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O	3021.5	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O	4119.4	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #8	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3241.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #8	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3010.8	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #8	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4343.1	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #9	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3218.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #9	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3027.2	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,6TMS,isomer #9	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4382.6	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,7TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3257.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,7TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3004.6	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,7TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4057.6	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,7TMS,isomer #2	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3232.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,7TMS,isomer #2	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3036.9	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,7TMS,isomer #2	C[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4121.3	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,7TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	3258.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,7TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	3028.3	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,7TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	3822.4	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,7TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C	3260.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,7TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C	3026.4	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,7TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C	3786.5	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,7TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3260.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,7TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3026.9	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,7TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3833.0	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,7TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3264.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,7TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3027.9	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,7TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3776.8	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,7TMS,isomer #7	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=N1)[Si](C)(C)C	3260.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,7TMS,isomer #7	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=N1)[Si](C)(C)C	3041.7	Standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,7TMS,isomer #7	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=N1)[Si](C)(C)C	3759.4	Standard polar	33892256
Succinylaminoimidazole carboxamide riboside,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N)[C@H](O)[C@@H]1O	3563.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N)[C@@H]1O	3588.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C1N	3564.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)C(=O)O	3575.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1	3542.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O	3605.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)[C@@H](CC(=O)O)C(=O)O	3566.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)=C2N)[C@H](O)[C@@H]1O	3736.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3764.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)=C2N)[C@@H]1O	3742.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C=N1)C(=O)O	3730.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C=N1	3715.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3762.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)=C1N	3731.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)C(=O)O[Si](C)(C)C(C)(C)C	3722.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O	3766.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC(=O)C[C@@H](C(=O)O)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)[Si](C)(C)C(C)(C)C	3713.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O	3728.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)=C2N)[C@H](O)[C@@H]1O	3714.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=O)O)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)[Si](C)(C)C(C)(C)C	3704.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)N(C1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3764.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O	3804.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3717.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3714.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O	3775.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)=C2N)[C@H](O)[C@@H]1O	3731.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C=N1)C(=O)O	3740.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C=N1	3730.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N)[C@@H]1O[Si](C)(C)C(C)(C)C	3711.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=C2N)[C@H](O)[C@@H]1O	3889.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3857.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3922.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)=C2N)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3885.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3918.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)=C2N)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3883.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O	3916.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O	3957.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C=N1)C(=O)O	3851.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C=N1)C(=O)O[Si](C)(C)C(C)(C)C	3879.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3926.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)=C2N)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3875.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC(=O)C[C@@H](C(=O)O)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C=N1)[Si](C)(C)C(C)(C)C	3890.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C=N1	3842.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #22	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3909.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=O)O)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C=N1)[Si](C)(C)C(C)(C)C	3887.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #24	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3911.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #25	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)=C2N)[C@@H]1O[Si](C)(C)C(C)(C)C	3887.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #26	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3917.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #27	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3952.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C=N1)C(=O)O[Si](C)(C)C(C)(C)C	3864.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #29	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3916.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)=C2N)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3870.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC(=O)C[C@@H](C(=O)O)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C=N1)[Si](C)(C)C(C)(C)C	3884.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #31	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3898.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=O)O)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C=N1)[Si](C)(C)C(C)(C)C	3881.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #33	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C1N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3912.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #34	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3949.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #35	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O	3914.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OC(=O)C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)[Si](C)(C)C(C)(C)C	3868.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #37	CC(C)(C)[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)C(=O)O	3898.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #38	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O	3933.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1	3874.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O	3922.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #40	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O	3922.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #41	CC(C)(C)[Si](C)(C)N(C(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)[C@@H](CC(=O)O)C(=O)O	3924.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)=C2N)[C@H](O)[C@@H]1O	3882.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)=C2N)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3861.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)=C2N)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3860.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O	3899.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N)[C@H](O)[C@@H]1O	3877.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=C2N)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4007.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O	4051.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O	4065.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)=C2N)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	4008.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4054.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4002.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4051.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3997.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O	4037.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O	4057.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #19	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	4070.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=C2N)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4000.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)=C2N)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	4021.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4082.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #22	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4077.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4088.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #24	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4078.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O	4080.8	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C=N1)C(=O)O[Si](C)(C)C(C)(C)C	3990.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #27	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	4057.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC(=O)C[C@@H](C(=O)O)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C=N1)[Si](C)(C)C(C)(C)C	3992.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #29	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4061.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O	4053.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC(=O)C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C=N1)[Si](C)(C)C(C)(C)C	3981.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C=N1)C(=O)O	4075.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #32	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4070.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #33	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	4046.7	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=O)O)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C=N1)[Si](C)(C)C(C)(C)C	3992.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C=N1	4065.3	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #36	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4067.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #37	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O)C(=O)O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	4093.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #38	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	4071.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #39	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	4087.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N)[C@H](O)[C@@H]1O	3991.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #40	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4057.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #41	CC(C)(C)[Si](C)(C)OC(=O)C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C1=C(N)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C=N1)[Si](C)(C)C(C)(C)C	3972.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #42	CC(C)(C)[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C=N1)C(=O)O	4068.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #43	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4064.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #44	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C=N1	4059.2	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #45	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4062.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #46	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=NC(C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)=C1N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4081.1	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #47	CC(C)(C)[Si](C)(C)OC(=O)C[C@H](NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)C(=O)O[Si](C)(C)C(C)(C)C	4032.6	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #48	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O	4047.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #49	CC(C)(C)[Si](C)(C)OC(=O)C[C@@H](C(=O)O)N(C(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)[Si](C)(C)C(C)(C)C	4039.4	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)=C2N)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	4017.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #50	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=O)O)N(C(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=N1)[Si](C)(C)C(C)(C)C	4032.0	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4067.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)=C2N)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4003.9	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)N=CN1[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4063.5	Semi standard non polar	33892256
Succinylaminoimidazole carboxamide riboside,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC(C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)=C2N)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4000.2	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Succinylaminoimidazole carboxamide riboside GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Succinylaminoimidazole carboxamide riboside GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Succinylaminoimidazole carboxamide riboside 10V, Negative-QTOF	splash10-00di-0369000000-b4f58840f4f79eec6eb6	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Succinylaminoimidazole carboxamide riboside 20V, Negative-QTOF	splash10-001v-2960000000-b43fa287aa16e1a4123b	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Succinylaminoimidazole carboxamide riboside 40V, Negative-QTOF	splash10-05fs-2910000000-6734a1447cc68e9af042	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Succinylaminoimidazole carboxamide riboside 10V, Positive-QTOF	splash10-004l-0191000000-85c8aeded29efc7ea28f	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Succinylaminoimidazole carboxamide riboside 20V, Positive-QTOF	splash10-03fr-3960000000-8952d8599499d506c881	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Succinylaminoimidazole carboxamide riboside 40V, Positive-QTOF	splash10-03k9-2920000000-8417c33d91e7ee906f02	2021-09-25	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Urine

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Urine	Detected and Quantified	214 umol/mmol creatinine	Adult (>18 years old)	Both	Adenylosuccinate lyase deficiency	10102915	details

Associated Disorders and Diseases

Disease References

Adenylosuccinate lyase deficiency
Wevers RA, Engelke UF, Moolenaar SH, Brautigam C, de Jong JG, Duran R, de Abreu RA, van Gennip AH: 1H-NMR spectroscopy of body fluids: inborn errors of purine and pyrimidine metabolism. Clin Chem. 1999 Apr;45(4):539-48. [PubMed:10102915 ]

Associated OMIM IDs

103050 (Adenylosuccinate lyase deficiency)

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

57562912

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

54478644

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Keller KE, Tan IS, Lee YS: SAICAR stimulates pyruvate kinase isoform M2 and promotes cancer cell survival in glucose-limited conditions. Science. 2012 Nov 23;338(6110):1069-72. doi: 10.1126/science.1224409. Epub 2012 Oct 18. [PubMed:23086999 ]

Showing metabocard for Succinylaminoimidazole carboxamide riboside (HMDB0240295)

MOL for HMDB0240295 (Succinylaminoimidazole carboxamide riboside)

3D MOL for HMDB0240295 (Succinylaminoimidazole carboxamide riboside)

3D SDF for HMDB0240295 (Succinylaminoimidazole carboxamide riboside)

3D-SDF for HMDB0240295 (Succinylaminoimidazole carboxamide riboside)

PDB for HMDB0240295 (Succinylaminoimidazole carboxamide riboside)

3D PDB for HMDB0240295 (Succinylaminoimidazole carboxamide riboside)

SMILES for HMDB0240295 (Succinylaminoimidazole carboxamide riboside)

INCHI for HMDB0240295 (Succinylaminoimidazole carboxamide riboside)

Structure for HMDB0240295 (Succinylaminoimidazole carboxamide riboside)

3D Structure for HMDB0240295 (Succinylaminoimidazole carboxamide riboside)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra