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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 01:14:31 UTC

Update Date

2021-09-26 22:58:09 UTC

HMDB ID

HMDB0248071

Secondary Accession Numbers

None

Metabolite Identification

Common Name

1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-

Description

1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-, also known as acadesine 5'-monophosphoric acid, 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. 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- has been detected, but not quantified in, herbs and spices. This could make 1H-imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-. This compound has been identified in human blood as reported by (PMID: 31557052 ). 1h-imidazole-4-carboxamide, 5-amino-1-(5-o-phosphono-beta-d-ribofuranosyl)- is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

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

HMDB0248071
     RDKit          3D
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-
 37 38  0  0  0  0  0  0  0  0999 V2000
    5.8994    0.9288   -0.9063 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4193   -0.2204   -0.5945 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3697   -1.2539   -0.4737 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0047   -0.4948   -0.3698 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4622   -1.6964   -0.0391 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1332   -1.5518    0.0821 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7799   -0.2789   -0.1610 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4509    0.2998   -0.1367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4216   -0.3438   -0.9691 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5504   -0.6965   -0.2909 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7678    0.1052   -0.6713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8848   -0.2924    0.0455 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2575    0.5716   -0.3458 P   0  0  0  0  0  5  0  0  0  0  0  0
   -6.0551    0.7961    0.9218 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2523   -0.2481   -1.4386 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9136    2.0943   -1.0010 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2979   -0.6107    1.1772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9032   -1.8410    1.6782 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1270    0.3730    1.2335 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7463   -0.0298    2.2368 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9520    0.3663   -0.4404 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0354    1.7595   -0.7608 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3744    1.7901   -1.0378 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4221   -1.8429    0.3459 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4541   -2.3697    0.3430 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5400    1.3616   -0.5128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7796   -1.7654   -0.5281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6005    1.1879   -0.4333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9961    0.0002   -1.7501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0808   -1.2106   -1.3853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7233    2.6740   -0.8892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1815   -0.2022    1.7470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0293   -2.5454    0.9733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5838    1.3629    1.4619 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2478   -0.6188    2.8672 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8221    2.0091   -1.7531 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2927    2.4330   -0.0265 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 13 16  1  0
 10 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
  7 21  1  0
 21 22  1  0
 21  4  2  0
 19  8  1  0
  1 23  1  0
  3 24  1  0
  6 25  1  0
  8 26  1  0
 10 27  1  0
 11 28  1  0
 11 29  1  0
 15 30  1  0
 16 31  1  0
 17 32  1  0
 18 33  1  0
 19 34  1  0
 20 35  1  0
 22 36  1  0
 22 37  1  0
M  END


  Mrv1652305221919592D          

 22 23  0  0  0  0            999 V2000
   -1.5056    0.2572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6689    1.9642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7209    0.5122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2564    3.2338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0535    0.0273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6139    0.5122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5890    2.7489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2564    4.0588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3590    1.2968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1956    3.0038    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9709    4.4713    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9239    2.7489    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8439    1.9642    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0535   -0.7977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3986    0.2572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5420    4.4713    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6879    0.2994    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1582    1.3390    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6483   -0.2303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1187    0.8093    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4660    1.2968    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9033    0.5543    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  5  3  1  0  0  0  0
  6  5  1  0  0  0  0
  7  4  2  0  0  0  0
  8  4  1  0  0  0  0
  9  6  1  0  0  0  0
 10  7  1  0  0  0  0
 11  8  2  0  0  0  0
 12  2  2  0  0  0  0
 12  4  1  0  0  0  0
 13  2  1  0  0  0  0
 13  7  1  0  0  0  0
 13  9  1  0  0  0  0
 14  5  1  0  0  0  0
 15  6  1  0  0  0  0
 16  8  1  0  0  0  0
 20  1  1  0  0  0  0
 21  3  1  0  0  0  0
 21  9  1  0  0  0  0
 22 17  1  0  0  0  0
 22 18  1  0  0  0  0
 22 19  2  0  0  0  0
 22 20  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0248071

> <DATABASE_NAME>
hmdb

> <SMILES>
NC1=C(N=CN1C1OC(COP(O)(O)=O)C(O)C1O)C(O)=N

> <INCHI_IDENTIFIER>
InChI=1S/C9H15N4O8P/c10-7-4(8(11)16)12-2-13(7)9-6(15)5(14)3(21-9)1-20-22(17,18)19/h2-3,5-6,9,14-15H,1,10H2,(H2,11,16)(H2,17,18,19)

> <INCHI_KEY>
NOTGFIUVDGNKRI-UHFFFAOYSA-N

> <FORMULA>
C9H15N4O8P

> <MOLECULAR_WEIGHT>
338.2112

> <EXACT_MASS>
338.062749988

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
28.92912715523955

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-amino-1-{3,4-dihydroxy-5-[(phosphonooxy)methyl]oxolan-2-yl}-1H-imidazole-4-carboximidic acid

> <ALOGPS_LOGP>
-2.20

> <JCHEM_LOGP>
-4.697606410580134

> <ALOGPS_LOGS>
-2.09

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
5.595061710832443

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.2241311496964489

> <JCHEM_PKA_STRONGEST_BASIC>
6.322411117073653

> <JCHEM_POLAR_SURFACE_AREA>
204.36999999999995

> <JCHEM_REFRACTIVITY>
80.0787

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.74e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-amino-1-{3,4-dihydroxy-5-[(phosphonooxy)methyl]oxolan-2-yl}imidazole-4-carboximidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0248071
     RDKit          3D
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-
 37 38  0  0  0  0  0  0  0  0999 V2000
    5.8994    0.9288   -0.9063 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4193   -0.2204   -0.5945 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3697   -1.2539   -0.4737 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0047   -0.4948   -0.3698 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4622   -1.6964   -0.0391 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1332   -1.5518    0.0821 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7799   -0.2789   -0.1610 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4509    0.2998   -0.1367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4216   -0.3438   -0.9691 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5504   -0.6965   -0.2909 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7678    0.1052   -0.6713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8848   -0.2924    0.0455 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2575    0.5716   -0.3458 P   0  0  0  0  0  5  0  0  0  0  0  0
   -6.0551    0.7961    0.9218 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2523   -0.2481   -1.4386 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9136    2.0943   -1.0010 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2979   -0.6107    1.1772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9032   -1.8410    1.6782 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1270    0.3730    1.2335 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7463   -0.0298    2.2368 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9520    0.3663   -0.4404 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0354    1.7595   -0.7608 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3744    1.7901   -1.0378 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4221   -1.8429    0.3459 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4541   -2.3697    0.3430 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5400    1.3616   -0.5128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7796   -1.7654   -0.5281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6005    1.1879   -0.4333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9961    0.0002   -1.7501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0808   -1.2106   -1.3853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7233    2.6740   -0.8892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1815   -0.2022    1.7470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0293   -2.5454    0.9733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5838    1.3629    1.4619 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2478   -0.6188    2.8672 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8221    2.0091   -1.7531 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2927    2.4330   -0.0265 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 13 16  1  0
 10 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
  7 21  1  0
 21 22  1  0
 21  4  2  0
 19  8  1  0
  1 23  1  0
  3 24  1  0
  6 25  1  0
  8 26  1  0
 10 27  1  0
 11 28  1  0
 11 29  1  0
 15 30  1  0
 16 31  1  0
 17 32  1  0
 18 33  1  0
 19 34  1  0
 20 35  1  0
 22 36  1  0
 22 37  1  0
M  END

HEADER    PROTEIN                                 22-MAY-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   22-MAY-19         0                                  
HETATM    1  C   UNK     0      -2.810   0.480   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.115   3.667   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.346   0.956   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.345   6.036   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.100   0.051   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.146   0.956   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.099   5.131   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.345   7.576   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.670   2.421   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0      -0.365   5.607   0.000  0.00  0.00           N+0
HETATM   11  N   UNK     0       3.679   8.346   0.000  0.00  0.00           N+0
HETATM   12  N   UNK     0       3.591   5.131   0.000  0.00  0.00           N+0
HETATM   13  N   UNK     0       1.575   3.667   0.000  0.00  0.00           N+0
HETATM   14  O   UNK     0      -0.100  -1.489   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       2.611   0.480   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       1.012   8.346   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -6.884   0.559   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      -5.895   2.499   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -4.944  -0.430   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -3.955   1.511   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -0.870   2.421   0.000  0.00  0.00           O+0
HETATM   22  P   UNK     0      -5.419   1.035   0.000  0.00  0.00           P+0
CONECT    1    3   20                                                       
CONECT    2   12   13                                                       
CONECT    3    1    5   21                                                  
CONECT    4    7    8   12                                                  
CONECT    5    3    6   14                                                  
CONECT    6    5    9   15                                                  
CONECT    7    4   10   13                                                  
CONECT    8    4   11   16                                                  
CONECT    9    6   13   21                                                  
CONECT   10    7                                                            
CONECT   11    8                                                            
CONECT   12    2    4                                                       
CONECT   13    2    7    9                                                  
CONECT   14    5                                                            
CONECT   15    6                                                            
CONECT   16    8                                                            
CONECT   17   22                                                            
CONECT   18   22                                                            
CONECT   19   22                                                            
CONECT   20    1   22                                                       
CONECT   21    3    9                                                       
CONECT   22   17   18   19   20                                             
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

COMPND    HMDB0248071
HETATM    1  N1  UNL     1       5.899   0.929  -0.906  1.00  0.00           N  
HETATM    2  C1  UNL     1       5.419  -0.220  -0.594  1.00  0.00           C  
HETATM    3  O1  UNL     1       6.370  -1.254  -0.474  1.00  0.00           O  
HETATM    4  C2  UNL     1       4.005  -0.495  -0.370  1.00  0.00           C  
HETATM    5  N2  UNL     1       3.462  -1.696  -0.039  1.00  0.00           N  
HETATM    6  C3  UNL     1       2.133  -1.552   0.082  1.00  0.00           C  
HETATM    7  N3  UNL     1       1.780  -0.279  -0.161  1.00  0.00           N  
HETATM    8  C4  UNL     1       0.451   0.300  -0.137  1.00  0.00           C  
HETATM    9  O2  UNL     1      -0.422  -0.344  -0.969  1.00  0.00           O  
HETATM   10  C5  UNL     1      -1.550  -0.697  -0.291  1.00  0.00           C  
HETATM   11  C6  UNL     1      -2.768   0.105  -0.671  1.00  0.00           C  
HETATM   12  O3  UNL     1      -3.885  -0.292   0.045  1.00  0.00           O  
HETATM   13  P1  UNL     1      -5.258   0.572  -0.346  1.00  0.00           P  
HETATM   14  O4  UNL     1      -6.055   0.796   0.922  1.00  0.00           O  
HETATM   15  O5  UNL     1      -6.252  -0.248  -1.439  1.00  0.00           O  
HETATM   16  O6  UNL     1      -4.914   2.094  -1.001  1.00  0.00           O  
HETATM   17  C7  UNL     1      -1.298  -0.611   1.177  1.00  0.00           C  
HETATM   18  O7  UNL     1      -0.903  -1.841   1.678  1.00  0.00           O  
HETATM   19  C8  UNL     1      -0.127   0.373   1.234  1.00  0.00           C  
HETATM   20  O8  UNL     1       0.746  -0.030   2.237  1.00  0.00           O  
HETATM   21  C9  UNL     1       2.952   0.366  -0.440  1.00  0.00           C  
HETATM   22  N4  UNL     1       3.035   1.759  -0.761  1.00  0.00           N  
HETATM   23  H1  UNL     1       5.374   1.790  -1.038  1.00  0.00           H  
HETATM   24  H2  UNL     1       6.422  -1.843   0.346  1.00  0.00           H  
HETATM   25  H3  UNL     1       1.454  -2.370   0.343  1.00  0.00           H  
HETATM   26  H4  UNL     1       0.540   1.362  -0.513  1.00  0.00           H  
HETATM   27  H5  UNL     1      -1.780  -1.765  -0.528  1.00  0.00           H  
HETATM   28  H6  UNL     1      -2.600   1.188  -0.433  1.00  0.00           H  
HETATM   29  H7  UNL     1      -2.996   0.000  -1.750  1.00  0.00           H  
HETATM   30  H8  UNL     1      -6.081  -1.211  -1.385  1.00  0.00           H  
HETATM   31  H9  UNL     1      -5.723   2.674  -0.889  1.00  0.00           H  
HETATM   32  H10 UNL     1      -2.181  -0.202   1.747  1.00  0.00           H  
HETATM   33  H11 UNL     1      -1.029  -2.545   0.973  1.00  0.00           H  
HETATM   34  H12 UNL     1      -0.584   1.363   1.462  1.00  0.00           H  
HETATM   35  H13 UNL     1       0.248  -0.619   2.867  1.00  0.00           H  
HETATM   36  H14 UNL     1       2.822   2.009  -1.753  1.00  0.00           H  
HETATM   37  H15 UNL     1       3.293   2.433  -0.026  1.00  0.00           H  
CONECT    1    2    2   23
CONECT    2    3    4
CONECT    3   24
CONECT    4    5   21   21
CONECT    5    6    6
CONECT    6    7   25
CONECT    7    8   21
CONECT    8    9   19   26
CONECT    9   10
CONECT   10   11   17   27
CONECT   11   12   28   29
CONECT   12   13
CONECT   13   14   14   15   16
CONECT   15   30
CONECT   16   31
CONECT   17   18   19   32
CONECT   18   33
CONECT   19   20   34
CONECT   20   35
CONECT   21   22
CONECT   22   36   37
END

HMDB0248071
     RDKit          3D
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-
 37 38  0  0  0  0  0  0  0  0999 V2000
    5.8994    0.9288   -0.9063 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4193   -0.2204   -0.5945 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3697   -1.2539   -0.4737 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0047   -0.4948   -0.3698 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4622   -1.6964   -0.0391 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1332   -1.5518    0.0821 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7799   -0.2789   -0.1610 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4509    0.2998   -0.1367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4216   -0.3438   -0.9691 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5504   -0.6965   -0.2909 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7678    0.1052   -0.6713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8848   -0.2924    0.0455 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2575    0.5716   -0.3458 P   0  0  0  0  0  5  0  0  0  0  0  0
   -6.0551    0.7961    0.9218 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2523   -0.2481   -1.4386 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9136    2.0943   -1.0010 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2979   -0.6107    1.1772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9032   -1.8410    1.6782 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1270    0.3730    1.2335 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7463   -0.0298    2.2368 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9520    0.3663   -0.4404 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0354    1.7595   -0.7608 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3744    1.7901   -1.0378 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4221   -1.8429    0.3459 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4541   -2.3697    0.3430 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5400    1.3616   -0.5128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7796   -1.7654   -0.5281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6005    1.1879   -0.4333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9961    0.0002   -1.7501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0808   -1.2106   -1.3853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7233    2.6740   -0.8892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1815   -0.2022    1.7470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0293   -2.5454    0.9733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5838    1.3629    1.4619 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2478   -0.6188    2.8672 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8221    2.0091   -1.7531 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2927    2.4330   -0.0265 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 13 16  1  0
 10 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
  7 21  1  0
 21 22  1  0
 21  4  2  0
 19  8  1  0
  1 23  1  0
  3 24  1  0
  6 25  1  0
  8 26  1  0
 10 27  1  0
 11 28  1  0
 11 29  1  0
 15 30  1  0
 16 31  1  0
 17 32  1  0
 18 33  1  0
 19 34  1  0
 20 35  1  0
 22 36  1  0
 22 37  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
Acadesine 5'-monophosphoric acid	HMDB

Chemical Formula

C₉H₁₅N₄O₈P

Average Molecular Weight

338.2112

Monoisotopic Molecular Weight

338.062749988

IUPAC Name

5-amino-1-{3,4-dihydroxy-5-[(phosphonooxy)methyl]oxolan-2-yl}-1H-imidazole-4-carboximidic acid

Traditional Name

5-amino-1-{3,4-dihydroxy-5-[(phosphonooxy)methyl]oxolan-2-yl}imidazole-4-carboximidic acid

CAS Registry Number

Not Available

SMILES

NC1=C(N=CN1C1OC(COP(O)(O)=O)C(O)C1O)C(O)=N

InChI Identifier

InChI=1S/C9H15N4O8P/c10-7-4(8(11)16)12-2-13(7)9-6(15)5(14)3(21-9)1-20-22(17,18)19/h2-3,5-6,9,14-15H,1,10H2,(H2,11,16)(H2,17,18,19)

InChI Key

NOTGFIUVDGNKRI-UHFFFAOYSA-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
Pentose phosphate
Pentose-5-phosphate
Glycosyl compound
N-glycosyl compound
Monosaccharide phosphate
Pentose monosaccharide
2-heteroaryl carboxamide
Imidazole-4-carbonyl group
Monoalkyl phosphate
Aminoimidazole
Monosaccharide
N-substituted imidazole
Organic phosphoric acid derivative
Alkyl phosphate
Phosphoric acid ester
Azole
Imidazole
Heteroaromatic compound
Vinylogous amide
Tetrahydrofuran
Primary carboxylic acid amide
Secondary alcohol
Amino acid or derivatives
1,2-diol
Carboxamide group
Organoheterocyclic compound
Azacycle
Oxacycle
Carboxylic acid derivative
Primary amine
Organonitrogen compound
Organopnictogen compound
Organooxygen compound
Organic oxygen compound
Amine
Organic oxide
Hydrocarbon derivative
Organic nitrogen compound
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

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	-2.2	ALOGPS
logP	-4.7	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	1.22	ChemAxon
pKa (Strongest Basic)	6.32	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	204.37 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	80.08 m³·mol⁻¹	ChemAxon
Polarizability	28.93 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]+	165.071	30932474
DeepCCS	[M-H]-	162.713	30932474
DeepCCS	[M-2H]-	196.262	30932474
DeepCCS	[M+Na]+	171.398	30932474
AllCCS	[M+H]+	172.4	32859911
AllCCS	[M+H-H2O]+	169.4	32859911
AllCCS	[M+NH4]+	175.1	32859911
AllCCS	[M+Na]+	175.9	32859911
AllCCS	[M-H]-	167.8	32859911
AllCCS	[M+Na-2H]-	167.6	32859911
AllCCS	[M+HCOO]-	167.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-	NC1=C(N=CN1C1OC(COP(O)(O)=O)C(O)C1O)C(O)=N	3967.2	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-	NC1=C(N=CN1C1OC(COP(O)(O)=O)C(O)C1O)C(O)=N	2732.8	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-	NC1=C(N=CN1C1OC(COP(O)(O)=O)C(O)C1O)C(O)=N	3361.0	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #1	C[Si](C)(C)OC(=N)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3074.0	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #1	C[Si](C)(C)OC(=N)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2858.8	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #1	C[Si](C)(C)OC(=N)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	4718.7	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #10	C[Si](C)(C)NC1=C(C(=N)O)N=CN1C1OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3242.8	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #10	C[Si](C)(C)NC1=C(C(=N)O)N=CN1C1OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2896.7	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #10	C[Si](C)(C)NC1=C(C(=N)O)N=CN1C1OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4160.5	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #11	C[Si](C)(C)N=C(O)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3019.8	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #11	C[Si](C)(C)N=C(O)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2893.9	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #11	C[Si](C)(C)N=C(O)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	4598.3	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #12	C[Si](C)(C)OC1C(COP(=O)(O)O)OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	3282.5	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #12	C[Si](C)(C)OC1C(COP(=O)(O)O)OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	2963.9	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #12	C[Si](C)(C)OC1C(COP(=O)(O)O)OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4405.6	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #13	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3084.4	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #13	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2997.9	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #13	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	4570.4	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #14	C[Si](C)(C)NC1=C(C(=N)O)N=CN1C1OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3255.0	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #14	C[Si](C)(C)NC1=C(C(=N)O)N=CN1C1OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2947.0	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #14	C[Si](C)(C)NC1=C(C(=N)O)N=CN1C1OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4032.1	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #15	C[Si](C)(C)N=C(O)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3034.4	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #15	C[Si](C)(C)N=C(O)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	2928.7	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #15	C[Si](C)(C)N=C(O)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	4494.3	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #16	C[Si](C)(C)OC1C(COP(=O)(O)O[Si](C)(C)C)OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O	3336.9	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #16	C[Si](C)(C)OC1C(COP(=O)(O)O[Si](C)(C)C)OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O	2997.3	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #16	C[Si](C)(C)OC1C(COP(=O)(O)O[Si](C)(C)C)OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O	4225.2	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #17	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3087.2	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #17	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	2990.1	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #17	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	4387.9	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #18	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O)C=N1	3115.9	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #18	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O)C=N1	3133.9	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #18	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O)C=N1	4629.2	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #19	C[Si](C)(C)OC(=N)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3062.2	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #19	C[Si](C)(C)OC(=N)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	2911.3	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #19	C[Si](C)(C)OC(=N)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	4622.9	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #2	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O)O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3118.3	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #2	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O)O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2899.1	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #2	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O)O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4732.4	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #20	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3122.5	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #20	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2946.7	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #20	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4570.4	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #21	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	2988.4	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #21	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	2914.9	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #21	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	4707.8	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #22	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O[Si](C)(C)C)C=N1	3134.8	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #22	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O[Si](C)(C)C)C=N1	3023.9	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #22	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O[Si](C)(C)C)C=N1	4774.0	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #23	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O[Si](C)(C)C)C=N1	3041.8	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #23	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O[Si](C)(C)C)C=N1	3020.0	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #23	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O[Si](C)(C)C)C=N1	4839.6	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #24	C[Si](C)(C)NC1=C(C(=N)O)N=CN1C1OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3243.2	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #24	C[Si](C)(C)NC1=C(C(=N)O)N=CN1C1OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2951.3	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #24	C[Si](C)(C)NC1=C(C(=N)O)N=CN1C1OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4063.9	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #25	C[Si](C)(C)N=C(O)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3006.7	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #25	C[Si](C)(C)N=C(O)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	2940.0	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #25	C[Si](C)(C)N=C(O)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	4507.1	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #26	C[Si](C)(C)OC1C(O)C(COP(=O)(O)O[Si](C)(C)C)OC1N1C=NC(C(=N)O)=C1N([Si](C)(C)C)[Si](C)(C)C	3325.3	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #26	C[Si](C)(C)OC1C(O)C(COP(=O)(O)O[Si](C)(C)C)OC1N1C=NC(C(=N)O)=C1N([Si](C)(C)C)[Si](C)(C)C	3000.0	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #26	C[Si](C)(C)OC1C(O)C(COP(=O)(O)O[Si](C)(C)C)OC1N1C=NC(C(=N)O)=C1N([Si](C)(C)C)[Si](C)(C)C	4240.6	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #27	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3071.5	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #27	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	2997.2	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #27	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	4412.1	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #28	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O[Si](C)(C)C)C=N1	3106.1	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #28	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O[Si](C)(C)C)C=N1	3137.0	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #28	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O[Si](C)(C)C)C=N1	4641.6	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #29	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	3127.2	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #29	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	3012.2	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #29	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	4400.6	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #3	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2994.4	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #3	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2893.8	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #3	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	4904.7	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #30	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O)C=N1	2988.5	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #30	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O)C=N1	2968.7	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #30	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O)C=N1	4613.8	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #31	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O)C=N1	3169.0	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #31	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O)C=N1	3081.9	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #31	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O)C=N1	4551.6	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #32	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O)C=N1	3056.9	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #32	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O)C=N1	3025.7	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #32	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O)C=N1	4621.2	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #33	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O)C=N1	3017.0	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #33	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O)C=N1	3171.2	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #33	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O)C=N1	4764.3	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #34	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O)C1O)O[Si](C)(C)C	3350.8	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #34	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O)C1O)O[Si](C)(C)C	3072.3	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #34	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O)C1O)O[Si](C)(C)C	4083.8	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #35	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O)C=N1	3087.9	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #35	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O)C=N1	3050.0	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #35	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O)C=N1	4249.2	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #36	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O)C=N1	3125.8	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #36	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O)C=N1	3140.7	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #36	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O)C=N1	4435.1	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #4	C[Si](C)(C)OC(=N)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3088.8	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #4	C[Si](C)(C)OC(=N)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	2900.6	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #4	C[Si](C)(C)OC(=N)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	4609.7	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #5	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3138.4	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #5	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2943.4	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #5	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4545.3	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #6	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3006.4	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #6	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	2907.9	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #6	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	4697.5	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #7	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O)C=N1	3145.0	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #7	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O)C=N1	3025.1	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #7	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O)C=N1	4760.9	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #8	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O)C=N1	3060.0	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #8	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O)C=N1	3014.1	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #8	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O)C=N1	4818.7	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #9	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC(C(=N)O)=C2N)C1O[Si](C)(C)C	3194.5	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #9	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC(C(=N)O)=C2N)C1O[Si](C)(C)C	2845.5	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TMS,isomer #9	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC(C(=N)O)=C2N)C1O[Si](C)(C)C	4316.8	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #1	C[Si](C)(C)OC(=N)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3021.7	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #1	C[Si](C)(C)OC(=N)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2862.2	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #1	C[Si](C)(C)OC(=N)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	4378.8	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #10	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O)C=N1	3049.1	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #10	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O)C=N1	3104.7	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #10	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O)C=N1	4395.7	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #11	C[Si](C)(C)NC1=C(C(=N)O)N=CN1C1OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3182.1	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #11	C[Si](C)(C)NC1=C(C(=N)O)N=CN1C1OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2924.1	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #11	C[Si](C)(C)NC1=C(C(=N)O)N=CN1C1OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3740.5	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #12	C[Si](C)(C)N=C(O)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2992.6	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #12	C[Si](C)(C)N=C(O)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2887.4	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #12	C[Si](C)(C)N=C(O)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	4294.2	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #13	C[Si](C)(C)OC1C(COP(=O)(O)O[Si](C)(C)C)OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	3272.9	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #13	C[Si](C)(C)OC1C(COP(=O)(O)O[Si](C)(C)C)OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	2954.1	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #13	C[Si](C)(C)OC1C(COP(=O)(O)O[Si](C)(C)C)OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	3884.6	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #14	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3058.2	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #14	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2959.5	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #14	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	4097.6	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #15	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3097.6	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #15	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3090.3	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #15	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	4282.9	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #16	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O	3285.1	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #16	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O	2991.2	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #16	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O	3799.7	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #17	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3064.9	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #17	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	2982.6	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #17	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3992.5	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #18	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3110.0	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #18	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3060.3	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #18	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	4156.1	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #19	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3095.9	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #19	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2964.5	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #19	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4137.6	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #2	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3108.6	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #2	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2918.9	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #2	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4205.9	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #20	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	2951.5	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #20	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	2910.4	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #20	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	4386.4	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #21	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3135.0	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #21	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3007.9	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #21	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	4229.5	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #22	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3036.6	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #22	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	2982.6	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #22	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	4347.2	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #23	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O[Si](C)(C)C)C=N1	3023.8	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #23	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O[Si](C)(C)C)C=N1	3107.1	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #23	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O[Si](C)(C)C)C=N1	4407.1	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #24	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC(C(=N)O)=C1N([Si](C)(C)C)[Si](C)(C)C	3261.0	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #24	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC(C(=N)O)=C1N([Si](C)(C)C)[Si](C)(C)C	2998.1	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #24	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC(C(=N)O)=C1N([Si](C)(C)C)[Si](C)(C)C	3821.3	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #25	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3048.3	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #25	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	2995.6	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #25	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	4022.5	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #26	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3088.3	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #26	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3068.9	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #26	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	4170.2	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #27	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O)C=N1	3148.7	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #27	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O)C=N1	3058.1	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #27	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O)C=N1	4101.0	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #28	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O)C=N1	3040.5	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #28	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O)C=N1	3021.3	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #28	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O)C=N1	4203.2	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #29	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O)C=N1	3039.0	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #29	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O)C=N1	3097.4	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #29	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O)C=N1	4247.9	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #3	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2954.4	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #3	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2871.9	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #3	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	4475.6	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #30	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O)C=N1	3087.9	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #30	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O)C=N1	3104.6	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #30	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O)C=N1	4042.5	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #4	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3133.0	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #4	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2977.4	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #4	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	4337.3	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #5	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3035.9	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #5	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2984.7	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #5	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	4458.5	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #6	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3110.2	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #6	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2953.4	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #6	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4105.7	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #7	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	2973.2	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #7	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	2898.4	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #7	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	4373.3	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #8	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3159.4	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #8	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3003.0	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #8	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	4214.5	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #9	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3051.3	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #9	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	2973.1	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,5TMS,isomer #9	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	4323.5	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #1	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3073.1	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #1	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2938.4	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #1	C[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C)N=CN1C1OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3808.4	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #10	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3033.3	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #10	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2961.7	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #10	C[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3739.0	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #11	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3103.1	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #11	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3005.0	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #11	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3851.1	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #12	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3098.8	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #12	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3028.1	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #12	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3788.5	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #13	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3118.8	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #13	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	2989.4	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #13	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3832.2	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #14	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3031.2	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #14	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	2987.1	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #14	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3978.3	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #15	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3056.6	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #15	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3041.1	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #15	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3954.0	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #16	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3077.6	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #16	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3036.5	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #16	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3808.2	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #17	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O)C=N1	3055.8	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #17	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O)C=N1	3072.7	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #17	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O)C=N1	3859.8	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #2	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2948.3	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #2	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2867.0	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #2	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	4194.0	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #3	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3136.7	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #3	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2954.6	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #3	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3867.7	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #4	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3022.9	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #4	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2953.1	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #4	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	4023.1	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #5	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3056.3	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #5	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3049.9	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #5	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	4015.5	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #6	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3137.8	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #6	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	2982.9	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #6	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3811.5	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #7	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3044.1	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #7	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	2971.1	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #7	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3947.5	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #8	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3072.3	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #8	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3036.2	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #8	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3940.5	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #9	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	3238.5	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #9	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	2949.2	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,6TMS,isomer #9	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	3538.0	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,7TMS,isomer #1	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3116.7	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,7TMS,isomer #1	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2954.9	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,7TMS,isomer #1	C[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3561.1	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,7TMS,isomer #2	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3025.8	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,7TMS,isomer #2	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2965.0	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,7TMS,isomer #2	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3708.9	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,7TMS,isomer #3	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3078.1	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,7TMS,isomer #3	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2995.2	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,7TMS,isomer #3	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3665.8	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,7TMS,isomer #4	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3098.2	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,7TMS,isomer #4	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3017.4	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,7TMS,isomer #4	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3628.6	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,7TMS,isomer #5	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3083.2	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,7TMS,isomer #5	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2980.3	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,7TMS,isomer #5	C[Si](C)(C)N=C(O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3551.2	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,7TMS,isomer #6	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3082.8	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,7TMS,isomer #6	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3028.6	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,7TMS,isomer #6	C[Si](C)(C)N=C(O[Si](C)(C)C)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3646.8	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=N)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=N1	3899.7	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=N)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=N1	3588.0	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=N)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=N1	4742.9	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=C(C(=N)O)N=CN1C1OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4002.7	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=C(C(=N)O)N=CN1C1OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3650.5	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=C(C(=N)O)N=CN1C1OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4286.6	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(O)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=N1	3871.6	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(O)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=N1	3601.0	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(O)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=N1	4706.6	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)O)OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3989.1	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)O)OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3722.5	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)O)OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4428.8	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=N1	3890.8	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=N1	3721.8	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=N1	4629.1	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=C(C(=N)O)N=CN1C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4024.7	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=C(C(=N)O)N=CN1C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3643.9	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=C(C(=N)O)N=CN1C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4210.3	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N=C(O)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3897.6	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N=C(O)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3588.3	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N=C(O)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	4611.8	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	4023.1	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	3731.7	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	4317.9	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3913.5	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3702.2	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	4497.2	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #18	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(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3927.1	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #18	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(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3860.2	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #18	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(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	4658.1	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC(=N)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	3896.2	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC(=N)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	3587.9	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC(=N)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	4661.8	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C(C)(C)C)N=CN1C1OC(COP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3893.2	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C(C)(C)C)N=CN1C1OC(COP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3649.5	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C(C)(C)C)N=CN1C1OC(COP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4695.3	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #20	CC(C)(C)[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C(C)(C)C)N=CN1C1OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3949.4	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #20	CC(C)(C)[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C(C)(C)C)N=CN1C1OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3667.8	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #20	CC(C)(C)[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C(C)(C)C)N=CN1C1OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4589.2	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #21	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	3847.0	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #21	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	3600.5	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #21	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	4768.5	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	3905.7	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	3747.3	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	4686.8	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #23	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	3839.3	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #23	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	3735.1	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #23	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	4810.7	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #24	CC(C)(C)[Si](C)(C)NC1=C(C(=N)O)N=CN1C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4015.6	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #24	CC(C)(C)[Si](C)(C)NC1=C(C(=N)O)N=CN1C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3650.7	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #24	CC(C)(C)[Si](C)(C)NC1=C(C(=N)O)N=CN1C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4238.1	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #25	CC(C)(C)[Si](C)(C)N=C(O)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	3881.2	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #25	CC(C)(C)[Si](C)(C)N=C(O)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	3605.6	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #25	CC(C)(C)[Si](C)(C)N=C(O)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	4623.8	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)OC1N1C=NC(C(=N)O)=C1N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4016.5	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)OC1N1C=NC(C(=N)O)=C1N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3732.5	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)OC1N1C=NC(C(=N)O)=C1N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4330.6	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #27	CC(C)(C)[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	3902.8	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #27	CC(C)(C)[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	3716.9	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #27	CC(C)(C)[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	4518.7	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #28	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(C2OC(COP(=O)(O)O)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	3919.0	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #28	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(C2OC(COP(=O)(O)O)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	3865.1	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #28	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(C2OC(COP(=O)(O)O)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	4668.1	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #29	CC(C)(C)[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C(C)(C)C)N=CN1C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C1O	3956.6	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #29	CC(C)(C)[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C(C)(C)C)N=CN1C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C1O	3660.7	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #29	CC(C)(C)[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C(C)(C)C)N=CN1C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C1O	4487.1	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=N1	3792.3	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=N1	3592.8	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=N1	4928.6	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #30	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C2O)C=N1	3843.0	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #30	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C2O)C=N1	3591.4	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #30	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C2O)C=N1	4694.6	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C2O)C=N1	3940.8	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C2O)C=N1	3765.5	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C2O)C=N1	4555.3	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #32	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C2O)C=N1	3885.2	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #32	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C2O)C=N1	3708.8	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #32	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C2O)C=N1	4665.5	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #33	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O)C=N1	3859.3	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #33	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O)C=N1	3862.7	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #33	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O)C(O)C2O)C=N1	4724.7	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O)C1O)O[Si](C)(C)C(C)(C)C	4033.9	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O)C1O)O[Si](C)(C)C(C)(C)C	3744.7	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C=NC(C(=N)O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O)C1O)O[Si](C)(C)C(C)(C)C	4254.7	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #35	CC(C)(C)[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C2O)C=N1	3922.4	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #35	CC(C)(C)[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C2O)C=N1	3683.6	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #35	CC(C)(C)[Si](C)(C)N=C(O)C1=C(N[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C2O)C=N1	4418.9	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #36	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(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C2O)C=N1	3938.1	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #36	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(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C2O)C=N1	3833.8	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #36	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(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C2O)C=N1	4537.1	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=N)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3913.2	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=N)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3573.2	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=N)C1=C(N)N(C2OC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	4649.4	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C(C)(C)C)N=CN1C1OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3967.1	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C(C)(C)C)N=CN1C1OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3662.4	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=C(C(=N)O[Si](C)(C)C(C)(C)C)N=CN1C1OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4566.3	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3857.7	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3590.8	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N)N(C2OC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	4759.9	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3911.8	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3745.6	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=N)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	4676.3	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3848.5	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3722.7	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)C1=C(N[Si](C)(C)C(C)(C)C)N(C2OC(COP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	4792.2	Standard polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)OC(N2C=NC(C(=N)O)=C2N)C1O[Si](C)(C)C(C)(C)C	3976.7	Semi standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)OC(N2C=NC(C(=N)O)=C2N)C1O[Si](C)(C)C(C)(C)C	3562.0	Standard non polar	33892256
1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)OC(N2C=NC(C(=N)O)=C2N)C1O[Si](C)(C)C(C)(C)C	4437.7	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (Non-derivatized) - 70eV, Positive	splash10-0002-9613000000-e58f9c8b6a55e4f5a202	2016-09-22	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_2_14) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_2_15) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_2_16) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- GC-MS (TMS_2_17) - 70eV, Positive	Not Available	2021-11-03	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 - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- 10V, Positive-QTOF	splash10-004i-0914000000-3f9f36edeef89d71a3ea	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- 20V, Positive-QTOF	splash10-004i-1900000000-59f0993d53f2b3a0df55	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- 40V, Positive-QTOF	splash10-056r-6900000000-5d814182d3f1cbb7b775	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- 10V, Negative-QTOF	splash10-004r-9617000000-d4df2b34274e0f689bc3	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- 20V, Negative-QTOF	splash10-004i-9400000000-ed6fd97e03721be9836e	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- 40V, Negative-QTOF	splash10-004i-9000000000-9646a76a3e1fea1b56a2	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- 10V, Positive-QTOF	splash10-000i-0639000000-178ad9c357925b86b452	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- 20V, Positive-QTOF	splash10-053r-5900000000-b920fbfbdbcfef210667	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- 40V, Positive-QTOF	splash10-0a4i-3900000000-c0d43b5a09c0faa3a83e	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- 10V, Negative-QTOF	splash10-000i-2009000000-47ccd1d49f5222b04197	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- 20V, Negative-QTOF	splash10-004i-9000000000-b043d7ebca027c26892a	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- 40V, Negative-QTOF	splash10-004i-9000000000-7e80b614e5b2fa8cc0e3	2021-10-12	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB001213

KNApSAcK ID

Not Available

Chemspider ID

195

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

200

PDB ID

Not Available

ChEBI ID

93885

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

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for 1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)- (HMDB0248071)

MOL for HMDB0248071 (1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-)

3D MOL for HMDB0248071 (1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-)

3D SDF for HMDB0248071 (1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-)

3D-SDF for HMDB0248071 (1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-)

PDB for HMDB0248071 (1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-)

3D PDB for HMDB0248071 (1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-)

SMILES for HMDB0248071 (1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-)

INCHI for HMDB0248071 (1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-)

Structure for HMDB0248071 (1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-)

3D Structure for HMDB0248071 (1H-Imidazole-4-carboxamide, 5-amino-1-(5-O-phosphono-beta-D-ribofuranosyl)-)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra