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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 18:40:25 UTC

Update Date

2021-09-26 23:14:08 UTC

HMDB ID

HMDB0257644

Secondary Accession Numbers

None

Metabolite Identification

Common Name

5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide

Description

5-amino-1-{[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-1H-imidazole-4-carboximidic acid belongs to the class of organic compounds known as pentoses. These are monosaccharides in which the carbohydrate moiety contains five carbon atoms. Based on a literature review very few articles have been published on 5-amino-1-{[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-1H-imidazole-4-carboximidic acid. This compound has been identified in human blood as reported by (PMID: 31557052 ). 5-amino-1-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide 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

HMDB0257644
     RDKit          3D
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidaz...
 33 34  0  0  0  0  0  0  0  0999 V2000
    5.9398   -0.0260   -0.6647 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7486   -0.5815   -0.1415 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6959   -1.7507    0.2968 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5330    0.2427   -0.1119 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3807    1.5116   -0.5309 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1200    1.9439   -0.3470 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4462    0.9233    0.2050 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1247    0.9223    0.5624 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8352    0.0356    0.0436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8382    0.7415   -0.5943 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9643   -0.0610   -0.5711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1684    0.8246   -0.8161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2754    1.8054    0.1656 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9510   -0.5681    0.8612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6092   -1.7834    0.9441 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4836   -0.8037    1.1135 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0738   -0.3961    2.3658 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2791   -0.1187    0.3579 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0061   -1.4026    0.8972 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.7125    0.2190   -0.0162 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0816    0.1511   -1.6769 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7106    2.9299   -0.5940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3112   -0.6262   -0.6798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9240   -0.8976   -1.2946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0511    1.3413   -1.7808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0836    0.1674   -0.7890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3383    2.0325    0.4523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3678    0.1817    1.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5852   -1.6964    1.0980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2101   -1.8842    1.0201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5097    0.4064    2.3070 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0413   -1.6033    1.9282 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7600   -2.1806    0.2424 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  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
 11 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
  7 18  1  0
 18 19  1  0
 18  4  2  0
 16  9  1  0
  1 20  1  0
  1 21  1  0
  6 22  1  0
  9 23  1  0
 11 24  1  0
 12 25  1  0
 12 26  1  0
 13 27  1  0
 14 28  1  0
 15 29  1  0
 16 30  1  0
 17 31  1  0
 19 32  1  0
 19 33  1  0
M  END


  Mrv1652309112120402D          

 19 20  0  0  0  0            999 V2000
    3.2004   -1.1401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9455   -1.9248    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1205   -1.9248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8655   -1.1401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5330   -0.6552    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5330    0.1698    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2475    0.5823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3337    1.4028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1407    1.5743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5532    0.8598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0011    0.2467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3736    0.7736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8586    1.4410    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4762    2.3280    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7206    1.9548    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0809   -0.8852    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6356   -2.5922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9711   -3.3459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8151   -2.5060    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  1  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  7 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
  9 14  1  0  0  0  0
  8 15  1  0  0  0  0
  4 16  1  0  0  0  0
  3 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0257644

> <DATABASE_NAME>
hmdb

> <SMILES>
NC(=O)C1=C(N)N(OC2OC(CO)C(O)C2O)C=N1

> <INCHI_IDENTIFIER>
InChI=1S/C9H14N4O6/c10-7-4(8(11)17)12-2-13(7)19-9-6(16)5(15)3(1-14)18-9/h2-3,5-6,9,14-16H,1,10H2,(H2,11,17)

> <INCHI_KEY>
XBCNSMSXIDLRDD-UHFFFAOYSA-N

> <FORMULA>
C9H14N4O6

> <MOLECULAR_WEIGHT>
274.233

> <EXACT_MASS>
274.091334187

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
25.125155809449737

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-amino-1-{[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-1H-imidazole-4-carboxamide

> <ALOGPS_LOGP>
-1.75

> <JCHEM_LOGP>
-3.076340061666667

> <ALOGPS_LOGS>
-1.01

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.589318998880945

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.209052859461913

> <JCHEM_PKA_STRONGEST_BASIC>
3.374945356455717

> <JCHEM_POLAR_SURFACE_AREA>
166.08

> <JCHEM_REFRACTIVITY>
61.030100000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.67e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-amino-1-{[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}imidazole-4-carboxamide

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0257644
     RDKit          3D
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidaz...
 33 34  0  0  0  0  0  0  0  0999 V2000
    5.9398   -0.0260   -0.6647 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7486   -0.5815   -0.1415 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6959   -1.7507    0.2968 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5330    0.2427   -0.1119 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3807    1.5116   -0.5309 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1200    1.9439   -0.3470 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4462    0.9233    0.2050 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1247    0.9223    0.5624 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8352    0.0356    0.0436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8382    0.7415   -0.5943 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9643   -0.0610   -0.5711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1684    0.8246   -0.8161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2754    1.8054    0.1656 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9510   -0.5681    0.8612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6092   -1.7834    0.9441 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4836   -0.8037    1.1135 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0738   -0.3961    2.3658 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2791   -0.1187    0.3579 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0061   -1.4026    0.8972 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.7125    0.2190   -0.0162 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0816    0.1511   -1.6769 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7106    2.9299   -0.5940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3112   -0.6262   -0.6798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9240   -0.8976   -1.2946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0511    1.3413   -1.7808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0836    0.1674   -0.7890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3383    2.0325    0.4523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3678    0.1817    1.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5852   -1.6964    1.0980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2101   -1.8842    1.0201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5097    0.4064    2.3070 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0413   -1.6033    1.9282 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7600   -2.1806    0.2424 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  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
 11 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
  7 18  1  0
 18 19  1  0
 18  4  2  0
 16  9  1  0
  1 20  1  0
  1 21  1  0
  6 22  1  0
  9 23  1  0
 11 24  1  0
 12 25  1  0
 12 26  1  0
 13 27  1  0
 14 28  1  0
 15 29  1  0
 16 30  1  0
 17 31  1  0
 19 32  1  0
 19 33  1  0
M  END

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0       5.974  -2.128   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       5.498  -3.593   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       3.958  -3.593   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.482  -2.128   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       4.728  -1.223   0.000  0.00  0.00           N+0
HETATM    6  O   UNK     0       4.728   0.317   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       6.062   1.087   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.223   2.619   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.729   2.939   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.499   1.605   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       7.469   0.461   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      10.031   1.444   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      10.936   2.690   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       8.356   4.346   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       5.078   3.649   0.000  0.00  0.00           O+0
HETATM   16  N   UNK     0       2.018  -1.652   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       3.053  -4.839   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.679  -6.246   0.000  0.00  0.00           O+0
HETATM   19  N   UNK     0       1.521  -4.678   0.000  0.00  0.00           N+0
CONECT    1    2    5                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   17                                                  
CONECT    4    3    5   16                                                  
CONECT    5    4    1    6                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   11                                                  
CONECT    8    7    9   15                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10    7                                                       
CONECT   12   10   13                                                       
CONECT   13   12                                                            
CONECT   14    9                                                            
CONECT   15    8                                                            
CONECT   16    4                                                            
CONECT   17    3   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
MASTER        0    0    0    0    0    0    0    0   19    0   40    0
END

COMPND    HMDB0257644
HETATM    1  N1  UNL     1       5.940  -0.026  -0.665  1.00  0.00           N  
HETATM    2  C1  UNL     1       4.749  -0.582  -0.141  1.00  0.00           C  
HETATM    3  O1  UNL     1       4.696  -1.751   0.297  1.00  0.00           O  
HETATM    4  C2  UNL     1       3.533   0.243  -0.112  1.00  0.00           C  
HETATM    5  N2  UNL     1       3.381   1.512  -0.531  1.00  0.00           N  
HETATM    6  C3  UNL     1       2.120   1.944  -0.347  1.00  0.00           C  
HETATM    7  N3  UNL     1       1.446   0.923   0.205  1.00  0.00           N  
HETATM    8  O2  UNL     1       0.125   0.922   0.562  1.00  0.00           O  
HETATM    9  C4  UNL     1      -0.835   0.036   0.044  1.00  0.00           C  
HETATM   10  O3  UNL     1      -1.838   0.742  -0.594  1.00  0.00           O  
HETATM   11  C5  UNL     1      -2.964  -0.061  -0.571  1.00  0.00           C  
HETATM   12  C6  UNL     1      -4.168   0.825  -0.816  1.00  0.00           C  
HETATM   13  O4  UNL     1      -4.275   1.805   0.166  1.00  0.00           O  
HETATM   14  C7  UNL     1      -2.951  -0.568   0.861  1.00  0.00           C  
HETATM   15  O5  UNL     1      -3.609  -1.783   0.944  1.00  0.00           O  
HETATM   16  C8  UNL     1      -1.484  -0.804   1.114  1.00  0.00           C  
HETATM   17  O6  UNL     1      -1.074  -0.396   2.366  1.00  0.00           O  
HETATM   18  C9  UNL     1       2.279  -0.119   0.358  1.00  0.00           C  
HETATM   19  N4  UNL     1       2.006  -1.403   0.897  1.00  0.00           N  
HETATM   20  H1  UNL     1       6.713   0.219  -0.016  1.00  0.00           H  
HETATM   21  H2  UNL     1       6.082   0.151  -1.677  1.00  0.00           H  
HETATM   22  H3  UNL     1       1.711   2.930  -0.594  1.00  0.00           H  
HETATM   23  H4  UNL     1      -0.311  -0.626  -0.680  1.00  0.00           H  
HETATM   24  H5  UNL     1      -2.924  -0.898  -1.295  1.00  0.00           H  
HETATM   25  H6  UNL     1      -4.051   1.341  -1.781  1.00  0.00           H  
HETATM   26  H7  UNL     1      -5.084   0.167  -0.789  1.00  0.00           H  
HETATM   27  H8  UNL     1      -3.338   2.033   0.452  1.00  0.00           H  
HETATM   28  H9  UNL     1      -3.368   0.182   1.538  1.00  0.00           H  
HETATM   29  H10 UNL     1      -4.585  -1.696   1.098  1.00  0.00           H  
HETATM   30  H11 UNL     1      -1.210  -1.884   1.020  1.00  0.00           H  
HETATM   31  H12 UNL     1      -0.510   0.406   2.307  1.00  0.00           H  
HETATM   32  H13 UNL     1       2.041  -1.603   1.928  1.00  0.00           H  
HETATM   33  H14 UNL     1       1.760  -2.181   0.242  1.00  0.00           H  
CONECT    1    2   20   21
CONECT    2    3    3    4
CONECT    4    5   18   18
CONECT    5    6    6
CONECT    6    7   22
CONECT    7    8   18
CONECT    8    9
CONECT    9   10   16   23
CONECT   10   11
CONECT   11   12   14   24
CONECT   12   13   25   26
CONECT   13   27
CONECT   14   15   16   28
CONECT   15   29
CONECT   16   17   30
CONECT   17   31
CONECT   18   19
CONECT   19   32   33
END

HMDB0257644
     RDKit          3D
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidaz...
 33 34  0  0  0  0  0  0  0  0999 V2000
    5.9398   -0.0260   -0.6647 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7486   -0.5815   -0.1415 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6959   -1.7507    0.2968 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5330    0.2427   -0.1119 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3807    1.5116   -0.5309 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1200    1.9439   -0.3470 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4462    0.9233    0.2050 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1247    0.9223    0.5624 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8352    0.0356    0.0436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8382    0.7415   -0.5943 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9643   -0.0610   -0.5711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1684    0.8246   -0.8161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2754    1.8054    0.1656 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9510   -0.5681    0.8612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6092   -1.7834    0.9441 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4836   -0.8037    1.1135 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0738   -0.3961    2.3658 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2791   -0.1187    0.3579 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0061   -1.4026    0.8972 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.7125    0.2190   -0.0162 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0816    0.1511   -1.6769 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7106    2.9299   -0.5940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3112   -0.6262   -0.6798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9240   -0.8976   -1.2946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0511    1.3413   -1.7808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0836    0.1674   -0.7890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3383    2.0325    0.4523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3678    0.1817    1.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5852   -1.6964    1.0980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2101   -1.8842    1.0201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5097    0.4064    2.3070 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0413   -1.6033    1.9282 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7600   -2.1806    0.2424 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  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
 11 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
  7 18  1  0
 18 19  1  0
 18  4  2  0
 16  9  1  0
  1 20  1  0
  1 21  1  0
  6 22  1  0
  9 23  1  0
 11 24  1  0
 12 25  1  0
 12 26  1  0
 13 27  1  0
 14 28  1  0
 15 29  1  0
 16 30  1  0
 17 31  1  0
 19 32  1  0
 19 33  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
5-Amino-1-{[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-1H-imidazole-4-carboximidate	Generator

Chemical Formula

C₉H₁₄N₄O₆

Average Molecular Weight

274.233

Monoisotopic Molecular Weight

274.091334187

IUPAC Name

5-amino-1-{[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-1H-imidazole-4-carboxamide

Traditional Name

5-amino-1-{[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}imidazole-4-carboxamide

CAS Registry Number

Not Available

SMILES

NC(=O)C1=C(N)N(OC2OC(CO)C(O)C2O)C=N1

InChI Identifier

InChI=1S/C9H14N4O6/c10-7-4(8(11)17)12-2-13(7)19-9-6(16)5(15)3(1-14)18-9/h2-3,5-6,9,14-16H,1,10H2,(H2,11,17)

InChI Key

XBCNSMSXIDLRDD-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pentoses. These are monosaccharides in which the carbohydrate moiety contains five carbon atoms.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Pentoses

Alternative Parents

Substituents

Pentose monosaccharide
Aminoimidazole
N-substituted imidazole
Azole
Heteroaromatic compound
Imidazole
Oxolane
Secondary alcohol
Carboximidic acid
Carboximidic acid derivative
Oxacycle
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Amine
Alcohol
Organonitrogen compound
Hydrocarbon derivative
Primary amine
Primary 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	-1.8	ALOGPS
logP	-3.1	ChemAxon
logS	-1	ALOGPS
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	3.37	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	166.08 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	61.03 m³·mol⁻¹	ChemAxon
Polarizability	25.13 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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]+	165.939	30932474
DeepCCS	[M-H]-	163.581	30932474
DeepCCS	[M-2H]-	196.468	30932474
DeepCCS	[M+Na]+	172.032	30932474

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide	NC(=O)C1=C(N)N(OC2OC(CO)C(O)C2O)C=N1	3583.5	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide	NC(=O)C1=C(N)N(OC2OC(CO)C(O)C2O)C=N1	2549.5	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide	NC(=O)C1=C(N)N(OC2OC(CO)C(O)C2O)C=N1	2792.4	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #1	C[Si](C)(C)NC(=O)C1=C(N)N(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2608.2	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #1	C[Si](C)(C)NC(=O)C1=C(N)N(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2569.2	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #1	C[Si](C)(C)NC(=O)C1=C(N)N(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3928.9	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #10	C[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO[Si](C)(C)C)C(O)C2O)C=N1	2717.5	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #10	C[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO[Si](C)(C)C)C(O)C2O)C=N1	2790.9	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #10	C[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO[Si](C)(C)C)C(O)C2O)C=N1	3949.1	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #11	C[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C)N(OC2OC(CO)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2677.4	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #11	C[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C)N(OC2OC(CO)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2642.1	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #11	C[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C)N(OC2OC(CO)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3971.4	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #12	C[Si](C)(C)OC1C(CO)OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N)C1O[Si](C)(C)C	2736.2	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #12	C[Si](C)(C)OC1C(CO)OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N)C1O[Si](C)(C)C	2712.9	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #12	C[Si](C)(C)OC1C(CO)OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N)C1O[Si](C)(C)C	3993.4	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #13	C[Si](C)(C)OC1C(CO)OC(ON2C=NC(C(N)=O)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	2691.2	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #13	C[Si](C)(C)OC1C(CO)OC(ON2C=NC(C(N)=O)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	2660.2	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #13	C[Si](C)(C)OC1C(CO)OC(ON2C=NC(C(N)=O)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	3818.8	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #14	C[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N=CN1OC1OC(CO)C(O[Si](C)(C)C)C1O	2796.6	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #14	C[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N=CN1OC1OC(CO)C(O[Si](C)(C)C)C1O	2816.4	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #14	C[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N=CN1OC1OC(CO)C(O[Si](C)(C)C)C1O	3971.5	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #15	C[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO)C(O[Si](C)(C)C)C2O)C=N1	2699.4	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #15	C[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO)C(O[Si](C)(C)C)C2O)C=N1	2760.7	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #15	C[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO)C(O[Si](C)(C)C)C2O)C=N1	3889.8	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #16	C[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N=CN1OC1OC(CO)C(O)C1O[Si](C)(C)C	2803.7	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #16	C[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N=CN1OC1OC(CO)C(O)C1O[Si](C)(C)C	2822.7	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #16	C[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N=CN1OC1OC(CO)C(O)C1O[Si](C)(C)C	4027.8	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #17	C[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO)C(O)C2O[Si](C)(C)C)C=N1	2713.2	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #17	C[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO)C(O)C2O[Si](C)(C)C)C=N1	2765.0	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #17	C[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO)C(O)C2O[Si](C)(C)C)C=N1	3928.4	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #18	C[Si](C)(C)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO)C(O)C2O)C=N1)[Si](C)(C)C	2819.9	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #18	C[Si](C)(C)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO)C(O)C2O)C=N1)[Si](C)(C)C	2975.7	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #18	C[Si](C)(C)N(C(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO)C(O)C2O)C=N1)[Si](C)(C)C	3796.6	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #2	C[Si](C)(C)NC1=C(C(N)=O)N=CN1OC1OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2652.7	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #2	C[Si](C)(C)NC1=C(C(N)=O)N=CN1OC1OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2567.0	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #2	C[Si](C)(C)NC1=C(C(N)=O)N=CN1OC1OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3832.8	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #3	C[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C)N(OC2OC(CO[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	2682.4	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #3	C[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C)N(OC2OC(CO[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	2667.0	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #3	C[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C)N(OC2OC(CO[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	4075.2	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #4	C[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N)C(O[Si](C)(C)C)C1O	2748.9	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #4	C[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N)C(O[Si](C)(C)C)C1O	2741.0	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #4	C[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N)C(O[Si](C)(C)C)C1O	4063.1	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #5	C[Si](C)(C)OCC1OC(ON2C=NC(C(N)=O)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2706.4	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #5	C[Si](C)(C)OCC1OC(ON2C=NC(C(N)=O)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2686.9	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #5	C[Si](C)(C)OCC1OC(ON2C=NC(C(N)=O)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3890.1	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #6	C[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C)N(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	2673.9	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #6	C[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C)N(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	2663.1	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #6	C[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C)N(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	4028.7	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #7	C[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N)C(O)C1O[Si](C)(C)C	2740.5	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #7	C[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N)C(O)C1O[Si](C)(C)C	2731.5	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #7	C[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N)C(O)C1O[Si](C)(C)C	4035.2	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #8	C[Si](C)(C)OCC1OC(ON2C=NC(C(N)=O)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2693.8	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #8	C[Si](C)(C)OCC1OC(ON2C=NC(C(N)=O)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2677.4	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #8	C[Si](C)(C)OCC1OC(ON2C=NC(C(N)=O)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3863.8	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #9	C[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N=CN1OC1OC(CO[Si](C)(C)C)C(O)C1O	2791.6	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #9	C[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N=CN1OC1OC(CO[Si](C)(C)C)C(O)C1O	2857.2	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TMS,isomer #9	C[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N=CN1OC1OC(CO[Si](C)(C)C)C(O)C1O	4032.8	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #1	C[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C)N(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2667.7	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #1	C[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C)N(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2661.9	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #1	C[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C)N(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3665.1	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #10	C[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2713.9	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #10	C[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2737.0	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #10	C[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3535.4	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #11	C[Si](C)(C)OC1C(CO)OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O	2807.4	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #11	C[Si](C)(C)OC1C(CO)OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O	2919.4	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #11	C[Si](C)(C)OC1C(CO)OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O	3459.6	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #12	C[Si](C)(C)OC1C(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)OC(CO)C1O	2821.8	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #12	C[Si](C)(C)OC1C(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)OC(CO)C1O	2936.3	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #12	C[Si](C)(C)OC1C(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)OC(CO)C1O	3492.5	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #2	C[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2687.5	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #2	C[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2698.5	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #2	C[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3792.4	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #3	C[Si](C)(C)OCC1OC(ON2C=NC(C(N)=O)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2675.1	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #3	C[Si](C)(C)OCC1OC(ON2C=NC(C(N)=O)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2656.3	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #3	C[Si](C)(C)OCC1OC(ON2C=NC(C(N)=O)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3618.5	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #4	C[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N=CN1OC1OC(CO[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2794.1	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #4	C[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N=CN1OC1OC(CO[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2800.8	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #4	C[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N=CN1OC1OC(CO[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3732.2	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #5	C[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	2736.6	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #5	C[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	2764.0	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #5	C[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=N1	3630.7	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #6	C[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N=CN1OC1OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2779.2	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #6	C[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N=CN1OC1OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2788.1	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #6	C[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N=CN1OC1OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3685.9	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #7	C[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	2716.9	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #7	C[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	2744.9	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #7	C[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=N1	3604.8	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #8	C[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O)C1O	2832.9	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #8	C[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O)C1O	2947.7	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #8	C[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O)C1O	3497.5	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #9	C[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N=CN1OC1OC(CO)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2784.7	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #9	C[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N=CN1OC1OC(CO)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2777.0	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TMS,isomer #9	C[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N=CN1OC1OC(CO)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3636.1	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,6TMS,isomer #1	C[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N=CN1OC1OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2769.1	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,6TMS,isomer #1	C[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N=CN1OC1OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2762.4	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,6TMS,isomer #1	C[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N=CN1OC1OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3415.0	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,6TMS,isomer #2	C[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2706.0	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,6TMS,isomer #2	C[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	2731.4	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,6TMS,isomer #2	C[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C)[Si](C)(C)C)N(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=N1	3314.1	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,6TMS,isomer #3	C[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2825.3	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,6TMS,isomer #3	C[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2882.7	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,6TMS,isomer #3	C[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3224.8	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,6TMS,isomer #4	C[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2808.8	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,6TMS,isomer #4	C[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2862.3	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,6TMS,isomer #4	C[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3204.5	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,6TMS,isomer #5	C[Si](C)(C)OC1C(CO)OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	2821.5	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,6TMS,isomer #5	C[Si](C)(C)OC1C(CO)OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	2854.3	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,6TMS,isomer #5	C[Si](C)(C)OC1C(CO)OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	3141.2	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,7TMS,isomer #1	C[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2811.5	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,7TMS,isomer #1	C[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2825.5	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,7TMS,isomer #1	C[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2978.0	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N)N(OC2OC(CO[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	3506.1	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N)N(OC2OC(CO[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	3329.6	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N)N(OC2OC(CO[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	4060.2	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C2O)C=N1	3518.7	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C2O)C=N1	3508.3	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C2O)C=N1	4027.3	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C(C)(C)C)N(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=N1	3527.4	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C(C)(C)C)N(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=N1	3373.0	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C(C)(C)C)N(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=N1	4063.5	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1C(CO)OC(ON2C=NC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N)C1O[Si](C)(C)C(C)(C)C	3565.5	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1C(CO)OC(ON2C=NC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N)C1O[Si](C)(C)C(C)(C)C	3444.2	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1C(CO)OC(ON2C=NC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N)C1O[Si](C)(C)C(C)(C)C	4067.6	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1C(CO)OC(ON2C=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	3514.2	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1C(CO)OC(ON2C=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	3395.1	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1C(CO)OC(ON2C=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	3940.8	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1OC1OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O	3599.0	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1OC1OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O	3537.1	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1OC1OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O	4016.8	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3510.8	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3483.6	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3978.9	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1OC1OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	3608.7	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1OC1OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	3546.2	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1OC1OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	4061.3	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(OC2OC(CO)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	3524.9	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(OC2OC(CO)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	3498.4	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(OC2OC(CO)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	4007.1	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,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(OC2OC(CO)C(O)C2O)C=N1)[Si](C)(C)C(C)(C)C	3595.0	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,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(OC2OC(CO)C(O)C2O)C=N1)[Si](C)(C)C(C)(C)C	3609.8	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,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(OC2OC(CO)C(O)C2O)C=N1)[Si](C)(C)C(C)(C)C	3874.3	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=C(C(N)=O)N=CN1OC1OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3551.3	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=C(C(N)=O)N=CN1OC1OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3334.6	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=C(C(N)=O)N=CN1OC1OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3984.0	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C(C)(C)C)N(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	3531.3	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C(C)(C)C)N(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	3420.7	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C(C)(C)C)N(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	4143.2	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N)C(O[Si](C)(C)C(C)(C)C)C1O	3577.4	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N)C(O[Si](C)(C)C(C)(C)C)C1O	3484.8	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N)C(O[Si](C)(C)C(C)(C)C)C1O	4125.4	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(ON2C=NC(C(N)=O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3524.1	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(ON2C=NC(C(N)=O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3445.1	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(ON2C=NC(C(N)=O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3998.5	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C(C)(C)C)N(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3522.8	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C(C)(C)C)N(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3408.0	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C(C)(C)C)N(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	4105.0	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N)C(O)C1O[Si](C)(C)C(C)(C)C	3566.6	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N)C(O)C1O[Si](C)(C)C(C)(C)C	3471.2	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N)C(O)C1O[Si](C)(C)C(C)(C)C	4103.1	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(ON2C=NC(C(N)=O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3520.7	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(ON2C=NC(C(N)=O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3427.9	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(ON2C=NC(C(N)=O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3982.5	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1OC1OC(CO[Si](C)(C)C(C)(C)C)C(O)C1O	3593.9	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1OC1OC(CO[Si](C)(C)C(C)(C)C)C(O)C1O	3568.8	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1OC1OC(CO[Si](C)(C)C(C)(C)C)C(O)C1O	4066.4	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C(C)(C)C)N(OC2OC(CO[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	3635.7	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C(C)(C)C)N(OC2OC(CO[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	3532.6	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N[Si](C)(C)C(C)(C)C)N(OC2OC(CO[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	3960.7	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=N1	3639.3	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=N1	3610.4	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=N1	3827.9	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1C(CO)OC(ON2C=NC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	3701.9	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1C(CO)OC(ON2C=NC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	3756.3	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1C(CO)OC(ON2C=NC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	3687.9	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1C(ON2C=NC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)OC(CO)C1O	3711.2	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1C(ON2C=NC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)OC(CO)C1O	3769.0	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1C(ON2C=NC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)OC(CO)C1O	3710.6	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3670.0	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3590.2	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4034.1	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(ON2C=NC(C(N)=O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3645.7	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(ON2C=NC(C(N)=O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3543.8	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(ON2C=NC(C(N)=O)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3908.6	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1OC1OC(CO[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3728.8	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1OC1OC(CO[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3697.3	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1OC1OC(CO[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3942.5	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	3655.9	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	3651.9	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=N1	3891.5	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1OC1OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3709.9	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1OC1OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3682.9	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1OC1OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3913.1	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3636.1	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3632.1	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)NC(=O)C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=N1	3876.1	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O)C1O	3695.8	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O)C1O	3774.1	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(ON2C=NC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O)C1O	3731.4	Standard polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1OC1OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3726.6	Semi standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1OC1OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3657.7	Standard non polar	33892256
5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC1=C(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN1OC1OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3879.6	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a4i-9230000000-6fe36107c5acbcab6204	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_3_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_3_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_3_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_3_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_3_5) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide GC-MS (TMS_3_6) - 70eV, Positive	Not Available	2021-11-05	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

Not Available

KNApSAcK ID

Not Available

Chemspider ID

10685477

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

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 5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide (HMDB0257644)

MOL for HMDB0257644 (5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide)

3D MOL for HMDB0257644 (5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide)

3D SDF for HMDB0257644 (5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide)

3D-SDF for HMDB0257644 (5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide)

PDB for HMDB0257644 (5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide)

3D PDB for HMDB0257644 (5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide)

SMILES for HMDB0257644 (5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide)

INCHI for HMDB0257644 (5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide)

Structure for HMDB0257644 (5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide)

3D Structure for HMDB0257644 (5-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyimidazole-4-carboxamide)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra