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Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (2) Show 2 proteins XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2005-11-16 15:48:42 UTC

Update Date

2021-09-14 15:39:01 UTC

HMDB ID

HMDB0001308

Secondary Accession Numbers

HMDB0006476
HMDB01308
HMDB06476

Metabolite Identification

Common Name

5'-Phosphoribosyl-N-formylglycinamide

Description

5'-Phosphoribosyl-N-formylglycinamide, also known as FGAR or N-formyl-GAR, belongs to the class of organic compounds known as glycinamide ribonucleotides. Glycinamide ribonucleotides are compounds in which the amide N atom of glycineamide is linked to the C-1 of a ribosyl (or deoxyribosyl) moiety. FGAR is an extremely weak basic (essentially neutral) compound (based on its pKa). FGAR is a substrate for phosphoribosylformylglycinamidine synthase. It is involved in aminoimidazole ribonucleotide biosynthesis and plays a vital role in purine metabolism as well as in the conversion of glutamine to glutamate.

Structure

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

HMDB0001308
     RDKit          3D
5'-Phosphoribosyl-N-formylglycinamide
 35 35  0  0  0  0  0  0  0  0999 V2000
    5.9051    2.2268    1.0242 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7095    2.5532    0.8857 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6977    1.5266    0.8699 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0640    0.1387    1.0127 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8935   -0.7346    0.9701 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1870   -1.9936    1.0960 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5607   -0.3385    0.8132 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4346   -1.2483    0.7777 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1585   -1.1457   -0.4789 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5337   -1.1876   -0.2688 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3209   -0.6698   -1.4230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0325    0.6554   -1.7315 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9446    1.1822   -3.0332 P   0  0  0  0  0  5  0  0  0  0  0  0
   -4.0069    2.1323   -2.5025 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7347   -0.0630   -3.8344 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9394    1.9874   -4.1174 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6814   -0.3333    0.9769 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9206   -0.4349    1.5516 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5930   -1.0210    1.8121 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1435   -2.2491    2.1999 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4203    3.5705    0.7790 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7259    1.8794    0.7504 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8151   -0.0855    0.2210 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5673    0.0667    2.0167 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2715    0.6491    0.7088 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8476   -2.2727    0.8972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8699   -2.1940   -0.0095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0743   -1.2922   -2.3072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3941   -0.7318   -1.1610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7205    0.0285   -3.8301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9159    2.9449   -3.8227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3848    0.7132    0.7356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6086   -0.8176    0.9782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3182   -0.4730    2.6918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8038   -2.9685    1.6402 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  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
 19  8  1  0
  2 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  7 25  1  0
  8 26  1  1
 10 27  1  1
 11 28  1  0
 11 29  1  0
 15 30  1  0
 16 31  1  0
 17 32  1  6
 18 33  1  0
 19 34  1  1
 20 35  1  0
M  END


  Mrv1652304082023362D          

 20 20  0  0  0  0            999 V2000
 9999.311810000.5633    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9998.597210000.1510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.882610000.5633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.7787 9998.7115    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10002.079110000.5633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.5699 9998.7033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10002.792510000.1510    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10003.507810000.5633    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
10003.095510001.2766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10004.221210000.1510    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10003.920210001.2766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10000.692010000.6450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10000.024610000.1600    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10000.2795 9999.3754    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10001.1045 9999.3754    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10001.359410000.1600    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9998.5972 9999.3257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9995.738710000.1510    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.453310000.5633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.168110000.1510    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  8 11  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 12 13  1  0  0  0  0
 12 16  1  0  0  0  0
 13  1  1  6  0  0  0
 14  4  1  1  0  0  0
 16  5  1  6  0  0  0
 15  6  1  1  0  0  0
  2  3  1  0  0  0  0
 19 18  2  0  0  0  0
 20 19  1  0  0  0  0
  3 20  1  0  0  0  0
  2 17  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0001308

> <DATABASE_NAME>
hmdb

> <SMILES>
O[C@H]1[C@@H](O)[C@H](NC(=O)CNC=O)O[C@@H]1COP(O)(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C8H15N2O9P/c11-3-9-1-5(12)10-8-7(14)6(13)4(19-8)2-18-20(15,16)17/h3-4,6-8,13-14H,1-2H2,(H,9,11)(H,10,12)(H2,15,16,17)/t4-,6-,7-,8-/m1/s1

> <INCHI_KEY>
VDXLUNDMVKSKHO-XVFCMESISA-N

> <FORMULA>
C8H15N2O9P

> <MOLECULAR_WEIGHT>
314.1865

> <EXACT_MASS>
314.0515166

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
25.651467502321367

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[(2R,3S,4R,5R)-3,4-dihydroxy-5-(2-formamidoacetamido)oxolan-2-yl]methoxy}phosphonic acid

> <ALOGPS_LOGP>
-2.28

> <JCHEM_LOGP>
-3.867787448666667

> <ALOGPS_LOGS>
-1.68

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.251389402211153

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.2263355568590275

> <JCHEM_PKA_STRONGEST_BASIC>
-1.5302762200112934

> <JCHEM_POLAR_SURFACE_AREA>
174.64999999999998

> <JCHEM_REFRACTIVITY>
60.248099999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.52e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,3S,4R,5R)-3,4-dihydroxy-5-(2-formamidoacetamido)oxolan-2-yl]methoxyphosphonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0001308
     RDKit          3D
5'-Phosphoribosyl-N-formylglycinamide
 35 35  0  0  0  0  0  0  0  0999 V2000
    5.9051    2.2268    1.0242 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7095    2.5532    0.8857 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6977    1.5266    0.8699 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0640    0.1387    1.0127 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8935   -0.7346    0.9701 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1870   -1.9936    1.0960 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5607   -0.3385    0.8132 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4346   -1.2483    0.7777 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1585   -1.1457   -0.4789 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5337   -1.1876   -0.2688 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3209   -0.6698   -1.4230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0325    0.6554   -1.7315 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9446    1.1822   -3.0332 P   0  0  0  0  0  5  0  0  0  0  0  0
   -4.0069    2.1323   -2.5025 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7347   -0.0630   -3.8344 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9394    1.9874   -4.1174 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6814   -0.3333    0.9769 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9206   -0.4349    1.5516 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5930   -1.0210    1.8121 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1435   -2.2491    2.1999 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4203    3.5705    0.7790 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7259    1.8794    0.7504 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8151   -0.0855    0.2210 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5673    0.0667    2.0167 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2715    0.6491    0.7088 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8476   -2.2727    0.8972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8699   -2.1940   -0.0095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0743   -1.2922   -2.3072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3941   -0.7318   -1.1610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7205    0.0285   -3.8301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9159    2.9449   -3.8227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3848    0.7132    0.7356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6086   -0.8176    0.9782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3182   -0.4730    2.6918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8038   -2.9685    1.6402 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  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
 19  8  1  0
  2 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  7 25  1  0
  8 26  1  1
 10 27  1  1
 11 28  1  0
 11 29  1  0
 15 30  1  0
 16 31  1  0
 17 32  1  6
 18 33  1  0
 19 34  1  1
 20 35  1  0
M  END

HEADER    PROTEIN                                 08-APR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-APR-20         0                                  
HETATM    1  N   UNK     0    8665.3828667.718   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0    8664.0488666.949   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0    8662.7148667.718   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0    8666.2548664.261   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0    8670.5488667.718   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0    8669.5978664.246   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0    8671.8798666.949   0.000  0.00  0.00           O+0
HETATM    8  P   UNK     0    8673.2158667.718   0.000  0.00  0.00           P+0
HETATM    9  O   UNK     0    8672.4458669.050   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0    8674.5468666.949   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0    8673.9848669.050   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0    8667.9588667.871   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0    8666.7138666.965   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8667.1888665.501   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0    8668.7288665.501   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0    8669.2048666.965   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0    8664.0488665.408   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0    8658.7128666.949   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0    8660.0468667.718   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0    8661.3808666.949   0.000  0.00  0.00           N+0
CONECT    1    2   13                                                       
CONECT    2    1    3   17                                                  
CONECT    3    2   20                                                       
CONECT    4   14                                                            
CONECT    5    7   16                                                       
CONECT    6   15                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   10   11                                             
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    8                                                            
CONECT   12   13   16                                                       
CONECT   13   14   12    1                                                  
CONECT   14   13   15    4                                                  
CONECT   15   14   16    6                                                  
CONECT   16   15   12    5                                                  
CONECT   17    2                                                            
CONECT   18   19                                                            
CONECT   19   18   20                                                       
CONECT   20   19    3                                                       
MASTER        0    0    0    0    0    0    0    0   20    0   40    0
END

COMPND    HMDB0001308
HETATM    1  O1  UNL     1       5.905   2.227   1.024  1.00  0.00           O  
HETATM    2  C1  UNL     1       4.710   2.553   0.886  1.00  0.00           C  
HETATM    3  N1  UNL     1       3.698   1.527   0.870  1.00  0.00           N  
HETATM    4  C2  UNL     1       4.064   0.139   1.013  1.00  0.00           C  
HETATM    5  C3  UNL     1       2.893  -0.735   0.970  1.00  0.00           C  
HETATM    6  O2  UNL     1       3.187  -1.994   1.096  1.00  0.00           O  
HETATM    7  N2  UNL     1       1.561  -0.338   0.813  1.00  0.00           N  
HETATM    8  C4  UNL     1       0.435  -1.248   0.778  1.00  0.00           C  
HETATM    9  O3  UNL     1      -0.159  -1.146  -0.479  1.00  0.00           O  
HETATM   10  C5  UNL     1      -1.534  -1.188  -0.269  1.00  0.00           C  
HETATM   11  C6  UNL     1      -2.321  -0.670  -1.423  1.00  0.00           C  
HETATM   12  O4  UNL     1      -2.033   0.655  -1.732  1.00  0.00           O  
HETATM   13  P1  UNL     1      -2.945   1.182  -3.033  1.00  0.00           P  
HETATM   14  O5  UNL     1      -4.007   2.132  -2.502  1.00  0.00           O  
HETATM   15  O6  UNL     1      -3.735  -0.063  -3.834  1.00  0.00           O  
HETATM   16  O7  UNL     1      -1.939   1.987  -4.117  1.00  0.00           O  
HETATM   17  C7  UNL     1      -1.681  -0.333   0.977  1.00  0.00           C  
HETATM   18  O8  UNL     1      -2.921  -0.435   1.552  1.00  0.00           O  
HETATM   19  C8  UNL     1      -0.593  -1.021   1.812  1.00  0.00           C  
HETATM   20  O9  UNL     1      -1.143  -2.249   2.200  1.00  0.00           O  
HETATM   21  H1  UNL     1       4.420   3.570   0.779  1.00  0.00           H  
HETATM   22  H2  UNL     1       2.726   1.879   0.750  1.00  0.00           H  
HETATM   23  H3  UNL     1       4.815  -0.086   0.221  1.00  0.00           H  
HETATM   24  H4  UNL     1       4.567   0.067   2.017  1.00  0.00           H  
HETATM   25  H5  UNL     1       1.271   0.649   0.709  1.00  0.00           H  
HETATM   26  H6  UNL     1       0.848  -2.273   0.897  1.00  0.00           H  
HETATM   27  H7  UNL     1      -1.870  -2.194  -0.010  1.00  0.00           H  
HETATM   28  H8  UNL     1      -2.074  -1.292  -2.307  1.00  0.00           H  
HETATM   29  H9  UNL     1      -3.394  -0.732  -1.161  1.00  0.00           H  
HETATM   30  H10 UNL     1      -4.720   0.028  -3.830  1.00  0.00           H  
HETATM   31  H11 UNL     1      -1.916   2.945  -3.823  1.00  0.00           H  
HETATM   32  H12 UNL     1      -1.385   0.713   0.736  1.00  0.00           H  
HETATM   33  H13 UNL     1      -3.609  -0.818   0.978  1.00  0.00           H  
HETATM   34  H14 UNL     1      -0.318  -0.473   2.692  1.00  0.00           H  
HETATM   35  H15 UNL     1      -0.804  -2.968   1.640  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   21
CONECT    3    4   22
CONECT    4    5   23   24
CONECT    5    6    6    7
CONECT    7    8   25
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
END

HMDB0001308
     RDKit          3D
5'-Phosphoribosyl-N-formylglycinamide
 35 35  0  0  0  0  0  0  0  0999 V2000
    5.9051    2.2268    1.0242 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7095    2.5532    0.8857 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6977    1.5266    0.8699 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0640    0.1387    1.0127 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8935   -0.7346    0.9701 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1870   -1.9936    1.0960 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5607   -0.3385    0.8132 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4346   -1.2483    0.7777 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1585   -1.1457   -0.4789 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5337   -1.1876   -0.2688 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3209   -0.6698   -1.4230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0325    0.6554   -1.7315 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9446    1.1822   -3.0332 P   0  0  0  0  0  5  0  0  0  0  0  0
   -4.0069    2.1323   -2.5025 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7347   -0.0630   -3.8344 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9394    1.9874   -4.1174 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6814   -0.3333    0.9769 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9206   -0.4349    1.5516 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5930   -1.0210    1.8121 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1435   -2.2491    2.1999 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4203    3.5705    0.7790 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7259    1.8794    0.7504 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8151   -0.0855    0.2210 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5673    0.0667    2.0167 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2715    0.6491    0.7088 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8476   -2.2727    0.8972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8699   -2.1940   -0.0095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0743   -1.2922   -2.3072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3941   -0.7318   -1.1610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7205    0.0285   -3.8301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9159    2.9449   -3.8227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3848    0.7132    0.7356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6086   -0.8176    0.9782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3182   -0.4730    2.6918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8038   -2.9685    1.6402 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  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
 19  8  1  0
  2 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  7 25  1  0
  8 26  1  1
 10 27  1  1
 11 28  1  0
 11 29  1  0
 15 30  1  0
 16 31  1  0
 17 32  1  6
 18 33  1  0
 19 34  1  1
 20 35  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
N-Formyl-gar	Kegg
N-Formylglycinamide ribonucleotide	Kegg
N2-Formyl-N1-(5-phospho-D-ribosyl)glycinamide	Kegg
5'-p-Ribosyl-N-formylglycineamide	HMDB
5'-Phosphoribosyl-formylglycinamide	HMDB
5'-Phosphoribosyl-N-formylglycineamide	HMDB
5-Phosphoribosyl-N-formalglycineamide	HMDB
FGAR	HMDB
N(2)-Formyl-N(1)-(5-phospho-D-ribosyl)glycinamide	HMDB
Formylglycinamide ribonucleotide	HMDB
Formylglycineamideribotide	HMDB
Phosphoribosyl-N-formylglycineamide	HMDB
2-(Formylamino)-N-(5-O-phosphono-beta-D-ribofuranosyl)acetamide	HMDB
2-(Formylamino)-N-(5-O-phosphono-β-D-ribofuranosyl)acetamide	HMDB
5'-Phosphoribosyl-N-formylglycinamide	HMDB
5’-Phosphoribosyl-N-formylglycinamide	HMDB
Formylglycinamide ribotide	HMDB
Phosphoribosylformylglycinamide	HMDB
alpha-N-Formylglycinamide ribonucleotide	HMDB
α-N-Formylglycinamide ribonucleotide	HMDB

Chemical Formula

C₈H₁₅N₂O₉P

Average Molecular Weight

314.1865

Monoisotopic Molecular Weight

314.0515166

IUPAC Name

{[(2R,3S,4R,5R)-3,4-dihydroxy-5-(2-formamidoacetamido)oxolan-2-yl]methoxy}phosphonic acid

Traditional Name

[(2R,3S,4R,5R)-3,4-dihydroxy-5-(2-formamidoacetamido)oxolan-2-yl]methoxyphosphonic acid

CAS Registry Number

349-34-8

SMILES

O[C@H]1[C@@H](O)[C@H](NC(=O)CNC=O)O[C@@H]1COP(O)(O)=O

InChI Identifier

InChI=1S/C8H15N2O9P/c11-3-9-1-5(12)10-8-7(14)6(13)4(19-8)2-18-20(15,16)17/h3-4,6-8,13-14H,1-2H2,(H,9,11)(H,10,12)(H2,15,16,17)/t4-,6-,7-,8-/m1/s1

InChI Key

VDXLUNDMVKSKHO-XVFCMESISA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as glycinamide ribonucleotides. Glycinamide ribonucleotides are compounds in which the amide N atom of glycineamide is linked to the C-1 of a ribosyl (or deoxyribosyl) moiety. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.

Kingdom

Organic compounds

Super Class

Nucleosides, nucleotides, and analogues

Class

Glycinamide ribonucleotides

Sub Class

Not Available

Direct Parent

Glycinamide ribonucleotides

Alternative Parents

Substituents

Glycinamide-ribonucleotide
Pentose phosphate
Pentose-5-phosphate
N-formyl-alpha amino acid or derivatives
Alpha-amino acid amide
N-formyl-alpha-amino acid
N-substituted-alpha-amino acid
Alpha-amino acid or derivatives
Monosaccharide phosphate
Pentose monosaccharide
Monoalkyl phosphate
Organic phosphoric acid derivative
Alkyl phosphate
Monosaccharide
Phosphoric acid ester
Tetrahydrofuran
Secondary carboxylic acid amide
1,2-diol
Carboxamide group
Secondary alcohol
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Alcohol
Organic nitrogen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

N-glycosyl compound (CHEBI:42411 )
ribose monophosphate (CHEBI:42411 )
amido monocarboxylic acid amide (CHEBI:42411 )

Ontology

Not Available

Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)
Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)

Equine

Horse (FooDB: FOOD00378)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Process

Naturally occurring process

Biological process

Biochemical pathway

Metabolic pathway

Purine Metabolism (HMDB: HMDB0001308)
Purine Nucleotides De Novo Biosynthesis (PathBank: SMP0000927)
One Carbon Pool by Folate (PathBank: SMP0001750)
Thiamin Diphosphate Biosynthesis (PathBank: SMP0002042)
Purine Nucleotides De Novo Biosynthesis 2 (PathBank: SMP0002047)
Tetrahydrofolate Biosynthesis (PathBank: SMP0002334)
One Carbon Pool by Folate I (PathBank: SMP0002369)
Purine Nucleotides De Novo Biosynthesis (PathBank: SMP0002377)

Disease pathway

Adenosine Deaminase Deficiency (PathBank: SMP0000144)
Adenylosuccinate Lyase Deficiency (PathBank: SMP0000167)
Gout or Kelley-Seegmiller Syndrome (PathBank: SMP0000365)
Lesch-Nyhan Syndrome (LNS) (PathBank: SMP0000364)
Molybdenum Cofactor Deficiency (PathBank: SMP0000203)
Xanthine Dehydrogenase Deficiency (Xanthinuria) (PathBank: SMP0000220)
Purine Nucleoside Phosphorylase Deficiency (PathBank: SMP0000210)
AICA-Ribosiduria (PathBank: SMP0000168)
Xanthinuria Type I (PathBank: SMP0000512)
Xanthinuria Type II (PathBank: SMP0000513)
Adenine Phosphoribosyltransferase Deficiency (APRT) (PathBank: SMP0000535)
Mitochondrial DNA Depletion Syndrome (PathBank: SMP0000536)
Myoadenylate Deaminase Deficiency (PathBank: SMP0000537)
Mitochondrial DNA Depletion Syndrome (PathBank: SMP0120601)

Drug action pathway

Azathioprine Action Pathway (PathBank: SMP0000427)
Mercaptopurine Action Pathway (PathBank: SMP0000428)
Thioguanine Action Pathway (PathBank: SMP0000430)

Role

Not Available

Physical Properties

State

Solid

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
Water Solubility	6.52 g/L	ALOGPS
logP	-2.3	ALOGPS
logP	-3.9	ChemAxon
logS	-1.7	ALOGPS
pKa (Strongest Acidic)	1.23	ChemAxon
pKa (Strongest Basic)	-1.5	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	174.65 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	60.25 m³·mol⁻¹	ChemAxon
Polarizability	25.65 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	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
DarkChem	[M+H]+	172.573	31661259
DarkChem	[M-H]-	166.448	31661259
AllCCS	[M+H]+	165.428	32859911
AllCCS	[M-H]-	162.781	32859911
DeepCCS	[M+H]+	162.196	30932474
DeepCCS	[M-H]-	159.838	30932474
DeepCCS	[M-2H]-	193.078	30932474
DeepCCS	[M+Na]+	168.305	30932474
AllCCS	[M+H]+	165.4	32859911
AllCCS	[M+H-H2O]+	162.4	32859911
AllCCS	[M+NH4]+	168.2	32859911
AllCCS	[M+Na]+	169.0	32859911
AllCCS	[M-H]-	162.8	32859911
AllCCS	[M+Na-2H]-	162.7	32859911
AllCCS	[M+HCOO]-	162.8	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
5'-Phosphoribosyl-N-formylglycinamide	O[C@H]1[C@@H](O)[C@H](NC(=O)CNC=O)O[C@@H]1COP(O)(O)=O	3912.4	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide	O[C@H]1[C@@H](O)[C@H](NC(=O)CNC=O)O[C@@H]1COP(O)(O)=O	2273.7	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide	O[C@H]1[C@@H](O)[C@H](NC(=O)CNC=O)O[C@@H]1COP(O)(O)=O	2996.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
5'-Phosphoribosyl-N-formylglycinamide,1TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CNC=O)[C@@H]1O	2603.5	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,1TMS,isomer #2	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CNC=O)O[C@H](COP(=O)(O)O)[C@H]1O	2608.8	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,1TMS,isomer #3	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](NC(=O)CNC=O)[C@H](O)[C@@H]1O	2680.3	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,1TMS,isomer #4	C[Si](C)(C)N(C(=O)CNC=O)[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O	2579.4	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,1TMS,isomer #5	C[Si](C)(C)N(C=O)CC(=O)N[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O	2732.2	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CNC=O)[C@@H]1O[Si](C)(C)C	2575.8	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TMS,isomer #10	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C)[C@H](O)[C@@H]1O	2783.4	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TMS,isomer #11	C[Si](C)(C)N(C=O)CC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)[Si](C)(C)C	2635.4	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](NC(=O)CNC=O)[C@@H]1O	2680.7	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C)[C@@H]1O	2560.1	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C)[C@@H]1O	2714.5	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TMS,isomer #5	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CNC=O)O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@H]1O	2687.0	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N(C(=O)CNC=O)[Si](C)(C)C	2568.7	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TMS,isomer #7	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CN(C=O)[Si](C)(C)C)O[C@H](COP(=O)(O)O)[C@H]1O	2715.9	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TMS,isomer #8	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](NC(=O)CNC=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C	2718.2	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TMS,isomer #9	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C)[C@H](O)[C@@H]1O	2607.0	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](NC(=O)CNC=O)[C@@H]1O[Si](C)(C)C	2644.0	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](NC(=O)CNC=O)[C@@H]1O[Si](C)(C)C	2596.0	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](NC(=O)CNC=O)[C@@H]1O[Si](C)(C)C	3826.3	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #10	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CN(C=O)[Si](C)(C)C)O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@H]1O	2755.3	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #10	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CN(C=O)[Si](C)(C)C)O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@H]1O	2711.4	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #10	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CN(C=O)[Si](C)(C)C)O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@H]1O	3838.2	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #11	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C	2628.0	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #11	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C	2804.0	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #11	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C	4146.6	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #12	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C	2633.8	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #12	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C	2671.5	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #12	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3601.8	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #13	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C	2781.6	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #13	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C	2739.2	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #13	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3675.2	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #14	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O	2651.0	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #14	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O	2758.9	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #14	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O	3890.7	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2542.0	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2689.0	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4094.7	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2673.2	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2728.5	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4178.1	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CNC=O)[C@@H]1O	2710.9	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CNC=O)[C@@H]1O	2626.6	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CNC=O)[C@@H]1O	3580.5	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C)[C@@H]1O	2595.5	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C)[C@@H]1O	2658.0	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C)[C@@H]1O	3766.9	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C)[C@@H]1O	2756.8	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C)[C@@H]1O	2705.0	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C)[C@@H]1O	3872.3	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	2614.4	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	2808.6	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	4144.3	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #8	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CNC=O)O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@H]1O	2728.3	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #8	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CNC=O)O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@H]1O	2631.1	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #8	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CNC=O)O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@H]1O	3570.2	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #9	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N(C(=O)CNC=O)[Si](C)(C)C	2594.4	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #9	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N(C(=O)CNC=O)[Si](C)(C)C	2659.0	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TMS,isomer #9	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N(C(=O)CNC=O)[Si](C)(C)C	3784.6	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CNC=O)[C@@H]1O[Si](C)(C)C	2720.1	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CNC=O)[C@@H]1O[Si](C)(C)C	2612.6	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CNC=O)[C@@H]1O[Si](C)(C)C	3315.3	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #10	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C	2656.8	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #10	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C	2736.3	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #10	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C	3565.0	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #11	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C	2681.2	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #11	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C	2744.9	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #11	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3422.9	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2585.6	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2643.9	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3466.8	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2726.9	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2692.9	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3590.5	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2615.6	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2784.4	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3789.4	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C)[C@@H]1O	2644.7	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C)[C@@H]1O	2643.2	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C)[C@@H]1O	3257.3	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C)[C@@H]1O	2776.8	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C)[C@@H]1O	2698.1	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C)[C@@H]1O	3390.6	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	2651.7	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	2735.3	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	3560.8	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N(C(=O)CNC=O)[Si](C)(C)C	2628.3	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N(C(=O)CNC=O)[Si](C)(C)C	2642.7	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N(C(=O)CNC=O)[Si](C)(C)C	3283.7	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #9	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CN(C=O)[Si](C)(C)C)O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@H]1O	2781.0	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #9	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CN(C=O)[Si](C)(C)C)O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@H]1O	2712.4	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TMS,isomer #9	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CN(C=O)[Si](C)(C)C)O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@H]1O	3370.0	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2635.1	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2624.1	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3059.7	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2757.3	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2686.7	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3195.2	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2659.2	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2728.8	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3326.6	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	2702.1	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	2717.4	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	3173.0	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C	2700.2	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C	2718.6	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C	3186.0	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,6TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2697.7	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,6TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2705.7	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,6TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3011.2	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CNC=O)[C@@H]1O	2827.2	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CNC=O)O[C@H](COP(=O)(O)O)[C@H]1O	2831.7	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](NC(=O)CNC=O)[C@H](O)[C@@H]1O	2913.5	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N(C(=O)CNC=O)[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O	2808.8	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N(C=O)CC(=O)N[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O	2932.4	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CNC=O)[C@@H]1O[Si](C)(C)C(C)(C)C	2983.0	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O	3194.3	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N(C=O)CC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3048.4	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CNC=O)[C@@H]1O	3098.3	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C)[C@@H]1O	2975.6	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[C@@H]1O	3102.8	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CNC=O)O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@H]1O	3103.7	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C	2973.2	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)O[C@H](COP(=O)(O)O)[C@H]1O	3109.6	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](NC(=O)CNC=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3152.3	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O	3068.7	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CNC=O)[C@@H]1O[Si](C)(C)C(C)(C)C	3276.7	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CNC=O)[C@@H]1O[Si](C)(C)C(C)(C)C	3182.5	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CNC=O)[C@@H]1O[Si](C)(C)C(C)(C)C	3891.5	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@H]1O	3375.7	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@H]1O	3292.7	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@H]1O	3916.5	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3232.2	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3365.4	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4145.6	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3291.6	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3211.6	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3725.3	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3414.0	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3276.9	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3822.2	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O	3290.2	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O	3330.0	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O	3976.3	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3186.9	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3255.0	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	4051.3	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3280.5	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3312.4	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	4165.6	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CNC=O)[C@@H]1O	3335.7	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CNC=O)[C@@H]1O	3175.2	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CNC=O)[C@@H]1O	3716.2	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C)[C@@H]1O	3246.3	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C)[C@@H]1O	3234.5	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C)[C@@H]1O	3823.5	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[C@@H]1O	3373.7	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[C@@H]1O	3289.2	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[C@@H]1O	3944.9	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3233.4	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3366.0	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	4143.6	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CNC=O)O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H]1O	3335.6	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CNC=O)O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H]1O	3178.8	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CNC=O)O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H]1O	3713.6	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C	3241.4	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C	3233.3	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C	3834.0	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CNC=O)[C@@H]1O[Si](C)(C)C(C)(C)C	3523.9	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CNC=O)[C@@H]1O[Si](C)(C)C(C)(C)C	3276.4	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CNC=O)[C@@H]1O[Si](C)(C)C(C)(C)C	3539.5	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3459.9	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3451.4	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3709.2	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3495.5	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3430.4	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3640.3	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3441.2	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3341.5	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3607.2	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3543.9	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3404.0	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3714.3	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3424.6	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3488.0	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3851.9	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C)[C@@H]1O	3478.8	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C)[C@@H]1O	3319.7	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C)[C@@H]1O	3485.8	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[C@@H]1O	3579.4	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[C@@H]1O	3389.5	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[C@@H]1O	3593.7	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3466.4	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3456.2	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3705.8	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@H]1N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C	3466.1	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@H]1N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C	3313.0	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@H]1N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C	3506.0	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H]1O	3573.7	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H]1O	3399.8	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H]1O	3586.4	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3653.3	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3397.1	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CNC=O)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3403.7	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3739.2	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3481.7	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3499.6	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3661.4	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3566.8	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3580.5	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3680.8	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3529.1	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3491.8	Standard polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@H]1N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3670.5	Semi standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@H]1N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3522.6	Standard non polar	33892256
5'-Phosphoribosyl-N-formylglycinamide,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@H]1N(C(=O)CN(C=O)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3507.4	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 5'-Phosphoribosyl-N-formylglycinamide GC-MS (Non-derivatized) - 70eV, Positive	splash10-0002-9330000000-47bd3a51454a22349c16	2016-09-22	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5'-Phosphoribosyl-N-formylglycinamide GC-MS (2 TMS) - 70eV, Positive	splash10-0089-5972200000-28cbe677e79c994d5692	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5'-Phosphoribosyl-N-formylglycinamide GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5'-Phosphoribosyl-N-formylglycinamide GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5'-Phosphoribosyl-N-formylglycinamide 10V, Positive-QTOF	splash10-0a4i-9121000000-70e7f7e392d67c9062d7	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5'-Phosphoribosyl-N-formylglycinamide 20V, Positive-QTOF	splash10-0a4i-9110000000-24b14d3360fd37fa0b5a	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5'-Phosphoribosyl-N-formylglycinamide 40V, Positive-QTOF	splash10-0a4i-9100000000-6c2f243f9e36f7267013	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5'-Phosphoribosyl-N-formylglycinamide 10V, Negative-QTOF	splash10-01r6-8914000000-411b5cf47e3e7e5511fd	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5'-Phosphoribosyl-N-formylglycinamide 20V, Negative-QTOF	splash10-004i-9200000000-fc9464d8ad7b3b1ac820	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5'-Phosphoribosyl-N-formylglycinamide 40V, Negative-QTOF	splash10-004i-9000000000-ccc93e5e04249a7f1425	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5'-Phosphoribosyl-N-formylglycinamide 10V, Positive-QTOF	splash10-014i-0079000000-0c457b0a6a5c25c65962	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5'-Phosphoribosyl-N-formylglycinamide 20V, Positive-QTOF	splash10-001i-2920000000-569fd550eacc61a8bd6c	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5'-Phosphoribosyl-N-formylglycinamide 40V, Positive-QTOF	splash10-0udi-2900000000-32e3418d15835aba1b7b	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5'-Phosphoribosyl-N-formylglycinamide 10V, Negative-QTOF	splash10-01t9-9036000000-b8480e9ce9f70df638e9	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5'-Phosphoribosyl-N-formylglycinamide 20V, Negative-QTOF	splash10-004i-9100000000-14698f4417bb19153972	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5'-Phosphoribosyl-N-formylglycinamide 40V, Negative-QTOF	splash10-004i-9000000000-e93ac01407977ed80740	2021-09-24	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)	2022-08-18	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	2022-08-18	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	2022-08-18	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	2022-08-18	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)	2022-08-18	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	2022-08-18	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)	2022-08-18	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	2022-08-18	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)	2022-08-18	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	2022-08-18	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)	2022-08-18	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	2022-08-18	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)	2022-08-18	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	2022-08-18	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)	2022-08-18	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	2022-08-18	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)	2022-08-18	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	2022-08-18	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)	2022-08-18	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	2022-08-18	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Name	SMPDB/PathBank	KEGG
Purine metabolism	Not Available
Adenosine Deaminase Deficiency		Not Available
Adenylosuccinate Lyase Deficiency		Not Available
Gout or Kelley-Seegmiller Syndrome		Not Available
Lesch-Nyhan Syndrome (LNS)		Not Available

Normal Concentrations

Not Available

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

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

5-P-RIBOSYL-N-FORMYLGLYCINEAMIDE

BiGG ID

43690

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

130805

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

FGAM

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Not Available

Enzymes

Enzyme Details

1. Trifunctional purine biosynthetic protein adenosine-3

General function:: Involved in catalytic activity
Specific function:: Not Available
Gene Name:: GART
Uniprot ID:: P22102
Molecular weight:: 107766.295

Reactions

10-Formyltetrahydrofolate + Glycineamideribotide → Tetrahydrofolic acid + 5'-Phosphoribosyl-N-formylglycinamide	details
Glycineamideribotide + 5,10-Methenyltetrahydrofolic acid + Water → 5'-Phosphoribosyl-N-formylglycinamide + Tetrahydrofolic acid	details

Enzyme Details

2. Phosphoribosylformylglycinamidine synthase

General function:: Involved in catalytic activity
Specific function:: Not Available
Gene Name:: PFAS
Uniprot ID:: O15067
Molecular weight:: 144733.165

Reactions

Adenosine triphosphate + 5'-Phosphoribosyl-N-formylglycinamide + L-Glutamine + Water → ADP + Phosphate + Phosphoribosylformylglycinamidine + L-Glutamic acid	details

Showing metabocard for 5'-Phosphoribosyl-N-formylglycinamide (HMDB0001308)

MOL for HMDB0001308 (5'-Phosphoribosyl-N-formylglycinamide)

3D MOL for HMDB0001308 (5'-Phosphoribosyl-N-formylglycinamide)

3D SDF for HMDB0001308 (5'-Phosphoribosyl-N-formylglycinamide)

3D-SDF for HMDB0001308 (5'-Phosphoribosyl-N-formylglycinamide)

PDB for HMDB0001308 (5'-Phosphoribosyl-N-formylglycinamide)

3D PDB for HMDB0001308 (5'-Phosphoribosyl-N-formylglycinamide)

SMILES for HMDB0001308 (5'-Phosphoribosyl-N-formylglycinamide)

INCHI for HMDB0001308 (5'-Phosphoribosyl-N-formylglycinamide)

Structure for HMDB0001308 (5'-Phosphoribosyl-N-formylglycinamide)

3D Structure for HMDB0001308 (5'-Phosphoribosyl-N-formylglycinamide)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes

Reactions

Reactions