MiMeDB: Showing metabocard for N(2)-(1-hydroxy-2-oxoethyl)-GDP (MMDBc0056169)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2022-06-17 20:18:39 UTC

Update Date

2022-08-12 20:09:36 UTC

Metabolite ID

MMDBc0056169

Metabolite Identification

Common Name

N(2)-(1-hydroxy-2-oxoethyl)-GDP

Description

9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-({[hydroxy(phosphonatooxy)phosphoryl]oxy}methyl)oxolan-2-yl]-2-[(1-hydroxy-2-oxoethyl)imino]-3,9-dihydro-2H-purin-6-olate belongs to the class of organic compounds known as purine ribonucleoside diphosphates. These are purine ribobucleotides with diphosphate group linked to the ribose moiety. Based on a literature review very few articles have been published on 9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-({[hydroxy(phosphonatooxy)phosphoryl]oxy}methyl)oxolan-2-yl]-2-[(1-hydroxy-2-oxoethyl)imino]-3,9-dihydro-2H-purin-6-olate.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652306172222182D          

 37 39  0  0  1  0            999 V2000
    4.2135   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8505   -3.7149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1831   -3.2299    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4990   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984   -3.4849    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0865   -2.8174    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6411   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984   -2.1500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0701   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -0.0305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -1.5229    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -1.5229    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -0.2854    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -1.3654    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279   -1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -0.2854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -4.2695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9115   -2.8174    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.9521    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -2.9267   -7.1462    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -3.8334   -6.4119    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -2.1924   -6.2394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9166   -4.3528    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9468   -5.6877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7643   -4.5353    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1831   -2.4049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0991   -5.5052    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0129   -6.3257    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4317   -5.0203    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0540   -4.0448    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -1.9354    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4164   -3.6139    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4610   -2.0824    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9818   -1.5666    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  2  1  1  0  0  0
  5  1  1  0  0  0  0
  7  4  1  0  0  0  0
  8  7  1  0  0  0  0
  9  6  2  0  0  0  0
 10  6  1  0  0  0  0
 11  8  1  0  0  0  0
 13  3  2  0  0  0  0
 13  6  1  0  0  0  0
 14  5  1  4  0  0  0
 14 12  2  0  0  0  0
 15  9  1  0  0  0  0
 15 12  1  0  0  0  0
 16 10  2  0  0  0  0
 16 12  1  0  0  0  0
 17  3  1  0  0  0  0
 17  9  1  0  0  0  0
 11 17  1  1  0  0  0
 18  1  2  0  0  0  0
 19  5  1  0  0  0  0
  7 20  1  6  0  0  0
  8 21  1  6  0  0  0
 22 10  1  0  0  0  0
 28  2  1  0  0  0  0
 29  4  1  0  0  0  0
 29 11  1  0  0  0  0
 31 23  1  0  0  0  0
 31 24  1  0  0  0  0
 31 25  2  0  0  0  0
 31 30  1  0  0  0  0
 32 26  1  0  0  0  0
 32 27  2  0  0  0  0
 32 28  1  0  0  0  0
 32 30  1  0  0  0  0
  4 33  1  6  0  0  0
 34  5  1  0  0  0  0
  7 35  1  1  0  0  0
  8 36  1  1  0  0  0
 11 37  1  6  0  0  0
M  CHG  3  22  -1  23  -1  24  -1
M  END


  Mrv1652306172222182D          

 37 39  0  0  1  0            999 V2000
    4.2135   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8505   -3.7149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1831   -3.2299    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4990   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984   -3.4849    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0865   -2.8174    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6411   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984   -2.1500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0701   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -0.0305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -1.5229    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -1.5229    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -0.2854    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -1.3654    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279   -1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -0.2854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -4.2695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9115   -2.8174    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.9521    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -2.9267   -7.1462    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -3.8334   -6.4119    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -2.1924   -6.2394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9166   -4.3528    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9468   -5.6877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7643   -4.5353    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1831   -2.4049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0991   -5.5052    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0129   -6.3257    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4317   -5.0203    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0540   -4.0448    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -1.9354    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4164   -3.6139    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4610   -2.0824    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9818   -1.5666    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  2  1  1  0  0  0
  5  1  1  0  0  0  0
  7  4  1  0  0  0  0
  8  7  1  0  0  0  0
  9  6  2  0  0  0  0
 10  6  1  0  0  0  0
 11  8  1  0  0  0  0
 13  3  2  0  0  0  0
 13  6  1  0  0  0  0
 14  5  1  4  0  0  0
 14 12  2  0  0  0  0
 15  9  1  0  0  0  0
 15 12  1  0  0  0  0
 16 10  2  0  0  0  0
 16 12  1  0  0  0  0
 17  3  1  0  0  0  0
 17  9  1  0  0  0  0
 11 17  1  1  0  0  0
 18  1  2  0  0  0  0
 19  5  1  0  0  0  0
  7 20  1  6  0  0  0
  8 21  1  6  0  0  0
 22 10  1  0  0  0  0
 28  2  1  0  0  0  0
 29  4  1  0  0  0  0
 29 11  1  0  0  0  0
 31 23  1  0  0  0  0
 31 24  1  0  0  0  0
 31 25  2  0  0  0  0
 31 30  1  0  0  0  0
 32 26  1  0  0  0  0
 32 27  2  0  0  0  0
 32 28  1  0  0  0  0
 32 30  1  0  0  0  0
  4 33  1  6  0  0  0
 34  5  1  0  0  0  0
  7 35  1  1  0  0  0
  8 36  1  1  0  0  0
 11 37  1  6  0  0  0
M  CHG  3  22  -1  23  -1  24  -1
M  END
> <DATABASE_ID>
MMDBc0056169

> <DATABASE_NAME>
MIME

> <SMILES>
[H]C(O)(C=O)N=C1NC2=C(N=CN2[C@]2([H])O[C@]([H])(COP(O)(=O)OP([O-])([O-])=O)[C@@]([H])(O)[C@@]2([H])O)C([O-])=N1

> <INCHI_IDENTIFIER>
InChI=1S/C12H17N5O13P2/c18-1-5(19)14-12-15-9-6(10(22)16-12)13-3-17(9)11-8(21)7(20)4(29-11)2-28-32(26,27)30-31(23,24)25/h1,3-5,7-8,11,19-21H,2H2,(H,26,27)(H2,23,24,25)(H2,14,15,16,22)/p-3/t4-,5?,7-,8-,11-/m1/s1

> <INCHI_KEY>
QDSKEQBPIYYJRK-VXSOYKKHSA-K

> <FORMULA>
C12H14N5O13P2

> <MOLECULAR_WEIGHT>
498.215

> <EXACT_MASS>
498.007980267

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
39.73387120663648

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
-3

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-({[hydroxy(phosphonooxy)phosphoryl]oxy}methyl)oxolan-2-yl]-2-[(1-hydroxy-2-oxoethyl)imino]-3,9-dihydro-2H-purin-6-olate

> <JCHEM_LOGP>
-4.475322889686381

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-3

> <JCHEM_PKA>
2.783805198611709

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.743425690481418

> <JCHEM_PKA_STRONGEST_BASIC>
3.3947011810149412

> <JCHEM_POLAR_SURFACE_AREA>
283.57000000000005

> <JCHEM_REFRACTIVITY>
106.09429999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-({[hydroxy(phosphonooxy)phosphoryl]oxy}methyl)oxolan-2-yl]-2-[(1-hydroxy-2-oxoethyl)imino]-3H-purin-6-olate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-JUN-22         0                                  
HETATM    1  C   UNK     0       7.865  -2.843   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.454  -6.934   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.173  -1.303   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.208  -6.029   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.531  -2.073   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.197  -0.533   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.744  -6.505   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.161  -5.259   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.197  -2.073   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.530   0.237   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.744  -4.013   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.864  -2.073   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      -0.268  -0.057   0.000  0.00  0.00           N+0
HETATM   14  N   UNK     0       5.198  -2.843   0.000  0.00  0.00           N+0
HETATM   15  N   UNK     0       2.530  -2.843   0.000  0.00  0.00           N+0
HETATM   16  N   UNK     0       3.864  -0.533   0.000  0.00  0.00           N+0
HETATM   17  N   UNK     0      -0.268  -2.549   0.000  0.00  0.00           N+0
HETATM   18  O   UNK     0       9.199  -2.073   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       6.531  -0.533   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -0.268  -7.970   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       1.701  -5.259   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       2.530   1.777   0.000  0.00  0.00           O-1
HETATM   23  O   UNK     0      -5.463 -13.339   0.000  0.00  0.00           O-1
HETATM   24  O   UNK     0      -7.156 -11.969   0.000  0.00  0.00           O-1
HETATM   25  O   UNK     0      -4.093 -11.647   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      -5.444  -8.125   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      -3.634 -10.617   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      -3.293  -8.466   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -2.208  -4.489   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -5.785 -10.276   0.000  0.00  0.00           O+0
HETATM   31  P   UNK     0      -5.624 -11.808   0.000  0.00  0.00           P+0
HETATM   32  P   UNK     0      -4.539  -9.371   0.000  0.00  0.00           P+0
HETATM   33  H   UNK     0      -1.967  -7.550   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0       6.531  -3.613   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.777  -6.746   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.861  -3.887   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0      -1.833  -2.924   0.000  0.00  0.00           H+0
CONECT    1    5   18                                                       
CONECT    2    4   28                                                       
CONECT    3   13   17                                                       
CONECT    4    2    7   29   33                                             
CONECT    5    1   14   19   34                                             
CONECT    6    9   10   13                                                  
CONECT    7    4    8   20   35                                             
CONECT    8    7   11   21   36                                             
CONECT    9    6   15   17                                                  
CONECT   10    6   16   22                                                  
CONECT   11    8   17   29   37                                             
CONECT   12   14   15   16                                                  
CONECT   13    3    6                                                       
CONECT   14    5   12                                                       
CONECT   15    9   12                                                       
CONECT   16   10   12                                                       
CONECT   17    3    9   11                                                  
CONECT   18    1                                                            
CONECT   19    5                                                            
CONECT   20    7                                                            
CONECT   21    8                                                            
CONECT   22   10                                                            
CONECT   23   31                                                            
CONECT   24   31                                                            
CONECT   25   31                                                            
CONECT   26   32                                                            
CONECT   27   32                                                            
CONECT   28    2   32                                                       
CONECT   29    4   11                                                       
CONECT   30   31   32                                                       
CONECT   31   23   24   25   30                                             
CONECT   32   26   27   28   30                                             
CONECT   33    4                                                            
CONECT   34    5                                                            
CONECT   35    7                                                            
CONECT   36    8                                                            
CONECT   37   11                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   78    0
END

Synonyms

Value	Source
9-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-({[hydroxy(phosphonatooxy)phosphoryl]oxy}methyl)oxolan-2-yl]-2-[(1-hydroxy-2-oxoethyl)imino]-3,9-dihydro-2H-purin-6-olic acid	Generator

Molecular Formula

C₁₂H₁₄N₅O₁₃P₂

Average Mass

498.215

Monoisotopic Mass

498.007980267

IUPAC Name

9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-({[hydroxy(phosphonooxy)phosphoryl]oxy}methyl)oxolan-2-yl]-2-[(1-hydroxy-2-oxoethyl)imino]-3,9-dihydro-2H-purin-6-olate

Traditional Name

9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-({[hydroxy(phosphonooxy)phosphoryl]oxy}methyl)oxolan-2-yl]-2-[(1-hydroxy-2-oxoethyl)imino]-3H-purin-6-olate

CAS Registry Number

Not Available

SMILES

[H]C(O)(C=O)N=C1NC2=C(N=CN2[C@]2([H])O[C@]([H])(COP(O)(=O)OP([O-])([O-])=O)[C@@]([H])(O)[C@@]2([H])O)C([O-])=N1

InChI Identifier

InChI=1S/C12H17N5O13P2/c18-1-5(19)14-12-15-9-6(10(22)16-12)13-3-17(9)11-8(21)7(20)4(29-11)2-28-32(26,27)30-31(23,24)25/h1,3-5,7-8,11,19-21H,2H2,(H,26,27)(H2,23,24,25)(H2,14,15,16,22)/p-3/t4-,5?,7-,8-,11-/m1/s1

InChI Key

QDSKEQBPIYYJRK-VXSOYKKHSA-K

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as purine ribonucleoside diphosphates. These are purine ribobucleotides with diphosphate group linked to the ribose moiety.

Kingdom

Organic compounds

Super Class

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Sub Class

Purine ribonucleotides

Direct Parent

Purine ribonucleoside diphosphates

Alternative Parents

Substituents

Purine ribonucleoside diphosphate
Purine ribonucleoside monophosphate
Pentose-5-phosphate
Pentose phosphate
N-glycosyl compound
Glycosyl compound
Pentose monosaccharide
Organic pyrophosphate
Monosaccharide phosphate
Purine
Imidazopyrimidine
Monoalkyl phosphate
Alkyl phosphate
Pyrimidine
Phosphoric acid ester
Organic phosphoric acid derivative
N-substituted imidazole
Monosaccharide
Heteroaromatic compound
Tetrahydrofuran
Imidazole
Azole
Secondary alcohol
1,2-diol
Oxacycle
Azacycle
Organoheterocyclic compound
Alkanolamine
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Aldehyde
Alcohol
Organic anion
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
logP	-4.5	ChemAxon
pKa (Strongest Acidic)	1.74	ChemAxon
pKa (Strongest Basic)	3.39	ChemAxon
Physiological Charge	-3	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	283.57 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	106.09 m³·mol⁻¹	ChemAxon
Polarizability	39.73 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Spectra

Not Available

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria	Proteobacteria	28	Human ; Human feces
Bacteria	Firmicutes	14	Human ; Cattle

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

134716613

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Bansal P, Morgat A, Axelsen KB, Muthukrishnan V, Coudert E, Aimo L, Hyka-Nouspikel N, Gasteiger E, Kerhornou A, Neto TB, Pozzato M, Blatter MC, Ignatchenko A, Redaschi N, Bridge A: Rhea, the reaction knowledgebase in 2022. Nucleic Acids Res. 2022 Jan 7;50(D1):D693-D700. doi: 10.1093/nar/gkab1016. [PubMed:34755880 ]

Showing metabocard for N(2)-(1-hydroxy-2-oxoethyl)-GDP (MMDBc0056169)

MOL for #<Metabolite:0x00007fecf4033c50>

3D MOL for #<Metabolite:0x00007fecf4033c50>

3D SDF for #<Metabolite:0x00007fecf4033c50>

3D-SDF for #<Metabolite:0x00007fecf4033c50>

PDB for #<Metabolite:0x00007fecf4033c50>

3D PDB for #<Metabolite:0x00007fecf4033c50>

SMILES for #<Metabolite:0x00007fecf4033c50>

INCHI for #<Metabolite:0x00007fecf4033c50>

Structure for #<Metabolite:0x00007fecf4033c50>

3D Structure for #<Metabolite:0x00007fecf4033c50>