MiMeDB: Showing metabocard for Fosfocytocin (MMDBc0021310)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 11:25:41 UTC

Update Date

2022-08-31 06:47:20 UTC

MiMeDB ID

MMDBc0021310

Metabolite Identification

Common Name

Fosfocytocin

Description

Fosfocytocin belongs to the class of organic compounds known as pyrimidine ribonucleoside diphosphates. These are pyrimidine ribonucleotides with diphosphate group linked to the ribose moiety. Based on a literature review very few articles have been published on Fosfocytocin.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152113252D          

 35 36  0  0  1  0            999 V2000
   -2.7777   -8.8346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4421   -8.0810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0175   -5.6678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3030   -5.2553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9838   -5.2553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4464   -5.6678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6983   -5.6678    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5982   -8.9209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4520   -5.3323    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0040   -5.9454    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5915   -6.6599    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7475   -7.4998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9337   -9.6746    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0831   -8.2534    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7319   -5.2553    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9271   -7.4135    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1609   -5.2553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6235   -4.5253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8245   -5.8592    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2325   -6.8323    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7319   -4.4303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4616   -5.9698    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2866   -4.5409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8576   -5.9698    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0326   -4.5409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5885   -5.6678    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2694   -5.6678    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7845   -6.4883    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1596   -4.8428    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8741   -5.2553    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    0.4451   -5.2553    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7415   -4.8440    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2489   -5.1188    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4533   -6.6373    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0723   -7.3010    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  4  3  1  0  0  0  0
  7  5  1  1  0  0  0
  8  1  1  0  0  0  0
  9  7  1  0  0  0  0
 10  9  1  0  0  0  0
 11 10  1  0  0  0  0
 13  8  2  0  0  0  0
 14  8  1  0  0  0  0
 14 12  2  0  0  0  0
 15  3  1  0  0  0  0
 15  6  1  0  0  0  0
 16  2  1  0  0  0  0
 11 16  1  1  0  0  0
 16 12  1  0  0  0  0
 17  6  2  0  0  0  0
  9 18  1  6  0  0  0
 10 19  1  6  0  0  0
 20 12  1  0  0  0  0
 21 15  1  0  0  0  0
 26  4  1  0  0  0  0
 27  5  1  0  0  0  0
 28  7  1  0  0  0  0
 28 11  1  0  0  0  0
 30 22  1  0  0  0  0
 30 23  2  0  0  0  0
 30 26  1  0  0  0  0
 30 29  1  0  0  0  0
 31 24  1  0  0  0  0
 31 25  2  0  0  0  0
 31 27  1  0  0  0  0
 31 29  1  0  0  0  0
  7 32  1  6  0  0  0
  9 33  1  1  0  0  0
 10 34  1  1  0  0  0
 11 35  1  6  0  0  0
M  END


  Mrv1652305152113252D          

 35 36  0  0  1  0            999 V2000
   -2.7777   -8.8346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4421   -8.0810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0175   -5.6678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3030   -5.2553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9838   -5.2553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4464   -5.6678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6983   -5.6678    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5982   -8.9209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4520   -5.3323    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0040   -5.9454    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5915   -6.6599    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7475   -7.4998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9337   -9.6746    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0831   -8.2534    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7319   -5.2553    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9271   -7.4135    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1609   -5.2553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6235   -4.5253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8245   -5.8592    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2325   -6.8323    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7319   -4.4303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4616   -5.9698    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2866   -4.5409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8576   -5.9698    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0326   -4.5409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5885   -5.6678    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2694   -5.6678    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7845   -6.4883    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1596   -4.8428    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8741   -5.2553    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    0.4451   -5.2553    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7415   -4.8440    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2489   -5.1188    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4533   -6.6373    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0723   -7.3010    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  4  3  1  0  0  0  0
  7  5  1  1  0  0  0
  8  1  1  0  0  0  0
  9  7  1  0  0  0  0
 10  9  1  0  0  0  0
 11 10  1  0  0  0  0
 13  8  2  0  0  0  0
 14  8  1  0  0  0  0
 14 12  2  0  0  0  0
 15  3  1  0  0  0  0
 15  6  1  0  0  0  0
 16  2  1  0  0  0  0
 11 16  1  1  0  0  0
 16 12  1  0  0  0  0
 17  6  2  0  0  0  0
  9 18  1  6  0  0  0
 10 19  1  6  0  0  0
 20 12  1  0  0  0  0
 21 15  1  0  0  0  0
 26  4  1  0  0  0  0
 27  5  1  0  0  0  0
 28  7  1  0  0  0  0
 28 11  1  0  0  0  0
 30 22  1  0  0  0  0
 30 23  2  0  0  0  0
 30 26  1  0  0  0  0
 30 29  1  0  0  0  0
 31 24  1  0  0  0  0
 31 25  2  0  0  0  0
 31 27  1  0  0  0  0
 31 29  1  0  0  0  0
  7 32  1  6  0  0  0
  9 33  1  1  0  0  0
 10 34  1  1  0  0  0
 11 35  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0021310

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@]1(COP(O)(=O)OP(O)(=O)OCCN(O)C=O)O[C@@]([H])(N2C=CC(=N)N=C2O)[C@]([H])(O)[C@]1([H])O

> <INCHI_IDENTIFIER>
InChI=1S/C12H20N4O13P2/c13-8-1-2-16(12(20)14-8)11-10(19)9(18)7(28-11)5-27-31(24,25)29-30(22,23)26-4-3-15(21)6-17/h1-2,6-7,9-11,18-19,21H,3-5H2,(H,22,23)(H,24,25)(H2,13,14,20)/t7-,9-,10-,11-/m1/s1

> <INCHI_KEY>
BWGMNVJUNKPELE-QCNRFFRDSA-N

> <FORMULA>
C12H20N4O13P2

> <MOLECULAR_WEIGHT>
490.255

> <EXACT_MASS>
490.050210716

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
40.40671857406255

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[({[(2R,3S,4R,5R)-3,4-dihydroxy-5-(2-hydroxy-4-imino-1,4-dihydropyrimidin-1-yl)oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy][2-(N-hydroxyformamido)ethoxy]phosphinic acid

> <ALOGPS_LOGP>
-1.43

> <JCHEM_LOGP>
-3.9167220052714162

> <ALOGPS_LOGS>
-1.85

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
2.554676444851374

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.7807523904116063

> <JCHEM_PKA_STRONGEST_BASIC>
3.349870948002279

> <JCHEM_POLAR_SURFACE_AREA>
252.19999999999993

> <JCHEM_REFRACTIVITY>
106.85309999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.97e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
{[(2R,3S,4R,5R)-3,4-dihydroxy-5-(2-hydroxy-4-iminopyrimidin-1-yl)oxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(2-(N-hydroxyformamido)ethoxy)phosphinic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAY-21         0                                  
HETATM    1  C   UNK     0      -5.185 -16.491   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.559 -15.084   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.499 -10.580   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.166  -9.810   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.836  -9.810   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.167 -10.580   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.170 -10.580   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -6.717 -16.652   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.577  -9.954   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -5.607 -11.098   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.837 -12.432   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -6.995 -14.000   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      -7.343 -18.059   0.000  0.00  0.00           N+0
HETATM   14  N   UNK     0      -7.622 -15.406   0.000  0.00  0.00           N+0
HETATM   15  N   UNK     0       8.833  -9.810   0.000  0.00  0.00           N+0
HETATM   16  N   UNK     0      -5.464 -13.839   0.000  0.00  0.00           N+0
HETATM   17  O   UNK     0      11.500  -9.810   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      -4.897  -8.447   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -7.139 -10.937   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -7.901 -12.754   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       8.833  -8.270   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       2.728 -11.144   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       4.268  -8.476   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       1.601 -11.144   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       0.061  -8.476   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       4.832 -10.580   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      -0.503 -10.580   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      -3.331 -12.112   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       2.165  -9.040   0.000  0.00  0.00           O+0
HETATM   30  P   UNK     0       3.498  -9.810   0.000  0.00  0.00           P+0
HETATM   31  P   UNK     0       0.831  -9.810   0.000  0.00  0.00           P+0
HETATM   32  H   UNK     0      -3.251  -9.042   0.000  0.00  0.00           H+0
HETATM   33  H   UNK     0      -6.065  -9.555   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0      -6.446 -12.390   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0      -3.868 -13.629   0.000  0.00  0.00           H+0
CONECT    1    2    8                                                       
CONECT    2    1   16                                                       
CONECT    3    4   15                                                       
CONECT    4    3   26                                                       
CONECT    5    7   27                                                       
CONECT    6   15   17                                                       
CONECT    7    5    9   28   32                                             
CONECT    8    1   13   14                                                  
CONECT    9    7   10   18   33                                             
CONECT   10    9   11   19   34                                             
CONECT   11   10   16   28   35                                             
CONECT   12   14   16   20                                                  
CONECT   13    8                                                            
CONECT   14    8   12                                                       
CONECT   15    3    6   21                                                  
CONECT   16    2   11   12                                                  
CONECT   17    6                                                            
CONECT   18    9                                                            
CONECT   19   10                                                            
CONECT   20   12                                                            
CONECT   21   15                                                            
CONECT   22   30                                                            
CONECT   23   30                                                            
CONECT   24   31                                                            
CONECT   25   31                                                            
CONECT   26    4   30                                                       
CONECT   27    5   31                                                       
CONECT   28    7   11                                                       
CONECT   29   30   31                                                       
CONECT   30   22   23   26   29                                             
CONECT   31   24   25   27   29                                             
CONECT   32    7                                                            
CONECT   33    9                                                            
CONECT   34   10                                                            
CONECT   35   11                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   72    0
END

Synonyms

Not Available

Chemical Formula

C₁₂H₂₀N₄O₁₃P₂

Average Molecular Weight

490.255

Monoisotopic Molecular Weight

490.050210716

IUPAC Name

[({[(2R,3S,4R,5R)-3,4-dihydroxy-5-(2-hydroxy-4-imino-1,4-dihydropyrimidin-1-yl)oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy][2-(N-hydroxyformamido)ethoxy]phosphinic acid

Traditional Name

{[(2R,3S,4R,5R)-3,4-dihydroxy-5-(2-hydroxy-4-iminopyrimidin-1-yl)oxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(2-(N-hydroxyformamido)ethoxy)phosphinic acid

CAS Registry Number

Not Available

SMILES

[H][C@]1(COP(O)(=O)OP(O)(=O)OCCN(O)C=O)O[C@@]([H])(N2C=CC(=N)N=C2O)[C@]([H])(O)[C@]1([H])O

InChI Identifier

InChI=1S/C12H20N4O13P2/c13-8-1-2-16(12(20)14-8)11-10(19)9(18)7(28-11)5-27-31(24,25)29-30(22,23)26-4-3-15(21)6-17/h1-2,6-7,9-11,18-19,21H,3-5H2,(H,22,23)(H,24,25)(H2,13,14,20)/t7-,9-,10-,11-/m1/s1

InChI Key

BWGMNVJUNKPELE-QCNRFFRDSA-N

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleotides

Sub Class

Pyrimidine ribonucleotides

Direct Parent

Pyrimidine ribonucleoside diphosphates

Alternative Parents

Substituents

Pyrimidine ribonucleoside diphosphate
Pentose-5-phosphate
Pentose phosphate
N-glycosyl compound
Glycosyl compound
Pentose monosaccharide
Organic pyrophosphate
Monosaccharide phosphate
Phosphoethanolamine
Monoalkyl phosphate
Pyrimidone
Aminopyrimidine
Imidolactam
Alkyl phosphate
Pyrimidine
Phosphoric acid ester
Organic phosphoric acid derivative
Monosaccharide
Hydropyrimidine
Heteroaromatic compound
Tetrahydrofuran
Secondary alcohol
Hydroxamic acid
Amino acid or derivatives
1,2-diol
Oxacycle
Azacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Primary amine
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	6.97 g/L	ALOGPS
logP	-1.4	ALOGPS
logP	-3.9	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	1.78	ChemAxon
pKa (Strongest Basic)	3.35	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	252.2 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	106.85 m³·mol⁻¹	ChemAxon
Polarizability	40.41 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

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

Proteins

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Not Available

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Related Health Condition	Evidence Type	Measured in Matrix	Data Source	Reference

Microbial Sources

Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
	Proteobacteria	2	Human	Metabolic reconstruction

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference	Details

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

C00017576

Chemspider ID

169502

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

195506

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for Fosfocytocin (MMDBc0021310)

MOL for #<Metabolite:0x000055b76de4d250>

3D MOL for #<Metabolite:0x000055b76de4d250>

3D SDF for #<Metabolite:0x000055b76de4d250>

3D-SDF for #<Metabolite:0x000055b76de4d250>

PDB for #<Metabolite:0x000055b76de4d250>

3D PDB for #<Metabolite:0x000055b76de4d250>

SMILES for #<Metabolite:0x000055b76de4d250>

INCHI for #<Metabolite:0x000055b76de4d250>

Structure for #<Metabolite:0x000055b76de4d250>

3D Structure for #<Metabolite:0x000055b76de4d250>