MiMeDB: Showing metabocard for 12alpha,13alpha-dihydroxyfumitremorgin C (MMDBc0055167)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2022-06-17 19:45:16 UTC

Update Date

2022-08-12 20:09:15 UTC

Metabolite ID

MMDBc0055167

Metabolite Identification

Common Name

12alpha,13alpha-dihydroxyfumitremorgin C

Description

12,13-dihydroxyfumitremorgin C belongs to the class of organic compounds known as beta carbolines. Beta carbolines are compounds containing a 9H-pyrido[3,4-b]indole moiety. Based on a literature review a small amount of articles have been published on 12,13-dihydroxyfumitremorgin C.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652306172221452D          

 33 37  0  0  1  0            999 V2000
    2.3189   -0.6027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2088    0.5153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4749    1.9560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3352    2.8644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9545    2.1325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8893    3.4561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0651    3.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7567    3.4526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7957    0.7270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8265    2.0285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4411    0.2132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2700    2.7242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6216    2.7967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0023    2.0648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1407    2.2684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9179    1.5429    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8078    2.6608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6856    1.8450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1624    3.1746    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5047    1.7546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7492    3.3864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3947    2.8726    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4238    1.4766    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0185    3.0843    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2724    2.0567    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2846    3.9905    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3825    0.9387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8714    4.2023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5169    3.6885    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0942    2.6879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3476    1.4697    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5634    1.0291    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9301    3.4767    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
  7  6  2  0  0  0  0
  8  4  1  0  0  0  0
 11  1  1  0  0  0  0
 11  2  1  0  0  0  0
 11  9  2  0  0  0  0
 12  6  1  0  0  0  0
 12 10  2  0  0  0  0
 13  7  1  0  0  0  0
 14 10  1  0  0  0  0
 14 13  2  0  0  0  0
 15  5  1  0  0  0  0
 16  9  1  6  0  0  0
 17 13  1  0  0  0  0
 18 16  1  0  0  0  0
 18 17  2  0  0  0  0
 19 17  1  0  0  0  0
 20 15  1  0  0  0  0
 22 19  1  0  0  0  0
 22 21  1  0  0  0  0
 23 14  1  0  0  0  0
 23 18  1  0  0  0  0
 24  8  1  0  0  0  0
 24 15  1  0  0  0  0
 24 21  1  0  0  0  0
 25 16  1  0  0  0  0
 25 20  1  0  0  0  0
 25 22  1  0  0  0  0
 19 26  1  1  0  0  0
 27 20  2  0  0  0  0
 28 21  2  0  0  0  0
 22 29  1  1  0  0  0
 30  3  1  0  0  0  0
 30 12  1  0  0  0  0
 15 31  1  1  0  0  0
 16 32  1  1  0  0  0
 19 33  1  6  0  0  0
M  END


  Mrv1652306172221452D          

 33 37  0  0  1  0            999 V2000
    2.3189   -0.6027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2088    0.5153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4749    1.9560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3352    2.8644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9545    2.1325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8893    3.4561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0651    3.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7567    3.4526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7957    0.7270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8265    2.0285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4411    0.2132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2700    2.7242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6216    2.7967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0023    2.0648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1407    2.2684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9179    1.5429    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8078    2.6608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6856    1.8450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1624    3.1746    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5047    1.7546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7492    3.3864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3947    2.8726    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4238    1.4766    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0185    3.0843    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2724    2.0567    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2846    3.9905    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3825    0.9387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8714    4.2023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5169    3.6885    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0942    2.6879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3476    1.4697    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5634    1.0291    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9301    3.4767    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
  7  6  2  0  0  0  0
  8  4  1  0  0  0  0
 11  1  1  0  0  0  0
 11  2  1  0  0  0  0
 11  9  2  0  0  0  0
 12  6  1  0  0  0  0
 12 10  2  0  0  0  0
 13  7  1  0  0  0  0
 14 10  1  0  0  0  0
 14 13  2  0  0  0  0
 15  5  1  0  0  0  0
 16  9  1  6  0  0  0
 17 13  1  0  0  0  0
 18 16  1  0  0  0  0
 18 17  2  0  0  0  0
 19 17  1  0  0  0  0
 20 15  1  0  0  0  0
 22 19  1  0  0  0  0
 22 21  1  0  0  0  0
 23 14  1  0  0  0  0
 23 18  1  0  0  0  0
 24  8  1  0  0  0  0
 24 15  1  0  0  0  0
 24 21  1  0  0  0  0
 25 16  1  0  0  0  0
 25 20  1  0  0  0  0
 25 22  1  0  0  0  0
 19 26  1  1  0  0  0
 27 20  2  0  0  0  0
 28 21  2  0  0  0  0
 22 29  1  1  0  0  0
 30  3  1  0  0  0  0
 30 12  1  0  0  0  0
 15 31  1  1  0  0  0
 16 32  1  1  0  0  0
 19 33  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0055167

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]12CCCN1C(=O)[C@@]1(O)N(C2=O)[C@@]([H])(C=C(C)C)C2=C(C3=C(N2)C=C(OC)C=C3)[C@]1([H])O

> <INCHI_IDENTIFIER>
InChI=1S/C22H25N3O5/c1-11(2)9-16-18-17(13-7-6-12(30-3)10-14(13)23-18)19(26)22(29)21(28)24-8-4-5-15(24)20(27)25(16)22/h6-7,9-10,15-16,19,23,26,29H,4-5,8H2,1-3H3/t15-,16-,19-,22+/m0/s1

> <INCHI_KEY>
CPHRCQUGNAGVIB-FWJAZRMLSA-N

> <FORMULA>
C22H25N3O5

> <MOLECULAR_WEIGHT>
411.458

> <EXACT_MASS>
411.179420917

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
43.95072654905872

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,12S,15S)-1,2-dihydroxy-7-methoxy-12-(2-methylprop-1-en-1-yl)-10,13,19-triazapentacyclo[11.7.0.0^{3,11}.0^{4,9}.0^{15,19}]icosa-3(11),4,6,8-tetraene-14,20-dione

> <JCHEM_LOGP>
1.1564713573333343

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.517653698745935

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.132294938117656

> <JCHEM_PKA_STRONGEST_BASIC>
-3.787766808953516

> <JCHEM_POLAR_SURFACE_AREA>
106.10000000000001

> <JCHEM_REFRACTIVITY>
109.31970000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,12S,15S)-1,2-dihydroxy-7-methoxy-12-(2-methylprop-1-en-1-yl)-10,13,19-triazapentacyclo[11.7.0.0^{3,11}.0^{4,9}.0^{15,19}]icosa-3(11),4,6,8-tetraene-14,20-dione

> <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       4.329  -1.125   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.990   0.962   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.086   3.651   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.492   5.347   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.782   3.981   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.127   6.451   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.588   6.519   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.413   6.445   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.352   1.357   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.009   3.787   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.557   0.398   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.837   5.085   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.760   5.221   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.471   3.854   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.263   4.234   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.580   2.880   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.241   4.967   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.013   3.444   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.036   5.926   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.942   3.275   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.398   6.321   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.603   5.362   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0       6.391   2.756   0.000  0.00  0.00           N+0
HETATM   24  N   UNK     0      -0.035   5.757   0.000  0.00  0.00           N+0
HETATM   25  N   UNK     0       2.375   3.839   0.000  0.00  0.00           N+0
HETATM   26  O   UNK     0       4.265   7.449   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       0.714   1.752   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       1.627   7.844   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       2.832   6.885   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      11.376   5.017   0.000  0.00  0.00           O+0
HETATM   31  H   UNK     0      -0.649   2.743   0.000  0.00  0.00           H+0
HETATM   32  H   UNK     0       4.785   1.921   0.000  0.00  0.00           H+0
HETATM   33  H   UNK     0       5.469   6.490   0.000  0.00  0.00           H+0
CONECT    1   11                                                            
CONECT    2   11                                                            
CONECT    3   30                                                            
CONECT    4    5    8                                                       
CONECT    5    4   15                                                       
CONECT    6    7   12                                                       
CONECT    7    6   13                                                       
CONECT    8    4   24                                                       
CONECT    9   11   16                                                       
CONECT   10   12   14                                                       
CONECT   11    1    2    9                                                  
CONECT   12    6   10   30                                                  
CONECT   13    7   14   17                                                  
CONECT   14   10   13   23                                                  
CONECT   15    5   20   24   31                                             
CONECT   16    9   18   25   32                                             
CONECT   17   13   18   19                                                  
CONECT   18   16   17   23                                                  
CONECT   19   17   22   26   33                                             
CONECT   20   15   25   27                                                  
CONECT   21   22   24   28                                                  
CONECT   22   19   21   25   29                                             
CONECT   23   14   18                                                       
CONECT   24    8   15   21                                                  
CONECT   25   16   20   22                                                  
CONECT   26   19                                                            
CONECT   27   20                                                            
CONECT   28   21                                                            
CONECT   29   22                                                            
CONECT   30    3   12                                                       
CONECT   31   15                                                            
CONECT   32   16                                                            
CONECT   33   19                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   74    0
END

Synonyms

Value	Source
12alpha,13alpha-Dihydroxyfumitremorgin C	ChEBI
12a,13a-Dihydroxyfumitremorgin C	Generator
12Α,13α-dihydroxyfumitremorgin C	Generator

Molecular Formula

C₂₂H₂₅N₃O₅

Average Mass

411.458

Monoisotopic Mass

411.179420917

IUPAC Name

(1R,2S,12S,15S)-1,2-dihydroxy-7-methoxy-12-(2-methylprop-1-en-1-yl)-10,13,19-triazapentacyclo[11.7.0.0^{3,11}.0^{4,9}.0^{15,19}]icosa-3(11),4,6,8-tetraene-14,20-dione

Traditional Name

(1R,2S,12S,15S)-1,2-dihydroxy-7-methoxy-12-(2-methylprop-1-en-1-yl)-10,13,19-triazapentacyclo[11.7.0.0^{3,11}.0^{4,9}.0^{15,19}]icosa-3(11),4,6,8-tetraene-14,20-dione

CAS Registry Number

Not Available

SMILES

[H][C@@]12CCCN1C(=O)[C@@]1(O)N(C2=O)[C@@]([H])(C=C(C)C)C2=C(C3=C(N2)C=C(OC)C=C3)[C@]1([H])O

InChI Identifier

InChI=1S/C22H25N3O5/c1-11(2)9-16-18-17(13-7-6-12(30-3)10-14(13)23-18)19(26)22(29)21(28)24-8-4-5-15(24)20(27)25(16)22/h6-7,9-10,15-16,19,23,26,29H,4-5,8H2,1-3H3/t15-,16-,19-,22+/m0/s1

InChI Key

CPHRCQUGNAGVIB-FWJAZRMLSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as beta carbolines. Beta carbolines are compounds containing a 9H-pyrido[3,4-b]indole moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Pyridoindoles

Direct Parent

Beta carbolines

Alternative Parents

Substituents

Beta-carboline
Alpha-amino acid or derivatives
3-alkylindole
Indole
Anisole
Dioxopiperazine
2,5-dioxopiperazine
Alkyl aryl ether
N-alkylpiperazine
1,4-diazinane
Benzenoid
Piperazine
Heteroaromatic compound
Tertiary carboxylic acid amide
Pyrrolidine
Pyrrole
Carboxamide group
Secondary alcohol
Lactam
Alkanolamine
Ether
Azacycle
Carboxylic acid derivative
Hydrocarbon derivative
Alcohol
Carbonyl group
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

aromatic ether (CHEBI:72764 )
organic heteropentacyclic compound (CHEBI:72764 )
indole alkaloid (CHEBI:72764 )
diol (CHEBI:72764 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
logP	1.16	ChemAxon
pKa (Strongest Acidic)	10.13	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	106.1 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	109.32 m³·mol⁻¹	ChemAxon
Polarizability	43.95 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-09	View Spectrum
MS	Mass Spectrum (Electron Ionization)	Not Available	2022-08-06	View Spectrum

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

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference
MMDBr0015464	Fumitremorgin C	12alpha,13alpha-dihydroxyfumitremorgin C	Fumitremorgin C monooxygenase	Oxygenation	RHEA	34755880
MMDBr0015465	12alpha,13alpha-dihydroxyfumitremorgin C	diphosphate	12-alpha,13-alpha-dihydroxyfumitremorgin C prenyltransferase	Synthesis; Reverse C-prenylation of phenalenone	RHEA	34755880

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
Eukaryota/Fungi	Ascomycota	3	Human feces

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

C00038128

Chemspider ID

8177229

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10001648

PDB ID

Not Available

ChEBI ID

72764

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 12alpha,13alpha-dihydroxyfumitremorgin C (MMDBc0055167)

MOL for #<Metabolite:0x00007fa4b01c0a78>

3D MOL for #<Metabolite:0x00007fa4b01c0a78>

3D SDF for #<Metabolite:0x00007fa4b01c0a78>

3D-SDF for #<Metabolite:0x00007fa4b01c0a78>

PDB for #<Metabolite:0x00007fa4b01c0a78>

3D PDB for #<Metabolite:0x00007fa4b01c0a78>

SMILES for #<Metabolite:0x00007fa4b01c0a78>

INCHI for #<Metabolite:0x00007fa4b01c0a78>

Structure for #<Metabolite:0x00007fa4b01c0a78>

3D Structure for #<Metabolite:0x00007fa4b01c0a78>