MiMeDB: Showing metabocard for Versicolactone A (MMDBc0006113)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 23:27:21 UTC

Update Date

2022-08-31 06:24:53 UTC

Metabolite ID

MMDBc0006113

Metabolite Identification

Common Name

Versicolactone A

Description

CHEMBL4449926 belongs to the class of organic compounds known as phenylpropanes. These are organic compounds containing a phenylpropane moiety. Based on a literature review very few articles have been published on CHEMBL4449926.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152101272D          

 31 33  0  0  1  0            999 V2000
    0.1211    7.0964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0968    2.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2333    3.3448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8321    3.8594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7429    1.5082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3014    2.8672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5275    1.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0860    3.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0871    4.6440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1760    5.6987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4731    4.3010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7702    2.9033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4310    6.4833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0251    3.6879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1298    2.0602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7280    5.0856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6991    2.5701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5350    5.2571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6548    1.8053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9097    1.0206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7347    1.0206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8743    2.9033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3222    2.2902    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2379    6.6549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7900    6.0418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4248    0.3532    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2197    0.3532    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1292    3.6879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4837    2.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6812    2.7317    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9897    1.8053    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  5  1  0  0  0  0
  8  6  2  0  0  0  0
  9  4  2  0  0  0  0
 13  1  1  0  0  0  0
 13 10  1  0  0  0  0
 14  4  1  0  0  0  0
 14 11  2  0  0  0  0
 14 12  1  0  0  0  0
 15  5  2  0  0  0  0
 15  6  1  0  0  0  0
 16 10  1  0  0  0  0
 16 11  1  0  0  0  0
 17  7  2  0  0  0  0
 17  8  1  0  0  0  0
 18  9  1  0  0  0  0
 18 16  2  0  0  0  0
 19 15  1  0  0  0  0
 20 19  2  0  0  0  0
 21 20  1  0  0  0  0
 23 12  1  6  0  0  0
 23 19  1  0  0  0  0
 23 22  1  1  0  0  0
 24 13  2  0  0  0  0
 25 18  1  0  0  0  0
 26 20  1  0  0  0  0
 27 21  2  0  0  0  0
 28 22  2  0  0  0  0
 29  2  1  0  0  0  0
 29 17  1  0  0  0  0
 30  3  1  0  0  0  0
 30 22  1  0  0  0  0
 31 21  1  0  0  0  0
 31 23  1  0  0  0  0
M  END


  Mrv1652305152101272D          

 31 33  0  0  1  0            999 V2000
    0.1211    7.0964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0968    2.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2333    3.3448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8321    3.8594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7429    1.5082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3014    2.8672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5275    1.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0860    3.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0871    4.6440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1760    5.6987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4731    4.3010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7702    2.9033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4310    6.4833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0251    3.6879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1298    2.0602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7280    5.0856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6991    2.5701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5350    5.2571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6548    1.8053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9097    1.0206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7347    1.0206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8743    2.9033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3222    2.2902    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2379    6.6549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7900    6.0418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4248    0.3532    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2197    0.3532    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1292    3.6879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4837    2.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6812    2.7317    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9897    1.8053    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  5  1  0  0  0  0
  8  6  2  0  0  0  0
  9  4  2  0  0  0  0
 13  1  1  0  0  0  0
 13 10  1  0  0  0  0
 14  4  1  0  0  0  0
 14 11  2  0  0  0  0
 14 12  1  0  0  0  0
 15  5  2  0  0  0  0
 15  6  1  0  0  0  0
 16 10  1  0  0  0  0
 16 11  1  0  0  0  0
 17  7  2  0  0  0  0
 17  8  1  0  0  0  0
 18  9  1  0  0  0  0
 18 16  2  0  0  0  0
 19 15  1  0  0  0  0
 20 19  2  0  0  0  0
 21 20  1  0  0  0  0
 23 12  1  6  0  0  0
 23 19  1  0  0  0  0
 23 22  1  1  0  0  0
 24 13  2  0  0  0  0
 25 18  1  0  0  0  0
 26 20  1  0  0  0  0
 27 21  2  0  0  0  0
 28 22  2  0  0  0  0
 29  2  1  0  0  0  0
 29 17  1  0  0  0  0
 30  3  1  0  0  0  0
 30 22  1  0  0  0  0
 31 21  1  0  0  0  0
 31 23  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0006113

> <DATABASE_NAME>
MIME

> <SMILES>
COC(=O)[C@]1(CC2=CC(CC(C)=O)=C(O)C=C2)OC(=O)C(O)=C1C1=CC=C(OC)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C23H22O8/c1-13(24)10-16-11-14(4-9-18(16)25)12-23(22(28)30-3)19(20(26)21(27)31-23)15-5-7-17(29-2)8-6-15/h4-9,11,25-26H,10,12H2,1-3H3/t23-/m1/s1

> <INCHI_KEY>
GBICKRVPGNZDMS-HSZRJFAPSA-N

> <FORMULA>
C23H22O8

> <MOLECULAR_WEIGHT>
426.421

> <EXACT_MASS>
426.131467668

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
41.91716539092583

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (2R)-4-hydroxy-2-{[4-hydroxy-3-(2-oxopropyl)phenyl]methyl}-3-(4-methoxyphenyl)-5-oxo-2,5-dihydrofuran-2-carboxylate

> <ALOGPS_LOGP>
2.63

> <JCHEM_LOGP>
2.9649196153333337

> <ALOGPS_LOGS>
-4.31

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.361895346907687

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.55844711490668

> <JCHEM_PKA_STRONGEST_BASIC>
-3.324483076847221

> <JCHEM_POLAR_SURFACE_AREA>
119.36

> <JCHEM_REFRACTIVITY>
110.82589999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.10e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2R)-4-hydroxy-2-{[4-hydroxy-3-(2-oxopropyl)phenyl]methyl}-3-(4-methoxyphenyl)-5-oxofuran-2-carboxylate

> <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       0.226  13.247   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.781   4.243   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -6.035   6.244   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.420   7.204   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.387   2.815   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.563   5.352   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.851   3.291   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.027   5.828   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.896   8.669   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.329  10.638   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.883   8.029   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.438   5.419   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.804  12.102   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.914   6.884   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.242   3.846   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.359   9.493   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.172   4.797   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.865   9.813   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.222   3.370   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.698   1.905   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -3.238   1.905   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.499   5.419   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.468   4.275   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -2.311  12.422   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      -3.341  11.278   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      -0.793   0.659   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      -4.143   0.659   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      -3.975   6.884   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       4.636   5.273   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -5.005   5.099   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -3.714   3.370   0.000  0.00  0.00           O+0
CONECT    1   13                                                            
CONECT    2   29                                                            
CONECT    3   30                                                            
CONECT    4    9   14                                                       
CONECT    5    7   15                                                       
CONECT    6    8   15                                                       
CONECT    7    5   17                                                       
CONECT    8    6   17                                                       
CONECT    9    4   18                                                       
CONECT   10   13   16                                                       
CONECT   11   14   16                                                       
CONECT   12   14   23                                                       
CONECT   13    1   10   24                                                  
CONECT   14    4   11   12                                                  
CONECT   15    5    6   19                                                  
CONECT   16   10   11   18                                                  
CONECT   17    7    8   29                                                  
CONECT   18    9   16   25                                                  
CONECT   19   15   20   23                                                  
CONECT   20   19   21   26                                                  
CONECT   21   20   27   31                                                  
CONECT   22   23   28   30                                                  
CONECT   23   12   19   22   31                                             
CONECT   24   13                                                            
CONECT   25   18                                                            
CONECT   26   20                                                            
CONECT   27   21                                                            
CONECT   28   22                                                            
CONECT   29    2   17                                                       
CONECT   30    3   22                                                       
CONECT   31   21   23                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

Synonyms

Value	Source
Methyl (2R)-4-hydroxy-2-{[4-hydroxy-3-(2-oxopropyl)phenyl]methyl}-3-(4-methoxyphenyl)-5-oxo-2,5-dihydrofuran-2-carboxylic acid	Generator

Molecular Formula

C₂₃H₂₂O₈

Average Mass

426.421

Monoisotopic Mass

426.131467668

IUPAC Name

methyl (2R)-4-hydroxy-2-{[4-hydroxy-3-(2-oxopropyl)phenyl]methyl}-3-(4-methoxyphenyl)-5-oxo-2,5-dihydrofuran-2-carboxylate

Traditional Name

methyl (2R)-4-hydroxy-2-{[4-hydroxy-3-(2-oxopropyl)phenyl]methyl}-3-(4-methoxyphenyl)-5-oxofuran-2-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@]1(CC2=CC(CC(C)=O)=C(O)C=C2)OC(=O)C(O)=C1C1=CC=C(OC)C=C1

InChI Identifier

InChI=1S/C23H22O8/c1-13(24)10-16-11-14(4-9-18(16)25)12-23(22(28)30-3)19(20(26)21(27)31-23)15-5-7-17(29-2)8-6-15/h4-9,11,25-26H,10,12H2,1-3H3/t23-/m1/s1

InChI Key

GBICKRVPGNZDMS-HSZRJFAPSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenylpropanes. These are organic compounds containing a phenylpropane moiety.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Phenylpropanes

Direct Parent

Phenylpropanes

Alternative Parents

Substituents

Phenylpropane
Phenoxy compound
Methoxybenzene
Phenol ether
Anisole
1-hydroxy-2-unsubstituted benzenoid
Phenol
Fatty acid ester
Alkyl aryl ether
Fatty acyl
Dicarboxylic acid or derivatives
2-furanone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Dihydrofuran
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Enol
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	0.021 g/L	ALOGPS
logP	2.63	ALOGPS
logP	2.96	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	8.56	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	119.36 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	110.83 m³·mol⁻¹	ChemAxon
Polarizability	41.92 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_2) - 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
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	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

Not Available

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	1	Human feces	Metabolic reconstruction

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

78440898

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139584625

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 Versicolactone A (MMDBc0006113)

MOL for #<Metabolite:0x00007f468e7c9af8>

3D MOL for #<Metabolite:0x00007f468e7c9af8>

3D SDF for #<Metabolite:0x00007f468e7c9af8>

3D-SDF for #<Metabolite:0x00007f468e7c9af8>

PDB for #<Metabolite:0x00007f468e7c9af8>

3D PDB for #<Metabolite:0x00007f468e7c9af8>

SMILES for #<Metabolite:0x00007f468e7c9af8>

INCHI for #<Metabolite:0x00007f468e7c9af8>

Structure for #<Metabolite:0x00007f468e7c9af8>

3D Structure for #<Metabolite:0x00007f468e7c9af8>