MiMeDB: Showing metabocard for Oxisterigmatocystin A (MMDBc0005032)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 22:46:57 UTC

Update Date

2025-10-07 16:04:57 UTC

Metabolite ID

MMDBc0005032

Metabolite Identification

Common Name

Oxisterigmatocystin A

Description

Oxisterigmatocystin A is a polyketide, a chemical class characterized by its complex structure derived from the condensation of acetyl and malonyl units. This metabolite was identified in the context of fungal secondary metabolites, specifically isolated from the deep-sea-derived fungus Aspergillus versicolor, alongside other sterigmatocystin derivatives (PMID:21119680 ). Its chemical structure and potential biological activities have garnered interest due to the presence of similar compounds known for their bioactive properties. Oxisterigmatocystin A is part of a broader family of metabolites that may exhibit various pharmacological effects, although specific biological functions remain to be fully elucidated. The compound is often studied in conjunction with other related metabolites, such as sterigmatocystin and its derivatives, which have been linked to significant biological activities, including cytotoxicity and antimicrobial effects (PMID:25038471 ). Understanding the chemistry and potential applications of oxisterigmatocystin A could provide insights into the development of new therapeutic agents derived from natural sources.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152100462D          

 31 35  0  0  1  0            999 V2000
    6.1772    0.5383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0732    5.5555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4031    0.6023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5443    2.6015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0886    1.9137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1575    2.1514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9707    4.9693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2940    2.9651    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1765    3.3400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2651    1.9645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7941    4.9185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5150    4.2815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3415    2.0299    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8828    3.5430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3531    3.3907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1619    4.1800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9853    4.1292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8974    2.7030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7062    3.4923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5624    3.3464    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.6322    4.0277    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4410    4.8170    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8095    1.2768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2498    5.6062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9602    1.2983    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6990    4.1600    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9737    2.7684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0739    2.7538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0256    2.5838    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5165    2.0375    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8308    3.7277    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  2  0  0  0  0
  8  6  1  0  0  0  0
  9  4  1  0  0  0  0
 10  5  1  0  0  0  0
 11  7  2  0  0  0  0
 12  7  1  0  0  0  0
 13  6  1  0  0  0  0
 14  8  1  0  0  0  0
 14 12  2  0  0  0  0
 15  9  2  0  0  0  0
 16 11  1  0  0  0  0
 17 15  1  0  0  0  0
 17 16  1  0  0  0  0
 18 10  2  0  0  0  0
 18 15  1  0  0  0  0
 19 14  1  0  0  0  0
 19 16  2  0  0  0  0
 20  8  1  0  0  0  0
 21  9  1  0  0  0  0
 22 17  2  0  0  0  0
 23  1  1  0  0  0  0
 23 10  1  0  0  0  0
 24  2  1  0  0  0  0
 24 11  1  0  0  0  0
 25  3  1  0  0  0  0
 13 25  1  6  0  0  0
 26 12  1  0  0  0  0
 26 20  1  0  0  0  0
 27 13  1  0  0  0  0
 27 20  1  0  0  0  0
 28 18  1  0  0  0  0
 28 19  1  0  0  0  0
  8 29  1  1  0  0  0
 13 30  1  1  0  0  0
 20 31  1  1  0  0  0
M  END


  Mrv1652305152100462D          

 31 35  0  0  1  0            999 V2000
    6.1772    0.5383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0732    5.5555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4031    0.6023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5443    2.6015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0886    1.9137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1575    2.1514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9707    4.9693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2940    2.9651    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1765    3.3400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2651    1.9645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7941    4.9185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5150    4.2815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3415    2.0299    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8828    3.5430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3531    3.3907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1619    4.1800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9853    4.1292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8974    2.7030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7062    3.4923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5624    3.3464    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.6322    4.0277    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4410    4.8170    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8095    1.2768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2498    5.6062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9602    1.2983    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6990    4.1600    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9737    2.7684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0739    2.7538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0256    2.5838    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5165    2.0375    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8308    3.7277    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  2  0  0  0  0
  8  6  1  0  0  0  0
  9  4  1  0  0  0  0
 10  5  1  0  0  0  0
 11  7  2  0  0  0  0
 12  7  1  0  0  0  0
 13  6  1  0  0  0  0
 14  8  1  0  0  0  0
 14 12  2  0  0  0  0
 15  9  2  0  0  0  0
 16 11  1  0  0  0  0
 17 15  1  0  0  0  0
 17 16  1  0  0  0  0
 18 10  2  0  0  0  0
 18 15  1  0  0  0  0
 19 14  1  0  0  0  0
 19 16  2  0  0  0  0
 20  8  1  0  0  0  0
 21  9  1  0  0  0  0
 22 17  2  0  0  0  0
 23  1  1  0  0  0  0
 23 10  1  0  0  0  0
 24  2  1  0  0  0  0
 24 11  1  0  0  0  0
 25  3  1  0  0  0  0
 13 25  1  6  0  0  0
 26 12  1  0  0  0  0
 26 20  1  0  0  0  0
 27 13  1  0  0  0  0
 27 20  1  0  0  0  0
 28 18  1  0  0  0  0
 28 19  1  0  0  0  0
  8 29  1  1  0  0  0
 13 30  1  1  0  0  0
 20 31  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0005032

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]1(C[C@@]2([H])C3=C(O[C@@]2([H])O1)C=C(OC)C1=C3OC2=C(OC)C=CC(O)=C2C1=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C20H18O8/c1-23-10-5-4-9(21)15-17(22)16-11(24-2)7-12-14(19(16)28-18(10)15)8-6-13(25-3)27-20(8)26-12/h4-5,7-8,13,20-21H,6H2,1-3H3/t8-,13+,20-/m0/s1

> <INCHI_KEY>
JOXQRCQSTGKMFA-IBXPANGUSA-N

> <FORMULA>
C20H18O8

> <MOLECULAR_WEIGHT>
386.356

> <EXACT_MASS>
386.10016754

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
38.415002961462186

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,5R,7S)-15-hydroxy-5,11,18-trimethoxy-6,8,20-trioxapentacyclo[10.8.0.0^{2,9}.0^{3,7}.0^{14,19}]icosa-1,9,11,14,16,18-hexaen-13-one

> <ALOGPS_LOGP>
2.31

> <JCHEM_LOGP>
2.9791424763333336

> <ALOGPS_LOGS>
-3.22

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.859330265712536

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5742363766740364

> <JCHEM_POLAR_SURFACE_AREA>
92.68

> <JCHEM_REFRACTIVITY>
95.96419999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.32e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,5R,7S)-15-hydroxy-5,11,18-trimethoxy-6,8,20-trioxapentacyclo[10.8.0.0^{2,9}.0^{3,7}.0^{14,19}]icosa-1,9,11,14,16,18-hexaen-13-one

> <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      11.531   1.005   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.337  10.370   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.486   1.124   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.083   4.856   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.232   3.572   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.894   4.016   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.412   9.276   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.149   5.535   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.396   6.235   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.695   3.667   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.949   9.181   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.561   7.992   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.371   3.789   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.248   6.614   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.859   6.329   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.635   7.803   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.173   7.708   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.008   5.046   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.785   6.519   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.783   6.247   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      14.247   7.518   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      12.023   8.992   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      10.844   2.383   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       9.800  10.465   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       3.659   2.423   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       5.038   7.765   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       3.684   5.168   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       9.471   5.140   0.000  0.00  0.00           O+0
HETATM   29  H   UNK     0       7.515   4.823   0.000  0.00  0.00           H+0
HETATM   30  H   UNK     0       2.831   3.803   0.000  0.00  0.00           H+0
HETATM   31  H   UNK     0       3.418   6.958   0.000  0.00  0.00           H+0
CONECT    1   23                                                            
CONECT    2   24                                                            
CONECT    3   25                                                            
CONECT    4    5    9                                                       
CONECT    5    4   10                                                       
CONECT    6    8   13                                                       
CONECT    7   11   12                                                       
CONECT    8    6   14   20   29                                             
CONECT    9    4   15   21                                                  
CONECT   10    5   18   23                                                  
CONECT   11    7   16   24                                                  
CONECT   12    7   14   26                                                  
CONECT   13    6   25   27   30                                             
CONECT   14    8   12   19                                                  
CONECT   15    9   17   18                                                  
CONECT   16   11   17   19                                                  
CONECT   17   15   16   22                                                  
CONECT   18   10   15   28                                                  
CONECT   19   14   16   28                                                  
CONECT   20    8   26   27   31                                             
CONECT   21    9                                                            
CONECT   22   17                                                            
CONECT   23    1   10                                                       
CONECT   24    2   11                                                       
CONECT   25    3   13                                                       
CONECT   26   12   20                                                       
CONECT   27   13   20                                                       
CONECT   28   18   19                                                       
CONECT   29    8                                                            
CONECT   30   13                                                            
CONECT   31   20                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

Synonyms

Not Available

Molecular Formula

C₂₀H₁₈O₈

Average Mass

386.356

Monoisotopic Mass

386.10016754

IUPAC Name

(3S,5R,7S)-15-hydroxy-5,11,18-trimethoxy-6,8,20-trioxapentacyclo[10.8.0.0^{2,9}.0^{3,7}.0^{14,19}]icosa-1,9,11,14,16,18-hexaen-13-one

Traditional Name

(3S,5R,7S)-15-hydroxy-5,11,18-trimethoxy-6,8,20-trioxapentacyclo[10.8.0.0^{2,9}.0^{3,7}.0^{14,19}]icosa-1,9,11,14,16,18-hexaen-13-one

CAS Registry Number

Not Available

SMILES

[H][C@@]1(C[C@@]2([H])C3=C(O[C@@]2([H])O1)C=C(OC)C1=C3OC2=C(OC)C=CC(O)=C2C1=O)OC

InChI Identifier

InChI=1S/C20H18O8/c1-23-10-5-4-9(21)15-17(22)16-11(24-2)7-12-14(19(16)28-18(10)15)8-6-13(25-3)27-20(8)26-12/h4-5,7-8,13,20-21H,6H2,1-3H3/t8-,13+,20-/m0/s1

InChI Key

JOXQRCQSTGKMFA-IBXPANGUSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sterigmatocystins. These are a group of closely related fungal metabolites chemically characterized by a xanthone moiety fused to a dihydrodifurano or a tetrahydrodifurano moiety. The chemical difference among the various sterigmagocystins are the presence or absence of unsaturation at positions 2 and 3 of the difurano ring system, the substitution pattern on positions 6, 7, and 10 of the xanthone system and/or the substituent on position 3 of the difurano system. They are produced by Aspergilus spp. And Bipolaris spp.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Sterigmatocystins

Sub Class

Not Available

Direct Parent

Sterigmatocystins

Alternative Parents

Substituents

Sterigmatocystin backbone
Xanthone
Dibenzopyran
Xanthene
Chromone
Benzopyran
1-benzopyran
Coumaran
Anisole
Pyranone
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Pyran
Benzenoid
Vinylogous acid
Vinylogous ester
Oxolane
Heteroaromatic compound
Ether
Acetal
Organoheterocyclic compound
Oxacycle
Organic oxide
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
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
Water Solubility	0.23 g/L	ALOGPS
logP	2.31	ALOGPS
logP	2.98	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	8.86	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	92.68 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	95.96 m³·mol⁻¹	ChemAxon
Polarizability	38.42 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_1_1) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	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

Microbial Pathways

Pathways

This table shows at most 5 pathways. For the full list of associated pathways:

See All Associated Bacterial Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated 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
Eukaryota/Fungi	Ascomycota	1	Human feces	Metabolic reconstruction

Exposure Sources

Other Exposures

Source Type	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

27025653

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101802788

PDB ID

Not Available

ChEBI ID

Not Available

CMMC Knowledgebase

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 Oxisterigmatocystin A (MMDBc0005032)

MOL for #<Metabolite:0x00007fd4487a5660>

3D MOL for #<Metabolite:0x00007fd4487a5660>

3D SDF for #<Metabolite:0x00007fd4487a5660>

3D-SDF for #<Metabolite:0x00007fd4487a5660>

PDB for #<Metabolite:0x00007fd4487a5660>

3D PDB for #<Metabolite:0x00007fd4487a5660>

SMILES for #<Metabolite:0x00007fd4487a5660>

INCHI for #<Metabolite:0x00007fd4487a5660>

Structure for #<Metabolite:0x00007fd4487a5660>

3D Structure for #<Metabolite:0x00007fd4487a5660>