MiMeDB: Showing metabocard for Anhydroophiobolin A (MMDBc0015251)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 06:07:23 UTC

Update Date

2025-10-07 16:06:23 UTC

Metabolite ID

MMDBc0015251

Metabolite Identification

Common Name

Anhydroophiobolin A

Description

Anhydroophiobolin A is a member of the chemical class of metabolites known as ophiobolins, which are characterized by their unique structural features and biological activities. This compound has been identified as a product of the fermentation process of the fungus Cochliobolus heterostrophus, alongside other related compounds such as Ophiobolin A, 3-anhydroophiobolin A, Ophiobolin B, and Ophiobolin L (PMID:7760080 ). The structural uniqueness of anhydroophiobolin A contributes to its potential biological significance, as ophiobolins have been studied for their various effects, including antifungal and phytotoxic properties. The exploration of anhydroophiobolin A within the context of its biosynthetic origins and its interactions in biological systems may provide insights into its functional roles and applications in biotechnology and medicine. Further research is necessary to elucidate the specific mechanisms by which anhydroophiobolin A exerts its effects and to explore its potential therapeutic uses.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152108072D          

 34 37  0  0  1  0            999 V2000
    1.1811    0.8973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2787   -0.0177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7082   -3.4415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0482   -3.4127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6763   -3.4477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5681   -0.7204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9196   -1.2304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8726   -3.3835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0788   -3.1587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9375   -0.5107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1089   -2.0270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7630   -1.9705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1509   -2.7960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7912   -0.0990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4657    0.1230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5482   -2.6322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2730   -2.6190    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3872   -0.8183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2221   -1.2851    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7994   -2.2860    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7066   -1.3067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8217   -2.0496    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8973   -1.4668    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3317   -2.6981    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0474   -2.3343    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6161   -0.0891    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0528   -0.5579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0159   -1.5099    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3450    0.0739    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4637   -2.7790    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7828   -0.6799    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0800   -1.8820    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6160   -1.8266    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1837   -0.6931    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0  0  0  0
  9  8  1  0  0  0  0
 15  1  1  0  0  0  0
 15  2  1  0  0  0  0
 15 10  2  0  0  0  0
 16  3  1  0  0  0  0
 16 11  2  0  0  0  0
 17  4  1  1  0  0  0
 17 12  1  0  0  0  0
 18  6  2  0  0  0  0
 18 14  1  0  0  0  0
 19 10  1  6  0  0  0
 19 12  1  0  0  0  0
 20 13  1  0  0  0  0
 20 16  1  0  0  0  0
 21 11  1  0  0  0  0
 22  7  1  0  0  0  0
 23 18  1  0  0  0  0
 23 20  1  0  0  0  0
 23 21  1  0  0  0  0
 24  5  1  6  0  0  0
 24  8  1  0  0  0  0
 24 13  1  0  0  0  0
 24 22  1  0  0  0  0
 25  9  1  0  0  0  0
 25 17  1  0  0  0  0
 25 22  1  0  0  0  0
 26 14  2  0  0  0  0
 27 21  2  0  0  0  0
 28 19  1  0  0  0  0
 25 28  1  1  0  0  0
 29  6  1  0  0  0  0
 17 30  1  6  0  0  0
 19 31  1  1  0  0  0
 20 32  1  6  0  0  0
 22 33  1  1  0  0  0
 23 34  1  6  0  0  0
M  END


  Mrv1652305152108072D          

 34 37  0  0  1  0            999 V2000
    1.1811    0.8973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2787   -0.0177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7082   -3.4415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0482   -3.4127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6763   -3.4477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5681   -0.7204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9196   -1.2304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8726   -3.3835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0788   -3.1587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9375   -0.5107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1089   -2.0270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7630   -1.9705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1509   -2.7960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7912   -0.0990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4657    0.1230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5482   -2.6322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2730   -2.6190    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3872   -0.8183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2221   -1.2851    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7994   -2.2860    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7066   -1.3067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8217   -2.0496    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8973   -1.4668    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3317   -2.6981    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0474   -2.3343    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6161   -0.0891    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0528   -0.5579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0159   -1.5099    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3450    0.0739    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4637   -2.7790    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7828   -0.6799    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0800   -1.8820    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6160   -1.8266    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1837   -0.6931    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0  0  0  0
  9  8  1  0  0  0  0
 15  1  1  0  0  0  0
 15  2  1  0  0  0  0
 15 10  2  0  0  0  0
 16  3  1  0  0  0  0
 16 11  2  0  0  0  0
 17  4  1  1  0  0  0
 17 12  1  0  0  0  0
 18  6  2  0  0  0  0
 18 14  1  0  0  0  0
 19 10  1  6  0  0  0
 19 12  1  0  0  0  0
 20 13  1  0  0  0  0
 20 16  1  0  0  0  0
 21 11  1  0  0  0  0
 22  7  1  0  0  0  0
 23 18  1  0  0  0  0
 23 20  1  0  0  0  0
 23 21  1  0  0  0  0
 24  5  1  6  0  0  0
 24  8  1  0  0  0  0
 24 13  1  0  0  0  0
 24 22  1  0  0  0  0
 25  9  1  0  0  0  0
 25 17  1  0  0  0  0
 25 22  1  0  0  0  0
 26 14  2  0  0  0  0
 27 21  2  0  0  0  0
 28 19  1  0  0  0  0
 25 28  1  1  0  0  0
 29  6  1  0  0  0  0
 17 30  1  6  0  0  0
 19 31  1  1  0  0  0
 20 32  1  6  0  0  0
 22 33  1  1  0  0  0
 23 34  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0015251

> <DATABASE_NAME>
MIME

> <SMILES>
[H]\C1=C(C=O)\[C@@]2([H])C(=O)C=C(C)[C@@]2([H])C[C@@]2(C)CC[C@@]3(O[C@]([H])(C[C@]3([H])C)C=C(C)C)[C@]2([H])C1

> <INCHI_IDENTIFIER>
InChI=1S/C25H34O3/c1-15(2)10-19-12-17(4)25(28-19)9-8-24(5)13-20-16(3)11-21(27)23(20)18(14-26)6-7-22(24)25/h6,10-11,14,17,19-20,22-23H,7-9,12-13H2,1-5H3/b18-6-/t17-,19-,20+,22+,23+,24+,25-/m0/s1

> <INCHI_KEY>
MDYSLOGZXCWLSL-CWPAWFJGSA-N

> <FORMULA>
C25H34O3

> <MOLECULAR_WEIGHT>
382.544

> <EXACT_MASS>
382.250794955

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
43.779739328126404

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1'S,2S,3S,3'R,5R,7'R,9'E,11'S)-3,3',14'-trimethyl-5-(2-methylprop-1-en-1-yl)-12'-oxospiro[oxolane-2,6'-tricyclo[9.3.0.0^{3,7}]tetradecane]-9',13'-diene-10'-carbaldehyde

> <ALOGPS_LOGP>
5.12

> <JCHEM_LOGP>
4.6487224026666665

> <ALOGPS_LOGS>
-5.01

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.493587773966375

> <JCHEM_PKA_STRONGEST_BASIC>
-4.086520987085461

> <JCHEM_POLAR_SURFACE_AREA>
43.370000000000005

> <JCHEM_REFRACTIVITY>
114.3424

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.72e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,2S,3S,3'R,5R,7'R,9'E,11'S)-3,3',14'-trimethyl-5-(2-methylprop-1-en-1-yl)-12'-oxospiro[oxolane-2,6'-tricyclo[9.3.0.0^{3,7}]tetradecane]-9',13'-diene-10'-carbaldehyde

> <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       2.205   1.675   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.253  -0.033   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.655  -6.424   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.957  -6.370   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.862  -6.436   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.660  -1.345   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.450  -2.297   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.362  -6.316   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.880  -5.896   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.750  -0.953   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.403  -3.784   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.424  -3.678   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.748  -5.219   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.943  -0.185   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.736   0.230   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.357  -4.913   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.376  -4.889   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.190  -1.528   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.281  -2.399   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.959  -4.267   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.652  -2.439   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.267  -3.826   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.142  -2.738   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.219  -5.036   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.822  -4.357   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      10.483  -0.166   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      11.299  -1.041   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       3.763  -2.818   0.000  0.00  0.00           O+0
HETATM   29  H   UNK     0       6.244   0.138   0.000  0.00  0.00           H+0
HETATM   30  H   UNK     0       0.866  -5.187   0.000  0.00  0.00           H+0
HETATM   31  H   UNK     0       3.328  -1.269   0.000  0.00  0.00           H+0
HETATM   32  H   UNK     0       7.616  -3.513   0.000  0.00  0.00           H+0
HETATM   33  H   UNK     0       6.750  -3.410   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0       9.676  -1.294   0.000  0.00  0.00           H+0
CONECT    1   15                                                            
CONECT    2   15                                                            
CONECT    3   16                                                            
CONECT    4   17                                                            
CONECT    5   24                                                            
CONECT    6    7   18   29                                                  
CONECT    7    6   22                                                       
CONECT    8    9   24                                                       
CONECT    9    8   25                                                       
CONECT   10   15   19                                                       
CONECT   11   16   21                                                       
CONECT   12   17   19                                                       
CONECT   13   20   24                                                       
CONECT   14   18   26                                                       
CONECT   15    1    2   10                                                  
CONECT   16    3   11   20                                                  
CONECT   17    4   12   25   30                                             
CONECT   18    6   14   23                                                  
CONECT   19   10   12   28   31                                             
CONECT   20   13   16   23   32                                             
CONECT   21   11   23   27                                                  
CONECT   22    7   24   25   33                                             
CONECT   23   18   20   21   34                                             
CONECT   24    5    8   13   22                                             
CONECT   25    9   17   22   28                                             
CONECT   26   14                                                            
CONECT   27   21                                                            
CONECT   28   19   25                                                       
CONECT   29    6                                                            
CONECT   30   17                                                            
CONECT   31   19                                                            
CONECT   32   20                                                            
CONECT   33   22                                                            
CONECT   34   23                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

Synonyms

Not Available

Molecular Formula

C₂₅H₃₄O₃

Average Mass

382.544

Monoisotopic Mass

382.250794955

IUPAC Name

(1'S,2S,3S,3'R,5R,7'R,9'E,11'S)-3,3',14'-trimethyl-5-(2-methylprop-1-en-1-yl)-12'-oxospiro[oxolane-2,6'-tricyclo[9.3.0.0^{3,7}]tetradecane]-9',13'-diene-10'-carbaldehyde

Traditional Name

(1'S,2S,3S,3'R,5R,7'R,9'E,11'S)-3,3',14'-trimethyl-5-(2-methylprop-1-en-1-yl)-12'-oxospiro[oxolane-2,6'-tricyclo[9.3.0.0^{3,7}]tetradecane]-9',13'-diene-10'-carbaldehyde

CAS Registry Number

Not Available

SMILES

[H]\C1=C(C=O)\[C@@]2([H])C(=O)C=C(C)[C@@]2([H])C[C@@]2(C)CC[C@@]3(O[C@]([H])(C[C@]3([H])C)C=C(C)C)[C@]2([H])C1

InChI Identifier

InChI=1S/C25H34O3/c1-15(2)10-19-12-17(4)25(28-19)9-8-24(5)13-20-16(3)11-21(27)23(20)18(14-26)6-7-22(24)25/h6,10-11,14,17,19-20,22-23H,7-9,12-13H2,1-5H3/b18-6-/t17-,19-,20+,22+,23+,24+,25-/m0/s1

InChI Key

MDYSLOGZXCWLSL-CWPAWFJGSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ophiobolane sesterterpenoids. These are sesterterpnoids with a structure based on the ophiobolane backbone. Ophiobolane is a tricyclic compound consisting of two cyclopentane rings joined by a cyclooctane ring, and carries a methyl group at the 1-, 4-, and 8-position, as well as a 6-methylheptane group at the 12-position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesterterpenoids

Direct Parent

Ophiobolane sesterterpenoids

Alternative Parents

Substituents

Ophiobolane sesterterpenoid
Oxolane
Ketone
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aldehyde
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.0037 g/L	ALOGPS
logP	5.12	ALOGPS
logP	4.65	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	13.49	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	43.37 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	114.34 m³·mol⁻¹	ChemAxon
Polarizability	43.78 Å³	ChemAxon
Number of Rings	4	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
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

Not Available

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
Bacteria/Eubacteria	Proteobacteria	1	Human ; Human sputum; Human subgingival plaque; 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

30829421

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

12306827

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

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 Anhydroophiobolin A (MMDBc0015251)

MOL for #<Metabolite:0x00007f8d89337480>

3D MOL for #<Metabolite:0x00007f8d89337480>

3D SDF for #<Metabolite:0x00007f8d89337480>

3D-SDF for #<Metabolite:0x00007f8d89337480>

PDB for #<Metabolite:0x00007f8d89337480>

3D PDB for #<Metabolite:0x00007f8d89337480>

SMILES for #<Metabolite:0x00007f8d89337480>

INCHI for #<Metabolite:0x00007f8d89337480>

Structure for #<Metabolite:0x00007f8d89337480>

3D Structure for #<Metabolite:0x00007f8d89337480>