MiMeDB: Showing metabocard for Asperiene B (MMDBc0026449)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 16:05:35 UTC

Update Date

2025-10-07 16:07:40 UTC

Metabolite ID

MMDBc0026449

Metabolite Identification

Common Name

Asperiene B

Description

Asperiene B is a secondary metabolite belonging to the class of terpenoids. Currently, there is limited literature available on this metabolite, indicating a need for further research to elucidate its properties and potential biological significance.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152118052D          

 34 36  0  0  1  0            999 V2000
   -1.8114    4.1335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8607    0.3353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9261    0.8367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4901   -1.4507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7070    2.7825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5316    2.8083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1393   -1.3992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2724    3.4837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9662    2.1070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5293   -0.6722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3147   -1.4249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0109    0.6788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8196   -0.2449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9868    4.1592    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6209   -0.0482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5522    3.4580    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8355    0.7045    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7908    2.1328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2701    0.0033    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5229   -1.3795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0947    0.0291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8801   -0.7237    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0555   -0.7495    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5968    4.8862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9422    2.7310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1808    2.8598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7195   -2.1807    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1673   -1.5669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7591   -1.0676    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2254    1.4315    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3768    3.4322    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1622    4.1850    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6601    0.7303    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7047   -0.6979    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  6  1  4  0  0  0
  8  5  2  0  0  0  0
  9  6  2  0  0  0  0
 10  7  1  0  0  0  0
 11  7  1  0  0  0  0
 14  1  1  0  0  0  0
 15 12  2  0  0  0  0
 15 13  1  0  0  0  0
 16  8  1  0  0  0  0
 16 14  1  0  0  0  0
 17 12  1  0  0  0  0
  9 18  1  4  0  0  0
 19 17  1  0  0  0  0
 21  2  1  0  0  0  0
 21  3  1  0  0  0  0
 21 10  1  0  0  0  0
 21 19  1  0  0  0  0
 22  4  1  1  0  0  0
 22 11  1  0  0  0  0
 22 19  1  0  0  0  0
 23 15  1  0  0  0  0
 23 20  1  0  0  0  0
 23 22  1  0  0  0  0
 14 24  1  1  0  0  0
 16 25  1  1  0  0  0
 26 18  2  0  0  0  0
 27 20  2  0  0  0  0
 23 28  1  6  0  0  0
 29 13  1  0  0  0  0
 29 20  1  0  0  0  0
 17 30  1  1  0  0  0
 30 18  1  0  0  0  0
 14 31  1  1  0  0  0
 16 32  1  1  0  0  0
 17 33  1  6  0  0  0
 19 34  1  6  0  0  0
M  END


  Mrv1652305152118052D          

 34 36  0  0  1  0            999 V2000
   -1.8114    4.1335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8607    0.3353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9261    0.8367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4901   -1.4507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7070    2.7825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5316    2.8083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1393   -1.3992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2724    3.4837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9662    2.1070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5293   -0.6722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3147   -1.4249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0109    0.6788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8196   -0.2449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9868    4.1592    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6209   -0.0482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5522    3.4580    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8355    0.7045    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7908    2.1328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2701    0.0033    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5229   -1.3795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0947    0.0291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8801   -0.7237    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0555   -0.7495    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5968    4.8862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9422    2.7310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1808    2.8598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7195   -2.1807    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1673   -1.5669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7591   -1.0676    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2254    1.4315    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3768    3.4322    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1622    4.1850    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6601    0.7303    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7047   -0.6979    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  6  1  4  0  0  0
  8  5  2  0  0  0  0
  9  6  2  0  0  0  0
 10  7  1  0  0  0  0
 11  7  1  0  0  0  0
 14  1  1  0  0  0  0
 15 12  2  0  0  0  0
 15 13  1  0  0  0  0
 16  8  1  0  0  0  0
 16 14  1  0  0  0  0
 17 12  1  0  0  0  0
  9 18  1  4  0  0  0
 19 17  1  0  0  0  0
 21  2  1  0  0  0  0
 21  3  1  0  0  0  0
 21 10  1  0  0  0  0
 21 19  1  0  0  0  0
 22  4  1  1  0  0  0
 22 11  1  0  0  0  0
 22 19  1  0  0  0  0
 23 15  1  0  0  0  0
 23 20  1  0  0  0  0
 23 22  1  0  0  0  0
 14 24  1  1  0  0  0
 16 25  1  1  0  0  0
 26 18  2  0  0  0  0
 27 20  2  0  0  0  0
 23 28  1  6  0  0  0
 29 13  1  0  0  0  0
 29 20  1  0  0  0  0
 17 30  1  1  0  0  0
 30 18  1  0  0  0  0
 14 31  1  1  0  0  0
 16 32  1  1  0  0  0
 17 33  1  6  0  0  0
 19 34  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0026449

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@](C)(O)[C@@]([H])(O)C=CC=CC(=O)O[C@]1([H])C=C2COC(=O)[C@]2(O)[C@@]2(C)CCCC(C)(C)[C@]12[H]

> <INCHI_IDENTIFIER>
InChI=1S/C23H32O7/c1-14(24)16(25)8-5-6-9-18(26)30-17-12-15-13-29-20(27)23(15,28)22(4)11-7-10-21(2,3)19(17)22/h5-6,8-9,12,14,16-17,19,24-25,28H,7,10-11,13H2,1-4H3/t14-,16-,17+,19-,22-,23-/m0/s1

> <INCHI_KEY>
AVBLSPPEZPLINV-GNZHWTDASA-N

> <FORMULA>
C23H32O7

> <MOLECULAR_WEIGHT>
420.502

> <EXACT_MASS>
420.21480337

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
44.51443243009119

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5R,5aS,9aS,9bS)-9b-hydroxy-6,6,9a-trimethyl-1-oxo-1H,3H,5H,5aH,6H,7H,8H,9H,9aH,9bH-naphtho[1,2-c]furan-5-yl (6S,7S)-6,7-dihydroxyocta-2,4-dienoate

> <ALOGPS_LOGP>
2.31

> <JCHEM_LOGP>
2.1475553873333317

> <ALOGPS_LOGS>
-3.45

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.745140887721888

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.44301016598953

> <JCHEM_PKA_STRONGEST_BASIC>
-3.034380622792873

> <JCHEM_POLAR_SURFACE_AREA>
113.29

> <JCHEM_REFRACTIVITY>
112.15459999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.49e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5R,5aS,9aS,9bS)-9b-hydroxy-6,6,9a-trimethyl-1-oxo-3H,5H,5aH,7H,8H,9H-naphtho[1,2-c]furan-5-yl (6S,7S)-6,7-dihydroxyocta-2,4-dienoate

> <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      -3.381   7.716   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.073   0.626   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.329   1.562   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.648  -2.708   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.320   5.194   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.859   5.242   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.727  -2.612   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.509   6.503   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.670   3.933   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.455  -1.255   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.187  -2.660   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.754   1.267   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.530  -0.457   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.842   7.764   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.026  -0.090   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.031   6.455   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.293   1.315   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.210   3.981   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.104   0.006   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.843  -2.575   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.643   0.054   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.376  -1.351   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.837  -1.399   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -1.114   9.121   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      -1.759   5.098   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       5.938   5.338   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       3.210  -4.071   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       4.046  -2.925   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       1.417  -1.993   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       6.021   2.672   0.000  0.00  0.00           O+0
HETATM   31  H   UNK     0      -2.570   6.407   0.000  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.303   7.812   0.000  0.00  0.00           H+0
HETATM   33  H   UNK     0       6.832   1.363   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0       6.915  -1.303   0.000  0.00  0.00           H+0
CONECT    1   14                                                            
CONECT    2   21                                                            
CONECT    3   21                                                            
CONECT    4   22                                                            
CONECT    5    6    8                                                       
CONECT    6    5    9                                                       
CONECT    7   10   11                                                       
CONECT    8    5   16                                                       
CONECT    9    6   18                                                       
CONECT   10    7   21                                                       
CONECT   11    7   22                                                       
CONECT   12   15   17                                                       
CONECT   13   15   29                                                       
CONECT   14    1   16   24   31                                             
CONECT   15   12   13   23                                                  
CONECT   16    8   14   25   32                                             
CONECT   17   12   19   30   33                                             
CONECT   18    9   26   30                                                  
CONECT   19   17   21   22   34                                             
CONECT   20   23   27   29                                                  
CONECT   21    2    3   10   19                                             
CONECT   22    4   11   19   23                                             
CONECT   23   15   20   22   28                                             
CONECT   24   14                                                            
CONECT   25   16                                                            
CONECT   26   18                                                            
CONECT   27   20                                                            
CONECT   28   23                                                            
CONECT   29   13   20                                                       
CONECT   30   17   18                                                       
CONECT   31   14                                                            
CONECT   32   16                                                            
CONECT   33   17                                                            
CONECT   34   19                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   72    0
END

Synonyms

Not Available

Molecular Formula

C₂₃H₃₂O₇

Average Mass

420.502

Monoisotopic Mass

420.21480337

IUPAC Name

(5R,5aS,9aS,9bS)-9b-hydroxy-6,6,9a-trimethyl-1-oxo-1H,3H,5H,5aH,6H,7H,8H,9H,9aH,9bH-naphtho[1,2-c]furan-5-yl (6S,7S)-6,7-dihydroxyocta-2,4-dienoate

Traditional Name

(5R,5aS,9aS,9bS)-9b-hydroxy-6,6,9a-trimethyl-1-oxo-3H,5H,5aH,7H,8H,9H-naphtho[1,2-c]furan-5-yl (6S,7S)-6,7-dihydroxyocta-2,4-dienoate

CAS Registry Number

Not Available

SMILES

[H][C@@](C)(O)[C@@]([H])(O)C=CC=CC(=O)O[C@]1([H])C=C2COC(=O)[C@]2(O)[C@@]2(C)CCCC(C)(C)[C@]12[H]

InChI Identifier

InChI=1S/C23H32O7/c1-14(24)16(25)8-5-6-9-18(26)30-17-12-15-13-29-20(27)23(15,28)22(4)11-7-10-21(2,3)19(17)22/h5-6,8-9,12,14,16-17,19,24-25,28H,7,10-11,13H2,1-4H3/t14-,16-,17+,19-,22-,23-/m0/s1

InChI Key

AVBLSPPEZPLINV-GNZHWTDASA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthofurans

Sub Class

Not Available

Direct Parent

Naphthofurans

Alternative Parents

Substituents

Naphthofuran
Fatty alcohol
Fatty acid ester
Fatty acyl
Gamma butyrolactone
Dicarboxylic acid or derivatives
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Tertiary alcohol
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	0.15 g/L	ALOGPS
logP	2.31	ALOGPS
logP	2.15	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	11.44	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	113.29 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	112.15 m³·mol⁻¹	ChemAxon
Polarizability	44.51 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_2_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)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-23	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
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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

146683069

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 Asperiene B (MMDBc0026449)

MOL for #<Metabolite:0x00007f8dc9f02108>

3D MOL for #<Metabolite:0x00007f8dc9f02108>

3D SDF for #<Metabolite:0x00007f8dc9f02108>

3D-SDF for #<Metabolite:0x00007f8dc9f02108>

PDB for #<Metabolite:0x00007f8dc9f02108>

3D PDB for #<Metabolite:0x00007f8dc9f02108>

SMILES for #<Metabolite:0x00007f8dc9f02108>

INCHI for #<Metabolite:0x00007f8dc9f02108>

Structure for #<Metabolite:0x00007f8dc9f02108>

3D Structure for #<Metabolite:0x00007f8dc9f02108>