MiMeDB: Showing metabocard for Asperversiamide B (MMDBc0024215)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 14:02:40 UTC

Update Date

2025-10-07 16:07:25 UTC

Metabolite ID

MMDBc0024215

Metabolite Identification

Common Name

Asperversiamide B

Description

Asperversiamide B is a secondary metabolite belonging to the class of alkaloids. There is limited literature available on this compound, indicating that further research is needed to fully understand its properties and potential applications.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152116022D          

 34 40  0  0  1  0            999 V2000
    6.4760    0.0104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7398    1.0376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2102    3.2882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2803    3.4987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2113    0.4151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6195    0.2968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7026    1.0833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4186    0.0917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3900    0.5572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5985    1.2966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7529    2.4755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4592    1.8478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4644    1.6353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3976    1.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3766    2.0912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9538    2.6806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9748    1.6809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2659    2.1821    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8315    0.2664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7581    3.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7762    1.3151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9958    0.6811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8647    2.7860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2368    0.9037    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6376    2.4580    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6341    1.4013    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5716    3.4117    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6289    0.5393    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1543    1.4723    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6312   -0.5339    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1687    3.8513    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4951    0.5395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7739    1.4757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8060    2.8670    0.0000 H   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  5  1  0  0  0  0
 14  6  1  0  0  0  0
 14 10  1  0  0  0  0
 15 10  2  0  0  0  0
 16 11  2  0  0  0  0
 16 15  1  0  0  0  0
 17 11  1  0  0  0  0
 17 14  2  0  0  0  0
 18 12  1  0  0  0  0
 22  1  1  0  0  0  0
 22  2  1  0  0  0  0
 22  8  1  0  0  0  0
 23  3  1  0  0  0  0
 23  4  1  0  0  0  0
 23 18  1  0  0  0  0
 24  7  1  0  0  0  0
 24 12  1  0  0  0  0
 24 19  1  0  0  0  0
 25 13  1  1  0  0  0
 25 15  1  0  0  0  0
 25 20  1  0  0  0  0
 25 23  1  0  0  0  0
 26 13  1  1  0  0  0
 26 18  1  0  0  0  0
 26 21  1  0  0  0  0
 27 16  1  0  0  0  0
 27 20  2  0  0  0  0
 28 19  2  0  0  0  0
 28 26  1  0  0  0  0
 29  9  1  0  0  0  0
 29 21  1  0  0  0  0
 24 29  1  1  0  0  0
 30 19  1  0  0  0  0
 31 20  1  0  0  0  0
 32 21  2  0  0  0  0
 33 17  1  0  0  0  0
 33 22  1  0  0  0  0
 18 34  1  1  0  0  0
M  END


  Mrv1652305152116022D          

 34 40  0  0  1  0            999 V2000
    6.4760    0.0104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7398    1.0376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2102    3.2882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2803    3.4987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2113    0.4151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6195    0.2968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7026    1.0833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4186    0.0917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3900    0.5572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5985    1.2966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7529    2.4755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4592    1.8478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4644    1.6353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3976    1.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3766    2.0912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9538    2.6806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9748    1.6809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2659    2.1821    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8315    0.2664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7581    3.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7762    1.3151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9958    0.6811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8647    2.7860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2368    0.9037    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6376    2.4580    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6341    1.4013    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5716    3.4117    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6289    0.5393    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1543    1.4723    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6312   -0.5339    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1687    3.8513    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4951    0.5395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7739    1.4757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8060    2.8670    0.0000 H   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  5  1  0  0  0  0
 14  6  1  0  0  0  0
 14 10  1  0  0  0  0
 15 10  2  0  0  0  0
 16 11  2  0  0  0  0
 16 15  1  0  0  0  0
 17 11  1  0  0  0  0
 17 14  2  0  0  0  0
 18 12  1  0  0  0  0
 22  1  1  0  0  0  0
 22  2  1  0  0  0  0
 22  8  1  0  0  0  0
 23  3  1  0  0  0  0
 23  4  1  0  0  0  0
 23 18  1  0  0  0  0
 24  7  1  0  0  0  0
 24 12  1  0  0  0  0
 24 19  1  0  0  0  0
 25 13  1  1  0  0  0
 25 15  1  0  0  0  0
 25 20  1  0  0  0  0
 25 23  1  0  0  0  0
 26 13  1  1  0  0  0
 26 18  1  0  0  0  0
 26 21  1  0  0  0  0
 27 16  1  0  0  0  0
 27 20  2  0  0  0  0
 28 19  2  0  0  0  0
 28 26  1  0  0  0  0
 29  9  1  0  0  0  0
 29 21  1  0  0  0  0
 24 29  1  1  0  0  0
 30 19  1  0  0  0  0
 31 20  1  0  0  0  0
 32 21  2  0  0  0  0
 33 17  1  0  0  0  0
 33 22  1  0  0  0  0
 18 34  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0024215

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@]12C[C@]34CCCN3C(=O)[C@@]1(C[C@]1(C(O)=NC3=CC5=C(C=CC(C)(C)O5)C=C13)C2(C)C)N=C4O

> <INCHI_IDENTIFIER>
InChI=1S/C26H29N3O4/c1-22(2)8-6-14-10-15-16(11-17(14)33-22)27-20(31)25(15)13-26-18(23(25,3)4)12-24(19(30)28-26)7-5-9-29(24)21(26)32/h6,8,10-11,18H,5,7,9,12-13H2,1-4H3,(H,27,31)(H,28,30)/t18-,24+,25+,26+/m1/s1

> <INCHI_KEY>
XLSISWUDRYYGNI-JTQLPTLWSA-N

> <FORMULA>
C26H29N3O4

> <MOLECULAR_WEIGHT>
447.535

> <EXACT_MASS>
447.215806426

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
48.701382278594195

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1'S,3'R,6S,7'S)-7,13'-dihydroxy-2,2,4',4'-tetramethyl-2H-9',14'-diazaspiro[chromeno[7,6-b]pyrrole-6,5'-tetracyclo[5.5.2.0^{1,9}.0^{3,7}]tetradecan]-13'-en-8'-one

> <ALOGPS_LOGP>
3.07

> <JCHEM_LOGP>
3.5894795163333324

> <ALOGPS_LOGS>
-4.22

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
4.601007482852141

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.8267019710262513

> <JCHEM_PKA_STRONGEST_BASIC>
1.083310371039041

> <JCHEM_POLAR_SURFACE_AREA>
94.72000000000001

> <JCHEM_REFRACTIVITY>
124.69679999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.73e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,3'R,6S,7'S)-7,13'-dihydroxy-2,2,4',4'-tetramethyl-9',14'-diazaspiro[chromeno[7,6-b]pyrrole-6,5'-tetracyclo[5.5.2.0^{1,9}.0^{3,7}]tetradecan]-13'-en-8'-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      12.691   0.690   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.909   2.658   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.193   5.594   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.170   6.121   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.219   0.945   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.185   0.734   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.750   2.238   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.715   0.564   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.619   2.585   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.036   2.314   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.861   4.795   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.734   3.389   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.997   2.641   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.566   2.144   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.418   3.724   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.330   4.965   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.479   3.385   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.444   3.523   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.172   0.492   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.965   5.749   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.179   1.579   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.628   1.804   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.478   4.745   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.061   1.684   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.956   4.209   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.483   2.174   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0       6.432   6.216   0.000  0.00  0.00           N+0
HETATM   28  N   UNK     0       2.865   0.577   0.000  0.00  0.00           N+0
HETATM   29  N   UNK     0       1.026   2.418   0.000  0.00  0.00           N+0
HETATM   30  O   UNK     0       0.630  -0.950   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       4.067   7.000   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       2.024   0.047   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      11.009   3.215   0.000  0.00  0.00           O+0
HETATM   34  H   UNK     0       1.742   4.893   0.000  0.00  0.00           H+0
CONECT    1   22                                                            
CONECT    2   22                                                            
CONECT    3   23                                                            
CONECT    4   23                                                            
CONECT    5    7    9                                                       
CONECT    6    8   14                                                       
CONECT    7    5   24                                                       
CONECT    8    6   22                                                       
CONECT    9    5   29                                                       
CONECT   10   14   15                                                       
CONECT   11   16   17                                                       
CONECT   12   18   24                                                       
CONECT   13   25   26                                                       
CONECT   14    6   10   17                                                  
CONECT   15   10   16   25                                                  
CONECT   16   11   15   27                                                  
CONECT   17   11   14   33                                                  
CONECT   18   12   23   26   34                                             
CONECT   19   24   28   30                                                  
CONECT   20   25   27   31                                                  
CONECT   21   26   29   32                                                  
CONECT   22    1    2    8   33                                             
CONECT   23    3    4   18   25                                             
CONECT   24    7   12   19   29                                             
CONECT   25   13   15   20   23                                             
CONECT   26   13   18   21   28                                             
CONECT   27   16   20                                                       
CONECT   28   19   26                                                       
CONECT   29    9   21   24                                                  
CONECT   30   19                                                            
CONECT   31   20                                                            
CONECT   32   21                                                            
CONECT   33   17   22                                                       
CONECT   34   18                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   80    0
END

Synonyms

Value	Source
(1S,3R,5S,7S)-2',2',4,4-Tetramethyl-2'H,13H-spiro(9,14-diazatetracyclo(5.5.2.01,9.03,7)tetradecane-5,6'-pyrano(3,2-F)indole)-7',8,13(8'H)-trione	MeSH

Molecular Formula

C₂₆H₂₉N₃O₄

Average Mass

447.535

Monoisotopic Mass

447.215806426

IUPAC Name

(1'S,3'R,6S,7'S)-7,13'-dihydroxy-2,2,4',4'-tetramethyl-2H-9',14'-diazaspiro[chromeno[7,6-b]pyrrole-6,5'-tetracyclo[5.5.2.0^{1,9}.0^{3,7}]tetradecan]-13'-en-8'-one

Traditional Name

(1'S,3'R,6S,7'S)-7,13'-dihydroxy-2,2,4',4'-tetramethyl-9',14'-diazaspiro[chromeno[7,6-b]pyrrole-6,5'-tetracyclo[5.5.2.0^{1,9}.0^{3,7}]tetradecan]-13'-en-8'-one

CAS Registry Number

Not Available

SMILES

[H][C@]12C[C@]34CCCN3C(=O)[C@@]1(C[C@]1(C(O)=NC3=CC5=C(C=CC(C)(C)O5)C=C13)C2(C)C)N=C4O

InChI Identifier

InChI=1S/C26H29N3O4/c1-22(2)8-6-14-10-15-16(11-17(14)33-22)27-20(31)25(15)13-26-18(23(25,3)4)12-24(19(30)28-26)7-5-9-29(24)21(26)32/h6,8,10-11,18H,5,7,9,12-13H2,1-4H3,(H,27,31)(H,28,30)/t18-,24+,25+,26+/m1/s1

InChI Key

XLSISWUDRYYGNI-JTQLPTLWSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2,2-dimethyl-1-benzopyrans. These are organic compounds containing a 1-benzopyran moiety that carries two methyl groups at the 2-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

2,2-dimethyl-1-benzopyrans

Alternative Parents

Substituents

2,2-dimethyl-1-benzopyran
Azaspirodecane
Alpha-amino acid or derivatives
Indolizidine
Dihydroindole
Indole or derivatives
2,5-dioxopiperazine
Dioxopiperazine
N-alkylpiperazine
Piperidinone
Delta-lactam
Alkyl aryl ether
Benzenoid
Piperidine
Piperazine
1,4-diazinane
Tertiary carboxylic acid amide
Pyrrolidine
Secondary carboxylic acid amide
Lactam
Carboxamide group
Oxacycle
Azacycle
Ether
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
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	0.027 g/L	ALOGPS
logP	3.07	ALOGPS
logP	3.59	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	3.83	ChemAxon
pKa (Strongest Basic)	1.08	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	94.72 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	124.7 m³·mol⁻¹	ChemAxon
Polarizability	48.7 Å³	ChemAxon
Number of Rings	7	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_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
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

40256727

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139591449

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 Asperversiamide B (MMDBc0024215)

MOL for #<Metabolite:0x00007f8dc77f10f0>

3D MOL for #<Metabolite:0x00007f8dc77f10f0>

3D SDF for #<Metabolite:0x00007f8dc77f10f0>

3D-SDF for #<Metabolite:0x00007f8dc77f10f0>

PDB for #<Metabolite:0x00007f8dc77f10f0>

3D PDB for #<Metabolite:0x00007f8dc77f10f0>

SMILES for #<Metabolite:0x00007f8dc77f10f0>

INCHI for #<Metabolite:0x00007f8dc77f10f0>

Structure for #<Metabolite:0x00007f8dc77f10f0>

3D Structure for #<Metabolite:0x00007f8dc77f10f0>