MiMeDB: Showing metabocard for Asterriquinone (MMDBc0012852)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 04:17:23 UTC

Update Date

2022-08-31 06:35:13 UTC

Metabolite ID

MMDBc0012852

Metabolite Identification

Common Name

Asterriquinone

Description

asterriquinone belongs to the class of organic compounds known as n-alkylindoles. N-alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 1-position. asterriquinone is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004171515352D          

 38 42  0  0  0  0            999 V2000
    6.2692   -1.4270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4846   -1.1721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6999   -0.9171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2296   -1.9567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7817   -2.5698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7395   -0.3875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2546    0.2800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7395    0.9474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4846    1.7320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6776    1.9036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1256    1.2905    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4227    2.6882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6157    2.8597    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9747    3.3013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7817    3.1298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3337    3.7429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0366    2.3451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8436    2.1736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7198    4.0859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9351    4.3409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9351    5.1659    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7198    5.4208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0553    6.1745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8758    6.2607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3607    5.5933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0252    4.8396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2047    4.7534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2677    5.6508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7526    6.3182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7828    4.9833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6003    6.1357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8466    5.8001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5241    0.6925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2386    1.1050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9531    0.6925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9531   -0.1325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2386   -0.5450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5241   -0.1325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  2  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
  9 17  1  0  0  0  0
 17 18  2  0  0  0  0
 14 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 19 27  1  0  0  0  0
 22 27  1  0  0  0  0
 21 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  2  0  0  0  0
  8 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
  6 38  1  0  0  0  0
 33 38  1  0  0  0  0
M  END


  Mrv1533004171515352D          

 38 42  0  0  0  0            999 V2000
    6.2692   -1.4270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4846   -1.1721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6999   -0.9171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2296   -1.9567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7817   -2.5698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7395   -0.3875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2546    0.2800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7395    0.9474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4846    1.7320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6776    1.9036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1256    1.2905    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4227    2.6882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6157    2.8597    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9747    3.3013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7817    3.1298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3337    3.7429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0366    2.3451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8436    2.1736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7198    4.0859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9351    4.3409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9351    5.1659    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7198    5.4208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0553    6.1745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8758    6.2607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3607    5.5933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0252    4.8396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2047    4.7534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2677    5.6508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7526    6.3182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7828    4.9833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6003    6.1357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8466    5.8001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5241    0.6925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2386    1.1050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9531    0.6925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9531   -0.1325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2386   -0.5450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5241   -0.1325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  2  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
  9 17  1  0  0  0  0
 17 18  2  0  0  0  0
 14 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 19 27  1  0  0  0  0
 22 27  1  0  0  0  0
 21 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  2  0  0  0  0
  8 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
  6 38  1  0  0  0  0
 33 38  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0012852

> <DATABASE_NAME>
MIME

> <SMILES>
CC(C)(C=C)N1C=C(C2=CC=CC=C12)C1=C(O)C(=O)C(C2=CN(C3=CC=CC=C23)C(C)(C)C=C)=C(O)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C32H30N2O4/c1-7-31(3,4)33-17-21(19-13-9-11-15-23(19)33)25-27(35)29(37)26(30(38)28(25)36)22-18-34(32(5,6)8-2)24-16-12-10-14-20(22)24/h7-18,35,38H,1-2H2,3-6H3

> <INCHI_KEY>
KMHWTYMNRHJTQG-UHFFFAOYSA-N

> <FORMULA>
C32H30N2O4

> <MOLECULAR_WEIGHT>
506.602

> <EXACT_MASS>
506.220557454

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
56.67696407656523

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2,5-dihydroxy-3,6-bis[1-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]cyclohexa-2,5-diene-1,4-dione

> <ALOGPS_LOGP>
5.20

> <JCHEM_LOGP>
6.8246531893333335

> <ALOGPS_LOGS>
-5.12

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.586804115510724

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.564461266595032

> <JCHEM_PKA_STRONGEST_BASIC>
-5.162694121887907

> <JCHEM_POLAR_SURFACE_AREA>
84.46000000000001

> <JCHEM_REFRACTIVITY>
152.27359999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.87e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
asterriquinone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      11.702  -2.664   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.238  -2.188   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.773  -1.712   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.762  -3.653   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.792  -4.797   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      10.714  -0.723   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       9.809   0.523   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.714   1.769   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.238   3.233   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.732   3.553   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       7.701   2.409   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       8.256   5.018   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.749   5.338   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       9.286   6.162   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.792   5.842   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      11.823   6.987   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      11.268   4.378   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      12.775   4.057   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.810   7.627   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.346   8.103   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       7.346   9.643   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       8.810  10.119   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.437  11.526   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.968  11.687   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.873  10.441   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.247   9.034   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.715   8.873   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.100  10.548   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.005  11.794   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.195   9.302   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.854  11.453   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.447  10.827   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      12.178   1.293   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      13.512   2.063   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      14.846   1.293   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      14.846  -0.247   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      13.512  -1.017   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      12.178  -0.247   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4    6                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4                                                            
CONECT    6    2    7   38                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   33                                                  
CONECT    9    8   10   17                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   19                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15    9   18                                                  
CONECT   18   17                                                            
CONECT   19   14   20   27                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   28                                                  
CONECT   22   21   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   19   22                                                  
CONECT   28   21   29   30   31                                             
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   28   32                                                       
CONECT   32   31                                                            
CONECT   33    8   34   38                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37    6   33                                                  
MASTER        0    0    0    0    0    0    0    0   38    0   84    0
END

Synonyms

Value	Source
2,5-Bis[1-(1,1-dimethylallyl)-1H-indol-3-yl]-3,6-dihydroxy-1,4-benzoquinone	ChEBI

Molecular Formula

C₃₂H₃₀N₂O₄

Average Mass

506.602

Monoisotopic Mass

506.220557454

IUPAC Name

2,5-dihydroxy-3,6-bis[1-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]cyclohexa-2,5-diene-1,4-dione

Traditional Name

asterriquinone

CAS Registry Number

Not Available

SMILES

CC(C)(C=C)N1C=C(C2=CC=CC=C12)C1=C(O)C(=O)C(C2=CN(C3=CC=CC=C23)C(C)(C)C=C)=C(O)C1=O

InChI Identifier

InChI=1S/C32H30N2O4/c1-7-31(3,4)33-17-21(19-13-9-11-15-23(19)33)25-27(35)29(37)26(30(38)28(25)36)22-18-34(32(5,6)8-2)24-16-12-10-14-20(22)24/h7-18,35,38H,1-2H2,3-6H3

InChI Key

KMHWTYMNRHJTQG-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-alkylindoles. N-alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 1-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

N-alkylindoles

Direct Parent

N-alkylindoles

Alternative Parents

Substituents

N-alkylindole
Indole
P-benzoquinone
Quinone
Benzenoid
Substituted pyrrole
Pyrrole
Heteroaromatic compound
Vinylogous acid
Ketone
Cyclic ketone
Enol
Azacycle
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

asterriquinones (CHEBI:51881 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.0039 g/L	ALOGPS
logP	5.2	ALOGPS
logP	6.82	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	5.56	ChemAxon
pKa (Strongest Basic)	-5.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	84.46 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	152.27 m³·mol⁻¹	ChemAxon
Polarizability	56.68 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Spectra

Not Available

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

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

100329

PDB ID

Not Available

ChEBI ID

51881

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 Asterriquinone (MMDBc0012852)

MOL for #<Metabolite:0x00005645ca20f718>

3D MOL for #<Metabolite:0x00005645ca20f718>

3D SDF for #<Metabolite:0x00005645ca20f718>

3D-SDF for #<Metabolite:0x00005645ca20f718>

PDB for #<Metabolite:0x00005645ca20f718>

3D PDB for #<Metabolite:0x00005645ca20f718>

SMILES for #<Metabolite:0x00005645ca20f718>

INCHI for #<Metabolite:0x00005645ca20f718>

Structure for #<Metabolite:0x00005645ca20f718>

3D Structure for #<Metabolite:0x00005645ca20f718>