MiMeDB: Showing metabocard for Cochlioquinone B (MMDBc0006910)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 00:16:14 UTC

Update Date

2025-10-07 16:05:15 UTC

Metabolite ID

MMDBc0006910

Metabolite Identification

Common Name

Cochlioquinone B

Description

Cochlioquinone B is a member of the terpenoid chemical class, specifically a natural product with notable biological activities. It has been synthesized alongside other terpenoid compounds, highlighting its structural significance in the realm of natural products (PMID:40523914 ). The compound is part of a diverse family of cochlioquinones, which includes unique structural variants such as bipolacochlioquinone A and B, characterized by their complex pentacyclic systems (PMID:35427653 ). Cochlioquinone B and its derivatives, particularly CoB1, have been isolated from the endophytic fungus Bipolaris sorokiniana found in Salvia miltiorrhiza, where they play a crucial role in modulating inflammatory responses and enhancing host defense against pulmonary pathogens (PMID:34624808 , PMID:32747503 ). Furthermore, Cochlioquinone B exhibits antimicrobial properties, demonstrating activity against methicillin-resistant Staphylococcus aureus (MRSA) and showing synergistic effects against other pathogens (PMID:32215711 ). Its isolation alongside other known compounds further underscores its relevance in the study of bioactive natural products (PMID:11908970 ).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152102162D          

 39 42  0  0  1  0            999 V2000
    6.1323    3.8327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5922    2.2736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5120    1.3382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8593    1.1823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8933    0.5280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0787    1.1823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7314    3.5209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3222    3.6768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6990    0.8704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8889    3.2091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8889    1.0264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0787    3.3650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8918    1.0264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7314    1.3382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0521    2.8973    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9720    1.9618    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1618    1.8059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5415    1.4941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0816    0.8704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1913    1.9618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2391    1.4941    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1589    2.4296    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2420    2.7414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6217    2.4296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8116    2.2736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0492    1.3382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6188    1.8059    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4614    2.7414    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8116    0.0909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7019    3.3650    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8918    3.2091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2051    2.1483    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9690    2.2736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2715    2.8973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8623    3.0532    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7019    1.1823    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0015    2.1177    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7792    2.1177    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3488    2.5855    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  1  1  0  0  0  0
 11  9  1  0  0  0  0
 12 10  1  0  0  0  0
 15  2  1  6  0  0  0
 15  8  1  0  0  0  0
 16  3  1  1  0  0  0
 17 13  2  0  0  0  0
 17 16  1  0  0  0  0
 18 14  1  0  0  0  0
 19 13  1  0  0  0  0
 19 18  1  0  0  0  0
 20 14  1  0  0  0  0
 21  9  1  0  0  0  0
 22 10  1  0  0  0  0
 23 15  1  0  0  0  0
 23 16  1  0  0  0  0
 24 17  1  0  0  0  0
 25 18  2  0  0  0  0
 25 24  1  0  0  0  0
 26  4  1  0  0  0  0
 26  5  1  0  0  0  0
 21 26  1  6  0  0  0
 27  6  1  6  0  0  0
 27 11  1  0  0  0  0
 27 20  1  0  0  0  0
 27 22  1  0  0  0  0
 28  7  1  6  0  0  0
 28 12  1  0  0  0  0
 28 20  1  0  0  0  0
 29 19  2  0  0  0  0
 30 23  2  0  0  0  0
 31 24  2  0  0  0  0
 32 26  1  0  0  0  0
 33 21  1  0  0  0  0
 33 22  1  0  0  0  0
 34 25  1  0  0  0  0
 34 28  1  0  0  0  0
 15 35  1  1  0  0  0
 16 36  1  6  0  0  0
 37 20  1  0  0  0  0
 21 38  1  1  0  0  0
 22 39  1  1  0  0  0
M  END


  Mrv1652305152102162D          

 39 42  0  0  1  0            999 V2000
    6.1323    3.8327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5922    2.2736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5120    1.3382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8593    1.1823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8933    0.5280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0787    1.1823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7314    3.5209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3222    3.6768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6990    0.8704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8889    3.2091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8889    1.0264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0787    3.3650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8918    1.0264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7314    1.3382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0521    2.8973    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9720    1.9618    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1618    1.8059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5415    1.4941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0816    0.8704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1913    1.9618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2391    1.4941    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1589    2.4296    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2420    2.7414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6217    2.4296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8116    2.2736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0492    1.3382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6188    1.8059    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4614    2.7414    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8116    0.0909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7019    3.3650    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8918    3.2091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2051    2.1483    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9690    2.2736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2715    2.8973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8623    3.0532    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7019    1.1823    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0015    2.1177    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7792    2.1177    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3488    2.5855    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  1  1  0  0  0  0
 11  9  1  0  0  0  0
 12 10  1  0  0  0  0
 15  2  1  6  0  0  0
 15  8  1  0  0  0  0
 16  3  1  1  0  0  0
 17 13  2  0  0  0  0
 17 16  1  0  0  0  0
 18 14  1  0  0  0  0
 19 13  1  0  0  0  0
 19 18  1  0  0  0  0
 20 14  1  0  0  0  0
 21  9  1  0  0  0  0
 22 10  1  0  0  0  0
 23 15  1  0  0  0  0
 23 16  1  0  0  0  0
 24 17  1  0  0  0  0
 25 18  2  0  0  0  0
 25 24  1  0  0  0  0
 26  4  1  0  0  0  0
 26  5  1  0  0  0  0
 21 26  1  6  0  0  0
 27  6  1  6  0  0  0
 27 11  1  0  0  0  0
 27 20  1  0  0  0  0
 27 22  1  0  0  0  0
 28  7  1  6  0  0  0
 28 12  1  0  0  0  0
 28 20  1  0  0  0  0
 29 19  2  0  0  0  0
 30 23  2  0  0  0  0
 31 24  2  0  0  0  0
 32 26  1  0  0  0  0
 33 21  1  0  0  0  0
 33 22  1  0  0  0  0
 34 25  1  0  0  0  0
 34 28  1  0  0  0  0
 15 35  1  1  0  0  0
 16 36  1  6  0  0  0
 37 20  1  0  0  0  0
 21 38  1  1  0  0  0
 22 39  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0006910

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@](C)(CC)C(=O)[C@@]([H])(C)C1=CC(=O)C2=C(O[C@]3(C)CC[C@@]4([H])O[C@]([H])(CC[C@]4(C)C3([H])C2)C(C)(C)O)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C28H40O6/c1-8-15(2)23(30)16(3)17-13-19(29)18-14-20-27(6)11-9-21(26(4,5)32)33-22(27)10-12-28(20,7)34-25(18)24(17)31/h13,15-16,20-22,32H,8-12,14H2,1-7H3/t15-,16-,20?,21+,22+,27+,28+/m0/s1

> <INCHI_KEY>
NTPNSKLZWVYKGK-DMBAJPFZSA-N

> <FORMULA>
C28H40O6

> <MOLECULAR_WEIGHT>
472.622

> <EXACT_MASS>
472.282489008

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
53.27430309606177

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,4aR,10aR,12aR)-2-(2-hydroxypropan-2-yl)-4a,10a-dimethyl-8-[(2S,4S)-4-methyl-3-oxohexan-2-yl]-2,3,4,4a,4b,5,6,9,10a,11,12,12a-dodecahydro-1,10-dioxatetraphene-6,9-dione

> <ALOGPS_LOGP>
4.37

> <JCHEM_LOGP>
4.668173634

> <ALOGPS_LOGS>
-5.26

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.88643114496645

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.326104959527221

> <JCHEM_PKA_STRONGEST_BASIC>
-3.093556462470996

> <JCHEM_POLAR_SURFACE_AREA>
89.9

> <JCHEM_REFRACTIVITY>
131.55609999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.58e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,4aR,10aR,12aR)-2-(2-hydroxypropan-2-yl)-4a,10a-dimethyl-8-[(2S,4S)-4-methyl-3-oxohexan-2-yl]-2,3,4,4b,5,11,12,12a-octahydro-1,10-dioxatetraphene-6,9-dione

> <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      11.447   7.154   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.439   4.244   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.422   2.498   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.204   2.207   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.401   0.986   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.147   2.207   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.365   6.572   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.935   6.863   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.171   1.625   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.659   5.990   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.659   1.916   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.147   6.281   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.398   1.916   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.365   2.498   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.431   5.408   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.414   3.662   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.902   3.371   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.878   2.789   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.886   1.625   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.357   3.662   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.180   2.789   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.163   4.535   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.918   5.117   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.894   4.535   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.382   4.244   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -5.692   2.498   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.155   3.371   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.861   5.117   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       3.382   0.170   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       6.910   6.281   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       5.398   5.990   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      -5.983   4.010   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      -3.676   4.244   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       2.373   5.408   0.000  0.00  0.00           O+0
HETATM   35  H   UNK     0      10.943   5.699   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0       6.910   2.207   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.869   3.953   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0      -5.188   3.953   0.000  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.651   4.826   0.000  0.00  0.00           H+0
CONECT    1    8                                                            
CONECT    2   15                                                            
CONECT    3   16                                                            
CONECT    4   26                                                            
CONECT    5   26                                                            
CONECT    6   27                                                            
CONECT    7   28                                                            
CONECT    8    1   15                                                       
CONECT    9   11   21                                                       
CONECT   10   12   22                                                       
CONECT   11    9   27                                                       
CONECT   12   10   28                                                       
CONECT   13   17   19                                                       
CONECT   14   18   20                                                       
CONECT   15    2    8   23   35                                             
CONECT   16    3   17   23   36                                             
CONECT   17   13   16   24                                                  
CONECT   18   14   19   25                                                  
CONECT   19   13   18   29                                                  
CONECT   20   14   27   28   37                                             
CONECT   21    9   26   33   38                                             
CONECT   22   10   27   33   39                                             
CONECT   23   15   16   30                                                  
CONECT   24   17   25   31                                                  
CONECT   25   18   24   34                                                  
CONECT   26    4    5   21   32                                             
CONECT   27    6   11   20   22                                             
CONECT   28    7   12   20   34                                             
CONECT   29   19                                                            
CONECT   30   23                                                            
CONECT   31   24                                                            
CONECT   32   26                                                            
CONECT   33   21   22                                                       
CONECT   34   25   28                                                       
CONECT   35   15                                                            
CONECT   36   16                                                            
CONECT   37   20                                                            
CONECT   38   21                                                            
CONECT   39   22                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   84    0
END

Synonyms

Not Available

Molecular Formula

C₂₈H₄₀O₆

Average Mass

472.622

Monoisotopic Mass

472.282489008

IUPAC Name

(2R,4aR,10aR,12aR)-2-(2-hydroxypropan-2-yl)-4a,10a-dimethyl-8-[(2S,4S)-4-methyl-3-oxohexan-2-yl]-2,3,4,4a,4b,5,6,9,10a,11,12,12a-dodecahydro-1,10-dioxatetraphene-6,9-dione

Traditional Name

(2R,4aR,10aR,12aR)-2-(2-hydroxypropan-2-yl)-4a,10a-dimethyl-8-[(2S,4S)-4-methyl-3-oxohexan-2-yl]-2,3,4,4b,5,11,12,12a-octahydro-1,10-dioxatetraphene-6,9-dione

CAS Registry Number

Not Available

SMILES

[H][C@](C)(CC)C(=O)[C@@]([H])(C)C1=CC(=O)C2=C(O[C@]3(C)CC[C@@]4([H])O[C@]([H])(CC[C@]4(C)C3([H])C2)C(C)(C)O)C1=O

InChI Identifier

InChI=1S/C28H40O6/c1-8-15(2)23(30)16(3)17-13-19(29)18-14-20-27(6)11-9-21(26(4,5)32)33-22(27)10-12-28(20,7)34-25(18)24(17)31/h13,15-16,20-22,32H,8-12,14H2,1-7H3/t15-,16-,20?,21+,22+,27+,28+/m0/s1

InChI Key

NTPNSKLZWVYKGK-DMBAJPFZSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxanes. Oxanes are compounds containing an oxane (tetrahydropyran) ring, which is a six-member saturated aliphatic heterocycle with one oxygen atom and five carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Oxanes

Sub Class

Not Available

Direct Parent

Oxanes

Alternative Parents

Substituents

Oxane
Vinylogous ester
Tertiary alcohol
Ketone
Oxacycle
Ether
Dialkyl ether
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	0.0026 g/L	ALOGPS
logP	4.37	ALOGPS
logP	4.67	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	14.33	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	89.9 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	131.56 m³·mol⁻¹	ChemAxon
Polarizability	53.27 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

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	Species

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	3	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

C00023741

Chemspider ID

78436999

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139584864

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

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 Cochlioquinone B (MMDBc0006910)

MOL for #<Metabolite:0x00007f288f6ed138>

3D MOL for #<Metabolite:0x00007f288f6ed138>

3D SDF for #<Metabolite:0x00007f288f6ed138>

3D-SDF for #<Metabolite:0x00007f288f6ed138>

PDB for #<Metabolite:0x00007f288f6ed138>

3D PDB for #<Metabolite:0x00007f288f6ed138>

SMILES for #<Metabolite:0x00007f288f6ed138>

INCHI for #<Metabolite:0x00007f288f6ed138>

Structure for #<Metabolite:0x00007f288f6ed138>

3D Structure for #<Metabolite:0x00007f288f6ed138>