MiMeDB: Showing metabocard for Epicorazine C (MMDBc0001995)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 20:35:05 UTC

Update Date

2025-10-07 16:04:32 UTC

Metabolite ID

MMDBc0001995

Metabolite Identification

Common Name

Epicorazine C

Description

Epicorazine C is a member of the chemical class of antimicrobial metabolites. This compound has been identified through spectral data, including NMR, ESI-MS, and DCI-MS, alongside its analogs epicorazine A and B, although it has not been reported as a constituent of any specific organism (PMID:16550228 ). Isolated from the fungus Stereum hirsutum HKI 0195, epicorazine C exhibits antimicrobial properties, indicating potential biological significance in combating microbial infections (PMID:11513044 ). Despite its identification and characterization, there is limited literature available regarding the specific biological mechanisms and broader applications of epicorazine C, suggesting that further research is warranted to fully understand its pharmacological potential and ecological role.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305142122352D          

 36 41  0  0  1  0            999 V2000
    9.6266    1.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3325    2.4306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9117    1.9372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5982    0.6749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9662    2.8672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2915    1.1504    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2565    2.4203    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.1061    1.0197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5179    2.5613    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4447    2.5670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1906    1.1608    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.9974    1.9212    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5354    1.6438    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0024    1.0141    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5548    2.6940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9664    0.8169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8517    1.0980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6803    2.4044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1368    1.9679    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3918    1.5400    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.4002    0.2489    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2238    3.3321    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1658    3.3434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6576    0.5310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2813    0.2377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7888    3.4851    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7258    0.0277    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1320    1.4014    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    6.4056    2.1038    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    8.4724    0.3455    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0994    3.2302    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0384    3.2014    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4695    0.3843    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8120    1.7905    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7236    1.7905    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8143    0.8674    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  6  4  1  0  0  0  0
  7  5  1  0  0  0  0
  8  1  1  0  0  0  0
  8  6  1  0  0  0  0
  9  2  1  0  0  0  0
 10  3  1  0  0  0  0
 10  7  1  0  0  0  0
 11  3  1  0  0  0  0
 12  6  1  0  0  0  0
 12  9  1  0  0  0  0
 13  7  1  0  0  0  0
 14 11  1  0  0  0  0
 14 13  1  0  0  0  0
 17  4  1  0  0  0  0
 17 16  1  0  0  0  0
 18  5  1  0  0  0  0
 18 15  1  0  0  0  0
 19 12  1  0  0  0  0
 19 15  1  0  0  0  0
 19 17  1  0  0  0  0
 20 13  1  0  0  0  0
 20 16  1  0  0  0  0
 20 18  1  0  0  0  0
 21  8  2  0  0  0  0
  9 22  1  1  0  0  0
 23 10  2  0  0  0  0
 11 24  1  1  0  0  0
 14 25  1  1  0  0  0
 26 15  2  0  0  0  0
 27 16  2  0  0  0  0
 28 17  1  0  0  0  0
 29 18  1  0  0  0  0
 29 28  1  0  0  0  0
  6 30  1  6  0  0  0
  7 31  1  1  0  0  0
  9 32  1  6  0  0  0
 11 33  1  6  0  0  0
 12 34  1  1  0  0  0
 13 35  1  1  0  0  0
 14 36  1  6  0  0  0
M  END


  Mrv1652305142122352D          

 36 41  0  0  1  0            999 V2000
    9.6266    1.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3325    2.4306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9117    1.9372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5982    0.6749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9662    2.8672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2915    1.1504    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2565    2.4203    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.1061    1.0197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5179    2.5613    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4447    2.5670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1906    1.1608    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.9974    1.9212    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5354    1.6438    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0024    1.0141    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5548    2.6940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9664    0.8169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8517    1.0980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6803    2.4044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1368    1.9679    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3918    1.5400    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.4002    0.2489    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2238    3.3321    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1658    3.3434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6576    0.5310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2813    0.2377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7888    3.4851    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7258    0.0277    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1320    1.4014    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    6.4056    2.1038    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    8.4724    0.3455    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0994    3.2302    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0384    3.2014    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4695    0.3843    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8120    1.7905    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7236    1.7905    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8143    0.8674    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  6  4  1  0  0  0  0
  7  5  1  0  0  0  0
  8  1  1  0  0  0  0
  8  6  1  0  0  0  0
  9  2  1  0  0  0  0
 10  3  1  0  0  0  0
 10  7  1  0  0  0  0
 11  3  1  0  0  0  0
 12  6  1  0  0  0  0
 12  9  1  0  0  0  0
 13  7  1  0  0  0  0
 14 11  1  0  0  0  0
 14 13  1  0  0  0  0
 17  4  1  0  0  0  0
 17 16  1  0  0  0  0
 18  5  1  0  0  0  0
 18 15  1  0  0  0  0
 19 12  1  0  0  0  0
 19 15  1  0  0  0  0
 19 17  1  0  0  0  0
 20 13  1  0  0  0  0
 20 16  1  0  0  0  0
 20 18  1  0  0  0  0
 21  8  2  0  0  0  0
  9 22  1  1  0  0  0
 23 10  2  0  0  0  0
 11 24  1  1  0  0  0
 14 25  1  1  0  0  0
 26 15  2  0  0  0  0
 27 16  2  0  0  0  0
 28 17  1  0  0  0  0
 29 18  1  0  0  0  0
 29 28  1  0  0  0  0
  6 30  1  6  0  0  0
  7 31  1  1  0  0  0
  9 32  1  6  0  0  0
 11 33  1  6  0  0  0
 12 34  1  1  0  0  0
 13 35  1  1  0  0  0
 14 36  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0001995

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]12CC34SSC5(C[C@]6([H])C(=O)C=C[C@]([H])(O)[C@@]6([H])N5C3=O)C(=O)N4[C@]1([H])[C@@]([H])(O)[C@@]([H])(O)CC2=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H18N2O7S2/c21-8-1-2-9(22)12-6(8)4-17-16(27)20-13-7(10(23)3-11(24)14(13)25)5-18(20,29-28-17)15(26)19(12)17/h1-2,6-7,9,11-14,22,24-25H,3-5H2/t6-,7+,9+,11+,12+,13+,14+,17?,18?/m1/s1

> <INCHI_KEY>
NCDIBOQDVNONGL-AONPJNASSA-N

> <FORMULA>
C18H18N2O7S2

> <MOLECULAR_WEIGHT>
438.47

> <EXACT_MASS>
438.055543276

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
40.90006147951051

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4S,5S,9S,14S,15R,16S,19R)-5,15,16-trihydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0^{1,13}.0^{3,11}.0^{4,9}.0^{14,19}]docos-6-ene-2,8,12,18-tetrone

> <ALOGPS_LOGP>
-0.71

> <JCHEM_LOGP>
-0.8634750440000001

> <ALOGPS_LOGS>
-0.94

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.944687444815788

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.093443759361794

> <JCHEM_PKA_STRONGEST_BASIC>
-3.178059655235966

> <JCHEM_POLAR_SURFACE_AREA>
135.45

> <JCHEM_REFRACTIVITY>
102.21319999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.05e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4S,5S,9S,14S,15R,16S,19R)-5,15,16-trihydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0^{1,13}.0^{3,11}.0^{4,9}.0^{14,19}]docos-6-ene-2,8,12,18-tetrone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 14-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   14-MAY-21         0                                  
HETATM    1  C   UNK     0      17.970   3.098   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      17.421   4.537   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.435   3.616   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.183   1.260   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.270   5.352   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      15.477   2.147   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.946   4.518   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      16.998   1.903   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      15.900   4.781   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.430   4.792   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.956   2.167   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.928   3.586   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.466   3.068   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.471   1.893   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.236   5.029   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.137   1.525   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.790   2.050   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.603   4.488   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0      13.322   3.673   0.000  0.00  0.00           N+0
HETATM   20  N   UNK     0      10.065   2.875   0.000  0.00  0.00           N+0
HETATM   21  O   UNK     0      17.547   0.465   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      15.351   6.220   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       5.909   6.241   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       4.961   0.991   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       7.992   0.444   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      12.672   6.505   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      10.688   0.052   0.000  0.00  0.00           O+0
HETATM   28  S   UNK     0      11.446   2.616   0.000  0.00  0.00           S+0
HETATM   29  S   UNK     0      11.957   3.927   0.000  0.00  0.00           S+0
HETATM   30  H   UNK     0      15.815   0.645   0.000  0.00  0.00           H+0
HETATM   31  H   UNK     0       7.652   6.030   0.000  0.00  0.00           H+0
HETATM   32  H   UNK     0      16.872   5.976   0.000  0.00  0.00           H+0
HETATM   33  H   UNK     0       6.476   0.717   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0      16.449   3.342   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0       6.951   3.342   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0       8.987   1.619   0.000  0.00  0.00           H+0
CONECT    1    2    8                                                       
CONECT    2    1    9                                                       
CONECT    3   10   11                                                       
CONECT    4    6   17                                                       
CONECT    5    7   18                                                       
CONECT    6    4    8   12   30                                             
CONECT    7    5   10   13   31                                             
CONECT    8    1    6   21                                                  
CONECT    9    2   12   22   32                                             
CONECT   10    3    7   23                                                  
CONECT   11    3   14   24   33                                             
CONECT   12    6    9   19   34                                             
CONECT   13    7   14   20   35                                             
CONECT   14   11   13   25   36                                             
CONECT   15   18   19   26                                                  
CONECT   16   17   20   27                                                  
CONECT   17    4   16   19   28                                             
CONECT   18    5   15   20   29                                             
CONECT   19   12   15   17                                                  
CONECT   20   13   16   18                                                  
CONECT   21    8                                                            
CONECT   22    9                                                            
CONECT   23   10                                                            
CONECT   24   11                                                            
CONECT   25   14                                                            
CONECT   26   15                                                            
CONECT   27   16                                                            
CONECT   28   17   29                                                       
CONECT   29   18   28                                                       
CONECT   30    6                                                            
CONECT   31    7                                                            
CONECT   32    9                                                            
CONECT   33   11                                                            
CONECT   34   12                                                            
CONECT   35   13                                                            
CONECT   36   14                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   82    0
END

Synonyms

Not Available

Molecular Formula

C₁₈H₁₈N₂O₇S₂

Average Mass

438.47

Monoisotopic Mass

438.055543276

IUPAC Name

(4S,5S,9S,14S,15R,16S,19R)-5,15,16-trihydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0^{1,13}.0^{3,11}.0^{4,9}.0^{14,19}]docos-6-ene-2,8,12,18-tetrone

Traditional Name

(4S,5S,9S,14S,15R,16S,19R)-5,15,16-trihydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0^{1,13}.0^{3,11}.0^{4,9}.0^{14,19}]docos-6-ene-2,8,12,18-tetrone

CAS Registry Number

Not Available

SMILES

[H][C@@]12CC34SSC5(C[C@]6([H])C(=O)C=C[C@]([H])(O)[C@@]6([H])N5C3=O)C(=O)N4[C@]1([H])[C@@]([H])(O)[C@@]([H])(O)CC2=O

InChI Identifier

InChI=1S/C18H18N2O7S2/c21-8-1-2-9(22)12-6(8)4-17-16(27)20-13-7(10(23)3-11(24)14(13)25)5-18(20,29-28-17)15(26)19(12)17/h1-2,6-7,9,11-14,22,24-25H,3-5H2/t6-,7+,9+,11+,12+,13+,14+,17?,18?/m1/s1

InChI Key

NCDIBOQDVNONGL-AONPJNASSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as epipolythiodioxopiperazines. Epipolythiodioxopiperazines are compounds containing an epipolythiodioxopiperazine moiety, which consists of a 2,3-dithia-5,7-diazabicyclo[2.2.2]Octane-6,8-dione ring system. One distinct characteristics of Epipolythiodioxopiperazines is the presence of unique di- or polysulfide bridges.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Diazinanes

Sub Class

Piperazines

Direct Parent

Epipolythiodioxopiperazines

Alternative Parents

Substituents

Alpha-amino acid or derivatives
Epipolythiodioxopiperazine
Indole or derivatives
Cyclohexenone
N-alkylpiperazine
Dithiazinane
Cyclic alcohol
Tertiary carboxylic acid amide
Pyrrolidine
Carboxamide group
Ketone
Secondary alcohol
Lactam
Organic disulfide
Carboxylic acid derivative
Azacycle
Polyol
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Alcohol
Organic oxygen compound
Carbonyl group
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
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	50.5 g/L	ALOGPS
logP	-0.71	ALOGPS
logP	-0.86	ChemAxon
logS	-0.94	ALOGPS
pKa (Strongest Acidic)	13.09	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	135.45 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	102.21 m³·mol⁻¹	ChemAxon
Polarizability	40.9 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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_3_4) - 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
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-18	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

This table shows at most 5 pathways. For the full list of associated pathways:

See All Associated Bacterial Pathways

Name	SMPDB/PathBank

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	Basidiomycota	2	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

78442458

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139583422

PDB ID

Not Available

ChEBI ID

Not Available

CMMC Knowledgebase

Not Available

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 Epicorazine C (MMDBc0001995)

MOL for #<Metabolite:0x00007fd4288b4490>

3D MOL for #<Metabolite:0x00007fd4288b4490>

3D SDF for #<Metabolite:0x00007fd4288b4490>

3D-SDF for #<Metabolite:0x00007fd4288b4490>

PDB for #<Metabolite:0x00007fd4288b4490>

3D PDB for #<Metabolite:0x00007fd4288b4490>

SMILES for #<Metabolite:0x00007fd4288b4490>

INCHI for #<Metabolite:0x00007fd4288b4490>

Structure for #<Metabolite:0x00007fd4288b4490>

3D Structure for #<Metabolite:0x00007fd4288b4490>