MiMeDB: Showing metabocard for 4â€²-epi-N-2-hydroxyethyl-azachaetoviridin A (MMDBc0006794)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 00:11:57 UTC

Update Date

2022-08-31 06:26:02 UTC

Metabolite ID

MMDBc0006794

Metabolite Identification

Common Name

4â€²-epi-N-2-hydroxyethyl-azachaetoviridin A

Description

CHEMBL2381973 belongs to the class of organic compounds known as isoquinolones and derivatives. These are aromatic polycyclic compounds containing a ketone bearing isoquinoline moiety. Based on a literature review very few articles have been published on CHEMBL2381973.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152102112D          

 38 40  0  0  1  0            999 V2000
    8.5134    1.7119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6442    0.3094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9729    2.2359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3661    3.8383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7565   -0.8892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6888    1.7377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4296    1.0622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9950    0.3610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2150    1.8150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8250    2.5420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7358   -0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9558    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2542    1.0365    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7651    2.4662    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9617    3.2674    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1704    0.3867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9112   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5212    0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1640    1.0941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6966    0.4640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4766   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3606    1.8953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6520   -0.9642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4002    0.7822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2620   -0.2372    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8666   -1.7170    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    4.7804    1.1137    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2596    3.2432    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7539    3.4977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1528    2.1256    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2174   -1.6655    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6989    1.2168    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4608   -0.0406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0396    1.7892    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3850   -0.3660    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0788    1.0107    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1695    3.0371    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1583    4.0686    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  1  0  0  0  0
  8  7  2  0  0  0  0
 10  9  1  0  0  0  0
 13  2  1  6  0  0  0
 13  6  1  0  0  0  0
 13  7  1  0  0  0  0
 14  3  1  6  0  0  0
 15  4  1  0  0  0  0
 15 14  1  0  0  0  0
 16  8  1  0  0  0  0
 16 11  2  0  0  0  0
 17 11  1  0  0  0  0
 18 12  2  0  0  0  0
 18 17  1  0  0  0  0
 20 18  1  0  0  0  0
 20 19  2  0  0  0  0
 21 17  2  0  0  0  0
 22 14  1  0  0  0  0
 22 19  1  0  0  0  0
 23 21  1  0  0  0  0
 24 19  1  0  0  0  0
 25  5  1  6  0  0  0
 25 20  1  0  0  0  0
 25 23  1  0  0  0  0
 26 21  1  0  0  0  0
 27  9  1  0  0  0  0
 27 12  1  0  0  0  0
 27 16  1  0  0  0  0
 28 10  1  0  0  0  0
 15 29  1  1  0  0  0
 30 22  2  0  0  0  0
 31 23  2  0  0  0  0
 32 24  2  0  0  0  0
 33 24  1  0  0  0  0
 33 25  1  0  0  0  0
 34  7  1  0  0  0  0
 35  8  1  0  0  0  0
 13 36  1  1  0  0  0
 14 37  1  1  0  0  0
 15 38  1  6  0  0  0
M  END


  Mrv1652305152102112D          

 38 40  0  0  1  0            999 V2000
    8.5134    1.7119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6442    0.3094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9729    2.2359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3661    3.8383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7565   -0.8892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6888    1.7377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4296    1.0622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9950    0.3610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2150    1.8150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8250    2.5420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7358   -0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9558    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2542    1.0365    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7651    2.4662    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9617    3.2674    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1704    0.3867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9112   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5212    0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1640    1.0941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6966    0.4640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4766   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3606    1.8953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6520   -0.9642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4002    0.7822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2620   -0.2372    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8666   -1.7170    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    4.7804    1.1137    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2596    3.2432    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7539    3.4977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1528    2.1256    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2174   -1.6655    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6989    1.2168    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4608   -0.0406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0396    1.7892    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3850   -0.3660    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0788    1.0107    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1695    3.0371    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1583    4.0686    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  1  0  0  0  0
  8  7  2  0  0  0  0
 10  9  1  0  0  0  0
 13  2  1  6  0  0  0
 13  6  1  0  0  0  0
 13  7  1  0  0  0  0
 14  3  1  6  0  0  0
 15  4  1  0  0  0  0
 15 14  1  0  0  0  0
 16  8  1  0  0  0  0
 16 11  2  0  0  0  0
 17 11  1  0  0  0  0
 18 12  2  0  0  0  0
 18 17  1  0  0  0  0
 20 18  1  0  0  0  0
 20 19  2  0  0  0  0
 21 17  2  0  0  0  0
 22 14  1  0  0  0  0
 22 19  1  0  0  0  0
 23 21  1  0  0  0  0
 24 19  1  0  0  0  0
 25  5  1  6  0  0  0
 25 20  1  0  0  0  0
 25 23  1  0  0  0  0
 26 21  1  0  0  0  0
 27  9  1  0  0  0  0
 27 12  1  0  0  0  0
 27 16  1  0  0  0  0
 28 10  1  0  0  0  0
 15 29  1  1  0  0  0
 30 22  2  0  0  0  0
 31 23  2  0  0  0  0
 32 24  2  0  0  0  0
 33 24  1  0  0  0  0
 33 25  1  0  0  0  0
 34  7  1  0  0  0  0
 35  8  1  0  0  0  0
 13 36  1  1  0  0  0
 14 37  1  1  0  0  0
 15 38  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0006794

> <DATABASE_NAME>
MIME

> <SMILES>
[H]\C(=C(\[H])[C@@]([H])(C)CC)C1=CC2=C(Cl)C(=O)[C@@]3(C)OC(=O)C(C(=O)[C@]([H])(C)[C@@]([H])(C)O)=C3C2=CN1CCO

> <INCHI_IDENTIFIER>
InChI=1S/C25H30ClNO6/c1-6-13(2)7-8-16-11-17-18(12-27(16)9-10-28)20-19(22(30)14(3)15(4)29)24(32)33-25(20,5)23(31)21(17)26/h7-8,11-15,28-29H,6,9-10H2,1-5H3/b8-7+/t13-,14+,15+,25-/m0/s1

> <INCHI_KEY>
CZNRWTXPKFAZAT-SUBMGMGCSA-N

> <FORMULA>
C25H30ClNO6

> <MOLECULAR_WEIGHT>
475.97

> <EXACT_MASS>
475.1761654

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
50.77375224413613

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(6aS)-5-chloro-9-[(2R,3R)-3-hydroxy-2-methylbutanoyl]-2-(2-hydroxyethyl)-6a-methyl-3-[(1E,3S)-3-methylpent-1-en-1-yl]-2H,6H,6aH,8H-furo[2,3-h]isoquinoline-6,8-dione

> <ALOGPS_LOGP>
3.05

> <JCHEM_LOGP>
2.780774542333332

> <ALOGPS_LOGS>
-4.10

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.684478621821402

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.957725716617212

> <JCHEM_PKA_STRONGEST_BASIC>
3.6687044153907893

> <JCHEM_POLAR_SURFACE_AREA>
104.14

> <JCHEM_REFRACTIVITY>
129.97699999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.75e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(6aS)-5-chloro-9-[(2R,3R)-3-hydroxy-2-methylbutanoyl]-2-(2-hydroxyethyl)-6a-methyl-3-[(1E,3S)-3-methylpent-1-en-1-yl]furo[2,3-h]isoquinoline-6,8-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      15.892   3.196   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.269   0.578   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.816   4.174   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.550   7.165   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.279  -1.660   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      14.352   3.244   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.002   1.983   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.191   0.674   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.735   3.388   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.007   4.745   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.840  -0.587   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.384   2.127   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.541   1.935   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.295   4.604   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.662   6.099   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.651   0.722   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.301  -0.539   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.573   0.818   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.039   2.042   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.034   0.866   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.490  -1.848   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.406   3.538   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.950  -1.800   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.614   1.460   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.222  -0.443   0.000  0.00  0.00           C+0
HETATM   26 Cl   UNK     0       7.218  -3.205   0.000  0.00  0.00          Cl+0
HETATM   27  N   UNK     0       8.923   2.079   0.000  0.00  0.00           N+0
HETATM   28  O   UNK     0       9.818   6.054   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       5.141   6.529   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       5.885   3.968   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       4.139  -3.109   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       1.305   2.271   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       2.727  -0.076   0.000  0.00  0.00           O+0
HETATM   34  H   UNK     0      11.274   3.340   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0      11.919  -0.683   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0      15.080   1.887   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0       2.183   5.669   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0       4.029   7.595   0.000  0.00  0.00           H+0
CONECT    1    6                                                            
CONECT    2   13                                                            
CONECT    3   14                                                            
CONECT    4   15                                                            
CONECT    5   25                                                            
CONECT    6    1   13                                                       
CONECT    7    8   13   34                                                  
CONECT    8    7   16   35                                                  
CONECT    9   10   27                                                       
CONECT   10    9   28                                                       
CONECT   11   16   17                                                       
CONECT   12   18   27                                                       
CONECT   13    2    6    7   36                                             
CONECT   14    3   15   22   37                                             
CONECT   15    4   14   29   38                                             
CONECT   16    8   11   27                                                  
CONECT   17   11   18   21                                                  
CONECT   18   12   17   20                                                  
CONECT   19   20   22   24                                                  
CONECT   20   18   19   25                                                  
CONECT   21   17   23   26                                                  
CONECT   22   14   19   30                                                  
CONECT   23   21   25   31                                                  
CONECT   24   19   32   33                                                  
CONECT   25    5   20   23   33                                             
CONECT   26   21                                                            
CONECT   27    9   12   16                                                  
CONECT   28   10                                                            
CONECT   29   15                                                            
CONECT   30   22                                                            
CONECT   31   23                                                            
CONECT   32   24                                                            
CONECT   33   24   25                                                       
CONECT   34    7                                                            
CONECT   35    8                                                            
CONECT   36   13                                                            
CONECT   37   14                                                            
CONECT   38   15                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   80    0
END

Synonyms

Not Available

Molecular Formula

C₂₅H₃₀ClNO₆

Average Mass

475.97

Monoisotopic Mass

475.1761654

IUPAC Name

(6aS)-5-chloro-9-[(2R,3R)-3-hydroxy-2-methylbutanoyl]-2-(2-hydroxyethyl)-6a-methyl-3-[(1E,3S)-3-methylpent-1-en-1-yl]-2H,6H,6aH,8H-furo[2,3-h]isoquinoline-6,8-dione

Traditional Name

(6aS)-5-chloro-9-[(2R,3R)-3-hydroxy-2-methylbutanoyl]-2-(2-hydroxyethyl)-6a-methyl-3-[(1E,3S)-3-methylpent-1-en-1-yl]furo[2,3-h]isoquinoline-6,8-dione

CAS Registry Number

Not Available

SMILES

[H]\C(=C(\[H])[C@@]([H])(C)CC)C1=CC2=C(Cl)C(=O)[C@@]3(C)OC(=O)C(C(=O)[C@]([H])(C)[C@@]([H])(C)O)=C3C2=CN1CCO

InChI Identifier

InChI=1S/C25H30ClNO6/c1-6-13(2)7-8-16-11-17-18(12-27(16)9-10-28)20-19(22(30)14(3)15(4)29)24(32)33-25(20,5)23(31)21(17)26/h7-8,11-15,28-29H,6,9-10H2,1-5H3/b8-7+/t13-,14+,15+,25-/m0/s1

InChI Key

CZNRWTXPKFAZAT-SUBMGMGCSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoquinolones and derivatives. These are aromatic polycyclic compounds containing a ketone bearing isoquinoline moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Isoquinolines and derivatives

Sub Class

Isoquinolones and derivatives

Direct Parent

Isoquinolones and derivatives

Alternative Parents

Substituents

Isoquinolone
Tetrahydroisoquinoline
Alpha-acyloxy ketone
Dihydropyridine
Cyclohexenone
2-furanone
Beta-hydroxy ketone
Dihydrofuran
Alpha-chloroketone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Alpha-haloketone
Carboxylic acid ester
Amino acid or derivatives
1,2-aminoalcohol
Ketone
Lactone
Secondary alcohol
Tertiary aliphatic amine
Tertiary amine
Alkanolamine
Allylamine
Carboxylic acid derivative
Oxacycle
Azacycle
Enamine
Chloroalkene
Haloalkene
Vinyl halide
Monocarboxylic acid or derivatives
Vinyl chloride
Amine
Organic nitrogen compound
Organic oxygen compound
Organic oxide
Alcohol
Carbonyl group
Organohalogen compound
Organochloride
Organonitrogen compound
Organooxygen compound
Primary alcohol
Hydrocarbon derivative
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	0.038 g/L	ALOGPS
logP	3.05	ALOGPS
logP	2.78	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	14.96	ChemAxon
pKa (Strongest Basic)	3.67	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	104.14 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	129.98 m³·mol⁻¹	ChemAxon
Polarizability	50.77 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

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

30815717

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73353406

PDB ID

Not Available

ChEBI ID

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 4â€²-epi-N-2-hydroxyethyl-azachaetoviridin A (MMDBc0006794)

MOL for #<Metabolite:0x00007f92326f72c0>

3D MOL for #<Metabolite:0x00007f92326f72c0>

3D SDF for #<Metabolite:0x00007f92326f72c0>

3D-SDF for #<Metabolite:0x00007f92326f72c0>

PDB for #<Metabolite:0x00007f92326f72c0>

3D PDB for #<Metabolite:0x00007f92326f72c0>

SMILES for #<Metabolite:0x00007f92326f72c0>

INCHI for #<Metabolite:0x00007f92326f72c0>

Structure for #<Metabolite:0x00007f92326f72c0>

3D Structure for #<Metabolite:0x00007f92326f72c0>