MiMeDB: Showing metabocard for Chaetoviridin H (MMDBc0001940)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-14 20:25:22 UTC

Update Date

2025-10-07 16:04:32 UTC

Metabolite ID

MMDBc0001940

Metabolite Identification

Common Name

Chaetoviridin H

Description

Chaetoviridin H is a secondary metabolite belonging to the class of alkaloids, specifically known for its unique structural features that contribute to its biological activity. This compound has been isolated from various fungal species, particularly those within the Chaetomium genus, and exhibits notable antifungal properties, making it of interest in the field of natural product chemistry. The biosynthetic pathways leading to its production involve complex enzymatic reactions, which have yet to be fully elucidated. Although research on Chaetoviridin H is limited, some studies have highlighted its potential as a lead compound for the development of new antifungal agents (PMID: 15305164 ). Further investigations are necessary to explore its mechanisms of action and potential applications in medicine, as well as to understand its ecological role in the environments where it is produced (PMID: 24572367 ). Overall, while the current literature on Chaetoviridin H is sparse, its chemical properties and biological activities warrant further exploration.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305142122252D          

 32 34  0  0  1  0            999 V2000
    7.8723    2.8224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0031    1.4199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3317    3.3463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7250    4.9488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1153    0.2213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0477    2.8481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7885    2.1727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3539    1.4714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0947    0.7959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8355    0.1205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3147    2.2499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6131    2.1469    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1239    3.5766    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3206    4.3779    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2701    0.8217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5293    1.4972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8801    1.5487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0109    0.1462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5229    2.2045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0555    1.5745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7195    3.0057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7591    1.8926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6209    0.8732    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1128    4.6082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5762   -0.5550    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5117    3.2360    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0578    2.3273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1393    2.2242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8196    1.0699    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4377    2.1211    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5284    4.1475    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5172    5.1791    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
 12  2  1  6  0  0  0
 12  6  1  0  0  0  0
 12  7  1  0  0  0  0
 13  3  1  1  0  0  0
 14  4  1  0  0  0  0
 14 13  1  0  0  0  0
 15  9  1  0  0  0  0
 15 10  2  0  0  0  0
  8 16  1  4  0  0  0
 16  9  2  0  0  0  0
 17 11  2  0  0  0  0
 17 15  1  0  0  0  0
 18 10  1  0  0  0  0
 20 17  1  0  0  0  0
 20 19  2  0  0  0  0
 21 13  1  0  0  0  0
 21 19  1  0  0  0  0
 22 19  1  0  0  0  0
 23  5  1  6  0  0  0
 23 18  1  0  0  0  0
 23 20  1  0  0  0  0
 14 24  1  1  0  0  0
 25 18  2  0  0  0  0
 26 21  2  0  0  0  0
 27 22  2  0  0  0  0
 28 11  1  0  0  0  0
 28 16  1  0  0  0  0
 29 22  1  0  0  0  0
 29 23  1  0  0  0  0
 12 30  1  1  0  0  0
 13 31  1  6  0  0  0
 14 32  1  6  0  0  0
M  END


  Mrv1652305142122252D          

 32 34  0  0  1  0            999 V2000
    7.8723    2.8224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0031    1.4199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3317    3.3463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7250    4.9488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1153    0.2213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0477    2.8481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7885    2.1727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3539    1.4714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0947    0.7959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8355    0.1205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3147    2.2499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6131    2.1469    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1239    3.5766    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3206    4.3779    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2701    0.8217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5293    1.4972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8801    1.5487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0109    0.1462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5229    2.2045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0555    1.5745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7195    3.0057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7591    1.8926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6209    0.8732    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1128    4.6082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5762   -0.5550    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5117    3.2360    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0578    2.3273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1393    2.2242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8196    1.0699    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4377    2.1211    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5284    4.1475    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5172    5.1791    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
 12  2  1  6  0  0  0
 12  6  1  0  0  0  0
 12  7  1  0  0  0  0
 13  3  1  1  0  0  0
 14  4  1  0  0  0  0
 14 13  1  0  0  0  0
 15  9  1  0  0  0  0
 15 10  2  0  0  0  0
  8 16  1  4  0  0  0
 16  9  2  0  0  0  0
 17 11  2  0  0  0  0
 17 15  1  0  0  0  0
 18 10  1  0  0  0  0
 20 17  1  0  0  0  0
 20 19  2  0  0  0  0
 21 13  1  0  0  0  0
 21 19  1  0  0  0  0
 22 19  1  0  0  0  0
 23  5  1  6  0  0  0
 23 18  1  0  0  0  0
 23 20  1  0  0  0  0
 14 24  1  1  0  0  0
 25 18  2  0  0  0  0
 26 21  2  0  0  0  0
 27 22  2  0  0  0  0
 28 11  1  0  0  0  0
 28 16  1  0  0  0  0
 29 22  1  0  0  0  0
 29 23  1  0  0  0  0
 12 30  1  1  0  0  0
 13 31  1  6  0  0  0
 14 32  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0001940

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@](C)(CC)C=CC1=CC2=CC(=O)[C@@]3(C)OC(=O)C(C(=O)[C@@]([H])(C)[C@@]([H])(C)O)=C3C2=CO1

> <INCHI_IDENTIFIER>
InChI=1S/C23H26O6/c1-6-12(2)7-8-16-9-15-10-18(25)23(5)20(17(15)11-28-16)19(22(27)29-23)21(26)13(3)14(4)24/h7-14,24H,6H2,1-5H3/t12-,13-,14+,23+/m0/s1

> <INCHI_KEY>
HKVYPGSRVJADQC-PJBDDNSMSA-N

> <FORMULA>
C23H26O6

> <MOLECULAR_WEIGHT>
398.455

> <EXACT_MASS>
398.172938557

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
42.74954942538916

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

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

> <ALOGPS_LOGP>
3.36

> <JCHEM_LOGP>
3.0163042069999992

> <ALOGPS_LOGS>
-4.49

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.096338043068148

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.047117925452437

> <JCHEM_PKA_STRONGEST_BASIC>
-2.756427634859798

> <JCHEM_POLAR_SURFACE_AREA>
89.9

> <JCHEM_REFRACTIVITY>
111.91779999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.29e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(6aS)-9-[(2S,3R)-3-hydroxy-2-methylbutanoyl]-6a-methyl-3-[(3S)-3-methylpent-1-en-1-yl]furo[2,3-h]isochromene-6,8-dione

> <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      14.695   5.268   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.072   2.650   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.619   6.246   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.353   9.238   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.082   0.413   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.156   5.317   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.805   4.056   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.994   2.747   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.643   1.486   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.293   0.225   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.187   4.200   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.344   4.008   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.098   6.676   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.465   8.172   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.104   1.534   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.455   2.795   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.376   2.891   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.754   0.273   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.843   4.115   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.837   2.939   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.210   5.611   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.417   3.533   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.026   1.630   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       3.944   8.602   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       2.942  -1.036   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       4.689   6.041   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       0.108   4.344   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       7.727   4.152   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       1.530   1.997   0.000  0.00  0.00           O+0
HETATM   30  H   UNK     0      13.884   3.959   0.000  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.986   7.742   0.000  0.00  0.00           H+0
HETATM   32  H   UNK     0       2.832   9.668   0.000  0.00  0.00           H+0
CONECT    1    6                                                            
CONECT    2   12                                                            
CONECT    3   13                                                            
CONECT    4   14                                                            
CONECT    5   23                                                            
CONECT    6    1   12                                                       
CONECT    7    8   12                                                       
CONECT    8    7   16                                                       
CONECT    9   15   16                                                       
CONECT   10   15   18                                                       
CONECT   11   17   28                                                       
CONECT   12    2    6    7   30                                             
CONECT   13    3   14   21   31                                             
CONECT   14    4   13   24   32                                             
CONECT   15    9   10   17                                                  
CONECT   16    8    9   28                                                  
CONECT   17   11   15   20                                                  
CONECT   18   10   23   25                                                  
CONECT   19   20   21   22                                                  
CONECT   20   17   19   23                                                  
CONECT   21   13   19   26                                                  
CONECT   22   19   27   29                                                  
CONECT   23    5   18   20   29                                             
CONECT   24   14                                                            
CONECT   25   18                                                            
CONECT   26   21                                                            
CONECT   27   22                                                            
CONECT   28   11   16                                                       
CONECT   29   22   23                                                       
CONECT   30   12                                                            
CONECT   31   13                                                            
CONECT   32   14                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

Synonyms

Not Available

Molecular Formula

C₂₃H₂₆O₆

Average Mass

398.455

Monoisotopic Mass

398.172938557

IUPAC Name

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

Traditional Name

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

CAS Registry Number

Not Available

SMILES

[H][C@](C)(CC)C=CC1=CC2=CC(=O)[C@@]3(C)OC(=O)C(C(=O)[C@@]([H])(C)[C@@]([H])(C)O)=C3C2=CO1

InChI Identifier

InChI=1S/C23H26O6/c1-6-12(2)7-8-16-9-15-10-18(25)23(5)20(17(15)11-28-16)19(22(27)29-23)21(26)13(3)14(4)24/h7-14,24H,6H2,1-5H3/t12-,13-,14+,23+/m0/s1

InChI Key

HKVYPGSRVJADQC-PJBDDNSMSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclohexenones. Cyclohexenones are compounds containing a cylohexenone moiety, which is a six-membered aliphatic ring that carries a ketone and has one endocyclic double bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Cyclohexenones

Alternative Parents

Substituents

Cyclohexenone
Alpha-acyloxy ketone
Pyran
2-furanone
Beta-hydroxy ketone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Dihydrofuran
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxide
Hydrocarbon derivative
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	0.013 g/L	ALOGPS
logP	3.36	ALOGPS
logP	3.02	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	15.05	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	89.9 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	111.92 m³·mol⁻¹	ChemAxon
Polarizability	42.75 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

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-09	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
MS	Mass Spectrum (Electron Ionization)	Not Available	2022-08-06	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	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	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

78440012

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139583405

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 Chaetoviridin H (MMDBc0001940)

MOL for #<Metabolite:0x0000564fa0238bd8>

3D MOL for #<Metabolite:0x0000564fa0238bd8>

3D SDF for #<Metabolite:0x0000564fa0238bd8>

3D-SDF for #<Metabolite:0x0000564fa0238bd8>

PDB for #<Metabolite:0x0000564fa0238bd8>

3D PDB for #<Metabolite:0x0000564fa0238bd8>

SMILES for #<Metabolite:0x0000564fa0238bd8>

INCHI for #<Metabolite:0x0000564fa0238bd8>

Structure for #<Metabolite:0x0000564fa0238bd8>

3D Structure for #<Metabolite:0x0000564fa0238bd8>