Page last updated: 2024-12-11
chaetoviridin a
Description
chaetoviridin A: from Chaetomium globosum; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
chaetoviridin A : An azaphilone that is 6H-furo[2,3-h]isochromene-6,8(6aH)-dione substituted by a chloro group at position 5, a 3-hydroxy-2-methylbutanoyl group at position 9, a methyl group at position 6a and a 3-methylpent-1-en-1yl group at position 3. Isolated from Chaetomium globosum, it exhibits natifungal activity against plant pathogenic fungi. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]
Cross-References
Synonyms (13)
Synonym |
6h-furo[2,3-h]-2-benzopyran-6,8(6ah)-dione, 5-chloro-9-[(2s,3r)-3-hydroxy-20methyl-1-oxobutyl]-6a-methyl-3-[(1e,3s)-3-methyl-1-pentenyl)-,(6as) |
(6as)-5-chloro-9-[(2s,3r)-3-hydroxy-2-methyl-butanoyl]-6a-methyl-3-[(e,3s)-3-methylpent-1-enyl]furo[2,3-h]isochromene-6,8-dione |
chaetoviridin a |
128252-98-2 |
(6as)-5-chloro-9-[(2s,3r)-3-hydroxy-2-methylbutanoyl]-6a-methyl-3-[(e,3s)-3-methylpent-1-enyl]furo[2,3-h]isochromene-6,8-dione |
chebi:67610 , |
CHEMBL1802150 |
ccris 7226 |
(6as)-5-chloro-9-[(2s,3r)-3-hydroxy-2-methylbutanoyl]-6a-methyl-3-[(1e,3s)-3-methylpent-1-en-1-yl]-6h-furo[2,3-h]isochromene-6,8(6ah)-dione |
HB3829 |
J-005582 |
DTXSID80893270 |
Q27136080 |
Roles (2)
Role | Description |
antifungal agent | An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce. |
Chaetomium metabolite | Any fungal metabolite produced during a metabolic reaction in the mould, Chaetomium. |
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] |
Drug Classes (7)
Class | Description |
azaphilone | Any member of a family of natural products which contains a 6H-isochromene-6,8(7H)-dione or an isoquinoline-6,8(2H,7H)-dione skeleton and its substituted derivatives thereof. |
gamma-lactone | A lactone having a five-membered lactone ring. |
organochlorine compound | An organochlorine compound is a compound containing at least one carbon-chlorine bond. |
enone | An alpha,beta-unsaturated ketone of general formula R(1)R(2)C=CR(3)-C(=O)R(4) (R(4) =/= H) in which the C=O function is conjugated to a C=C double bond at the alpha,beta position. |
secondary alcohol | A secondary alcohol is a compound in which a hydroxy group, -OH, is attached to a saturated carbon atom which has two other carbon atoms attached to it. |
beta-hydroxy ketone | A ketone containing a hydroxy group on the beta-carbon relative to the C=O group. |
organic heterotricyclic compound | An organic tricyclic compound in which at least one of the rings of the tricyclic skeleton contains one or more heteroatoms. |
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] |
Bioassays (5)
Assay ID | Title | Year | Journal | Article |
AID1651829 | Cytotoxicity against human AGS cells assessed as reduction in cell viability measured after 72 hrs by CCK8 assay | 2020 | Journal of natural products, 04-24, Volume: 83, Issue:4
| Cytotoxic Nitrogenated Azaphilones from the Deep-Sea-Derived Fungus |
AID606811 | Antibiotic activity against cytolysin-positive Enterococcus faecalis MMH594 infected in intestine of Caenorhabditis elegans glp-4(bn2ts);sek-1(km4) mutant infection model assessed as nematode survival at 50 to 100 ug/mL after 168 hrs by liquid infection a | 2011 | Journal of natural products, May-27, Volume: 74, Issue:5
| Azaphilones from the endophyte Chaetomium globosum. |
AID1651828 | Cytotoxicity against human MGC803 cells assessed as reduction in cell viability measured after 72 hrs by CCK8 assay | 2020 | Journal of natural products, 04-24, Volume: 83, Issue:4
| Cytotoxic Nitrogenated Azaphilones from the Deep-Sea-Derived Fungus |
AID606813 | Antimicrobial activity against Magnaporthe grisea mycelia assessed as growth inhibition | 2011 | Journal of natural products, May-27, Volume: 74, Issue:5
| Azaphilones from the endophyte Chaetomium globosum. |
AID606812 | Antimicrobial activity against Pythium ultimum mycelia assessed as growth inhibition | 2011 | Journal of natural products, May-27, Volume: 74, Issue:5
| Azaphilones from the endophyte Chaetomium globosum. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Research
Studies (6)
Timeframe | Studies, This Drug (%) | All Drugs % |
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 4 (66.67) | 24.3611 |
2020's | 2 (33.33) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Market Indicators
Research Demand Index: 12.63
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.
Metric | This Compound (vs All) |
---|
Research Demand Index | 12.63 (24.57) | Research Supply Index | 1.95 (2.92) | Research Growth Index | 4.57 (4.65) | Search Engine Demand Index | 0.00 (26.88) | Search Engine Supply Index | 0.00 (0.95) |
| |
Study Types
Publication Type | This drug (%) | All Drugs (%) |
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 6 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |