sordaricin : A tetracyclic diterpenoid that is produced by several fungi including Sordaria araneosa.
ID Source | ID |
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PubMed CID | 485853 |
CHEMBL ID | 4582916 |
CHEBI ID | 140259 |
MeSH ID | M0299924 |
Synonym |
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1,4-methano-s-indacene-3a(1h)-carboxylic acid, 4-formyl-4,4a,5,6,7,7a,8,8a-octahydro-8a-(hydroxymethyl)-7-methyl-3-(1-methylethyl)-,(1r,3ar,4s,4ar,7r,7ar,8as)- |
51493-69-7 |
formyl-(hydroxymethyl)-isopropyl-methyl-[?]carboxylic acid |
sordaricin |
(1r,3ar,4s,4ar,7r,7ar,8as)-4-formyl-8a-(hydroxymethyl)-7-methyl-3-(propan-2-yl)-4,4a,5,6,7,7a,8,8a-octahydro-1,4-methano-s-indacene-3a(1h)-carboxylic acid |
(-)-sordaricin |
CHEBI:140259 |
4-formyl-8a-(hydroxymethyl)-7-methyl-3-(propan-2-yl)-4,4a,5,6,7,7a,8,8a-octahydro-1,4-methano-s-indacene-3a(1h)-carboxylic acid |
DTXSID80965825 |
CHEMBL4582916 |
(1r,2s,4r,5r,8r,9s,11r)-9-formyl-2-(hydroxymethyl)-5-methyl-13-propan-2-yltetracyclo[7.4.0.02,11.04,8]tridec-12-ene-1-carboxylic acid |
Role | Description |
---|---|
fungal metabolite | Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds. |
antifungal agent | An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce. |
[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] |
Class | Description |
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tetracyclic diterpenoid | A diterpenoid with a tetracyclic skeleton. |
bridged compound | A polycyclic compound in which two rings have two or more atoms in common. |
3-oxo monocarboxylic acid | |
aldehyde | A compound RC(=O)H, in which a carbonyl group is bonded to one hydrogen atom and to one R group. |
primary alcohol | A primary alcohol is a compound in which a hydroxy group, -OH, is attached to a saturated carbon atom which has either three hydrogen atoms attached to it or only one other carbon atom and two hydrogen atoms attached to it. |
[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] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID1615874 | Antifungal activity against Candida albicans ATCC 10231 by NCCLS-protocol based microplate reader analysis | 2019 | Journal of natural products, 09-27, Volume: 82, Issue:9 | Sordarin Diterpene Glycosides with an Unusual 1,3-Dioxolan-4-one Ring from the Zoanthid-Derived Fungus |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (14.29) | 18.2507 |
2000's | 10 (71.43) | 29.6817 |
2010's | 1 (7.14) | 24.3611 |
2020's | 1 (7.14) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
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.
| This Compound (12.19) All Compounds (24.57) |
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 | 14 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |