Page last updated: 2024-12-11

mucidin

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

mucidin: produced by basidiomycete Oudemansiella mucida; strobilurin A produced by wood rot fungus Strobilurus tenacellus; [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

mucidin : An enoate ester that is the methyl ester of (2E,3Z,5E)-2-(methoxymethylene)-3-methyl-6-phenylhexa-3,5-dienoic acid. [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

ID SourceID
PubMed CID6437379
CHEBI ID78156
SCHEMBL ID1313193
MeSH IDM0052509

Synonyms (17)

Synonym
strobilurin a
om-1
3,5-hexadienoic acid, 2-(methoxymethylene)-3-methyl-6-phenyl-, methyl ester, (2e,3z,5e)-
3,5-hexadienoic acid, 2-(methoxymethylene)-3-methyl-6-phenyl-, methyl ester, (e,e,e)-
mucidin
methyl (2e,3z,5e)-2-(methoxymethylidene)-3-methyl-6-phenylhexa-3,5-dienoate
SCHEMBL1313193
unii-15143i0275
15143i0275 ,
52110-55-1
3,5-hexadienoic acid, 2-(methoxymethylene)-3-methyl-6-phenyl-, methyl ester, (e,z,e)-
strobilurin a [mi]
mucidermin
methyl (2e,3z,5e)-2-(methoxymethylene)-3-methyl-6-phenylhexa-3,5-dienoate
CHEBI:78156
Q27147658
DTXSID401025570
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
fungal metaboliteAny eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds.
antifungal agentAn 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]

Drug Classes (2)

ClassDescription
enoate esterAn alpha,beta-unsaturated carboxylic ester of general formula R(1)R(2)C=CR(3)-C(=O)OR(4) (R(4) =/= H) in which the ester C=O function is conjugated to a C=C double bond at the alpha,beta position.
enol etherEthers ROR' where R has a double bond adjacent to the oxygen of the ether linkage.
[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]

Research

Studies (51)

TimeframeStudies, This Drug (%)All Drugs %
pre-199026 (50.98)18.7374
1990's12 (23.53)18.2507
2000's6 (11.76)29.6817
2010's7 (13.73)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 34.21

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 moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index34.21 (24.57)
Research Supply Index3.99 (2.92)
Research Growth Index4.42 (4.65)
Search Engine Demand Index47.56 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (34.21)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews2 (3.77%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other51 (96.23%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]