Page last updated: 2024-12-07

culmorin

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

Description

Culmorin is a mycotoxin produced by the fungus Fusarium culmorum. It has been shown to have a variety of biological effects, including cytotoxic, anti-inflammatory, and antimicrobial activities. Culmorin is of interest to researchers due to its potential as a therapeutic agent, as well as its potential to contaminate food and feed. Culmorin is a potent inhibitor of the enzyme DNA polymerase, which is essential for DNA replication. This activity has led to research into its potential as an anticancer agent. Culmorin also inhibits the production of inflammatory cytokines, which suggests that it may have therapeutic potential for inflammatory diseases. In addition, culmorin has been shown to have antimicrobial activity against a variety of bacteria and fungi. The synthesis of culmorin has been studied in detail, and several methods have been developed for its production. However, the biosynthesis of culmorin is complex, and further research is needed to fully understand its mechanisms. Culmorin is a relatively rare mycotoxin, but it has been detected in a variety of food and feed products, including wheat, barley, and rice. The presence of culmorin in food can be a concern for human health, as it may have toxic effects. Therefore, it is important to monitor the levels of culmorin in food and feed products.'

culmorin: tricyclic sesquiterpene metabolite of fungus Fusarium culmorium; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

culmorin : A sesquiterpenoid fungal metabolite isolated from Fusarium culmorum. [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 CID115285
MeSH IDM0062031

Synonyms (4)

Synonym
18374-83-9
culmorin
DTXSID10891805
(1s,2r,7r,9s,11r)-2,6,6,9-tetramethyltricyclo[5.4.0.02,9]undecane-8,11-diol

Research Excerpts

Effects

ExcerptReferenceRelevance
"Culmorin has low toxicity in several in vitro assays and in one study in swine and is Ames test negative."( The fungal metabolite culmorin and related compounds.
Miller, JD; Pedersen, PB, 1999
)
1.34
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (15)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's1 (6.67)18.2507
2000's5 (33.33)29.6817
2010's7 (46.67)24.3611
2020's2 (13.33)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 22.65

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 Index22.65 (24.57)
Research Supply Index2.77 (2.92)
Research Growth Index4.84 (4.65)
Search Engine Demand Index21.17 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (22.65)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews2 (13.33%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other13 (86.67%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]