Page last updated: 2024-12-06

allyl thiocyanate

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

Description

Allyl thiocyanate is a pungent, colorless liquid that is a natural component of various plants, including mustard, horseradish, and wasabi. Its synthesis involves the reaction of allyl chloride with potassium thiocyanate. Allyl thiocyanate exhibits a variety of biological effects, including antimicrobial, insecticidal, and anti-inflammatory properties. It is of interest in research for its potential applications in agriculture and medicine. For example, its antimicrobial activity has been investigated for its use in controlling plant diseases, while its anti-inflammatory potential is being explored for therapeutic purposes. The compound is also studied for its role in the pungent flavor and aroma of mustard and other related foods.'

allyl thiocyanate: a glycosinolate degradation product that has insecticidal activity [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID69816
CHEBI ID183082
MeSH IDM0473314

Synonyms (22)

Synonym
CHEBI:183082
allyliso thiocyanate
allyl thiocyanate
brn 1739294
thiocyanic acid, allyl ester
allylrhodanid [german]
thiocyanic acid, 2-propenyl ester
einecs 212-126-5
allylrhodanid
prop-2-enyl thiocyanate
764-49-8
AKOS006279843
3-thiocyanatoprop-1-ene
allylthiocyanate
IFVYHJRLWCUVBB-UHFFFAOYSA-N
(prop-2-en-1-ylsulfanyl)carbonitrile
3-thiocyanato-1-propene
allylrhodamide
2-propenyl thiocyanate, 9ci
prop-2-en-1-yl thiocyanate
DTXSID00870765
EN300-3428770
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
thiocyanatesEsters of thiocyanic acid with general formula RSC#N.
[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 (6)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (50.00)29.6817
2010's2 (33.33)24.3611
2020's1 (16.67)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 25.98

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 Index25.98 (24.57)
Research Supply Index1.95 (2.92)
Research Growth Index4.59 (4.65)
Search Engine Demand Index26.67 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (25.98)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other6 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]