wasalexin a profile

wasalexin A: wasalexins A and B are geometrical isomers; isolated from Wasabia japonica; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID Source	ID
PubMed CID	44333108
CHEMBL ID	103746
CHEBI ID	174780
MeSH ID	M0354178

Synonyms (5)

Synonym
CHEBI:174780
(3e)-3-[[bis(methylsulanyl)methylideneamino]methylidene]-1-methoxyindol-2-one
wasalexin a
CHEMBL103746
(3e)-3-({[bis(methylsulfanyl)methylidene]amino}methylidene)-1-methoxy-2,3-dihydro-1h-indol-2-one

Drug Classes (1)

Class	Description
indoles	Any compound containing an indole skeleton.
[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 (1)

Assay ID	Title	Year	Journal	Article
AID155494	Antifungal activity against P. Lingam by spore germination assay after 24 hours; range is 40-50%	1999	Bioorganic & medicinal chemistry letters, Oct-18, Volume: 9, Issue:20	Wasalexins A and B, new phytoalexins from wasabi: isolation, synthesis, and antifungal activity.
[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	1 (16.67)	18.2507
2000's	2 (33.33)	29.6817
2010's	3 (50.00)	24.3611
2020's	0 (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: 12.99

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	12.99 (24.57)
Research Supply Index	1.95 (2.92)
Research Growth Index	4.94 (4.65)
Search Engine Demand Index	0.00 (26.88)
Search Engine Supply Index	0.00 (0.95)

This Compound (12.99)

All Compounds (24.57)

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]

Substance	Relationship Strength	Studies	Classes	Roles
thiazoles [no description available]	2.45	2	1,3-thiazoles; mancude organic heteromonocyclic parent; monocyclic heteroarene
deuterium Deuterium: The stable isotope of hydrogen. It has one neutron and one proton in the nucleus.	2.05	1	dihydrogen
glucose, (beta-d)-isomer beta-D-glucose : D-Glucopyranose with beta configuration at the anomeric centre.. (1->4)-beta-D-glucan : A beta-D-glucan in which the glucose units are connected by (1->4) linkages.. (1->3)-beta-D-glucan : A beta-D-glucan in which the glucose units are connected by (1->3) linkages.	2.05	1	D-glucopyranose	epitope; mouse metabolite
camalexin camalexin : An indole phytoalexin that is indole substituted at position 3 by a 1,3-thiazol-2-yl group.	2.04	1	1,3-thiazoles; indole phytoalexin	metabolite
glucobrassicin glucobrassicin: isolated from Brussels sprouts; structure given in first source. glucobrassicin : An indolylmethylglucosinolic acid that is 1-thio-beta-D-glucopyranose having a 2-(1H-indol-3-yl)-N-(sulfooxy)ethanimidoyl group attached to the anomeric sulfur.	2.05	1	indolyl carbohydrate; indolylmethylglucosinolic acid
sesquiterpenes [no description available]	2.96	4
brassinin [no description available]	2.05	1	dithiocarbamic ester; indole phytoalexin
rapalexin a rapalexin A: structure in first source	2.04	1
brassilexin brassilexin: structure in first source	2.05	1	indoles

wasalexin a

Description