Compounds > rapalexin a
Page last updated: 2024-11-12

rapalexin a

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

Description

rapalexin A: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID16102148
CHEMBL ID2253033
SCHEMBL ID19400912
MeSH IDM0507990

Synonyms (6)

Synonym
929083-72-7
CHEMBL2253033
rapalexin a
3-isothiocyanato-4-methoxy-1h-indole
DTXSID70582863
SCHEMBL19400912
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (3)

Assay IDTitleYearJournalArticle
AID1092145Antifungal activity against Leptosphaeria maculans assessed as mycelial radial growth inhibition on potato dextrose agar at 0.50 mM relative to control2012Bioorganic & medicinal chemistry, Jul-01, Volume: 20, Issue:13
The cruciferous phytoalexins rapalexin A, brussalexin A and erucalexin: chemistry and metabolism in Leptosphaeria maculans.
AID1092143Antifungal activity against Leptosphaeria maculans assessed as mycelial radial growth inhibition on potato dextrose agar at 0.10 mM relative to control2012Bioorganic & medicinal chemistry, Jul-01, Volume: 20, Issue:13
The cruciferous phytoalexins rapalexin A, brussalexin A and erucalexin: chemistry and metabolism in Leptosphaeria maculans.
AID1092144Antifungal activity against Leptosphaeria maculans assessed as mycelial radial growth inhibition on potato dextrose agar at 0.20 mM relative to control2012Bioorganic & medicinal chemistry, Jul-01, Volume: 20, Issue:13
The cruciferous phytoalexins rapalexin A, brussalexin A and erucalexin: chemistry and metabolism in Leptosphaeria maculans.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (7)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (28.57)29.6817
2010's4 (57.14)24.3611
2020's1 (14.29)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

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%
Other7 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
indole-3-carbinol
indole-3-carbinol: occurs in edible cruciferous vegetables. indole-3-methanol : An indolyl alcohol carrying a hydroxymethyl group at position 3. It is a constituent of the cruciferous vegetables and had anticancer activity.		2.0710indolyl alcoholantineoplastic agent;
plant metabolite
thiazoles
[no description available]		2.46201,3-thiazoles;
mancude organic heteromonocyclic parent;
monocyclic heteroarene
camalexin
camalexin : An indole phytoalexin that is indole substituted at position 3 by a 1,3-thiazol-2-yl group.		7.04101,3-thiazoles;
indole phytoalexin		metabolite
sesquiterpenes
[no description available]		3.1750
cysteine
Cysteine: A thiol-containing non-essential amino acid that is oxidized to form CYSTINE.. L-cysteinium : The L-enantiomer of cysteinium.. cysteine : A sulfur-containing amino acid that is propanoic acid with an amino group at position 2 and a sulfanyl group at position 3.		7.2510cysteiniumfundamental metabolite
wasalexin a
wasalexin A: wasalexins A and B are geometrical isomers; isolated from Wasabia japonica; structure in first source		2.0410indoles
ConditionIndicatedRelationship StrengthStudiesTrials