Page last updated: 2024-12-11

enanthotoxin

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Description

enanthotoxin: poisonous principle of Oenanthe crocata (Water Dropwort); RN given refers to (E,E,E)-isomer [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

FloraRankFlora DefinitionFamilyFamily Definition
OenanthegenusA plant genus of the family APIACEAE that is sometimes called Hemlock Water Dropwort but should not be confused with HEMLOCK. It contains enanthotoxin.[MeSH]ApiaceaeA large plant family in the order Apiales, also known as Umbelliferae. Most are aromatic herbs with alternate, feather-divided leaves that are sheathed at the base. The flowers often form a conspicuous flat-topped umbel. Each small individual flower is usually bisexual, with five sepals, five petals, and an enlarged disk at the base of the style. The fruits are ridged and are composed of two parts that split open at maturity.[MeSH]
Oenanthe crocataspecies[no description available]ApiaceaeA large plant family in the order Apiales, also known as Umbelliferae. Most are aromatic herbs with alternate, feather-divided leaves that are sheathed at the base. The flowers often form a conspicuous flat-topped umbel. Each small individual flower is usually bisexual, with five sepals, five petals, and an enlarged disk at the base of the style. The fruits are ridged and are composed of two parts that split open at maturity.[MeSH]

Cross-References

ID SourceID
PubMed CID44138996
CHEMBL ID550225
CHEBI ID144406
SCHEMBL ID1170273
MeSH IDM0056443

Synonyms (18)

Synonym
enanthotoxin
oenanthotoxin
CHEMBL550225
unii-4gd5a2rg2n
4gd5a2rg2n ,
20311-78-8
C20044
enanthotoxin [mi]
enanthotoxin, (+)-
(2e,8e,10e,14r)-2,8,10-heptadecatriene-4,6-diyne-1,14-diol
2,8,10-heptadecatriene-4,6-diyne-1,14-diol, (2e,8e,10e,14r)-
enanthotoxin, (r)-
SCHEMBL1170273
DTXSID60897236
Q3080860
(r,2e,8e,10e)-heptadeca-2,8,10-trien-4,6-diyne-1,14-diol
(2e,8e,10e,14r)-heptadeca-2,8,10-trien-4,6-diyne-1,14-diol
CHEBI:144406
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
long-chain fatty alcoholA fatty alcohol with a chain length ranging from C13 to C22.
[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 (8)

Assay IDTitleYearJournalArticle
AID424755Antagonist activity at GABAA receptor in Wistar rat neuronal cells assessed inhibition of GABA-evoked response by patch-clamp technique2009Journal of natural products, May-22, Volume: 72, Issue:5
Polyacetylenes from sardinian Oenanthe fistulosa: a molecular clue to risus sardonicus.
AID1239046Cytotoxicity against mouse NIH/3T3 cells after 96 hrs by sulforhodamine B assay2015Bioorganic & medicinal chemistry, Sep-01, Volume: 23, Issue:17
Chemoenzymatic synthesis and cytotoxicity of oenanthotoxin and analogues.
AID1239045Cytotoxicity against human MCF7 cells after 96 hrs by sulforhodamine B assay2015Bioorganic & medicinal chemistry, Sep-01, Volume: 23, Issue:17
Chemoenzymatic synthesis and cytotoxicity of oenanthotoxin and analogues.
AID1239042Cytotoxicity against human A2780 cells after 96 hrs by sulforhodamine B assay2015Bioorganic & medicinal chemistry, Sep-01, Volume: 23, Issue:17
Chemoenzymatic synthesis and cytotoxicity of oenanthotoxin and analogues.
AID1239041Cytotoxicity against human 8505C cells after 96 hrs by sulforhodamine B assay2015Bioorganic & medicinal chemistry, Sep-01, Volume: 23, Issue:17
Chemoenzymatic synthesis and cytotoxicity of oenanthotoxin and analogues.
AID1239043Cytotoxicity against human A549 cells after 96 hrs by sulforhodamine B assay2015Bioorganic & medicinal chemistry, Sep-01, Volume: 23, Issue:17
Chemoenzymatic synthesis and cytotoxicity of oenanthotoxin and analogues.
AID1239044Cytotoxicity against human HT-29 cells after 96 hrs by sulforhodamine B assay2015Bioorganic & medicinal chemistry, Sep-01, Volume: 23, Issue:17
Chemoenzymatic synthesis and cytotoxicity of oenanthotoxin and analogues.
AID1239040Cytotoxicity against human 518A2 cells after 96 hrs by sulforhodamine B assay2015Bioorganic & medicinal chemistry, Sep-01, Volume: 23, Issue:17
Chemoenzymatic synthesis and cytotoxicity of oenanthotoxin and analogues.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (20)

TimeframeStudies, This Drug (%)All Drugs %
pre-199010 (50.00)18.7374
1990's0 (0.00)18.2507
2000's4 (20.00)29.6817
2010's5 (25.00)24.3611
2020's1 (5.00)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%
Reviews1 (4.76%)6.00%
Case Studies4 (19.05%)4.05%
Observational0 (0.00%)0.25%
Other16 (76.19%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]