Page last updated: 2024-11-05

methyl linolenate

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

Cross-References

ID SourceID
PubMed CID5319706
CHEMBL ID1172198
CHEBI ID133634
SCHEMBL ID55951
MeSH IDM0136862

Synonyms (62)

Synonym
nsc607759
nsc-607759
linolenic acid, methyl ester
9,12,15-octadecatrienoic acid, methyl ester, (z,z,z)-
methyl linolenate, >=99% (gc)
methyl (9z,12z,15z)-9,12,15-octadecatrienoate
methyl (9z,12z,15z)-octadecatrienoate
methyl (9z,12z,15z)-octadeca-9,12,15-trienoate
CHEBI:133634
alpha-linolenic acid methyl ester
cis,cis,cis-9,12,15-octadecatrienoic acid, methyl ester
[z,z,z]-9,12,15-octadecadienoic acid methyl ester
methyl all-cis-9,12,15-octadecatrienoate
methyl alpha-linolenate
methyl cis,cis,cis-octadec-9,12,15-trienoate
octadecatrienoic acid methylester, 9,12,15-(z,z,z)-
0FE5A6DF-F28B-4F68-A34B-F46CBC4F91AD
methyl linolenate ,
301-00-8
S0324
L0051
CHEMBL1172198
ai3-26935
unii-0s1ns923k6
einecs 206-102-3
0s1ns923k6 ,
nsc 607759
(z,z,z)-9,12,15-octadecatrienoic acid methyl ester
fema no. 3411, methyl linolenate-
methyl cis,cis,cis-octadeca-9,12,15-trienoate
.alpha.-linolenic acid methyl ester
methyl .alpha.-linolenate
methyl linolenate [usp-rs]
9,?12,?15-?octadecatrienoic acid methyl ester
SCHEMBL55951
methyl linolenate, .alpha.
(z,z,z)-9,12,15-octadecatrienoic acid, methyl ester
methyl (9z,12z,15z)-9,12,15-octadecatrienoate #
dtxsid5041560 ,
cas-301-00-8
dtxcid3021560
NCGC00357264-01
tox21_303764
AC-33780
methyllinolenate
mfcd00135851
HY-21268
AKOS030526132
CS-5627
methyl linolenate, analytical standard
methyl linolenate, united states pharmacopeia (usp) reference standard
methyl linolenate, technical, 70-80% (gc)
linolenic acid-methyl ester
linolenic acid-methyl ester 10 microg/ml in acetonitrile
cis-9,cis-12,cis-15 octadecadienoic acid methyl ester
Q27237155
D91234
cis,cis,cis-octadeca-9,12,15-trienoic acid methyl ester
A912782
AS-56871
9z,12z,15z-octadecatrienoic acid methyl ester
methyl linolenate, tech grade
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
insect attractantA chemical that attracts insects.
[role 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]

Drug Classes (1)

ClassDescription
fatty acid methyl esterA fatty acid ester that is the carboxylic ester obtained by the formal condensation of a fatty acid with methanol.
[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]

Protein Targets (13)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
RAR-related orphan receptor gammaMus musculus (house mouse)Potency69.04470.006038.004119,952.5996AID1159521; AID1159523
GLI family zinc finger 3Homo sapiens (human)Potency34.77750.000714.592883.7951AID1259369; AID1259392
AR proteinHomo sapiens (human)Potency68.58960.000221.22318,912.5098AID1259243; AID1259247
caspase 7, apoptosis-related cysteine proteaseHomo sapiens (human)Potency68.58960.013326.981070.7614AID1346978
estrogen receptor 2 (ER beta)Homo sapiens (human)Potency61.53610.000657.913322,387.1992AID1259377; AID1259378
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency43.27710.003041.611522,387.1992AID1159555
retinoid X nuclear receptor alphaHomo sapiens (human)Potency21.87240.000817.505159.3239AID1159531
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency57.28060.001530.607315,848.9004AID1224841; AID1224842; AID1224848; AID1224849; AID1259401; AID1259403
pregnane X nuclear receptorHomo sapiens (human)Potency68.58960.005428.02631,258.9301AID1346982
caspase-3Homo sapiens (human)Potency68.58960.013326.981070.7614AID1346978
Histone H2A.xCricetulus griseus (Chinese hamster)Potency113.00400.039147.5451146.8240AID1224845
Caspase-7Cricetulus griseus (Chinese hamster)Potency54.48270.006723.496068.5896AID1346980
caspase-3Cricetulus griseus (Chinese hamster)Potency54.48270.006723.496068.5896AID1346980
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID492140Antioxidant activity assessed as formazan formation induced absorbance changes at 25 ppm at 570 nm at 37 degC for 6 hrs by MTT assay2010Journal of natural products, Jul-23, Volume: 73, Issue:7
An efficient and economical MTT assay for determining the antioxidant activity of plant natural product extracts and pure compounds.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (23)

TimeframeStudies, This Drug (%)All Drugs %
pre-19904 (17.39)18.7374
1990's2 (8.70)18.2507
2000's10 (43.48)29.6817
2010's6 (26.09)24.3611
2020's1 (4.35)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%
Other27 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]