Compounds > methyl ricinoleate
Page last updated: 2024-12-05

methyl ricinoleate

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

Description

methyl ricinoleate: structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID5354133
CHEMBL ID3183150
CHEBI ID156194
SCHEMBL ID290360
MeSH IDM0046637

Synonyms (58)

Synonym
nsc-1254
ricinoleic acid methyl ester
methyl ricinolate
flexricin p-1
nsc1254
ricinoleic acid, methyl ester
methyl ricinoleate
141-24-2
methyl ricinoleate, >=99% (gc)
methyl (9z,12r)-12-hydroxyoctadec-9-enoate
9-octadecenoic acid, 12-hydroxy-, methyl ester, (9z,12r)-
methyl (z,12r)-12-hydroxyoctadec-9-enoate
CHEBI:156194
R0029
ricinolic acid methyl ester
NCGC00248854-01
9-octadecenoic acid, 12-hydroxy-, methyl ester, [r-(z)]-
tox21_200861
dtxcid509169
dtxsid2029169 ,
NCGC00258415-01
cas-141-24-2
9-octadecenoic acid, 12-hydroxy-, methyl ester, (r-(z))-
einecs 205-472-3
hsdb 5636
9-octadecenoic acid, 12-hydroxy-, methyl ester, (theta-(z))-
9-octadecenoic acid, 12-hydroxy-, methyl ester
nsc 1254
unii-90fdr3o96y
90fdr3o96y ,
12-hydroxy-9-octadecenoic acid, methyl ester
ai3-10523
methyl 12-d-hydroxy-9-cis-octadecenoate
cis-ricinoleic acid methyl ester
methyl ricinoleate [inci]
ricinic acid methyl ester
dub rm
ricinoleic acid, methyl ester [hsdb]
methyl ricinoleate [usp-rs]
SCHEMBL290360
methyl (9z)-12-hydroxy-9-octadecenoate #
CHEMBL3183150
mfcd00046712
methyl 12-hydroxyoleate
9-octadecenoic acid,12-hydroxy-, methyl ester, (9z,12r)-
methyl ricinoleate, analytical standard
AKOS027320383
AS-70362
methyl ricinoleate, european pharmacopoeia (ep) reference standard
ricinoleic acid-methyl ester
41989-07-5
methyl ricinoleate, united states pharmacopeia (usp) reference standard
(r,z)-methyl 12-hydroxyoctadec-9-enoate
12r-hydroxy-9-cis-octadecenoic acid methyl ester
methyl 12-hydroxy-9(z)-octadecenoate
Q27271321
CS-0139029
HY-N8045
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
aliphatic alcoholAn alcohol derived from an aliphatic compound.
[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 (6)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
RAR-related orphan receptor gammaMus musculus (house mouse)Potency0.01220.006038.004119,952.5996AID1159521
GLI family zinc finger 3Homo sapiens (human)Potency30.76250.000714.592883.7951AID1259369
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency68.86870.003041.611522,387.1992AID1159553
retinoid X nuclear receptor alphaHomo sapiens (human)Potency55.21000.000817.505159.3239AID1159527
peroxisome proliferator activated receptor gammaHomo sapiens (human)Potency61.94660.001019.414170.9645AID743191
v-jun sarcoma virus 17 oncogene homolog (avian)Homo sapiens (human)Potency15.56030.057821.109761.2679AID1159526; AID1159528
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (22)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's5 (22.73)18.2507
2000's10 (45.45)29.6817
2010's7 (31.82)24.3611
2020's0 (0.00)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 (4.55%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other21 (95.45%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
acetone
methyl ketone : A ketone of formula RC(=O)CH3 (R =/= H).		2.0710ketone body;
methyl ketone;
propanones;
volatile organic compound		EC 3.5.1.4 (amidase) inhibitor;
human metabolite;
polar aprotic solvent
cetyltrimethylammonium ion
Cetrimonium: Cetyltrimethylammonium compound whose salts and derivatives are used primarily as topical antiseptics.. cetyltrimethylammonium ion : A quaternary ammonium ion in which the substituents on nitrogen are one hexadecyl and three methyl groups.		2.0210quaternary ammonium ion
methyl acrylate
[no description available]		7.0510enoate ester
pyrroles
1H-pyrrole : A tautomer of pyrrole that has the double bonds at positions 2 and 4.. pyrrole : A five-membered monocyclic heteroarene comprising one NH and four CH units which forms the parent compound of the pyrrole group of compounds. Its five-membered ring structure has three tautomers. A 'closed class'.. azole : Any monocyclic heteroarene consisting of a five-membered ring containing nitrogen. Azoles can also contain one or more other non-carbon atoms, such as nitrogen, sulfur or oxygen.		1.9810pyrrole;
secondary amine
decan-4-olide
gamma-decalactone : A gamma-lactone that is oxolan-2-one substituted by a hexyl group at position 5.		4.6380gamma-lactone;
tetrahydrofuranone		anticonvulsant;
flavouring agent;
food additive
ruthenium
Ruthenium: A hard, brittle, grayish-white rare earth metal with an atomic symbol Ru, atomic number 44, and atomic weight 101.07. It is used as a catalyst and hardener for PLATINUM and PALLADIUM.		2.0610iron group element atom;
platinum group metal atom
oleic acid
Oleic Acid: An unsaturated fatty acid that is the most widely distributed and abundant fatty acid in nature. It is used commercially in the preparation of oleates and lotions, and as a pharmaceutical solvent. (Stedman, 26th ed). oleic acid : An octadec-9-enoic acid in which the double bond at C-9 has Z (cis) stereochemistry.		1.9910octadec-9-enoic acidantioxidant;
Daphnia galeata metabolite;
EC 3.1.1.1 (carboxylesterase) inhibitor;
Escherichia coli metabolite;
mouse metabolite;
plant metabolite;
solvent
methyl linoleate
[no description available]		1.9810fatty acid methyl esterplant metabolite
methyl oleate
[no description available]		2.4120fatty acid methyl ester
phosphatidylcholines
Phosphatidylcholines: Derivatives of PHOSPHATIDIC ACIDS in which the phosphoric acid is bound in ester linkage to a CHOLINE moiety.		2101,2-diacyl-sn-glycero-3-phosphocholine
stearates
Stearates: Salts and esters of the 18-carbon saturated, monocarboxylic acid--stearic acid.		1.9810
ConditionIndicatedRelationship StrengthStudiesTrials