Page last updated: 2024-12-07

cholesteryl oleate

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

Description

cholesteryl oleate: RN given refers to ((Z)-isomer) [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

cholesteryl oleate : The (Z)-stereoisomer of cholesteryl octadec-9-enoate. [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]

Cross-References

ID SourceID
PubMed CID5283632
CHEMBL ID1097567
CHEBI ID46898
SCHEMBL ID132003
MeSH IDM0062919

Synonyms (62)

Synonym
3dpk9kfn2m ,
nsc 18186
cholest-5-en-3-ol (3beta)-, 3-((9z)-9-octadecenoate)
unii-3dpk9kfn2m
einecs 206-142-1
oleoylcholesterol
cholesteroyl-oleate
303-43-5
cholesteryl oleate
cholesteryl cis-9-octadecenoate
ce(18:1)
18:1 cholesteryl ester
cholest-5-en-3b-yl (9z-octadecenoate)
LMST01020003
cholest-5-en-3-ol (3beta)-, (9z)-9-octadecenoate
cholest-5-en-3-ol (3beta)-, (9z)-9-octadecenoate (9ci)
cholest-5-en-3-ol (3beta)-, 9-octadecenoate-9,10-t2, (z)- (9ci)
cholesteryl oleic ester
cholesterol, oleate (6ci,8ci)
9-octadecenoic acid, (3beta)-cholest-5-en-3-yl ester, (9z)-
oleic acid cholesteryl ester
cholest-5-en-3-beta-yl oleate
oleic acid, cholesteryl ester (6ci)
cholest-5-en-3-ol (3beta)-, 9-octadecenoate, (z)-
cholesterol, oleate (8ci)
cholesteryl oleate-9,10-t2
2ob ,
cholesteryl oleate, >=98% (hplc; detection at 205 nm)
ce(18:1(9z))
cholesteryl (9z-octadecenoate)
cholest-5-en-3-yl (9z)-9-octadecenoate
(3beta)-cholest-5-en-3-ol, (z)-9-octadecenoate
(3beta)-cholest-5-en-3-yl (9e)-octadec-9-enoate
CHEBI:46898 ,
(3beta)-cholest-5-en-3-yl (9z)-octadec-9-enoate
...cholesteryl-cis-9-octadecenoate
C-5830
cholesterol oleate
oleic acid cholesterol ester
CHEMBL1097567
[(3s,8s,9s,10r,13r,14s,17r)-10,13-dimethyl-17-[(2r)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl] (z)-octadec-9-enoate
AKOS025311525
cholesteryl oleate [inci]
oleic acid, cholesteryl ester
cholest-5-en-3-ol (3.beta.)-, 3-((9z)-9-octadecenoate)
yofco lc-co-d
cholesterol 3.beta.-oleate
cholest-5-en-3-.beta.-yl oleate
SCHEMBL132003
cholest-5-en-3-yl (9z)-9-octadecenoate #
5-cholesten-3beta-ol 3-oleate
cholesteryl oleate-13c18, 99 atom % 13c, 95% (cp)
(3beta,9beta,14beta,17alpha)-cholest-5-en-3-yl (9z)-octadec-9-enoate
'(3beta,9beta,14beta,17alpha)-cholest-5-en-3-yl (9z)-octadec-9-enoate'
Q27104577
DTXSID901014621
CS-0059332
HY-113217
cholest-5-en-3-ol (3beta)-, 3-[(9z)-9-octadecenoate]
F82232
BS-42184
BP-29625

Research Excerpts

Compound-Compound Interactions

ExcerptReferenceRelevance
" As apoE is a potent ligand for the LDL receptor, we next evaluated the effects of TOR in combination with the LDL-lowering drug berberine, which upregulates LDL receptor expression in dyslipidemic hamsters."( Upregulating reverse cholesterol transport with cholesteryl ester transfer protein inhibition requires combination with the LDL-lowering drug berberine in dyslipidemic hamsters.
Briand, F; Muzotte, E; Sulpice, T; Thieblemont, Q, 2013
)
0.39
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
mouse metaboliteAny mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
[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 (2)

ClassDescription
cholesteryl octadec-9-enoate
CE(18:1)
[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]

Pathways (1)

PathwayProteinsCompounds
Sterols biosynthesis pathway015

Bioassays (20)

Assay IDTitleYearJournalArticle
AID477324Antibacterial activity against Pseudomonas aeruginosa ATCC 27853 after 24 hrs by microdilution method2010European journal of medicinal chemistry, Apr, Volume: 45, Issue:4
Synthesis and characterization of novel fatty acid analogs of cholesterol: in vitro antimicrobial activity.
AID477321Antibacterial activity against Streptococcus mutans UA159 MTCC 497 after 24 hrs by microdilution method2010European journal of medicinal chemistry, Apr, Volume: 45, Issue:4
Synthesis and characterization of novel fatty acid analogs of cholesterol: in vitro antimicrobial activity.
AID477313Antibacterial activity against recultured Salmonella Typhimurium after 24 hrs by disk diffusion method2010European journal of medicinal chemistry, Apr, Volume: 45, Issue:4
Synthesis and characterization of novel fatty acid analogs of cholesterol: in vitro antimicrobial activity.
AID477312Antibacterial activity against Pseudomonas aeruginosa ATCC 27853 after 24 hrs by disk diffusion method2010European journal of medicinal chemistry, Apr, Volume: 45, Issue:4
Synthesis and characterization of novel fatty acid analogs of cholesterol: in vitro antimicrobial activity.
AID477329Antifungal activity against Candida parapsilosis ATCC 22019 after 48 to 72 hrs by disk diffusion method2010European journal of medicinal chemistry, Apr, Volume: 45, Issue:4
Synthesis and characterization of novel fatty acid analogs of cholesterol: in vitro antimicrobial activity.
AID477311Antibacterial activity against Staphylococcus aureus ATCC 25923 after 24 hrs by disk diffusion method2010European journal of medicinal chemistry, Apr, Volume: 45, Issue:4
Synthesis and characterization of novel fatty acid analogs of cholesterol: in vitro antimicrobial activity.
AID477325Antibacterial activity against recultured Salmonella Typhimurium after 24 hrs by microdilution method2010European journal of medicinal chemistry, Apr, Volume: 45, Issue:4
Synthesis and characterization of novel fatty acid analogs of cholesterol: in vitro antimicrobial activity.
AID477337Antifungal activity against Candida parapsilosis ATCC 22019 after 48 to 72 hrs by microdilution method2010European journal of medicinal chemistry, Apr, Volume: 45, Issue:4
Synthesis and characterization of novel fatty acid analogs of cholesterol: in vitro antimicrobial activity.
AID477326Antibacterial activity against Escherichia coli ATCC 25922 after 24 hrs by microdilution method2010European journal of medicinal chemistry, Apr, Volume: 45, Issue:4
Synthesis and characterization of novel fatty acid analogs of cholesterol: in vitro antimicrobial activity.
AID477327Antifungal activity against Candida albicans ATCC 24433 after 48 to 72 hrs by disk diffusion method2010European journal of medicinal chemistry, Apr, Volume: 45, Issue:4
Synthesis and characterization of novel fatty acid analogs of cholesterol: in vitro antimicrobial activity.
AID477338Antifungal activity Cryptococcus neoformans after 48 to 72 hrs by microdilution method2010European journal of medicinal chemistry, Apr, Volume: 45, Issue:4
Synthesis and characterization of novel fatty acid analogs of cholesterol: in vitro antimicrobial activity.
AID477335Antifungal activity against Candida albicans ATCC 24433 after 48 to 72 hrs by microdilution method2010European journal of medicinal chemistry, Apr, Volume: 45, Issue:4
Synthesis and characterization of novel fatty acid analogs of cholesterol: in vitro antimicrobial activity.
AID477309Antibacterial activity against Streptococcus mutans UA159 MTCC 497 after 24 hrs by disk diffusion method2010European journal of medicinal chemistry, Apr, Volume: 45, Issue:4
Synthesis and characterization of novel fatty acid analogs of cholesterol: in vitro antimicrobial activity.
AID477322Antibacterial activity against recultured Streptococcus pyogenes after 24 hrs by microdilution method2010European journal of medicinal chemistry, Apr, Volume: 45, Issue:4
Synthesis and characterization of novel fatty acid analogs of cholesterol: in vitro antimicrobial activity.
AID477310Antibacterial activity against recultured Streptococcus pyogenes after 24 hrs by disk diffusion method2010European journal of medicinal chemistry, Apr, Volume: 45, Issue:4
Synthesis and characterization of novel fatty acid analogs of cholesterol: in vitro antimicrobial activity.
AID477330Antifungal activity Cryptococcus neoformans after 48 to 72 hrs by disk diffusion method2010European journal of medicinal chemistry, Apr, Volume: 45, Issue:4
Synthesis and characterization of novel fatty acid analogs of cholesterol: in vitro antimicrobial activity.
AID477336Antifungal activity against Candida krusei ATCC 6528 after 48 to 72 hrs by microdilution method2010European journal of medicinal chemistry, Apr, Volume: 45, Issue:4
Synthesis and characterization of novel fatty acid analogs of cholesterol: in vitro antimicrobial activity.
AID477328Antifungal activity against Candida krusei ATCC 6528 after 48 to 72 hrs by disk diffusion method2010European journal of medicinal chemistry, Apr, Volume: 45, Issue:4
Synthesis and characterization of novel fatty acid analogs of cholesterol: in vitro antimicrobial activity.
AID477323Antibacterial activity against Staphylococcus aureus ATCC 25923 after 24 hrs by microdilution method2010European journal of medicinal chemistry, Apr, Volume: 45, Issue:4
Synthesis and characterization of novel fatty acid analogs of cholesterol: in vitro antimicrobial activity.
AID477314Antibacterial activity against Escherichia coli ATCC 25922 after 24 hrs by disk diffusion method2010European journal of medicinal chemistry, Apr, Volume: 45, Issue:4
Synthesis and characterization of novel fatty acid analogs of cholesterol: in vitro antimicrobial activity.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (285)

TimeframeStudies, This Drug (%)All Drugs %
pre-199094 (32.98)18.7374
1990's116 (40.70)18.2507
2000's44 (15.44)29.6817
2010's29 (10.18)24.3611
2020's2 (0.70)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 (%)
Trials6 (2.06%)5.53%
Reviews4 (1.37%)6.00%
Case Studies2 (0.69%)4.05%
Observational0 (0.00%)0.25%
Other279 (95.88%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]