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Details

Stereochemistry ABSOLUTE
Molecular Formula C45H78O2
Molecular Weight 651.0996
Optical Activity UNSPECIFIED
Defined Stereocenters 8 / 8
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CHOLESTERYL OLEATE

SMILES

[H][C@@]1(CC[C@@]2([H])[C@]3([H])CC=C4C[C@H](CC[C@]4(C)[C@@]3([H])CC[C@]12C)OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H](C)CCCC(C)C

InChI

InChIKey=RJECHNNFRHZQKU-RMUVNZEASA-N
InChI=1S/C45H78O2/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-25-43(46)47-38-30-32-44(5)37(34-38)26-27-39-41-29-28-40(36(4)24-22-23-35(2)3)45(41,6)33-31-42(39)44/h14-15,26,35-36,38-42H,7-13,16-25,27-34H2,1-6H3/b15-14-/t36-,38+,39+,40-,41+,42+,44+,45-/m1/s1

HIDE SMILES / InChI
Molecular Formula C45H78O2
Molecular Weight 651.0996
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 8 / 8
E/Z Centers 1
Optical Activity UNSPECIFIED

Approval Year

2013
596
PubMed

PubMed

TitleDatePubMed
Induced circular dichroism of incorporated fluorescent cholesteryl esters and polar lipids as a probe of human serum low density lipoprotein structure and melting.
1981 May 10
Accelerated transfer of cholesteryl esters in dyslipidemic plasma. Role of cholesteryl ester transfer protein.
1987 Apr
Plasma cholesteryl ester-triglyceride transfer protein. The catalytic domain is a low molecular weight proteolipid.
1987 Dec 25
Processing of cholesteryl ester from low-density lipoproteins in the rat. Hepatic metabolism and biliary secretion after uptake by different hepatic cell types.
1989 Feb 1
Rat adrenal uptake and metabolism of high density lipoprotein cholesteryl ester.
1989 May 15
Lecithin cholesterol acyltransferase in human cerebrospinal fluid: reduced level in patients with multiple sclerosis and evidence of direct synthesis in the brain.
1992
Cholesteryl esters in lymph chylomicrons: contribution from high density lipoprotein transferred from plasma into intestinal lymph.
1993 Oct
ACAT inhibitors as antiatherosclerotic agents: compounds and mechanisms.
1994 May
Kinetics of the incorporation of dietary fatty acids into serum cholesteryl esters, erythrocyte membranes, and adipose tissue: an 18-month controlled study.
1997 Oct
Cholesteryl ester transfer protein mediates selective uptake of high density lipoprotein cholesteryl esters by human adipose tissue.
1997 Sep 19
Effect of ursodeoxycholic acid on hepatic LDL binding and uptake in dietary hypercholesterolemic hamsters.
2000 Nov
Influence of dietary linoleic acid intake with different fat intakes on arachidonic acid concentrations in plasma and platelet lipids and eicosanoid biosynthesis in female volunteers.
2003
Fat mobilization in adipose tissue is promoted by adipose triglyceride lipase.
2004 Nov 19
Saturated fat-rich diet enhances selective uptake of LDL cholesteryl esters in the arterial wall.
2005 Aug
Improved HPLC assay for lipid peroxides in human plasma using the internal standard of hydroperoxide.
2005 May
Multiple functions as lipase, steryl ester hydrolase, phospholipase, and acyltransferase of Tgl4p from the yeast Saccharomyces cerevisiae.
2010 May 21
Patents

Patents

05219733
2
JPH04255800A
1
JPS59126492A
1
Substance Class Chemical
Created
by admin
on Sat Dec 16 20:10:22 GMT 2023
Edited
by admin
on Sat Dec 16 20:10:22 GMT 2023
Record UNII
3DPK9KFN2M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHOLESTERYL OLEATE
INCI  
INCI  
Official Name English
OLEIC ACID, CHOLESTERYL ESTER
Common Name English
YOFCO LC-CO-D
Brand Name English
CHOLEST-5-EN-3-OL (3.BETA.)-, 9-OCTADECENOATE, (Z)-
Common Name English
OLEOYLCHOLESTEROL
Common Name English
CHOLEST-5-EN-3-.BETA.-YL OLEATE
Common Name English
CHOLESTERYL OLEIC ESTER
Common Name English
CHOLESTEROL 3.BETA.-OLEATE
Common Name English
CHOLEST-5-EN-3-OL (3.BETA.)-, (9Z)-9-OCTADECENOATE
Common Name English
NSC-18186
Code English
CHOLESTERYL OLEATE [INCI]
Common Name English
CHOLESTERYL CIS-9-OCTADECENOATE
Common Name English
CHOLEST-5-EN-3-OL (3.BETA.)-, 3-((9Z)-9-OCTADECENOATE)
Common Name English
Code System Code Type Description
CAS
303-43-5
Created by admin on Sat Dec 16 20:10:22 GMT 2023 , Edited by admin on Sat Dec 16 20:10:22 GMT 2023
PRIMARY
MESH
C014409
Created by admin on Sat Dec 16 20:10:22 GMT 2023 , Edited by admin on Sat Dec 16 20:10:22 GMT 2023
PRIMARY
RXCUI
1368200
Created by admin on Sat Dec 16 20:10:22 GMT 2023 , Edited by admin on Sat Dec 16 20:10:22 GMT 2023
PRIMARY RxNorm
NSC
18186
Created by admin on Sat Dec 16 20:10:22 GMT 2023 , Edited by admin on Sat Dec 16 20:10:22 GMT 2023
PRIMARY
EPA CompTox
DTXSID901014621
Created by admin on Sat Dec 16 20:10:22 GMT 2023 , Edited by admin on Sat Dec 16 20:10:22 GMT 2023
PRIMARY
CHEBI
46898
Created by admin on Sat Dec 16 20:10:22 GMT 2023 , Edited by admin on Sat Dec 16 20:10:22 GMT 2023
PRIMARY
PUBCHEM
5283632
Created by admin on Sat Dec 16 20:10:22 GMT 2023 , Edited by admin on Sat Dec 16 20:10:22 GMT 2023
PRIMARY
ECHA (EC/EINECS)
206-142-1
Created by admin on Sat Dec 16 20:10:22 GMT 2023 , Edited by admin on Sat Dec 16 20:10:22 GMT 2023
PRIMARY
FDA UNII
3DPK9KFN2M
Created by admin on Sat Dec 16 20:10:22 GMT 2023 , Edited by admin on Sat Dec 16 20:10:22 GMT 2023
PRIMARY
DAILYMED
3DPK9KFN2M
Created by admin on Sat Dec 16 20:10:22 GMT 2023 , Edited by admin on Sat Dec 16 20:10:22 GMT 2023
PRIMARY
NIH
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