U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C43H76O2
Molecular Weight 625.0623
Optical Activity UNSPECIFIED
Defined Stereocenters 8 / 8
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHOLESTERYL PALMITATE

SMILES

CCCCCCCCCCCCCCCC(=O)O[C@H]1CC[C@]2(C)[C@H]3CC[C@]4(C)[C@H](CC[C@H]4[C@@H]3CC=C2C1)[C@H](C)CCCC(C)C

InChI

InChIKey=BBJQPKLGPMQWBU-JADYGXMDSA-N
InChI=1S/C43H76O2/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-23-41(44)45-36-28-30-42(5)35(32-36)24-25-37-39-27-26-38(34(4)22-20-21-33(2)3)43(39,6)31-29-40(37)42/h24,33-34,36-40H,7-23,25-32H2,1-6H3/t34-,36+,37+,38-,39+,40+,42+,43-/m1/s1

HIDE SMILES / InChI

Molecular Formula C43H76O2
Molecular Weight 625.0623
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 8 / 8
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Chemical warfare agents.
2010-07
Evolving neural network optimization of cholesteryl ester separation by reversed-phase HPLC.
2010-07
Clearance in vivo of instilled [h]cholesterol from the rat lung.
2010
Liquid crystals in tribology.
2009-09-18
Lipids including cholesteryl linoleate and cholesteryl arachidonate contribute to the inherent antibacterial activity of human nasal fluid.
2008-09-15
Thermodynamic studies of bovine lung surfactant extract mixing with cholesterol and its palmitate derivative.
2007-07-15
Interactions of poly(tert-butyl acrylate)-poly(styrene) diblock copolymers with lipids at the air-water interface.
2006-08-29
Purification, characterization, and molecular cloning of organic-solvent-tolerant cholesterol esterase from cyclohexane-tolerant Burkholderia cepacia strain ST-200.
2006-08
Percolation phenomenon in mixed reverse micelles: the effect of additives.
2006-03-01
[Determination of cholesteryl palmitate in Oviductus Ranae by HPLC].
2005-07
A single-step method of liposome preparation.
2004
Lipid peroxidation and vitamin E in human coronary atherosclerotic lesions.
2003-04
Anaerobic degradation kinetics of a cholesteryl ester.
2003
Gas chromatographic characterization of vegetable oil deodorization distillate.
2001-07-06
Biomarkers of dietary fat composition in young adults with a parental history of premature coronary heart disease compared with controls. The EARS Study.
1994-08
Semiautomated multisample analysis of amniotic fluid lipids by high-performance thin-layer chromatography-reflectance spectrodensitometry.
1993-05-19
The phase behavior of cholesteryl esters in intracellular inclusions.
1992-09-15
Serum cholesterol, cholesteryl ester, and high-density lipoprotein development in newborn infants: response to formulas supplemented with cholesterol and gamma-linolenic acid.
1992-04
Amniotic fluid cholesteryl palmitate in pregnancies complicated by diabetes mellitus.
1988-09
Cholesteryl palmitate as a predictor of fetal lung maturity.
1987-07
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:13:19 GMT 2025
Edited
by admin
on Mon Mar 31 18:13:19 GMT 2025
Record UNII
ZR4D53AD57
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHOLESTERYL PALMITATE
Common Name English
NSC-59692
Preferred Name English
CHOLEST-5-EN-3-OL (3.BETA.)-, HEXADECANOATE
Common Name English
CHOLESTERYL HEXADECANOATE
Common Name English
OP0201 COMPONENT CHOLESTERYL PALMITATE
Common Name English
HEXADECANOIC ACID, CHOLESTERYL ESTER
Common Name English
CHOLESTEROL PALMITATE
Common Name English
Code System Code Type Description
NSC
59692
Created by admin on Mon Mar 31 18:13:19 GMT 2025 , Edited by admin on Mon Mar 31 18:13:19 GMT 2025
PRIMARY
ECHA (EC/EINECS)
210-002-5
Created by admin on Mon Mar 31 18:13:19 GMT 2025 , Edited by admin on Mon Mar 31 18:13:19 GMT 2025
PRIMARY
SMS_ID
300000042416
Created by admin on Mon Mar 31 18:13:19 GMT 2025 , Edited by admin on Mon Mar 31 18:13:19 GMT 2025
PRIMARY
FDA UNII
ZR4D53AD57
Created by admin on Mon Mar 31 18:13:19 GMT 2025 , Edited by admin on Mon Mar 31 18:13:19 GMT 2025
PRIMARY
EPA CompTox
DTXSID40889356
Created by admin on Mon Mar 31 18:13:19 GMT 2025 , Edited by admin on Mon Mar 31 18:13:19 GMT 2025
PRIMARY
CAS
601-34-3
Created by admin on Mon Mar 31 18:13:19 GMT 2025 , Edited by admin on Mon Mar 31 18:13:19 GMT 2025
PRIMARY
CHEBI
3663
Created by admin on Mon Mar 31 18:13:19 GMT 2025 , Edited by admin on Mon Mar 31 18:13:19 GMT 2025
PRIMARY
PUBCHEM
246520
Created by admin on Mon Mar 31 18:13:19 GMT 2025 , Edited by admin on Mon Mar 31 18:13:19 GMT 2025
PRIMARY