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
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)CCCCCCCCCCCCCCC)[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
Approval Year
PubMed
Title | Date | PubMed |
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Serum cholesterol, cholesteryl ester, and high-density lipoprotein development in newborn infants: response to formulas supplemented with cholesterol and gamma-linolenic acid. | 1992 Apr |
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The phase behavior of cholesteryl esters in intracellular inclusions. | 1992 Sep 15 |
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Semiautomated multisample analysis of amniotic fluid lipids by high-performance thin-layer chromatography-reflectance spectrodensitometry. | 1993 May 19 |
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Gas chromatographic characterization of vegetable oil deodorization distillate. | 2001 Jul 6 |
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Anaerobic degradation kinetics of a cholesteryl ester. | 2003 |
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Lipid peroxidation and vitamin E in human coronary atherosclerotic lesions. | 2003 Apr |
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A single-step method of liposome preparation. | 2004 |
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[Determination of cholesteryl palmitate in Oviductus Ranae by HPLC]. | 2005 Jul |
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Lipids including cholesteryl linoleate and cholesteryl arachidonate contribute to the inherent antibacterial activity of human nasal fluid. | 2008 Sep 15 |
|
Liquid crystals in tribology. | 2009 Sep 18 |
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59692
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210-002-5
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300000042416
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ZR4D53AD57
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DTXSID40889356
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601-34-3
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3663
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246520
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SUBSTANCE RECORD