- Anacetrapib
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IUPACName = (4"S",5"R")-5- [3,5-bis(trifluoromethyl)phenyl] -
3-{ [4'-fluoro-2'-methoxy-5'-(propan-2-yl)-4-
(trifluoromethyl) [1,1'-biphenyl] -2-yl] methyl}-
4-methyl-1,3-oxazolidin-2-one
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Section1 = Chembox Identifiers
CASNo = 875446-37-0
PubChem = 11556427
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Section2 = Chembox Properties
Formula = C30H25F10NO3
MolarMass = 637.51 g·mol−1
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Section3 = Chembox Hazards
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Autoignition =Anacetrapib (USAN,cite web | url = http://www.ama-assn.org/ama1/pub/upload/mm/365/anacetrapib.pdf | title = Statement on a nonproprietary name adopted by the USAN Council: Anacetrapib | year = 2007 | accessdate = 2008-01-19 | publisher =
American Medical Association ] pINN; codenamed MK-0859, Merck) is aCETP inhibitor being developed to treathypercholesterolemia (elevated cholesterol levels) and preventcardiovascular disease . It has been in Phase Iclinical trial s; preliminary results appear encouraging,cite journal |author=Krishna R, Anderson MS, Bergman AJ, "et al" |title=Effect of the cholesteryl ester transfer protein inhibitor, anacetrapib, on lipoproteins in patients with dyslipidaemia and on 24-h ambulatory blood pressure in healthy individuals: two double-blind, randomised placebo-controlled phase I studies |journal=Lancet |volume=370 |issue=9603 |pages=1907–14 |year=2007 |pmid=18068514 |doi=10.1016/S0140-6736(07)61813-3] although long-term safety data are lacking.At the 16th International Symposium on Drugs Affecting Lipid Metabolism (New York, Oct 4-7, 2007), Merck reported on a Phase IIb study. The eight week study reported dosage correlated reduction in LDL-C and increases in HDL-C levels with no corresponding increases in blood pressure in any cohort. The increase in HDL was particularly significant, averaging 44 percent, 86 percent, 139 percent and 133 percent at doses of 10 mg, 40 mg, 150 mg and 300 mg.
ee also
*
Torcetrapib , another CETP inhibitor unsuccessfully developed byPfizer References
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