Joint effects of serum triglyceride and LDL cholesterol and HDL cholesterol concentrations on coronary heart disease risk in the helsinki heart study. Implications for treatment
Bis(2-(acylamino)phenyl) disulfides, 2(acylamino)benzenethiols, and S-(2-(acylamino)phenyl)alkanethioates as novel inhibitors of cholesteryl ester transfer protein
Genetic cholesteryl ester transfer protein deficiency is extremely frequent in omagari area of Japan; marked hyperalphalipoproteinemia caused by cholesteryl ester transfer protein gene mutation is not a longevity syndrome
Relationship of HDL and coronary heart desease to a common amino acid polymorphism in the cholesteryl ester transfer protein in men with and without hyperalphalipoproteinemia
Elevated HDL cholesterol is a risk factor for ischemic heart disease in white women when caused by a common mutation in the cholesteryl ester transfer protein gene
Stereo-selective mukaiyama-michael/michael/aldol domino cyclization as the key step in the synthesis of pentasubstituted arenes: An efficient access to highly active inhibitors of cholesteryl ester transfer protein (CETP)
Preparation of N-(1-Alkoxycarbonyl-1,2,3,4-Tetra-hydroquinolin-4-yl)Carbamates as Cholesteryl Ester Transfer Protein Inhibitors. WO0017164, March 30, 2000
Preparation of (2R,4S)-4-[(3,5-bistrifluoromethyl-benzyl)-methoxycarbonylamino] -2-ethyl-6-trifluoromethyl-3,4-dihydro-2H-quinoline-1-carboxylic acid ethyl ester as CETP inhibitor. WO0140190, June 7, 2001
Chiral synthesis via organoboranes. 40. Selective reductions. 55. A simple one-pot synthesis of the enantiomers of trifluoro-methyloxirane. A general synthesis in high optical purities of α-Trifluoro-methyl secondary alcohols via the ring-cleavage reactions of the epoxide
Novel heteroaryl replacements of aromatic 3-tetrafluoroethoxy substituents in trifluoro-3-(tertiaryamino)-2-propanols as potent inhibitors of cholesteryl ester transfer protein
2-Substituted (2SR)-2-amino-2-((1SR,2SR)-2-carboxycycloprop-1-yl)glycines as potent and selective antagonists of group ii metabotropic glutamate receptors. 2. Effects of aromatic substitution; pharmacological characterization, and bioavailability