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Fragment-based discovery of novel pentacyclic triterpenoid derivatives as cholesteryl ester transfer protein inhibitors.

China Pharmaceutical University
Design, synthesis and biological evaluation of novel cholesteryl ester transfer protein inhibitors bearing a cycloalkene scaffold.

Shenyang Pharmaceutical University
Discovery of hydroxyl 1,2-diphenylethanamine analogs as potent cholesterol ester transfer protein inhibitors.

Bristol-Myers Squibb Pharmaceutical Research Institute
Discovery of Novel Indoline Cholesterol Ester Transfer Protein Inhibitors (CETP) through a Structure-Guided Approach.

Merck Research Laboratories
Design, synthesis and biological evaluation of N,N-3-phenyl-3-benzylaminopropanamide derivatives as novel cholesteryl ester transfer protein inhibitor.

Shenyang Pharmaceutical University
Discovery of novel N,N-3-phenyl-3-benzylaminopropionanilides as potent inhibitors of cholesteryl ester transfer protein in vivo.

Shenyang Pharmaceutical University
Applications of Fluorine in Medicinal Chemistry.

Bristol-Myers Squibb Research and Development
Synthesis and biological evaluation of isoflavone amide derivatives with antihyperlipidemic and preadipocyte antiproliferative activities.

China Pharmaceutical University
Some molecular targets for antihyperlipidemic drug research.

Banasthali University
Potent cholesteryl ester transfer protein inhibitors of reduced lipophilicity: 1,1'-spiro-substituted hexahydrofuroquinoline derivatives.

Boehringer Ingelheim Pharma
Diphenylpyridylethanamine (DPPE)-based aminoheterocycles as cholesteryl ester transfer protein inhibitors.

Bristol-Myers Squibb
Diphenylpyridylethanamine (DPPE) derivatives as cholesteryl ester transfer protein (CETP) inhibitors.

Bristol-Myers Squibb
Identification of a potent and metabolically stable series of fluorinated diphenylpyridylethanamine-based cholesteryl ester transfer protein inhibitors.

Bristol-Myers Squibb
Design and synthesis of new tetrahydroquinolines derivatives as CETP inhibitors.

Eli Lilly
Design, synthesis and structure-activity-relationship of 1,5-tetrahydronaphthyridines as CETP inhibitors.

Eli Lilly
2-Arylbenzoxazoles as novel cholesteryl ester transfer protein inhibitors: optimization via array synthesis.

Bristol-Myers Squibb Pharmaceutical Research Institute
The biology and chemistry of hyperlipidemia.

Sinhgad College of Pharmacy
bis(2-(Acylamino)phenyl) disulfides, 2-(acylamino)benzenethiols, and S-(2-(acylamino)phenyl) alkanethioates as novel inhibitors of cholesteryl ester transfer protein.

Research Triangle Institute
CETP inhibitory activity of ceramides, isolated from the gorgonian Acabaria Undulata

TBA
Wiedendiol-A and -B, cholesteryl ester transfer protein inhibitors from the marine sponge Xestospongia wiedenmayeri

TBA
Discovery of substituted biphenyl oxazolidinone inhibitors of cholesteryl ester transfer protein.

TBA
SAR studies on the central phenyl ring of substituted biphenyl oxazolidinone-potent CETP inhibitors.

Merck Sharp & Dohme
Biphenyl-substituted oxazolidinones as cholesteryl ester transfer protein inhibitors: modifications of the oxazolidinone ring leading to the discovery of anacetrapib.

Merck Research Laboratories
2-(4-Carbonylphenyl)benzoxazole inhibitors of CETP: attenuation of hERG binding and improved HDLc-raising efficacy.

Merck Research Laboratories
2-(4-carbonylphenyl)benzoxazole inhibitors of CETP: scaffold design and advancement in HDLc-raising efficacy.

Merck Research Laboratories
2-Arylbenzoxazoles as CETP inhibitors: raising HDL-C in cynoCETP transgenic mice.

Merck Research Laboratories
Design of a novel class of biphenyl CETP inhibitors.

Merck Sharp & Dohme
Synthesis of a series of novel 2,4,5-trisubstituted selenazole compounds as potential PLTP inhibitors.

Beijing Institute of Pharmacology and Toxicology
Discovery of new cholesteryl ester transfer protein inhibitors via ligand-based pharmacophore modeling and QSAR analysis followed by synthetic exploration.

Al-Zaytoonah Private University of Jordan
Novel tetrahydrochinoline derived CETP inhibitors.

Bayer Healthcare
2-Arylbenzoxazoles as CETP inhibitors: substitution and modification of the alpha-alkoxyamide moiety.

Merck Research Laboratories
Synthesis and discovery of 2,3-dihydro-3,8-diphenylbenzo[1,4]oxazines as a novel class of potent cholesteryl ester transfer protein inhibitors.

Johnson & Johnson Pharmaceutical Research and Development
Substituted 1,3,5-triazines as cholesteryl ester transfer protein inhibitors

TBA
Phosphonate-containing analogs of cholesteryl ester as novel inhibitors of cholesteryl ester transfer protein

TBA
Novel inhibitors of cholesteryl ester transfer protein

TBA
Design and synthesis of potent inhibitors of cholesteryl ester transfer protein (CETP) exploiting a 1,2,3,4-tetrahydroquinoline platform.

Johnson & Johnson Pharmaceutical Research & Development
Design, synthesis, and biological evaluation of (2R,alphaS)-3,4-dihydro-2-[3-(1,1,2,2-tetrafluoroethoxy)phenyl]-5-[3-(trifluoromethoxy)-phenyl]-alpha-(trifluoromethyl)-1(2H)-quinolineethanol as potent and orally active cholesteryl ester transfer protein inhibitor.

Johnson and Johnson Pharmaceutical Research and Development
2D Quantitative structure-activity relationship studies on a series of cholesteryl ester transfer protein inhibitors.

Universidade Federal Da Bahia
Tetrazole and ester substituted tetrahydoquinoxalines as potent cholesteryl ester transfer protein inhibitors.

Array Biopharma
Dibenzodioxocinones--a new class of CETP inhibitors.

Bayer Healthcare Pharma Research
Invention of MK-8262, a Cholesteryl Ester Transfer Protein (CETP) Inhibitor Backup to Anacetrapib with Best-in-Class Properties.

Merck
S-(2-(acylamino)phenyl) 2,2-dimethylpropanethioates as CETP inhibitors.

Central Pharmaceutical Research Institute
Discovery of a simple picomolar inhibitor of cholesteryl ester transfer protein.

Pfizer
Chiral N,N-disubstituted trifluoro-3-amino-2-propanols are potent inhibitors of cholesteryl ester transfer protein.

Pharmacia
Cholesteryl ester transfer protein (CETP) inhibitors based on cyclic urea, bicyclic urea and bicyclic sulfamide cores.

Merck
Novel heteroaryl replacements of aromatic 3-tetrafluoroethoxy substituents in trifluoro-3-(tertiaryamino)-2-propanols as potent inhibitors of cholesteryl ester transfer protein.

Pharmacia
Discovery of chiral N,N-disubstituted trifluoro-3-amino-2-propanols as potent inhibitors of cholesteryl ester transfer protein.

Pfizer
Synthesis, biological evaluation and SAR studies of ursolic acid 3β-ester derivatives as novel CETP inhibitors.

Nanjing Medical University
Discovery of a Lead Triphenylethanamine Cholesterol Ester Transfer Protein (CETP) Inhibitor.

Bristol-Myers Squibb
A depsipeptide fungal metabolite inhibitor of cholesteryl ester transfer protein.

Schering-Plough Research Institute
Combinatorial synthesis of cholesterol ester transfer protein-mRNA ligands and screening by nondenaturating gel-electrophoresis.

Johann Wolfgang Goethe-Universit£T Frankfurt/Main
Discovery of pentacyclic triterpene 3β-ester derivatives as a new class of cholesterol ester transfer protein inhibitors.

China Pharmaceutical University
Discovery of a Novel Piperidine-Based Inhibitor of Cholesteryl Ester Transfer Protein (CETP) That Retains Activity in Hypertriglyceridemic Plasma.

Novartis Institutes For Biomedical Research
17-(1′propenyl)-17-3′-oxidoestra-4-en-3-one derivative, use thereof, and medicament containing said derivative

Bayer Intellectual Property
Aryl or N-heteroaryl substituted methanesulfonamide derivatives as vanilloid receptor ligands

Gruenenthal
Imidazole derivatives used as TAFIa inhibitors

Sanofi-Aventis Deutschland
Prolylcarboxypeptidase inhibitors

Merck Sharp & Dohme
Pharmacological characterization of the competitive GLUK5 receptor antagonist decahydroisoquinoline LY466195 in vitro and in vivo.

Eli Lilly
In vitro inhibition of cytosolic carbonic anhydrases I and II by some new dihydroxycoumarin compounds.

Balikesir University Science & Art Faculty
Antiparkinsonian agent piribedil displays antagonist properties at native, rat, and cloned, human alpha(2)-adrenoceptors: cellular and functional characterization.

Institut De Recherches Servier
Carbonic anhydrase activity modulators: synthesis of inhibitors and activators incorporating 2-substituted-thiazol-4-yl-methyl scaffolds.

UniversitÀ
Pharmacological characteristics of alpha 2-adrenergic receptors: comparison of pharmacologically defined subtypes with subtypes identified by molecular cloning.

University of Nebraska