Literature DB >> 23941686

Update on the discovery and development of cholesteryl ester transfer protein inhibitors for reducing residual cardiovascular risk.

Nathan B Mantlo1, Ana Escribano.   

Abstract

Cholesteryl ester transfer protein (CETP) facilitates the transfer of cholesteryl ester and triglycerides between plasma lipoprotein particles HDL and LDL/VLDL, resulting in equilibration between these lipoprotein fractions. Therapy that modulates HDL metabolism to increase HDL-c levels could be an effective strategy to reduce residual cardiovascular risk since it is estimated that for each mg/dL increase in plasma HDL cholesterol, there could be a 2-3% decrease in cardiovascular risk. Modification of the lipoprotein profile by CETP inhibitors is promising, but the beneficial effect of reducing coronary heart disease risk has not yet been proven. To date, four CETP inhibitors have advanced to phase 3 cardiovascular outcome clinical trials, and two have been terminated for off-target adverse effects and lack of efficacy. This perspective will summarize recent events, new research developments, and the discovery of new classes of CETP inhibitors.

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Year:  2013        PMID: 23941686     DOI: 10.1021/jm400574e

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  7 in total

Review 1.  The role of ligand efficiency metrics in drug discovery.

Authors:  Andrew L Hopkins; György M Keserü; Paul D Leeson; David C Rees; Charles H Reynolds
Journal:  Nat Rev Drug Discov       Date:  2014-02       Impact factor: 84.694

2.  Discovery of Novel Indoline Cholesterol Ester Transfer Protein Inhibitors (CETP) through a Structure-Guided Approach.

Authors:  Jonathan E Wilson; Ravi Kurukulasuriya; Mikhail Reibarkh; Maud Reiter; Aaron Zwicker; Kake Zhao; Fengqi Zhang; Rajan Anand; Vincent J Colandrea; Anne-Marie Cumiskey; Alejandro Crespo; Ruth A Duffy; Beth Ann Murphy; Kaushik Mitra; Douglas G Johns; Joseph L Duffy; Petr Vachal
Journal:  ACS Med Chem Lett       Date:  2016-01-04       Impact factor: 4.345

3.  Structural Plasticity of Cholesteryl Ester Transfer Protein Assists the Lipid Transfer Activity.

Authors:  Venkat R Chirasani; Prasanna D Revanasiddappa; Sanjib Senapati
Journal:  J Biol Chem       Date:  2016-07-20       Impact factor: 5.157

4.  Evacetrapib: in vitro and clinical disposition, metabolism, excretion, and assessment of drug interaction potential with strong CYP3A and CYP2C8 inhibitors.

Authors:  Ellen A Cannady; Ming-Dauh Wang; Stuart Friedrich; Jessica L F Rehmel; Ping Yi; David S Small; Wei Zhang; Jeffrey G Suico
Journal:  Pharmacol Res Perspect       Date:  2015-10-12

5.  Modular Entry to Functionalized Tetrahydrobenzo[b]azepines via the Palladium/Norbornene Cooperative Catalysis Enabled by a C7-Modified Norbornene.

Authors:  Xin Liu; Jianchun Wang; Guangbin Dong
Journal:  J Am Chem Soc       Date:  2021-06-23       Impact factor: 16.383

6.  Absolute bioavailability of evacetrapib in healthy subjects determined by simultaneous administration of oral evacetrapib and intravenous [(13) C8 ]-evacetrapib as a tracer.

Authors:  Ellen A Cannady; Aktham Aburub; Chris Ward; Chris Hinds; Boris Czeskis; Kenneth Ruterbories; Jeffrey G Suico; Jane Royalty; Demetrio Ortega; Brian W Pack; Syeda L Begum; William F Annes; Qun Lin; David S Small
Journal:  J Labelled Comp Radiopharm       Date:  2015-12-07       Impact factor: 1.921

7.  Design, Synthesis, and Biological Evaluation of N,N-Disubstituted-4-Arylthiazole-2-Methylamine Derivatives as Cholesteryl Ester Transfer Inhibitors.

Authors:  Xinran Wang; Xuehua Lin; Xuanqi Xu; Wei Li; Lijuan Hao; Chunchi Liu; Dongmei Zhao; Maosheng Cheng
Journal:  Molecules       Date:  2017-11-07       Impact factor: 4.411

  7 in total

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