1. Academic Validation
  2. Discovery of novel hepatoselective HMG-CoA reductase inhibitors for treating hypercholesterolemia: a bench-to-bedside case study on tissue selective drug distribution

Discovery of novel hepatoselective HMG-CoA reductase inhibitors for treating hypercholesterolemia: a bench-to-bedside case study on tissue selective drug distribution

  • Bioorg Med Chem Lett. 2011 May 1;21(9):2725-31. doi: 10.1016/j.bmcl.2010.11.103.
Jeffrey A Pfefferkorn 1 John Litchfield Richard Hutchings Xue-Min Cheng Scott D Larsen Bruce Auerbach Mark R Bush Chitase Lee Noe Erasga Daniel M Bowles David C Boyles Gina Lu Catherine Sekerke Valerie Askew Jeffrey C Hanselman Lisa Dillon Zhiwu Lin Andrew Robertson Karl Olsen Carine Boustany Karen Atkinson Theunis C Goosen Vaishali Sahasrabudhe Jonathan Chupka David B Duignan Bo Feng Renato Scialis Emi Kimoto Yi-An Bi Yurong Lai Ayman El-Kattan Rebecca Bakker-Arkema Paul Barclay Erick Kindt Vu Le Jaap W Mandema Mark Milad Bradley D Tait Robert Kennedy Bharat K Trivedi Mark Kowala
Affiliations

Affiliation

  • 1 Pfizer Global Research & Development, Eastern Point Road, Groton, CT 06340, USA. jeffrey.a.pfefferkorn@pfizer.com
Abstract

The design of drugs with selective tissue distribution can be an effective strategy for enhancing efficacy and safety, but understanding the translation of preclinical tissue distribution data to the clinic remains an important challenge. As part of a discovery program to identify next generation liver selective HMG-CoA reductase inhibitors we report the identification of (3R,5R)-7-(4-((3-fluorobenzyl)carbamoyl)-5-cyclopropyl-2-(4-fluorophenyl)-1H-imidazol-1-yl)-3,5-dihydroxyheptanoic acid (26) as a candidate for treating hypercholesterlemia. Clinical evaluation of 26 (PF-03491165), as well as the previously reported 2 (PF-03052334), provided an opportunity for a case study comparison of the preclinical and clinical pharmacokinetics as well as pharmacodynamics of tissue targeted HMG-CoA reductase inhibitors.

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