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Discovery of novel hepatoselective HMG-CoA reductase inhibitors for treating hypercholesterolemia: a bench-to-bedside case study on tissue selective drug distribution
Authors:Pfefferkorn Jeffrey A  Litchfield John  Hutchings Richard  Cheng Xue-Min  Larsen Scott D  Auerbach Bruce  Bush Mark R  Lee Chitase  Erasga Noe  Bowles Daniel M  Boyles David C  Lu Gina  Sekerke Catherine  Askew Valerie  Hanselman Jeffrey C  Dillon Lisa  Lin Zhiwu  Robertson Andrew  Olsen Karl  Boustany Carine  Atkinson Karen  Goosen Theunis C  Sahasrabudhe Vaishali  Chupka Jonathan  Duignan David B  Feng Bo  Scialis Renato  Kimoto Emi  Bi Yi-An  Lai Yurong  El-Kattan Ayman  Bakker-Arkema Rebecca  Barclay Paul  Kindt Erick  Le Vu  Mandema Jaap W  Milad Mark  Tait Bradley D  Kennedy Robert  Trivedi Bharat K  Kowala Mark
Affiliation:Pfizer Global Research & Development, Eastern Point Road, Groton, CT 06340, United States
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.
Keywords:HMG-CoA reductase inhibitor   Statin   Hypercholesterolemia   Liver selective   Hepatoselective
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