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首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Discovery of novel hepatoselective HMG-CoA reductase inhibitors for treating hypercholesterolemia: a bench-to-bedside case study on tissue selective drug distribution.
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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.

机译:发现用于治疗高胆固醇血症的新型肝选择性HMG-CoA还原酶抑制剂:组织选择性药物分布的逐案病例研究。

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摘要

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-imid azol-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.
机译:具有选择性组织分布的药物设计可以是提高疗效和安全性的有效策略,但是了解临床前组织分布数据到临床的转化仍然是一个重要的挑战。作为鉴定下一代肝脏选择性HMG-CoA还原酶抑制剂的发现计划的一部分,我们报告了对(3R,5R)-7-(4-((3-氟苄基)氨基甲酰基)-5-环丙基-2-(4)的鉴定-氟苯基)-1H-亚咪唑-1-基)-3,5-二羟基庚酸(26)作为治疗高胆固醇血症的候选药物。对26种药物(PF-03491165)以及先前报道的2种药物(PF-03052334)的临床评估为组织靶向HMG-CoA还原酶抑制剂的临床前和临床药代动力学以及药效学比较提供了案例研究的机会。

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