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1,4-环己烷羧酸酯:用于治疗哮喘的强效且选择性磷酸二酯酶4抑制剂。

1,4-Cyclohexanecarboxylates: potent and selective inhibitors of phosophodiesterase 4 for the treatment of asthma.

作者信息

Christensen S B, Guider A, Forster C J, Gleason J G, Bender P E, Karpinski J M, DeWolf W E, Barnette M S, Underwood D C, Griswold D E, Cieslinski L B, Burman M, Bochnowicz S, Osborn R R, Manning C D, Grous M, Hillegas L M, Bartus J O, Ryan M D, Eggleston D S, Haltiwanger R C, Torphy T J

机构信息

SmithKline Beecham Pharmaceuticals, King of Prussia, Pennsylvania 19406-0939, USA.

出版信息

J Med Chem. 1998 Mar 12;41(6):821-35. doi: 10.1021/jm970090r.

Abstract

Evaluation of a variety of PDE4 inhibitors in a series of cellular and in vivo assays suggested a strategy to improve the therapeutic index of PDE4 inhibitors by increasing their selectivity for the ability to inhibit PDE4 catalytic activity versus the ability to compete for high affinity [3H]rolipram-binding sites in the central nervous system. Use of this strategy led ultimately to the identification of cis-4-cyano-4-[3-(cyclopentyloxy)-4-methoxyphenyl]cyclohexane-1-carboxyl ic acid (1, SB 207499, Ariflo), a potent second-generation inhibitor of PDE4 with a decreased potential for side effects versus the archetypic first generation inhibitor, (R)-rolipram.

摘要

在一系列细胞和体内试验中对多种磷酸二酯酶4(PDE4)抑制剂进行评估,提出了一种提高PDE4抑制剂治疗指数的策略,即通过增强其对抑制PDE4催化活性能力的选择性,相对于在中枢神经系统中竞争高亲和力[3H]咯利普兰结合位点的能力。采用该策略最终鉴定出顺式-4-氰基-4-[3-(环戊氧基)-4-甲氧基苯基]环己烷-1-羧酸(1,SB 207499,阿立普唑),这是一种有效的第二代PDE4抑制剂,与原型第一代抑制剂(R)-咯利普兰相比,副作用潜力降低。

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