增强剂
化学
囊性纤维化
伊瓦卡夫托
突变
囊性纤维化跨膜传导调节器
基因
药理学
生物化学
内科学
医学
作者
Marc J. C. Scanio,Xenia B. Searle,Bo Liu,John R. Koenig,Robert J. Altenbach,Gregory A. Gfesser,Andrew R. Bogdan,Stephen N. Greszler,Gang Zhao,Ankita Singh,Yihong Fan,Andrew M. Swensen,Timothy A. Vortherms,Arlene M. Manelli,Corina Balut,Wenqing Gao,Hong Sae Yong,Michael R. Schrimpf,Chris Tse,Philip R. Kym,Xueqing Wang
标识
DOI:10.1016/j.bmcl.2022.128843
摘要
Cystic fibrosis (CF) is an autosomal recessive disease resulting from mutations on both copies of the CFTR gene. Phenylalanine deletion at position 508 of the CFTR protein (F508del-CFTR) is the most frequent mutation in CF patients. Currently, the most effective treatments of CF use a dual or triple combination of CFTR correctors and potentiators. In triple therapy, two correctors (C1 and C2) and a potentiator are employed. Herein, we describe the identification and exploration of the SAR of a series of 4-aminopyrrolidine-2-carboxylic acid C2 correctors of CFTR to be used in conjunction with our existing C1 corrector series for the treatment of CF.
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