作者
Peter T. W. Cheng,Robert F. Kaltenbach,Hao Zhang,Jun Shi,Shiwei Tao,Jun Li,Lawrence J. Kennedy,Steven J. Walker,Yan Shi,Ying Wang,Suresh Dhanusu,R. Ramesh Babu,K. Selvakumar,Sutjano Jusuf,Daniel Smith,Subramaniam Krishnananthan,Jianqing Li,Tao Wang,Rebekah Heiry,Chi Shing Sum,Stephen Kalinowski,Chen-Pin Hung,Ching-Hsuen Chu,Anthony V. Azzara,Milinda Ziegler,Lisa Burns,Bradley A. Zinker,Stephanie Boehm,Joseph R. Taylor,Julia Sapuppo,Kathy Mosure,Gerry Everlof,Victor R. Guarino,Lisa Zhang,Yanou Yang,Qian Ruan,Carrie Xu,Atsu Apedo,Sarah C. Traeger,Mary Ellen Cvijic,Kimberley A. Lentz,Giridhar Tirucherai,Lakshmi Sivaraman,Jeffrey A. Robl,Bruce A. Ellsworth,Glenn D. Rosen,David A. Gordon,Matthew G. Soars,Michael Gill,Brian J. Murphy
摘要
The oxycyclohexyl acid BMS-986278 (33) is a potent lysophosphatidic acid receptor 1 (LPA1) antagonist, with a human LPA1Kb of 6.9 nM. The structure-activity relationship (SAR) studies starting from the LPA1 antagonist clinical compound BMS-986020 (1), which culminated in the discovery of 33, are discussed. The detailed in vitro and in vivo preclinical pharmacology profiles of 33, as well as its pharmacokinetics/metabolism profile, are described. On the basis of its in vivo efficacy in rodent chronic lung fibrosis models and excellent overall ADME (absorption, distribution, metabolism, excretion) properties in multiple preclinical species, 33 was advanced into clinical trials, including an ongoing Phase 2 clinical trial in patients with lung fibrosis (NCT04308681).