Design and synthesis of novel proline based factor XIa selective inhibitors as leads for potential new anticoagulants. Issue 16 (15th August 2020)

• Record Type: Journal Article
• Authors: Hussain, Zahid; Cooke, Andrew J.; Neelamkavil, Santhosh; Brown, Lindsay; Carswell, Emma; Geissler, Wayne M.; Guo, Zhuyan; Hawes, Brian; Kelly, Terri M.; Kiyoi, Yasuko; Lai, KehDih; Lesburg, Charles; Pow, Eleanor; Zang, Yi; Wood, Harold B.; Edmondson, Scott D.; Liu, Weiguo
• Is Part Of: Bioorganic & medicinal chemistry letters. Volume 30:Issue 16(2020)
• Publication Date: 2020-08-15
• Subjects: Factor XIa (FXIa) inhibitor -- Thrombin (FIIa) -- Proline analogs -- Anticoagulants -- Thrombosis; Bioorganic chemistry -- Periodicals; Pharmaceutical chemistry -- Periodicals; 572
• DOI: 10.1016/j.bmcl.2020.127072
• Languages: English
• ISSNs: 0960-894X

Abstract

Graphical abstract: Abstract: A series of 4, 4-disubstituted proline analogs were designed, synthesized, and tested for selective inhibition of blood coagulation factor XIa in search of new non-vitamin K antagonists based oral anticoagulants for potential prevention and treatment of thrombotic diseases. Starting from a potent thrombin (FIIa) inhibitor chemotype with FIIa IC50 = 1 nM and FXIa IC50 = 160 nM, medicinal chemistry iterations guided by molecular modeling and structure-based drug design led to steady improvement of FXIa potency while dialing down thrombin activity and improving selectivity. Through this exercise, a thousand-fold enhancement of selectivity over thrombin was achieved with some analogs carrying factor XIa inhibition potencies in the 10 nM range. In this communication, we discuss the design principles and structure activity relationship (SAR) of these novel FXIa selective inhibitors.