| Literature DB >> 28430437 |
Kap-Sun Yeung1, Brett R Beno1, Kyle Parcella1, John A Bender1, Katherine A Grant-Young1, Andrew Nickel1, Prashantha Gunaga2, Prakash Anjanappa2, Rajesh Onkardas Bora2, Kumaravel Selvakumar2, Karen Rigat1, Ying-Kai Wang1, Mengping Liu1, Julie Lemm1, Kathy Mosure1, Steven Sheriff3, Changhong Wan3, Mark Witmer3, Kevin Kish3, Umesh Hanumegowda1, Xiaoliang Zhuo1, Yue-Zhong Shu3, Dawn Parker1, Roy Haskell1, Alicia Ng3, Qi Gao4, Elizabeth Colston3, Joseph Raybon3, Dennis M Grasela3, Kenneth Santone1, Min Gao1, Nicholas A Meanwell1, Michael Sinz1, Matthew G Soars1, Jay O Knipe1, Susan B Roberts1, John F Kadow1.
Abstract
The hepatitis C virus (HCV) NS5B replicase is a prime target for the development of direct-acting antiviral drugs for the treatment of chronic HCV infection. Inspired by the overlay of bound structures of three structurally distinct NS5B palm site allosteric inhibitors, the high-throughput screening hit anthranilic acid 4, the known benzofuran analogue 5, and the benzothiadiazine derivative 6, an optimization process utilizing the simple benzofuran template 7 as a starting point for a fragment growing approach was pursued. A delicate balance of molecular properties achieved via disciplined lipophilicity changes was essential to achieve both high affinity binding and a stringent targeted absorption, distribution, metabolism, and excretion profile. These efforts led to the discovery of BMS-929075 (37), which maintained ligand efficiency relative to early leads, demonstrated efficacy in a triple combination regimen in HCV replicon cells, and exhibited consistently high oral bioavailability and pharmacokinetic parameters across preclinical animal species. The human PK properties from the Phase I clinical studies of 37 were better than anticipated and suggest promising potential for QD administration.Entities:
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Year: 2017 PMID: 28430437 DOI: 10.1021/acs.jmedchem.7b00328
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446