Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10596175 | Bioorganic & Medicinal Chemistry Letters | 2013 | 5 Pages |
Abstract
A series of HIV-1 attachment inhibitors containing a 4,6-diazaindole core were examined in an effort to identify a compound which improved upon the potency and oral exposure of BMS-488043 (2). BMS-488043 (2) is a 6-azaindole-based HIV-1 attachment inhibitor which established proof-of-concept for this mechanism in human clinical studies but required high doses and concomitant administration of a high fat meal to achieve efficacious exposures. Based on previous studies in indole and azaindole scaffolds, SAR investigation was concentrated around the key 7-position in the 4,6-diazaindole series and led to the discovery of molecules with 5- to 20-fold increases in potency and three- to seven-fold increases in exposure over 2 in a rat PK studies.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
John A. Bender, Zhong Yang, Betsy Eggers, Yi-Fei Gong, Pin-Fang Lin, Dawn D. Parker, Sandhya Rahematpura, Ming Zheng, Nicholas A. Meanwell, John F. Kadow,