Novel Non-nucleoside Inhibitors of Human Immunodeficiency Virus Type 1 Reverse Transcriptase. 5. 4-Substituted and 2,4-Disubstituted Analogs of Nevirapine

• Published in: Journal of medicinal chemistry 1995-11, Vol.38 (24), p.4839-4847
• Main Authors: Kelly, Terence A, Proudfoot, John R, McNeil, Daniel W, Patel, Usha R, David, Eva, Hargrave, Karl D, Grob, Peter M, Cardozo, Mario, Agarwal, Atul, Adams, Julian
• Format: Article
• Language: English
• Subjects: AIDS/HIV; HIV-1; human immunodeficiency virus 1; Humans; Models, Molecular; Molecular Conformation; Nevirapine; Pyridines - chemical synthesis; Pyridines - chemistry; Reverse Transcriptase Inhibitors - chemical synthesis; Reverse Transcriptase Inhibitors - chemistry; Structure-Activity Relationship
• ISSN: 0022-2623; 1520-4804
• DOI: 10.1021/jm00024a011

Molecular modeling analysis of the recently published X-ray crystal structure of nevirapine bound to wild type human immunodeficiency virus type 1 reverse transcriptase (WT-RT) indicated the presence of a lipophilic cavity proximal to the 4-position of the inhibitor. A series of 4-substituted derivatives of nevirapine were thus synthesized to assess structure-activity relationships (SARs) and to see if increased binding to this region might translate into greater activity against mutant RTs. The results show that compounds with an appropriately spaced aryl ring appended to the 4-position of the dipyridodiazepinone ring system show good activity against WT-RT. Furthermore certain derivatives appear to inhibit the Y181C mutant RT. Attempts to combine these results with the recent discovery that 2-substituents enhance activity against the Y181C mutant led to a few compounds with moderate activity against both enzymes. The SAR of these two positions, however, could not be combined in a simple fashion.