Novel 4-arylaminoquinoline-3-carbonitriles as Inhibitors of HIV-1 Reverse Transcriptase
摘要:
This paper describes the synthesis of several new 4‐arylaminoquinoline‐3‐carbonitriles derivatives. These were evaluated on the activity reverse transcriptase (RT) of HIV‐1. Most of the synthesized compounds showed significant in vitro inhibition of RT enzyme, especially derivative 3h (IC50 = <8 μM). The derivatives showed low‐level cytotoxicity.