Design and optimisation of potent gp120-CD4 inhibitors
摘要:
The synthesis and structure-activity relationship of a series of novel gp120-CD4 inhibitors are described. Pharmacokinetic studies and antiviral spectrum assessment of lead compounds led to the identification of compound 36, a potent gp120-CD4 inhibitor which exhibited antiviral potency across a spectrum of 25 clade B isolates. (C) 2009 Elsevier Ltd. All rights reserved.