化学
肠道病毒71
人类免疫缺陷病毒(HIV)
病毒进入
衣壳
病毒
病毒学
吲哚试验
脚手架
脊髓灰质炎病毒
进入抑制剂
结构-活动关系
肠道病毒
病毒复制
立体化学
体外
生物化学
生物
生物医学工程
医学
作者
Belén Martínez-Gualda,Liang Sun,Olaia Martí‐Marí,Sam Noppen,Rana Abdelnabi,Carol M. Bator,Ernesto Quesada,Leen Delang,Carmen Mirabelli,Hyunwook Lee,Dominique Schols,Johan Neyts,Susan Hafenstein,María‐José Camarasa,Federico Gago,Ana San‐Félix
标识
DOI:10.1021/acs.jmedchem.9b01737
摘要
Currently, there are only three FDA-approved drugs that inhibit human immunodeficiency virus (HIV) entry-fusion into host cells. The situation is even worse for enterovirus EV71 infection for which no antiviral therapies are available. We describe here the discovery of potent entry dual inhibitors of HIV and EV71. These compounds contain in their structure three or four tryptophan (Trp) residues linked to a central scaffold. Critical for anti-HIV/EV71 activity is the presence of extra phenyl rings, bearing one or two carboxylates, at the C2 position of the indole ring of each Trp residue. The most potent derivatives, 22 and 30, inhibit early steps of the replicative cycles of HIV-1 and EV-A71 by interacting with their respective viral surfaces (glycoprotein gp120 of HIV and the fivefold axis of the EV-A71 capsid). The high potency, low toxicity, facile chemical synthesis, and great opportunities for chemical optimization make them useful prototypes for future medicinal chemistry studies.
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