Fehrentz J A, Chomier B, Bignon E, Venaud S, Chermann J C, Nisato D
Sanofi Recherche, Montpellier, France.
Biochem Biophys Res Commun. 1992 Oct 30;188(2):865-72. doi: 10.1016/0006-291x(92)91136-e.
Several series of chemically different inhibitors of the HIV-1 aspartyl protease have been described. Nevertheless despite the high in vitro potency showed, in most cases these inhibitors are unable to inhibit viral replication in infected cells. Penetration of the inhibitors across the cell membrane might account for their low antiviral activity. The relationship between inhibitory potency, antiviral activity and chemical structures of a series of oligopeptides containing statine or statine derivatives are presented here.
已经描述了几种化学结构不同的HIV-1天冬氨酸蛋白酶抑制剂系列。然而,尽管在体外显示出高效力,但在大多数情况下,这些抑制剂无法抑制感染细胞中的病毒复制。抑制剂穿过细胞膜的能力可能是其抗病毒活性较低的原因。本文介绍了一系列含有他汀或他汀衍生物的寡肽的抑制效力、抗病毒活性与化学结构之间的关系。