Witvrouw M, Balzarini J, Pannecouque C, Jhaumeer-Laulloo S, Esté J A, Schols D, Cherepanov P, Schmit J C, Debyser Z, Vandamme A M, Desmyter J, Ramadas S R, de Clercq E
Rega Institute for Medical Research, Katholieke Universiteit Leuven, Belgium.
Antimicrob Agents Chemother. 1997 Feb;41(2):262-8. doi: 10.1128/AAC.41.2.262.
From a series of macrocyclic diamides possessing the disulfide linkage, only SRR-SB3, a compound that complexes with zinc, was found to inhibit human immunodeficiency virus type 1 (HIV-1; strain IIIB) replication at a concentration of 1.8 to 6.5 micrograms/ml in MT-4, CEM, and peripheral blood mononuclear cells. SRR-SB3 was toxic to MT-4 cells at a concentration of 15.9 micrograms/ml, resulting in a selectivity index of 9 in these cells. This macrolide was also effective against various other HIV-1 strains, including clinical isolates and HIV-1 strains resistant to protease inhibitors and nucleoside and nonnucleoside reverse transcriptase inhibitors. It was also active against various HIV-2 strains, simian immunodeficiency virus (strain MAC251), and Moloney murine sarcoma virus, but not against viruses other than retroviruses. In addition, the compound was found to inhibit chronic HIV-1 infections in vitro. The compound in combination with other antiviral agents, such as zidovudine, zalcitabine, and stavudine, showed an effect that was between additive and synergistic. Time-of-addition experiments indicated that SRR-SB3 acts at a late stage of the HIV-1 replicative cycle.
在一系列具有二硫键的大环二酰胺中,只有与锌结合的化合物SRR-SB3在MT-4、CEM和外周血单核细胞中浓度为1.8至6.5微克/毫升时能抑制1型人类免疫缺陷病毒(HIV-1;IIIB株)复制。SRR-SB3在浓度为15.9微克/毫升时对MT-4细胞有毒,在这些细胞中的选择性指数为9。这种大环内酯对包括临床分离株以及对蛋白酶抑制剂、核苷和非核苷逆转录酶抑制剂耐药的HIV-1株在内的各种其他HIV-1毒株也有效。它对各种HIV-2毒株、猴免疫缺陷病毒(MAC251株)和莫洛尼鼠肉瘤病毒也有活性,但对逆转录病毒以外的病毒无活性。此外,该化合物在体外能抑制慢性HIV-1感染。该化合物与齐多夫定、扎西他滨和司他夫定等其他抗病毒药物联合使用时,显示出介于相加和协同之间的效果。添加时间实验表明,SRR-SB3作用于HIV-1复制周期的后期。