In vitro anti-human immunodeficiency virus activities of Z- and E- methylenecyclopropane nucleoside analogues and their phosphoro-L-alaninate diesters

Hiroyuki Uchida, Eiichi N. Kodama, Kazuhisa Yoshimura, Yosuke Maeda, Pope Kosalaraksa, Victor Maroun, Yao Ling Qiu, Jiri Zemlicka, Hiroaki Mitsuya

研究成果: Article査読

30 被引用数 (Scopus)

抄録

Nucleoside analogues with a Z- or an E-methylenecyclopropane moiety were synthesized and examined for activity against human immunodeficiency virus type 1 (HIV-1) in vitro. The addition of a methyl phenyl phosphoro-L- alaninate moiety to modestly active analogues resulted in potentiation of their anti-HIV-1 activity. Two such compounds, designated QYL-685 (with 2,6- diaminopurine) and QYL-609 (with adenine), were most potent against HIV-1 in vitro, with 50% inhibitory concentrations of 0.034 and 0.0026 μM, respectively, in MT-2 cell-based assays. Both compounds were active against zidovudine-resistant, didanosine-resistant, and multi-dideoxynucleoside- resistant infectious clones in vitro. Further development of these analogues as potential therapies for HIV-1 infection is warranted.

本文言語English
ページ(範囲)1487-1490
ページ数4
ジャーナルAntimicrobial agents and chemotherapy
43
6
DOI
出版ステータスPublished - 1999 6

ASJC Scopus subject areas

  • Pharmacology
  • Pharmacology (medical)
  • Infectious Diseases

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