Human immunodeficiency virus type 1 (HIV-1) strains selected for resistance against the HIV-1-specific [2',5'-bis-O-(tert-butyldimethylsilyl)-3'-spiro- 5''-(4''-amino-1'',2''-oxathiole-2'',2''-dioxide)]-beta-D-pentofurano syl (TSAO) nucleoside analogues retain sensitivity to HIV-1-specific nonnucleoside inhibitors.

We recently reported that a newly discovered class of nucleoside analogues--[2',5'-bis-O-(tert-butyldimethylsilyl)- 3'-spiro-5''-(4''-amino-1'',2''-oxathiole-2'',2''-dioxide)]-beta-D - pentofuranosyl derivatives of pyrimidines and purines (designated TSAO)--are highly specific inhibitors of human im...

詳細記述

書誌詳細

出版年:	Proc Natl Acad Sci U S A
主要な著者:	Balzarini, J, Karlsson, A, Vandamme, A M, Pérez-Pérez, M J, Zhang, H, Vrang, L, Oberg, B, Bäckbro, K, Unge, T, San-Félix, A
フォーマット:	Artigo
言語:	Inglês
出版事項:	National Academy of Sciences 1993
主題:	Research Article
オンライン･アクセス:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC47053/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7688467/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.90.15.6952
タグ:	タグ追加 タグなし, このレコードへの初めてのタグを付けませんか!