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In vitro drug combination of 1-beta-D-arabinofuranosyl-E-5-(2-bromovinyl)uracil with anti-human immunodeficiency virus or anticancer nucleosides.

1-beta-D-Arabinofuranosyl-E-5-(2-bromovinyl)uracil (BV-araU) and E-5-(2-bromovinyl)uracil, a metabolite of BV-araU, did not affect either the anti-human immunodeficiency virus activity or the cytotoxicity of azidothymidine in MT-4 and MOLT-4 cells. Similarly, the bromovinyl compounds did not affect...

詳細記述

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書誌詳細
出版年:Antimicrob Agents Chemother
主要な著者: Machida, H, Ashida, N, Ikeda, T, Sakata, S, Baba, M, Shigeta, S
フォーマット: Artigo
言語:Inglês
出版事項: American Society for Microbiology (ASM) 1992
主題:
オンライン・アクセス:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC189263/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1317147/
https://ncbi.nlm.nih.govhttps://doi.org/10.1128/aac.36.1.214
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