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The next ten stories on antiviral drug discovery (part E): advents, advances, and adventures.

机译:关于抗病毒药物发现的下十个故事(E部分):出现,进展和冒险。

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This review article presents the fifth part (part E) in the series of stories on antiviral drug discovery. The ten stories belonging to this fifth part are dealing with (i) aurintricarboxylic acid; (ii) alkenyldiarylmethanes; (iii) human immunodeficiency virus (HIV) integrase inhibitors; (iv) lens epithelium-derived growth factor as a potential target for HIV proviral DNA integration; (v) the status presens of neuraminidase inhibitors NAIs in the control of influenza virus infections; (vi) the status presens on respiratory syncytial virus inhibitors; (vii) tricyclic (1,N-2-ethenoguanine)-based acyclovir and ganciclovir derivatives; (viii) glycopeptide antibiotics as antivirals targeted at viral entry; (ix) the potential (off-label) use of cidofovir in the treatment of polyoma (JC and BK) virus infections; and (x) finally, thymidine phosphorylase as a target for both antiviral and anticancer agents.
机译:这篇评论文章介绍了有关抗病毒药物发现的一系列故事的第五部分(E部分)。属于第五部分的十个故事涉及(一)金三羧酸; (ii)烯基二芳基甲烷; (iii)人类免疫缺陷病毒(HIV)整合酶抑制剂; (iv)晶状体上皮来源的生长因子作为HIV前病毒DNA整合的潜在靶点; (v)神经氨酸酶抑制剂NAI在控制流感病毒感染中的状况; (vi)呼吸道合胞病毒抑制剂的状况; (vii)基于三环(1,N-2-乙鸟嘌呤)的阿昔洛韦和更昔洛韦衍生物; (viii)针对病毒进入的糖肽抗生素作为抗病毒剂; (ix)西多福韦在治疗多瘤(JC和BK)病毒感染中的潜在用途(标签外); (x)最后,胸苷磷酸化酶作为抗病毒药和抗癌药的靶标。

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