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抗痘病毒药物的发展历史。

Historical perspectives in the development of antiviral agents against poxviruses.

机构信息

Rega Institute for Medical Research, Department of Microbiology and Immunology, Minderbroedersstraat 10, B-3000 Leuven, Belgium.

出版信息

Viruses. 2010 Jun;2(6):1322-1339. doi: 10.3390/v2061322. Epub 2010 Jun 14.

Abstract

The poxvirus vaccinia virus (VV) served as the model virus for which the first antivirals, the thiosemicarbazones, were identified. This dates back to 1950; and, although there is at present no single antiviral drug specifically licensed for the chemotherapy or -prophylaxis of poxvirus infections, numerous candidate compounds have been described over the past 50 years. These compounds include interferon and inducers thereof (i.e., polyacrylic acid), 5-substituted 2'-deoxyuridines (i.e., idoxuridine), IMP dehydrogenase inhibitors, S-adenosylhomocysteine hydrolase inhibitors, acyclic nucleoside phosphonates (such as cidofovir) and alkoxyalkyl prodrugs thereof (such as CMX001), viral egress inhibitors (such as tecovirimat), and cellular kinase inhibitors (such as imatinib).

摘要

痘病毒牛痘病毒(VV)曾作为模型病毒,最初的抗病毒药物——噻唑烷酮类化合物就是在该病毒上被发现的。这可以追溯到 1950 年;尽管目前尚无专门用于化学治疗或预防痘病毒感染的单一抗病毒药物,但在过去的 50 年中已经描述了许多候选化合物。这些化合物包括干扰素及其诱导剂(即聚丙烯酸)、5 位取代的 2'-脱氧尿苷(即碘苷)、IMP 脱氢酶抑制剂、S-腺苷同型半胱氨酸水解酶抑制剂、无环核苷膦酸(如更昔洛韦)及其烷氧基烷基前药(如 CMX001)、病毒出芽抑制剂(如特考韦瑞)和细胞激酶抑制剂(如伊马替尼)。

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