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尿苷5'-二磷酸葡萄糖类似物在细胞培养中对某些包膜病毒的抗病毒活性。

Antiviral activity of uridine 5'-diphosphate glucose analogues against some enveloped viruses in cell culture.

作者信息

Gil-Fernández G, Pérez S, Vilas P, Pérez C, de las Heras F G, García Gancedo A

机构信息

Centro de Investigaciones Biológicas, Madrid, Spain.

出版信息

Antiviral Res. 1987 Dec;8(5-6):299-310. doi: 10.1016/s0166-3542(87)80007-4.

Abstract

Twenty five analogues of uridine 5'-diphosphate glucose were screened against herpes simplex type 2, vaccinia virus, Sindbis virus and African swine fever virus. After screening, the compound 5'-[[[[(2",3",4",6"-tetra-O-benzoyl-alpha-D- glucopyranosyl)oxi]carbonyl]amino]sulfonyl]uridine (2), the synthesis of which has been reported (Camarasa et al., J. Med. Chem. 28, 40-46, 1985), was selected for further study. This compound showed in vitro activity against all viruses tested. The replication of herpes virus type 2 and African swine fever virus was completely inhibited at 100 micrograms/ml and 150 micrograms/ml respectively; vaccinia virus and Sindbis virus were inhibited to a lesser extent. The compound may inhibit several steps in the viral replication process.

摘要

针对2型单纯疱疹病毒、痘苗病毒、辛德毕斯病毒和非洲猪瘟病毒,对25种尿苷5'-二磷酸葡萄糖类似物进行了筛选。筛选后,选择了化合物5'-[[[[(2",3",4",6"-四-O-苯甲酰基-α-D-吡喃葡萄糖基)氧基]羰基]氨基]磺酰基]尿苷(2)进行进一步研究,其合成方法已有报道(卡马拉萨等人,《药物化学杂志》28卷,40 - 46页,1985年)。该化合物对所有测试病毒均表现出体外活性。2型疱疹病毒和非洲猪瘟病毒的复制分别在100微克/毫升和150微克/毫升时被完全抑制;痘苗病毒和辛德毕斯病毒受到的抑制程度较小。该化合物可能会抑制病毒复制过程中的多个步骤。

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