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氨基糖衍生物对HIV复制的抑制作用。

Inhibition of HIV replication by amino-sugar derivatives.

作者信息

Fleet G W, Karpas A, Dwek R A, Fellows L E, Tyms A S, Petursson S, Namgoong S K, Ramsden N G, Smith P W, Son J C

机构信息

Dyson Perrins Laboratory, Department of Organic Chemistry, University of Oxford, England.

出版信息

FEBS Lett. 1988 Sep 12;237(1-2):128-32. doi: 10.1016/0014-5793(88)80185-6.

Abstract

The plant alkaloids castanospermine, dihydroxymethyldihydroxypyrrolidine and deoxynojirimycin have recently been shown to have potential anti-HIV activity [(1987) Proc. Natl. Acad. Sci. USA 84, 8120-8124; (1987) Nature 330, 74-77; (1987) Lancet i, 1025-1026]. They are thought to act by inhibiting alpha-glucosidase I, an enzyme involved in the processing of N-linked oligosaccharides on glycoproteins. We report here the relative efficacy of a spectrum of amino-sugar derivatives as inhibition of HIV cytopathicity. Several alpha-glucosidase inhibitors and alpha-fucosidase inhibitors were found to be active at concentrations which were non-cytotoxic.

摘要

植物生物碱栗精胺、二羟基甲基二羟基吡咯烷和脱氧野尻霉素最近已被证明具有潜在的抗HIV活性[(1987年)美国国家科学院院刊84,8120 - 8124;(1987年)自然330,74 - 77;(1987年)柳叶刀i,1025 - 1026]。它们被认为是通过抑制α-葡萄糖苷酶I起作用的,α-葡萄糖苷酶I是一种参与糖蛋白上N-连接寡糖加工的酶。我们在此报告一系列氨基糖衍生物作为HIV细胞病变抑制物的相对功效。发现几种α-葡萄糖苷酶抑制剂和α-岩藻糖苷酶抑制剂在无细胞毒性的浓度下具有活性。

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