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用于药物研发的水溶性富勒烯衍生物。

Water-soluble fullerene derivatives for drug discovery.

作者信息

Nakamura Shigeo, Mashino Tadahiko

机构信息

Department of Chemistry, Nippon Medical School, Kawasaki, Kanagawa, Japan.

出版信息

J Nippon Med Sch. 2012;79(4):248-54. doi: 10.1272/jnms.79.248.

Abstract

Fullerenes (represented by buckminsterfullerene, C(60)) are a new kind of organic compound with a cage-like structure. A great deal of attention has been focused on their unique properties. From the viewpoint of drug discovery, fullerenes could be novel lead compounds for drug discovery. However, fullerenes are poorly soluble in aqueous media. Incorporation of water-soluble groups into the fullerene core enables investigation of its biological activities. Certain fullerene derivatives show inhibitory activity against human immunodeficiency virus reverse transcriptase. Hepatitis C virus RNA polymerase is also inhibited by fullerene derivatives. Therefore, fullerene derivatives are candidate antiviral agents. In addition, fullerene derivatives exhibit antiproliferative activity by inducing apoptosis related to the generation of reactive oxygen species. Fullerene derivatives also have the potential to be anticancer drugs.

摘要

富勒烯(以巴克敏斯特富勒烯C(60)为代表)是一种具有笼状结构的新型有机化合物。人们对其独特性质给予了极大关注。从药物发现的角度来看,富勒烯可能是药物发现的新型先导化合物。然而,富勒烯在水性介质中的溶解度很差。将水溶性基团引入富勒烯核心能够研究其生物活性。某些富勒烯衍生物对人类免疫缺陷病毒逆转录酶具有抑制活性。富勒烯衍生物也能抑制丙型肝炎病毒RNA聚合酶。因此,富勒烯衍生物是候选抗病毒药物。此外,富勒烯衍生物通过诱导与活性氧生成相关的凋亡表现出抗增殖活性。富勒烯衍生物也有成为抗癌药物的潜力。

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