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一种N-羟基吡啶-2-硫酮衍生物的体外细胞毒性活性。

In vitro cytotoxic activity of an N-hydroxypyridine-2-thione derivative.

作者信息

Lepri E, Castagnino E, Binaglia L, Giampietri A, Corsano S, Fioretti M C

机构信息

Institute of Medical Pharmacology, University of Perugia, Italy.

出版信息

Arzneimittelforschung. 1993 Mar;43(3):381-3.

PMID:8489571
Abstract

The in vitro antitumor activity of N-(1-adamantoyloxy)pyridine-2-thione (APT), an N-hydroxypyridine-2-thione derivative, was investigated against a panel of both murine and human tumor cell lines growing in vitro. To evaluate the cytotoxic activity of APT the MTT ((4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) in vitro assay was used, which is considered to have predictive value for drug chemosensitivity evaluation. The results demonstrate that APT has antitumor activity, thus confirming theoretical suppositions about its cytoreductive potential.

摘要

N-(1-金刚烷氧基)吡啶-2-硫酮(APT)是一种N-羟基吡啶-2-硫酮衍生物,研究了其对一系列体外生长的小鼠和人类肿瘤细胞系的体外抗肿瘤活性。为了评估APT的细胞毒性活性,使用了MTT((4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐)体外测定法,该方法被认为对药物化学敏感性评估具有预测价值。结果表明,APT具有抗肿瘤活性,从而证实了关于其细胞还原潜力的理论假设。

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