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吩噻嗪和苯并[a]吩噻嗪衍生物的细胞毒性及诱导分化活性

Cytotoxicity and differentiation-inducing activity of phenothiazine and benzo[a]phenothiazine derivatives.

作者信息

Motohashi N, Sakagami H, Kamata K, Yamamoto Y

机构信息

Department of Medicinal Chemistry, Meiji College of Pharmacy, Tokyo, Japan.

出版信息

Anticancer Res. 1991 Sep-Oct;11(5):1933-7.

PMID:1662929
Abstract

The effects of 13 phenothiazines, and 8 benzo[a]phenothiazines on the growth and differentiation of various human cultured cell lines were investigated. Perphenazine dimaleate and chlorpromazine hydrochloride were more cytotoxic against human normal fibroblasts and glioma cells than 19 other related compounds. The differentiation of three human myelogenous leukemic cell lines (ML-1, U-937, THP-1) into maturing monocytes/macrophages was potently induced by 12H- benzo[a]phenothiazine and 5-oxo-5H-benzo[a]phenothiazine. The differentiation--inducing activity of phenothiazine, and other benzo[a]phenothiazine derivatives was much less, and that of phenothiazine derivatives without the benzyl group was undetectable. Simultaneous treatment with 12H- benzo[a]phenothiazine and tumor necrosis factor produced additive, but not synergistic differentiation--induction of these cells.

摘要

研究了13种吩噻嗪类化合物和8种苯并[a]吩噻嗪对多种人类培养细胞系生长和分化的影响。与其他19种相关化合物相比,马来酸奋乃静和盐酸氯丙嗪对人正常成纤维细胞和胶质瘤细胞的细胞毒性更强。12H-苯并[a]吩噻嗪和5-氧代-5H-苯并[a]吩噻嗪能有效诱导三种人骨髓白血病细胞系(ML-1、U-937、THP-1)分化为成熟的单核细胞/巨噬细胞。吩噻嗪和其他苯并[a]吩噻嗪衍生物的诱导分化活性要低得多,而没有苄基的吩噻嗪衍生物则未检测到诱导分化活性。12H-苯并[a]吩噻嗪与肿瘤坏死因子同时处理可产生相加作用,但对这些细胞的分化诱导无协同作用。

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