Facile microwave synthesis of a novel phenothiazine derivative and its cytotoxic activity

IF 1.6 Q3 CHEMISTRY, ORGANIC Organic Communications Pub Date : 2020-12-26 DOI:10.25135/acg.oc.86.20.10.1853
Cenk A Andac
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引用次数: 1

Abstract

Herein, a facile procedure for microwave synthesis and NMR characterization of phenothiazine derivatives 10-(3-hydroxypropyl)-2-(methylsulphanyl)-10H-phenothiazine (3) (25% yield) and 1-[3-(2-methylsulfanyl-10H-phenothiazine-10-yl)-propyl]pyrimidine-2,4-(1H,3H)-dione (6) (67% yield) is described. After successful microwave synthesis steps, MTT cytotoxicity experiments gave rise to greater anticancer effect of compound 6 in MCF-7 human breast adenocarcinoma cell line (IC50= 1.35 µM) as compared to literature values for tamoxifen (IC50= 8.3 µM) and doxorubicin (IC50= 27 µM).
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一种新型吩噻嗪衍生物的微波合成及其细胞毒活性研究
本文介绍了吩噻嗪衍生物10-(3-羟丙基)-2-(甲基磺酰基)-10H-吩噻津(3)(25%产率)和1-[3-(2-甲基硫烷基-10H-吩噻嗪-10-基)-丙基]嘧啶-2,4-(1H,3H)-二酮(6)(67%产率)的微波合成和NMR表征的简便方法。在成功的微波合成步骤之后,MTT细胞毒性实验在MCF-7人乳腺腺癌细胞系中产生了化合物6的更大的抗癌作用(IC50=1.35µM),与三苯氧胺(IC50=8.3µM)和阿霉素(IC50=27µM)的文献值相比。
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来源期刊
Organic Communications
Organic Communications CHEMISTRY, ORGANIC-
CiteScore
2.80
自引率
11.80%
发文量
21
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