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[含芳基哌嗪的新型苯并噻唑衍生物的设计、合成及活性]

[Design, synthesis and activities of novel benzothiazole derivatives containing arylpiperazine].

作者信息

Liu Wen-Hu, Chang Jin-Xia, Liu Yi, Luo Jie-Wei, Zhang Jian-Wu

机构信息

Department of Pharmacology, North Sichuan Medical College, Nanchong 637007, China.

出版信息

Yao Xue Xue Bao. 2013 Aug;48(8):1259-65.

Abstract

Twenty-four novel benzothiazole derivatives containing arylpiperazine were designed and synthesized by bioisosterism principle. Anti-proliferative effect of these synthesized compounds against four cancer cell and two normal cell lines were evaluated in vitro by the standard MTT assay. Pharmacological test showed that most of the compounds exhibited potent antitumor activity. Some of the compounds (II2, II3, II6, II7) showed strong anti-proliferation activities against HepG2 and HeLa229 cell lines with the IC 50 values of 1.6-4.5 micromol x L(-1) and 2.5-5.3 micromol x L(-1), respectively, and compounds having cyan in p-substituted benzene ring (I4, I8, I12, II4, II8 and II12) were found to have better antitumor activities against AsPC-1 cell lines with the IC50 values of 5.2-11.3 micromol x L(-1). The structure-activity relationship of benzothiazole derivatives containing arylpiperazine was also discussed preliminarily.

摘要

通过生物电子等排原理设计并合成了24种含芳基哌嗪的新型苯并噻唑衍生物。采用标准MTT法在体外评估了这些合成化合物对四种癌细胞系和两种正常细胞系的抗增殖作用。药理试验表明,大多数化合物表现出较强的抗肿瘤活性。其中一些化合物(II2、II3、II6、II7)对HepG2和HeLa229细胞系表现出较强的抗增殖活性,IC50值分别为1.6 - 4.5 μmol·L(-1)和2.5 - 5.3 μmol·L(-1),并且发现对苯环上有氰基的化合物(I4、I8、I12、II4、II8和II12)对AsPC-1细胞系具有更好的抗肿瘤活性,IC50值为5.2 - 11.3 μmol·L(-1)。还初步讨论了含芳基哌嗪的苯并噻唑衍生物的构效关系。

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