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首页> 外文期刊>Molecules >Synthesis and In Vitro Antiproliferative Activity of Novel Phenyl Ring-Substituted 5-Alkyl-12(H)-quino[3,4-b][1,4]benzothiazineDerivatives
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Synthesis and In Vitro Antiproliferative Activity of Novel Phenyl Ring-Substituted 5-Alkyl-12(H)-quino[3,4-b][1,4]benzothiazineDerivatives

机译:新型苯基环取代的5-烷基-12(H)-喹[3,4-b] [1,4]苯并噻嗪衍生物的合成及体外抗增殖活性

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摘要

A novel series of tetracyclic quinobenzothiazine derivatives was synthetized. Compounds containing a substituent (hydroxyl, methyl, phenyl, piperidyl, or piperazinyl) in positions 9 and 11 were obtained by cyclization of suitable 4-aminoquinolinium-3-thiolates. Quinobenzothiazine 10-O-substituted derivatives were obtained by alkylating the hydroxyl group in position 10 of the parent (quinobenzothiazine) system. Antiproliferative activity of the synthesized compounds was studied using cultured neoplastic cells (MDA-MB-231, SNB-19, and C-32 cell lines). Four selected compounds were investigated in more detail for cytotoxicity and antiproliferative effect. Transcriptional activity of genes regulating cell cycle (TP53), apoptosis (BAX, BCL-2), as well as proliferation (H3) were assessed. Finally, the ability of the selected compounds to bind DNA was checked in the presence of ethidium bromide.
机译:合成了一系列新的四环喹啉苯并噻嗪衍生物。通过使合适的4-氨基喹啉-3-硫醇盐环化获得在9和11位上含有取代基(羟基,甲基,苯基,哌啶基或哌嗪基)的化合物。通过将母体(喹啉苯并噻嗪)系统的10位上的羟基烷基化来获得喹啉苯并噻嗪10-O-取代的衍生物。使用培养的肿瘤细胞(MDA-MB-231,SNB-19和C-32细胞系)研究了合成化合物的抗增殖活性。对四种选定的化合物进行了细胞毒性和抗增殖作用的详细研究。评估调节细胞周期(TP53),细胞凋亡(BAX,BCL-2)和增殖(H3)的基因的转录活性。最后,在溴化乙锭存在下检查所选化合物结合DNA的能力。

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