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Synthesis, structural characterization and anti-carcinogenic activity of new cyclotriphosphazenes containing dioxybiphenyl and chalcone groups

机译:含二氧联苯和查耳酮基团的新型环三磷腈的合成,结构表征和抗癌活性

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摘要

2,2-Dichloro-4,4,6,6-bis[spiro(2',2 ''-dioxy-1',1 ''-biphenylyl]cyclotriphosphazene (2) was synthesized from hexachlorocyclotriphosphazene (HCCP) and 2,2'-dihydroxybiphenyl. The mixed substituent chalcone/dioxybiphenyl cyclophosphazenes (2a-h) were obtained from the reactions of (2) with hydroxy chalcone compounds in K2CO3/acetone system. The chalcone-cyclophosphazene compounds were characterized by elemental analysis, FT-IR, H-1, C-13, P-31 NMR techniques. In vitro anti-carcinogenic activities of all compounds were determined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MU) assay. Anti-carcinogenic activity of the compounds (2a-h) against androgen-dependent (LNCaP) and independent (PC-3) human prostate cancer cell lines were investigated. Our results indicate that the chalcone-phosphazene compounds (2a-h) have anti-carcinogenic activity on PC-3 and LNCaP cell lines (p < 0.05). The effective dose of the compounds was determined as 100 mu M. (C) 2015 Elsevier B.V. All rights reserved.
机译:2,6-Dichloro-4,4,6,6-bis [spiro(2',2''-dioxy-1',1''-biphenylyl] cyclotriphosphazene(2)由六氯环三磷腈(HCCP)和2,由(2)与羟基查尔酮化合物在K2CO3 /丙酮体系中的反应制得混合取代基查尔酮/二氧基联苯环磷腈(2a-h),并通过元素分析,FT-IR表征了查尔酮-环磷腈化合物。 ,H-1,C-13,P-31 NMR技术通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴化物(MU)测定所有化合物的体外抗癌活性研究了化合物(2a-h)对雄激素依赖性(LNCaP)和独立(PC-3)人前列腺癌细胞系的抗癌活性,我们的结果表明查尔酮-磷腈化合物(2a-h)对PC-3和LNCaP细胞系具有抗癌活性(p <0.05)。该化合物的有效剂量确定为100μM.(C)2015 Elsevier BV Al l保留权利。

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