首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Phosphorus-nitrogen compounds. Part 29. Syntheses, crystal structures, spectroscopic and stereogenic properties, electrochemical investigations, antituberculosis, antimicrobial and cytotoxic activities and DNA interactions of ansa-spiro-ansa cyclotetraphosphazenes
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Phosphorus-nitrogen compounds. Part 29. Syntheses, crystal structures, spectroscopic and stereogenic properties, electrochemical investigations, antituberculosis, antimicrobial and cytotoxic activities and DNA interactions of ansa-spiro-ansa cyclotetraphosphazenes

机译:磷氮化合物。第29部分。ansa-螺-ansa环四磷腈的合成,晶体结构,光谱和立体学性质,电化学研究,抗结核,抗微生物和细胞毒性活性以及DNA相互作用

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摘要

A number of novel ansa-spiro-ansa (asa) cyclotetraphosphazenes (1a-5b) was prepared in the range of 63-90% yields. The structures of the compounds were verified by MS, FTIR, H-1, C-13{H-1} and P-31{H-1} NMR, heteronuclear single quantum coherence (HSQC), and heteronuclear multiple-bond correlation (HMBC) techniques. The crystal structures of 1b, 2c and 5a were determined by X-ray crystallography. The compound 2c was analyzed by the changes in the P-31{H-1}NMR spectrum in addition of the chiral solvating agent; (R)-(+)-2,2,2-trifluoro-1-(9'-anthryl)-ethanol (CSA), to investigate its stereogenic properties. The result supports that compound 2c was found to be in the racemic mixture. Cyclic voltammetric and chronoamperometric data of the mono-ferrocenyl-spiro-asa-cyclotetraphosphazenes exhibited electrochemically reversible one-electron oxidation of Fe redox centres. The mono-ferrocenyl-spiro-asa compounds (3a-5b) were evaluated for antituberculosis activity against reference strain Mycobacterium tuberculosis H37Rv and M. tuberculosis clinical strain, which is resistant to rifampicin and isoniazid. These compounds appear not to be good candidates for being antituberculosis agents to clinical strains. All of the compounds were screened for antibacterial activities against G(+) and G(-) bacteria, and for antifungal activities against yeast strains. They seem to be more active against Gram positive bacteria than Gram negative. The interactions of the phosphazenes with plasmid DNA and the evaluations for cytotoxic activity against MCF-7 breast cancer cell lines were investigated. The compounds 1b, 2b, 3a and 4a were found to be more effective than Cisplatin against MCF-7 breast cancer cell lines at lower concentrations. (c) 2014 Elsevier Masson SAS. All rights reserved.
机译:制备了许多新颖的ansa-spiro-ansa(asa)环四磷腈(1a-5b),产率为63-90%。化合物的结构已通过MS,FTIR,H-1,C-13 {H-1}和P-31 {H-1} NMR,异核单量子相干(HSQC)和异核多键相关性( HMBC)技术。通过X射线晶体学测定1b,2c和5a的晶体结构。通过添加手性溶剂化剂,通过P-31 {H-1} NMR光谱的变化来分析化合物2c。 (R)-(+)-2,2,2-三氟-1-(9'-蒽基)-乙醇(CSA),以研究其立体感。结果支持发现化合物2c存在于外消旋混合物中。单二茂铁基-螺环-asa-环四磷腈的循环伏安和计时安培数据显示了Fe氧化还原中心的电化学可逆单电子氧化。评估了单二茂铁基-spiro-asa化合物(3a-5b)对参考菌株结核分枝杆菌H37Rv和结核分枝杆菌临床菌株的抗结核活性,该菌株对利福平和异烟肼具有抗性。这些化合物似乎不是临床菌株抗结核药的良好候选者。筛选所有化合物对G(+)和G(-)细菌的抗菌活性,以及​​对酵母菌株的抗真菌活性。他们似乎对革兰氏阳性细菌比对革兰氏阴性细菌更有活性。研究了磷腈与质粒DNA的相互作用以及对MCF-7乳腺癌细胞系的细胞毒活性评估。发现化合物1b,2b,3a和4a在较低浓度下比顺铂对MCF-7乳腺癌细胞株更有效。 (c)2014年Elsevier Masson SAS。版权所有。

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