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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis and antibacterial activity of some new thiadiaza/triazaphospholes, thiadiaza/triaza/tetrazaphosphinines and thiadiaza/tetrazaphosphepines containing 1,2,4-triazinone moiety.
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Synthesis and antibacterial activity of some new thiadiaza/triazaphospholes, thiadiaza/triaza/tetrazaphosphinines and thiadiaza/tetrazaphosphepines containing 1,2,4-triazinone moiety.

机译:一些含有1,2,4-三嗪酮部分的新的噻二氮杂/三氮杂氮磷,噻二氮杂/三氮杂/四氮杂膦和噻二氮杂/四氮杂五氮平的合成和抗菌活性。

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摘要

Some new thiadiaza/triazaphospholes, thiadiaza/triaza/tetrazaphosphinines and thiadiaza/tetrazaphosphepines fused with 6-methyl-1,2,4-triazin-5-one moiety were synthesized via reactions of alpha,beta-bifunctional compounds derived from 4-amino-3-mercapto-6-methyl-1,2,4-triazin-5(4H)-one (1) with various phosphorus reagents. The in vitro antibacterial activities of the synthesized compounds were evaluated against some bacterial strains. Compounds 16 and 21 exhibited good inhibitory activities against most the tested organisms with MIC values in the range 6.25-12.5 microg/mL and lower cytotoxicity in comparison with the reference drugs.
机译:通过与4-氨基-β-双官能团的α,β-双官能化合物反应合成了一些新的噻二氮杂/三氮杂磷,噻二氮杂/三氮杂/四氮杂膦和噻二氮杂/四氮杂五环素与6-甲基-1,2,4-三氮杂-5-一个部分融合。 3-巯基-6-甲基-1,2,4-三嗪-5(4H)-一(1)与各种磷试剂。评价了合成化合物对某些细菌菌株的体外抗菌活性。与参考药物相比,化合物16和21对大多数受测生物表现出良好的抑制活性,MIC值在6.25-12.5 microg / mL的范围内,并且具有较低的细胞毒性。

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