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一些新型含 5-咪唑并吡唑的多氢喹啉衍生物的合成、表征及药理学筛选。

Synthesis, characterization and pharmacological screening of some novel 5-imidazopyrazole incorporated polyhydroquinoline derivatives.

机构信息

Department of Chemistry, Sardar Patel University, Vallabh Vidyanagar 388 120, Gujarat, India.

Department of Chemistry, Sardar Patel University, Vallabh Vidyanagar 388 120, Gujarat, India.

出版信息

Eur J Med Chem. 2014 May 6;78:207-16. doi: 10.1016/j.ejmech.2014.02.015. Epub 2014 Mar 19.

Abstract

A new category of polyhydroquinoline derivatives 8a-t were synthesized in moderate to good yield (64-85%) by one-pot three-component cyclocondensation reaction of 5-(1H-imidazol-1-yl)-3-methyl-1-phenyl-1H-pyrazole-4-carbaldehyde 3 with various enaminones 6a-h and different active methylene compounds (malononitrile 7a, ethylcaynoacetate 7b and caynoacetamide 7c) in absolute ethanol. The newly synthesized compounds were evaluated for their in vitro antimalarial activity against Plasmodium falciparum, in vitro antibacterial activity against a panel of pathogenic strains of bacteria and fungi and also for their antitubercular activity against Mycobacterium tuberculosis H37Rv strain. Two of them (8n, 8t) exhibited excellent antimalarial activity. Some of them exhibited excellent antibacterial activity and moderate antituberculosis activity compared with the first line drugs.

摘要

一类新的多氢喹啉衍生物 8a-t 通过 5-(1H-咪唑-1-基)-3-甲基-1-苯基-1H-吡唑-4-甲醛 3 与各种烯胺酮 6a-h 和不同的活性亚甲基化合物(丙二腈 7a、氰基乙酸乙酯 7b 和氰基乙酰胺 7c)在绝对乙醇中的一锅三步环缩合反应以中等至良好的收率(64-85%)合成。新合成的化合物进行了体外抗疟原虫活性评价,对一组致病细菌和真菌菌株进行了体外抗菌活性评价,对结核分枝杆菌 H37Rv 菌株进行了体外抗结核活性评价。其中两种(8n、8t)表现出优异的抗疟原虫活性。与一线药物相比,它们中的一些表现出优异的抗菌活性和适度的抗结核活性。

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