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Synthesis of amide derivatives of quinolone and their antimicrobial studies

机译:喹诺酮酰胺衍生物的合成及其抗菌研究

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摘要

A series of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-[chloro/1-piperaziny 1/4-methyl-1-piperazinyl/4-ethyl-1-pipera-zinyl/ 4-hydroxyethyl-1-piperazinyl/imidazolyl/morpholinyl]-3 [N-(substituted phenyl amino) carbonyl]quinoline 5-11a-j have been prepared by using substituted arylamine at C-3 position and 1-piperazine/4-methyl-1-piperazine/4-ethyl-1-piperazine/4-hydroxyethyl-1-piperazine/imidazole/morpholine at C-7 position of newly synthesized quinolone 3.Biological profile like antibacterial activity against four different strain viz.S.aureus and B.subtilis (gram-positive bacteria) and E.coli and P.aeruginosa (gram-negative bacteria) and C.albicans (fungi) by cup plate method have been studied.
机译:一系列1-环丙基-6-氟-1,4-二氢-4-氧代-7- [氯/ 1-哌嗪基1 / 4-甲基-1-哌嗪基/ 4-乙基-1-哌嗪基/ 4 -羟乙基-1-哌嗪基/咪唑基/吗啉基] -3 [N-(取代的苯基氨基)羰基]喹啉5-11a-j是通过在C-3位使用取代的芳基胺和1-哌嗪/ 4-甲基-制备的。新合成喹诺酮C-7位的1-哌嗪/ 4-乙基-1-哌嗪/ 4-羟乙基-1-哌嗪/咪唑/吗啉3.对四种不同金黄色葡萄球菌和B菌株的抗菌活性通过杯板法研究了枯草杆菌(革兰氏阳性菌)和大肠杆菌,绿脓杆菌(革兰氏阴性菌)和白色念珠菌(真菌)。

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