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一些新型吡唑啉的合成及生物活性

Synthesis and biological activity of some novel pyrazolines.

作者信息

Venkataraman Setaraman, Jain Saras, Shah Kamal, Upmanyu Neeraj

机构信息

K. M. College of Pharmacy, Madurai, TN India.

出版信息

Acta Pol Pharm. 2010 Jul-Aug;67(4):361-6.

Abstract

Chalcones were prepared from substituted acetophenones and substituted benzaldehydes and condensed with hydrazine hydrate in ethanol to get the corresponding pyrazolines (Pdc1 to Pdc 14). The compounds were synthesized and characterizes by TLC, melting points, IR, and 1H-NMR spectra. All the synthesized compounds were screened for their antibacterial and anti-inflammatory activities. The in vitro antibacterial activity was checked against two Gram positive microorganisms ( S. aureus and B. subtilis) and two Gram negative microorganisms (E. coli and P. aureginosa). Some of tested compounds exhibited promising antibacterial and anti-inflammatory activities.

摘要

查耳酮由取代苯乙酮和取代苯甲醛制备,并在乙醇中与水合肼缩合得到相应的吡唑啉(Pdc1至Pdc 14)。通过薄层色谱法、熔点、红外光谱和1H-核磁共振光谱对这些化合物进行了合成和表征。对所有合成的化合物进行了抗菌和抗炎活性筛选。针对两种革兰氏阳性微生物(金黄色葡萄球菌和枯草芽孢杆菌)和两种革兰氏阴性微生物(大肠杆菌和铜绿假单胞菌)检测了体外抗菌活性。一些受试化合物表现出良好的抗菌和抗炎活性。

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