SYNTHESIS AND BIOLOGICAL EFFICACY OF NOVEL PIPERAZINE ANALOGUES BEARING QUINOLINE AND PYRIDINE MOIETIES
© 2015 M. Al-Ghorbani*, N. D. Rekha**, V. Lakshmi Ranganatha*, V. Prashanth*, T. Veerabasappagowda**, and S. A. Khanum*, #
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*Department of Chemistry, Yuvaraja’s College, University of Mysore, Mysore, Karnataka, India; **Department of Studies in Biotechnology, JSS College of Arts, Commerce and Science, Mysore, Karnataka, India
Received 24.08.2014; in final form 12.01.2015
A series of novel piperazine analogues bearing quinolin-8-yloxy-butan-1-ones/pyridin-2-yloxy-ethanones were synthesized by a simple and convenient approach based on various substituted piperazine incorporating quinoline and pyridine moieties. The analogues were evaluated for in vitro antioxidant activity against 2,2-diphenyl-1-picryl-hydrazyl (DPPH) and ferrous ion radical scavenging activities and anti-inflammatory activity by inhibition of Vipera russelli venom (PLA2) and gastric K+/H+-ATPase activities. Most of the title compounds exhibited promising activity. Best antioxidant and PLA2-inhibiting activities were found for piperazine analogues with phenyl and nitro phenyl groups, whereas methoxy group on phenyl piperazine indicated selectivity for the H+/K+-ATPase.
Keywords: piperazine analogues, antioxidant, PLA2, H+/K+-ATPase.
ÁÈÎÎÐÃÀÍÈ×ÅÑÊÀß ÕÈÌÈß, 2015, òîì 41, ¹ 5, ñ. 619–626