Synthesis and QSAR analysis of chalcone derivatives as nitric oxide inhibitory agent

…, A Syahida, MBA Rahman, Z Ul-Haq, NH Lajis

文献索引：Lam, Kok Wai; Lajis, Nordin H.; Uddin, Reaz; Ul-Haq, Zaheer; Liew, Choi Yi; Tham, Chau Ling; Israf, Daud A.; Syahida, Ahmad; Rahman, Mohd. Basyaruddin Abdul Medicinal Chemistry Research, 2012 , vol. 21, # 8 p. 1953 - 1966,14

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被引用次数: 14

摘要

Abstract In this study, thirty-eight chalcone analogs were synthesized and evaluated for nitric oxide (NO) inhibition activity on RAW 264.7 cells. Among these compounds, chalcones bearing furanyl group showed remarkable anti-inflammatory activity. Both compounds 2d and 2j were identified as the most potent NO inhibitor on IFN-γ/LPS-activated RAW 264.7 cells. In order to examine the structure–activity relationship, a 3D QSAR analysis was ...