Gacche R N, Dhole N A, Kamble S G, Bandgar B P
School of Life Sciences, Swami Ramanand Teerth Marathwada University, Nanded, MS, India.
J Enzyme Inhib Med Chem. 2008 Feb;23(1):28-31. doi: 10.1080/14756360701306370.
Synthetic chalcones (SCs) having different side chains on the 1-(2-Hydroxy-3-(2-hydroxy-cyclohexyl)-4,6 dimethoxy-phenyl(-methanone structure were examined in-vitro for their antioxidant abilities by DPPH (2,2-diphenyl-1-picryl hydrazine) radical scavenging activity, reducing ability, OH radical scavenging activity, inhibition of polyphenol oxidase (PPO) and formation of diene conjugates. Overall, with few exceptions, all the SCs showed moderate biological activity in all the parameters examined. The SCs were found to be reactive towards DPPH radical and had considerable reducing ability. With few exceptions, all the test compounds under study were found to possess moderate to poor OH radical scavenging activity and inhibited PPO significantly and all were found to be effective inhibitors of hydroperoxide formation. These findings suggest that these SCs can be considered as potential antioxidant agents which might be further explored for the design of lead antioxidant drug candidates.
对具有1-(2-羟基-3-(2-羟基环己基)-4,6-二甲氧基苯基)-甲酮结构且侧链不同的合成查耳酮(SCs)进行了体外研究,通过二苯基苦味酰基自由基(DPPH)清除活性、还原能力、羟基自由基清除活性、多酚氧化酶(PPO)抑制作用以及二烯共轭物的形成来考察其抗氧化能力。总体而言,除少数例外,所有SCs在所有检测参数中均表现出中等的生物活性。发现SCs对DPPH自由基具有反应性且具有相当的还原能力。除少数例外,所有研究的受试化合物均具有中等至较差的羟基自由基清除活性,能显著抑制PPO,并且均被发现是氢过氧化物形成的有效抑制剂。这些发现表明,这些SCs可被视为潜在的抗氧化剂,可能会在先导抗氧化药物候选物的设计中得到进一步探索。