首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Design, synthesis and biological evaluation of novel pyrazole sulfonamide derivatives as dual COX-2/5-LOX inhibitors
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Design, synthesis and biological evaluation of novel pyrazole sulfonamide derivatives as dual COX-2/5-LOX inhibitors

机译:新型吡唑磺胺胺衍生物作为双COX-2/5-LOX抑制剂的设计,合成及生物学评价

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摘要

The current therapeutic demand focuses more on the discovery of safer NSAIDs rather than exploring more potent alternatives. The dual COX-2/5 -LOX inhibition is a promising strategy for designing compounds with an enhanced efficacy, reduced side-effects and a broader anti-inflammatory spectrum in comparison to classical NSAIDs. In the present study, a hybridization strategy was adopted to combine the binding features of the non-selective COX inhibitor "sulindac" and the selective COX-2 inhibitor "celecoxib" which show 5 -LOX inhibitory activity with that of licofelone and a celecoxib pyridone analogue which show dual COX-2/5 -LOX inhibitory activity to design new series of pyrazole sulfonamide derivatives which, by design, should possess dual COX-2/5 -LOX inhibitory activity. All the newly synthesized compounds were initially tested for their potential analgesic activity, then candidates that showed potential analgesic activity, were selected for the subsequent anti-inflammatory activity evaluation, as well as, ulcerogenicity testing. Moreover, in vitro assessment of their COX-1, COX-2 and 5 -LOX inhibitory activities were performed. The benzothiophen-2-yl pyrazole carboxylic acid derivative 5b showed the most potent analgesic and anti-inflammatory activities surpassing that of celecoxib and indomethacin. It showed potent COX-1, COX-2 and 5-LOX inhibitory activity with IC50 of 5.40, 0.01 and 1.78 M, respectively, showing a selectivity index of 344.56 that was much better than the used reference standards and its parent compounds, confirming its selectivity towards COX-2 over COX-1. The prodrug ester derivatives 6c and 6d showed equipotent activity to their parent compound 5b with no gastric ulcerogenicity. Molecular docking simulations confirmed that the newly synthesized compounds possess the structural features required for binding to the target enzymes COX-2 and 5 -LOX. (C) 2020 Elsevier Masson SAS. All rights reserved.
机译:目前的治疗需求更多地侧重于发现更安全的NSAIDS,而不是探索更多有效的替代品。双COX-2/5 -LOX抑制是用于设计具有增强效力,减少副作用和更广泛的抗炎谱的化合物的有希望的策略与古典NSAID相比。在本研究中,采用杂交策略结合非选择性Cox抑制剂“舒林酸”和选择性Cox-2抑制剂“Celecoxib”的结合特征,其显示出5- XX抑制活性的含有LicoFelone和Celecoxib吡啶酮的抑制活性显示双COX-2/5 -LOX抑制活性的模拟,以设计新的吡唑磺胺胺衍生物,通过设计,应具有双COX-2/5 -LOX抑制活性。最初测试所有新合成的化合物,用于其潜在的镇痛活性,然后选择显示出势镇痛活性的候选物,用于随后的抗炎活性评估,以及溃疡性测试。此外,对其COX-1,COX-2和5-β抑制活性进行体外评估。苯并噻吩-2-基吡唑羧酸衍生物5b显示出最有效的镇痛和抗炎活动超过Celecoxib和Indomethacin。它表现出有效的COX-1,COX-2和5-LOX抑制活性,分别为5.40,0.01和1.78 m,显示344.56的选择性指数,比使用的参考标准和其母体化合物好得多,确认其在COX-1上对COX-2的选择性。前药酯衍生物6c和6d显示到它们的母体化合物5b的等渗活性,没有胃溃疡性。分子对接模拟证实,新合成的化合物具有与靶酶COX-2和5-1-结合所需的结构特征。 (c)2020 Elsevier Masson SAS。版权所有。

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