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首页> 外文期刊>Medicinal chemistry >Aryl/heteroaryl Substituted Celecoxib Derivatives as COX-2 Inhibitors: Synthesis, Anti-inflammatory Activity and Molecular Docking Studies
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Aryl/heteroaryl Substituted Celecoxib Derivatives as COX-2 Inhibitors: Synthesis, Anti-inflammatory Activity and Molecular Docking Studies

机译:芳基/杂芳基取代的Celecoxib衍生物作为COX-2抑制剂:合成,抗炎活性和分子对接研究

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摘要

Background: Cyclooxygenase (COX-2) inhibitors have been developed to provide better anti-inflammatory and analgesic efficacy than those of traditional NSAIDs. Several compounds having selective COX-2 inhibitors such as SC-558, Celecoxib, Rofecoxib, Valdecoxib and Etoricoxib are marketed as new generation NSAIDs and block the production of prostaglandins (PGs) in inflammatory cells. New anti-inflammatory agents with improved potency and safety profile are still needed.
机译:背景:已经开发了环加氧基酶(COX-2)抑制剂,以提供比传统NSAIDs的抗炎和镇痛效果更好。 具有选择性COX-2抑制剂如SC-558,Celecoxib,Rofecoxib,Valdecoxib和etoricoxib的几种化合物被销售为新一代NSAID,并阻止在炎性细胞中产生前列腺素(PGS)。 仍然需要具有改善的效力和安全性的新的抗炎剂。

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