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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis of new thiazolo-celecoxib analogues as dual cyclooxygenase-2/15-lipoxygenase inhibitors: Determination of regio-specific different pyrazole cyclization by 2D NMR
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Synthesis of new thiazolo-celecoxib analogues as dual cyclooxygenase-2/15-lipoxygenase inhibitors: Determination of regio-specific different pyrazole cyclization by 2D NMR

机译:作为双环氧合酶-2 / 15-脂氧合酶抑制剂的新型噻唑并-celecoxib类似物的合成:通过2D NMR测定区域特异性不同的吡唑环化

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摘要

Two new series of 1,5-diaryl pyrazoles (5a, 5b, 7a, 7b and 10) and 1,5-diaryl pyrazoline (12a and 12b) were prepared as both Cyclooxygenase-2 and 15-lipoxygenase inhibitors. Carrageenan-induced rat paw edema, ulcer index and anti-COX-1/COX-2 and 15-LOX inhibition assays were also included. Cyclization of different pyrazoles was discussed using 2D NMR such as HSQC, HMBC and NOSEY determinations. Compound 5a is more effective with ED50 = 0.98 and 3.98 mu M against COX-2 and 15-lipoxygenase respectively, than the references celecoxib (1.54 mu M) and meclofenamate sodium (5.64 mu M). (C) 2016 Elsevier Masson SAS. All rights reserved.
机译:制备了两个新系列的1,5-二芳基吡唑(5a,5b,7a,7b和10)和1,5-二芳基吡唑啉(12a和12b)作为环氧合酶-2和15-脂氧合酶抑制剂。还包括角叉菜胶诱导的大鼠爪水肿,溃疡指数以及抗COX-1 / COX-2和15-LOX抑制试验。使用2D NMR(例如HSQC,HMBC和NOSY测定)讨论了不同吡唑的环化反应。与参考塞来昔布(1.54μM)和甲氯芬那酸钠(5.64μM)相比,化合物5a分别具有ED50 = 0.98和3.98μM对抗COX-2和15-脂氧合酶更有效。 (C)2016 Elsevier Masson SAS。版权所有。

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