李瑞文, 张奕华, 季晖, 于晓琳, 彭司勋. 苯基呋咱氮氧化物与双氯芬酸偶联化合物的合成及其抗炎镇痛活性J. 药学学报, 2002, 37(1): 27-32.
引用本文: 李瑞文, 张奕华, 季晖, 于晓琳, 彭司勋. 苯基呋咱氮氧化物与双氯芬酸偶联化合物的合成及其抗炎镇痛活性J. 药学学报, 2002, 37(1): 27-32.
LI Rui-wen, ZHANG Yi-hua, JI Hui, YU Xiao-lin, PENG Si-xun. SYNTHESIS AND ANTI-INFLAMMATORY ANALGESIC ACTIVITIES OF PHENYLFUROXAN-COUPLED DICLOFENACJ. Acta Pharmaceutica Sinica, 2002, 37(1): 27-32.
Citation: LI Rui-wen, ZHANG Yi-hua, JI Hui, YU Xiao-lin, PENG Si-xun. SYNTHESIS AND ANTI-INFLAMMATORY ANALGESIC ACTIVITIES OF PHENYLFUROXAN-COUPLED DICLOFENACJ. Acta Pharmaceutica Sinica, 2002, 37(1): 27-32.

苯基呋咱氮氧化物与双氯芬酸偶联化合物的合成及其抗炎镇痛活性

SYNTHESIS AND ANTI-INFLAMMATORY ANALGESIC ACTIVITIES OF PHENYLFUROXAN-COUPLED DICLOFENAC

  • 摘要: 目的寻找能增强双氯芬酸(DC)抗炎镇痛活性,又能降低其胃肠道副作用的一氧化氮供体型DC(NO-DC)。方法以酯键将NO供体3-羟甲基-4-苯基-呋咱氮氧化物及其异构体与DC偶联,考察偶联物的抗炎镇痛活性及胃肠道毒副反应,研究偶联物体内外的NO释放作用。结果合成了15个新化合物,其中目标物(II1~9) 9个,其结构经IR,1HNMR,MS和元素分析确证。II3和II9的抗炎活性与DC相当,II2的抗炎镇痛活性强于DC,胃肠道副作用小于DC,并小于文献报道的硝酸酯类NO-DC,体内有明显的NO释放。结论II2值得深入研究。

     

    Abstract: AIMTo search for new derivatives of diclofenac (DC) having higher potency than the parent drug and lacking its undesirable effects. METHODSCoupling DC with NO donor 3-hydroxymethyl-4-phenylfuroxan and its isomer through esterification, evaluating anti-inflammatory and analgesic activities, observing side effects in the rat gastrointestinal (GI) tract and assessing NO releasing ability both in vitro and in vivo. RESULTSFifteen new compounds including nine target ones (II1~9) were synthesized, and their structures were determined by IR, 1HNMR, MS and elemental analysis. Compounds II3 and II9 showed anti-inflammatory activity comparable to DC. Compound II2 showed stronger anti-inflammatory and analgesic activities and less GI side effect than DC, and released NO in vivo. CONCLUSIONCompound II2 is worthy to be intensively studied.

     

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