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Synthesis and Biological Evaluation of New Heteroaryl Carboxylic Acid Derivatives as Anti-inflammatory-Analgesic Agents

机译:新型杂芳基羧酸衍生物作为抗炎镇痛药的合成及生物评价

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A series of nicotinic acid derivatives structurally related to niflumic acid and certain pyridazine-containing compounds have been synthesized and characterized by analytical and spectral data. All compounds were screened for their potential analgesic and anti-inflammatory activities. The compounds which displayed analgesic and anti-inflammatory activities were tested for ulcerogenicity and screened for in vivo inhibition of certain inflammatory cytokines such as tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6), and cyclooxygenase-2 (COX-2). Compounds 1c , 2a , 2b , and 5a have shown potent analgesic and anti-inflammatory activities.
机译:已经合成了一系列与烟酸和某些含哒嗪化合物有关的烟酸衍生物,并通过分析和光谱数据对其进行了表征。筛选所有化合物的潜在止痛和抗炎活性。测试了具有镇痛和抗炎活性的化合物的致溃疡性,并筛选了对某些炎性细胞因子的体内抑制作用,例如肿瘤坏死因子-α(TNF-α),白介素-6(IL-6)和环氧合酶-2。 (COX-2)。化合物1c,2a,2b和5a已显示出有效的止痛和抗炎活性。

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