Synthesis and pharmacological investigation of 5-substituted-3-methylsulfanyl-1H-pyrazole-4-carboxylic acid ethyl esters as new analgesic and anti-inflammatory agents.

Arzneimittel-Forschung-Drug Research Pub Date : 2012-10-01 Epub Date: 2012-08-29 DOI:10.1055/s-0032-1321830
P D Gokulan, B Jayakar, V Alagarsamy, V Raja Solomon
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引用次数: 7

Abstract

Purpose: To synthesize a new series of 5-substituted-3-methylsulfanyl-1H-pyrazole-4-carboxylic acid ethyl esters for their analgesic and anti-inflammatory activity.

Methods: The title compound synthesized by reacting the amino group of 5-amino-3-methylsulfanyl-1H-pyrazole-4-carboxylic acid ethyl ester with acid anhydrides, acid chlorides and phenyl dithiocarbamates. The synthesized compounds were characterized by IR, 1H-NMR and mass spectral data; the purity of the compounds was determined by elemental analysis. The title compounds were investigated for analgesic, anti-inflammatory and ulcerogenic behaviour.

Results: The compound 5-benzoylamino-3-methylsulfanyl-1-phenyl-1H-pyrazole-4-carboxylic acid ethyl ester (4c) emerged as the most active compound and exhibiting imperative analgesic and anti-inflammatory activities. Interestingly the test compounds showed only mild ulcerogenic potential when compared to indomethacin.

Conclusion: The compound (4c) could serve as a lead molecule for further modification to obtain a clinically useful novel class of analgesic and anti-inflammatory agents.

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新型镇痛抗炎药5-取代-3-甲基磺酰- 1h -吡唑-4-羧酸乙酯的合成及药理研究。
目的:合成一系列具有镇痛和抗炎活性的5-取代-3-甲基磺酰- 1h -吡唑-4-羧酸乙酯。方法:将5-氨基-3-甲基磺酰- 1h -吡唑-4-羧酸乙酯的氨基与酸酐、酸氯化物和苯基二硫代氨基甲酸酯反应合成标题化合物。通过IR、1H-NMR和质谱对合成的化合物进行了表征;通过元素分析确定了化合物的纯度。研究了标题化合物的镇痛、抗炎和致溃疡行为。结果:化合物5-苯甲酰氨基-3-甲基磺胺-1-苯基- 1h -吡唑-4-羧酸乙酯(4c)是活性最高的化合物,具有良好的镇痛和抗炎活性。有趣的是,与吲哚美辛相比,测试化合物仅显示出轻微的溃疡形成潜力。结论:化合物(4c)可作为进一步修饰的先导分子,获得具有临床应用价值的新型镇痛抗炎药。
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