首页> 外文期刊>Asian Journal of Chemistry: An International Quarterly Research Journal of Chemistry >Synthesis and Pharmacological Screening of Novel Ethyl(5-Substituted Acetamido)-3-methylthio-1-(4-chlorophenyl)-1H-pyrazole-4-carboxylate
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Synthesis and Pharmacological Screening of Novel Ethyl(5-Substituted Acetamido)-3-methylthio-1-(4-chlorophenyl)-1H-pyrazole-4-carboxylate

机译:新型(5-取代的乙酰氨基)-3-甲硫基-1-(4-氯苯基)-1H-吡唑-4-羧酸酯的合成及药理筛选

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摘要

Several novel ethyl(5-substituted acetamido)-3-methylthio-1-(4-chlorophenyl)-1H-pyrazole-4-carboxylate were synthesized and screened for their analgesic activity at a dose of 50 mg/kg and 10 mg/kg by acetic acid induced writhing method and hot plate method respectively. The compound 5j and 5k are prominent candidates, which showed good analgesic activity among the series. The compound 5j and 5k showed 54.20 % and 52.22 % analgesic activity to that of standard aspirin by acetic acid induced writhing method whereas 72.88 % and 69.7 % analgesic activity to that of standard pentazocine HCl by hot plate method respectively.
机译:合成了几种新型的(5-取代的乙酰胺基)-3-甲硫基-1-(4-氯苯基)-1H-吡唑-4-羧酸盐,并以50 mg / kg和10 mg / kg的剂量筛选了它们的镇痛活性。分别采用乙酸诱导扭体法和热板法。化合物5j和5k是突出的候选物,在系列中显示出良好的镇痛活性。化合物5j和5k通过乙酸诱导扭体法显示出比标准阿司匹林的镇痛活性分别为54.20%和52.22%,而通过热板法显示出的相对于标准喷他佐辛盐酸盐的镇痛活性分别为72.88%和69.7%。

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