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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis of amidine and amide derivatives and their evaluation for anti-inflammatory and analgesic activities.
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Synthesis of amidine and amide derivatives and their evaluation for anti-inflammatory and analgesic activities.

机译:idine和酰胺衍生物的合成及其抗炎和止痛活性的评估。

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摘要

A number of amidine derivatives (2a-i) have been synthesized by condensation of 2-cyanopyridine with various 3,4-diaryl-2-imino-4-thiazolines. Various amide derivatives (3a-h) were synthesized by condensation of orotic acid and hydantoin-5-acetic acid with a number of 3,4-diaryl-2-imino-4-thiazolines using microwave irradiation. All the compounds i.e. (2a-i) and (3a-h) synthesized were characterized by spectroscopic means and elemental analysis. Compounds (2a-i) and (3a-h) at 50 mg/kg p.o. were screened for anti-inflammatory activity whereas 2a-d, f, g, i and 3a, b, d, f at 50 mg/kg p.o. were evaluated for analgesic activity. Compounds 2e and 3g exhibited good anti-inflammatory activity (49% and 34%, respectively) and 2f, g showed interesting (50% in each case) analgesic activity.
机译:通过2-氰基吡啶与各种3,4-二芳基-2-亚氨基-4-噻唑啉的缩合合成了许多synthesized衍生物(2a-i)。通过使用微波辐射使乳清酸和乙内酰脲-5-乙酸与许多3,4-二芳基-2-亚氨基-4-噻唑啉缩合,合成了各种酰胺衍生物(3a-h)。通过光谱方法和元素分析表征所有合成的化合物,即(2a-i)和(3a-h)。剂量为50 mg / kg的化合物(2a-i)和(3a-h)。筛选抗炎活性,而2a-d,f,g,i和3a,b,d,f以50 mg / kg p.o.评估镇痛活性。化合物2e和3g显示出良好的抗炎活性(分别为49%和34%),而2f,g显示出令人感兴趣的镇痛活性(在每种情况下为50%)。

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