Synthesis of Some 4,5-Dihydrothieno[3,2-e][1,2,4]Triazolo[4,3-a] Pyrimi-dine-2-Carboxamides as Anti-Inflammatory and Analgesic Agents.

Q2 Pharmacology, Toxicology and Pharmaceutics Open Medicinal Chemistry Journal Pub Date : 2013-11-29 eCollection Date: 2013-01-01 DOI:10.2174/1874104501307010039
Omaima G Shaaban, Ola H Rizk, Aida E Bayad, Ibrahim M El-Ashmawy
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Abstract

A new series 4,5-dihydrothieno[3,2-e][1,2,4]triazolo[4,3-a]pyrimidine-2-carboxamide was synthesized. Twenty one newly synthesized compounds were investigated for their anti-inflammatory and analgesic activity using acute and subacute formalin-induced paw edema models and diclofenac Na as a reference. The acute toxicity (ALD50) and ulcerogenic effects of the active compounds were also determined. The thienotriazolopyrimidines 10a, 10c and 11c were found to exhibit remarkable anti-inflammatory activity at both models in addition to good analgesic activity with a delayed onset of action. Moreover, the active compounds showed high GI safety level and are well tolerated by experimental animals with high safety margin (ALD50 > 0.4 g/kg). Docking study using Molecular Operating Environment (MOE) version 2008.10 into COX-2 has been made for derivatives of highest anti-inflammatory activity.

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作为抗炎镇痛剂的一些 4,5-二氢噻吩并[3,2-e][1,2,4]三唑并[4,3-a]嘧啶-2-甲酰胺的合成。
合成了一系列新的 4,5-二氢噻吩并[3,2-e][1,2,4]三唑并[4,3-a]嘧啶-2-甲酰胺。以急性和亚急性福尔马林诱导的爪水肿模型和双氯芬酸钠为参照物,研究了 21 种新合成化合物的抗炎和镇痛活性。此外,还测定了活性化合物的急性毒性(ALD50)和致溃疡作用。结果发现,噻吩三唑嘧啶 10a、10c 和 11c 在这两种模型中均表现出显著的抗炎活性,此外还具有良好的镇痛活性和延迟起效的特点。此外,这些活性化合物显示出较高的消化道安全水平,实验动物耐受性良好,安全系数高(ALD50 > 0.4 g/kg)。利用分子操作环境(MOE)2008.10 版对 COX-2 进行了 Docking 研究,以找出抗炎活性最高的衍生物。
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来源期刊
Open Medicinal Chemistry Journal
Open Medicinal Chemistry Journal Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.40
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0.00%
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4
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