Synthesis and biological evaluation of thieno [2′,3′:4,5]pyrimido[1,2-b][1,2,4]triazines and thieno[2,3-d][1,2,4]triazolo[1,5-a]pyrimidines as anti-inflammatory and analgesic agents

被引:136
作者
Ashour, Hayam M. [1 ]
Shaaban, Omaima G. [1 ]
Rizk, Ola H. [1 ]
El-Ashmawy, Ibrahim M. [2 ]
机构
[1] Univ Alexandria, Fac Pharm, Dept Pharmaceut Chem, Alexandria 21521, Egypt
[2] Univ Alexandria, Fac Vet Med, Dept Pharmacol, Alexandria 21521, Egypt
关键词
Thienopyrimidotriazines; Thienotriazolopyrimidines; Anti-inflammatory activity; Ulcerogenic effect; Analgesic activity; ANTIMICROBIAL AGENTS; ACUTE GASTROLESIVITY; THIENOPYRIMIDINE DERIVATIVES; PYRAZOLE DERIVATIVES; CYCLOOXYGENASE; INHIBITORS; ANALOGS; DESIGN; DRUGS; ALKYL;
D O I
10.1016/j.ejmech.2012.12.003
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
A new series of thieno[2',3':4,5]pyrimido[1,2-b][1,2,4]triazines and thieno[2,3-d][1,2,4]triazolo[1,5-a] pyrimidines was synthesized. The newly synthesized compounds were evaluated for their anti-inflammatory and analgesic activity using diclofenac Na as a reference standard. Additionally, the ulcerogenic effects and acute toxicity (ALD(50)) values of the active compounds were also determined. In general, the thieno[2,3-d][1,2,4]triazolo[1,5-a]pyrimidine derivatives exhibited better biological activities than the thieno[2',3':4,5]pyrimido[1,2-b][1,2,4]triazines. Collectively, the thienotriazolopyrimidine derivatives 9, 13 and 14a were proved to display distinctive anti-inflammatory activity at the acute and subacute models as well as good analgesic profile with a delayed onset of action. Moreover, they revealed good gastrointestinal safety profile and are well tolerated by experimental animals with high safety margin (ALD(50) > 0.3 g/kg). (C) 2012 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:341 / 351
页数:11
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