Synthesis of 3,6-disubstituted 7H-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazines as novel analgesic/anti-inflammatory compounds

被引:53
作者
Aytac, S. Peri [1 ]
Tozkoparan, Birsen [1 ]
Kaynak, F. Betuel [2 ]
Aktay, Goeknur [3 ]
Goektas, Oezguer [3 ]
Uenuevar, Songuel [3 ]
机构
[1] Hacettepe Univ, Fac Pharm, Dept Pharmaceut Chem, TR-06100 Ankara, Turkey
[2] Hacettepe Univ, Fac Engn, Dept Engn Phys, TR-06800 Ankara, Turkey
[3] Inonu Univ, Fac Pharm, Dept Pharmacol, TR-44280 Malatya, Turkey
关键词
Aminomercaptotriazoles; Triazolothiadiazines; Analgesic/anti-inflammatory activity; Antioxidant activity; DERIVATIVES; IBUPROFEN;
D O I
10.1016/j.ejmech.2009.06.026
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In this study, a new class of 4-amino-3-substituted-1,2,4-triazole-5-thiones (1-4) and their corresponding condensed derivatives 3,6-disubstituted 7H-1,2,4-triazolo[3,4-bi-1,3,4-thiadiazines (1a-4c) were synthesized and evaluated for their analgesic/anti-inflammatory activities. All synthesized compounds were also tested for their gastric toxicity and antioxidant activity on acute administration. Most of the compounds showed significant activity in both carrageenan-induced oedema and acetic acid-induced writhing tests besides negligible gastrointestinal toxicity. The compounds showing less ulcerogenic effect also showed less lipid peroxidation (LPO) level. Most promising results were obtained with the compounds that placed a fluoro or a chloride on the phenyl ring at the sixth position of the fused ring. (C) 2009 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:4528 / 4538
页数:11
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