Synthesis, characterization and pharmacological activity of 4-{[1-substituted aminomethyl-4-arylideneamino-5-sulfanyl-4,5-dihydro-1H-1,2,4-triazol-3-yl]methyl}-2H-1,4-benzothiazin-3(4H)-ones

被引:46
|
作者
Gowda, J. [1 ]
Khader, A. M. A. [1 ]
Kalluraya, B. [1 ]
Shree, Padma [2 ]
Shabaraya, A. R. [2 ]
机构
[1] Mangalore Univ, Dept Studies Chem, Mangalagangothri 574199, India
[2] Srinivas Coll Pharm, Mangalore 574143, India
关键词
Analgesic activity; Anti-inflammatory activity; 1,4-Benzothiazin-3(4H)-one; REGIOSELECTIVE REACTION SYNTHESIS; MANNICH-BASES; ANTICONVULSANT ACTIVITY; DERIVATIVES; INHIBITORS; AGENTS; 1,2,4-TRIAZOLES; MOIETY;
D O I
10.1016/j.ejmech.2011.06.010
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A new series of Schiff and Mannich bases derivatives (6) of 4-[(4-amino-5-sulfanyl-4H-1,2,4-triazol-3-yl) methl]-2H-1,4-benzothiazin-3(4H)-one (4), derived from (3-oxo-2,3-dihydro-4H-1,4-benzothiazin-4-yl) acetic acid (3) were synthesized. The structures of all newly synthesized compounds were elucidated by elemental analysis, IR. (1)H NMR and mass spectral data. Synthesized compounds were evaluated for their anti-inflammatory and analgesic activity. Among the tested compounds, the (3-oxo-2,3-dihydro-4H-1,4-benzothiazin-4-yl)acetic acid (3) possess analgesic activity comparable to that of pentazocine; activity decreased on derivatization of the carboxylic acid group. However the anti-inflammatory activity of (3-oxo-2,3-dihydro-4H-1,4-benzothiazin-4-yl)acetic acid (3) increased by derivatization of the carboxylic acid group and some of the compounds showed anti-inflammatory activity comparable to that of indomethacin. (C) 2011 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:4100 / 4106
页数:7
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