New nitric oxide donating 1,2,4-triazole/oxime hybrids: Synthesis, investigation of anti-inflammatory, ulceroginic liability and antiproliferative activities

被引:41
作者
Abdel-Aziz, Mohamed [1 ]
Abuo-Rahma, Gamal El-Din A. A. [1 ]
Beshr, Eman A. M. [1 ]
Ali, Taha F. S. [1 ]
机构
[1] Minia Univ, Dept Med Chem, Fac Pharm, Al Minya 61519, Egypt
关键词
1,2,4-Triazole; Nitric oxide donors; Anti-inflammatory; Gastric ulceration; Antiproliferative; BIOLOGICAL EVALUATION; MUCOSAL DAMAGE; DERIVATIVES; CYTOTOXICITY; ULCER; PATHOGENESIS; SUPEROXIDE; DESIGN; INJURY; RAT;
D O I
10.1016/j.bmc.2013.04.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A series of novel nitric oxide (NO) donating triazole/oxime hybrids was prepared and evaluated for their anti-inflammatory activity. Most of the tested compounds showed significant anti-inflammatory activity using carrageenan-induced rat paw edema method compared to indomethacin. Calculation of the ulcer indices and histopathological investigation indicated that the prepared NO-donating oximes exhibited less ulcerogenicity compared to their intermediate ketones and indomethacin. The NO-donating oxime 6i revealed significant activity against renal cancer A498 cell lines with 50.52 cell growth inhibition. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3839 / 3849
页数:11
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