Synthesis and biological evaluation studies of novel quinazolinone derivatives as antibacterial and anti-inflammatory agents

被引:81
|
作者
Zayed, Mohamed F. [1 ,2 ]
Hassan, Memy H. [3 ,4 ]
机构
[1] Taibah Univ, Coll Pharm, Dept Pharmaceut Chem, Al Madinah Al Munawarah 41477, Saudi Arabia
[2] Al Azhar Univ, Fac Pharm, Dept Pharmaceut Chem, Cairo, Egypt
[3] Al Azhar Univ, Fac Pharm, Dept Pharmacol & Toxicol, Cairo, Egypt
[4] Taibah Univ, Dept Pharm, Coll Med Rehabil Sci, Al Madinah Al Munawarah 41477, Saudi Arabia
关键词
Quinazolinone; Antibacterial; Anti-inflammatory; Sulfonamides; Diiodo; Synthesis; INFLAMMATION;
D O I
10.1016/j.jsps.2013.03.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Some novel 6,8-diiodo-2-methyl-3-substituted-quinazolin-4(3II)-ones bearing sulfonamide derivatives (4-11) were synthesized in good yields and evaluated for their possible antibacterial, anti-inflammatory activities and acute toxicity. The structures of the synthesized compounds were confirmed on the basis of their spectral data and elemental analysis. Their antibacterial activities were evaluated by the agar well diffusion method while their anti-inflammatory activities were evaluated by the carrageenan-induced hind paw edema test. All the tested compounds showed considerable antibacterial activities and high to moderate anti-inflammatory activities that last for 12 h compared to ibuprofen. All the tested compounds showed no toxic symptoms or mortality rates 24 h post-administration at tested anti-inflammatory doses. In addition, LD50 for all tested compounds was higher than that for ibuprofen implying their good safety margin. The obtained results showed that the most active compounds could be useful as a template for future design, modification and investigation to produce more active analogs. (c) 2013 Production and hosting by Elsevier B.V. on behalf of King Saud University.
引用
收藏
页码:157 / 162
页数:6
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