Molecular modeling, enzyme activity, anti-inflammatory and antiarthritic activities of newly synthesized quinazoline derivatives

被引:15
作者
Abuelizz, Hatem A. [1 ]
El Hassane, Anouar [2 ]
Marzouk, Mohamed [2 ,3 ]
Ezzeldin, Essam [4 ]
Ali, Azza A. [5 ]
Al-Salahi, Rashad [1 ]
机构
[1] King Saud Univ, Coll Pharm, Dept Pharmaceut Chem, POB 2457, Riyadh 11451, Saudi Arabia
[2] Prince Sattam Bin Abdulaziz Univ, Coll Sci & Humanities, Dept Chem, 83 Al Kharj, Al Kharj, Saudi Arabia
[3] Natl Res Ctr, Ctr Excellence Adv Sci, Chem Nat Prod Grp, Cairo 12622, Egypt
[4] King Saud Univ, Coll Pharm, Drug Bioavailabil Lab, POB 2457, Riyadh 11451, Saudi Arabia
[5] Al Azhar Univ, Fac Pharm, Dept Pharmacol & Toxicol, Cairo, Egypt
关键词
2-thioxoquinazolin-4-(3H)-one; antiarthritic; anti-inflammatory; molecular modeling; IN-VITRO; ANTICONVULSANT ACTIVITY; INHIBITION; ARTHRITIS; DOCKING;
D O I
10.4155/fmc-2017-0157
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Aim: 16 thioxoquinazolines were evaluated in vivo for anti-inflammatory activity using carrageenan-induced paw edema assay. Results: In particular, out of the targets (1-16), compounds 4 and 6 displayed the highest anti-inflammatory activity (>= 80%) and furtherly tested against complete Freund's adjuvant-induced arthritic rats. Significant reduction in the serum level of IL-1 beta, COX-2 and prostaglandin E2 in the complete Freund's adjuvant rats is demonstrated by compounds 4 and 6. Furthermore, compound 4 showed non-selective activity against COX-1 and COX 2, however, compound 6 was specific toward COX-2. Molecular docking study has demonstrated the possible binding modes of the active quinazolines 4 and 6 in the COX-2 active site. Conclusion: These targets could be used as templates for further development of new derivatives with potent anti-inflammatory activity.
引用
收藏
页码:1995 / 2009
页数:15
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