Antimicrobial and anticancer activity of some novel fluorinated thiourea derivatives carrying sulfonamide moieties: synthesis, biological evaluation and molecular docking

被引:57
|
作者
Ghorab, Mostafa M. [1 ,2 ]
Alsaid, Mansour S. [1 ]
El-Gaby, Mohamed S. A. [3 ]
Elaasser, Mahmoud M. [4 ]
Nissan, Yassin M. [5 ]
机构
[1] King Saud Univ, Pharmacognosy Dept, Coll Pharm, POB 2457, Riyadh 11451, Saudi Arabia
[2] Natl Ctr Radiat Res & Technol, Dept Drug Radiat Res, Cairo 113701, Egypt
[3] Al Azhar Univ, Dept Chem, Fac Sci, Assiut 71524, Egypt
[4] Al Azhar Univ, Reg Ctr Mycol & Biotechnol, Cairo, Egypt
[5] Cairo Univ, Dept Pharmaceut Chem, Fac Pharm, Cairo, Egypt
来源
CHEMISTRY CENTRAL JOURNAL | 2017年 / 11卷
关键词
Isothiocyanate; Sulfonamide; Fluorinated thiourea; Antimicrobial and anticancer activity; MEDICINAL CHEMISTRY; KINASE; 2; AGENTS; INHIBITORS; POTENT; ANTIBACTERIAL; CHEMOTHERAPY; DESIGN; SERIES;
D O I
10.1186/s13065-017-0258-4
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Background: Various thiourea derivatives have been used as starting materials for compounds with better biological activities. Molecular modeling tools are used to explore their mechanism of action. Results: A new series of thioureas were synthesized. Fluorinated pyridine derivative 4a showed the highest antimicrobial activity (with MIC values ranged from 1.95 to 15.63 mu g/mL). Interestingly, thiadiazole derivative 4c and coumarin derivative 4d exhibited selective antibacterial activities against Gram positive bacteria. Fluorinated pyridine derivative 4a was the most active against HepG2 with IC50 value of 4.8 mu g/mL. Molecular docking was performed on the active site of MK-2 with good results. Conclusion: Novel compounds were obtained with good anticancer and antibacterial activity especially fluorinated pyridine derivative 4a and molecular docking study suggest good activity as mitogen activated protein kinase-2 inhibitor.
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页数:14
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