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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共 44 条
  • [31] ISOTHIOCYANATES IN THE CHEMISTRY OF HETEROCYCLES
    MUKERJEE, AK
    ASHARE, R
    [J]. CHEMICAL REVIEWS, 1991, 91 (01) : 1 - 24
  • [32] Discovery of indoles as potent and selective inhibitors of the deacetylase SIRT1
    Napper, AD
    Hixon, J
    McDonagh, T
    Keavey, K
    Pons, JF
    Barker, J
    Yau, WT
    Amouzegh, P
    Flegg, A
    Hamelin, E
    Thomas, RJ
    Kates, M
    Jones, S
    Navia, MA
    Saunders, J
    DiStefano, PS
    Curtis, R
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2005, 48 (25) : 8045 - 8054
  • [33] Parasca O., 2012, REV MED CHIR SOC MED, V117, P558
  • [34] Efficient synthesis and biological evaluation of 1,3-benzenedicarbonyl dithioureas
    Peng, Hao
    Liang, Yongju
    Chen, Le
    Fu, Liwu
    Wang, Haiqin
    He, Hongwu
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2011, 21 (04) : 1102 - 1104
  • [35] Petrov V.A., 2009, FLUORINATED HETEROCY
  • [36] Fluorine in medicinal chemistry
    Purser, Sophie
    Moore, Peter R.
    Swallow, Steve
    Gouverneur, Veronique
    [J]. CHEMICAL SOCIETY REVIEWS, 2008, 37 (02) : 320 - 330
  • [37] Vinyl sulfonate esters and vinyl sulfonamides: Potent, irreversible inhibitors of cysteine proteases
    Roush, WR
    Gwaltney, SL
    Cheng, JM
    Scheidt, KA
    McKerrow, JH
    Hansell, E
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (42) : 10994 - 10995
  • [38] The role of fluorine in medicinal chemistry
    Shah, Poonam
    Westwell, Andrew D.
    [J]. JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2007, 22 (05) : 527 - 540
  • [39] Shah SSA, 2013, MINI-REV MED CHEM, V13, P70
  • [40] Sharma S., 1989, Sulfur Rep, V8, P327