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
  • [11] SYNTHESIS AND ANTICANCER ACTIVITIES OF THIAZOLES, 1,3-THIAZINES, AND THIAZOLIDINE USING CHITOSAN-GRAFTEDPOLY(VINYLPYRIDINE) AS BASIC CATALYST
    Gomha, Sobhi M.
    Riyadh, Sayed M.
    Mahmmoud, Elmandi A.
    Elaasser, Mahmoud M.
    [J]. HETEROCYCLES, 2015, 91 (06) : 1227 - 1243
  • [12] Haddad J J, 2001, Curr Opin Investig Drugs, V2, P1070
  • [13] Novel (4-piperidin-1-yl)-phenyl sulfonamides as potent and selective human β3 agonists
    Hu, BH
    Ellingboe, J
    Han, S
    Largis, E
    Lim, K
    Malamas, M
    Mulvey, R
    Niu, CS
    Oliphant, A
    Pelletier, J
    Singanallore, T
    Sum, FW
    Tillett, J
    Wong, V
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2001, 9 (08) : 2045 - 2059
  • [14] Hu J., 2015, Rep. Org. Chem, V5, P19
  • [15] A Series of α-Heterocyclic Carboxaldehyde Thiosemicarbazones Inhibit Topoisomerase IIα Catalytic Activity
    Huang, He
    Chen, Qin
    Ku, Xin
    Meng, Linghua
    Lin, Liping
    Wang, Xiang
    Zhu, Caihua
    Wang, Yi
    Chen, Zhi
    Li, Ming
    Jiang, Hualiang
    Chen, Kaixian
    Ding, Jian
    Liu, Hong
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2010, 53 (08) : 3048 - 3064
  • [16] Improvement of antibacterial activity of some sulfa drugs through linkage to certain phthalazin-1(2H)-one scaffolds
    Ibrahim, Hany S.
    Eldehna, Wagdy M.
    Abdel-Aziz, Hatem A.
    Elaasser, Mahmoud M.
    Abdel-Aziz, Marwa M.
    [J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2014, 85 : 480 - 486
  • [17] Fluorine in medicinal chemistry: A review of anti-cancer agents
    Isanbor, C
    O'Hagan, D
    [J]. JOURNAL OF FLUORINE CHEMISTRY, 2006, 127 (03) : 303 - 319
  • [18] Synthesis and phosphodiesterase inhibitory activity of new sildenafil analogues containing a carboxylic acid group in the 5′-sulfonamide moiety of a phenyl ring
    Kim, DK
    Lee, JY
    Lee, N
    Ryu, DH
    Kim, JS
    Lee, S
    Choi, JY
    Ryu, JH
    Kim, NH
    Im, GJ
    Choi, WS
    Kim, TK
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2001, 9 (11) : 3013 - 3021
  • [19] Fluorine in medicinal chemistry: Recent therapeutic applications of fluorinated small molecules
    Kirk, Kenneth L.
    [J]. JOURNAL OF FLUORINE CHEMISTRY, 2006, 127 (08) : 1013 - 1029
  • [20] MAPKAP kinase 2 is essential for LPS-induced TNF-α biosynthesis
    Kotlyarov, A
    Neininger, A
    Schubert, C
    Eckert, R
    Birchmeier, C
    Volk, HD
    Gaestel, M
    [J]. NATURE CELL BIOLOGY, 1999, 1 (02) : 94 - 97