2-Anilinonicotinyl linked 1,3,4-oxadiazole derivatives: Synthesis, antitumour activity and inhibition of tubulin polymerization

被引:77
作者
Kamal, Ahmed [1 ]
Srikanth, Y. V. V. [1 ]
Shaik, Thokhir B. [2 ]
Khan, M. Naseer A. [1 ]
Ashraf, Md. [1 ]
Reddy, M. Kashi [1 ]
Kumar, K. Anil [2 ]
Kalivendi, Shasi V. [2 ]
机构
[1] Indian Inst Chem Technol, Div Organ Chem, Hyderabad 500607, Andhra Pradesh, India
[2] Indian Inst Chem Technol, Ctr Chem Biol, Hyderabad 500607, Andhra Pradesh, India
关键词
DNA-BINDING ABILITY; POTENTIAL ANTICANCER; BIOLOGICAL EVALUATION; GROWTH-INHIBITION; AGENTS; SULFONAMIDE; APOPTOSIS; SERIES; IDENTIFICATION; MICROTUBULES;
D O I
10.1039/c0md00177e
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A series of 2-anilinonicotinyl linked 1,3,4-oxadiazoles was synthesized and evaluated for their antitumour activity against various cancer cell lines, inhibition of tubulin polymerization and cell cycle effects. Some of these compounds showed good antiproliferative activity with GI(50) values ranging from 4.57 to 97.09 mu M in the human cancer cell lines and one of the compounds 5m showed potent antitumour efficacy in all the cell lines tested. This compound also inhibited tubulin polymerization under both in vitro and in vivo conditions. Analysis of tubulin by Western blot experiments demonstrated that 5m depolymerizes microtubules by causing disturbances in the ratio of soluble versus polymerized tubulin in cells, leading to the cell cycle arrest at G2/M phase of the cell cycle followed by activation of caspase-3 activity and apoptotic cell death.
引用
收藏
页码:819 / 823
页数:5
相关论文
共 42 条
[1]  
BELAUDROTUREAU MA, 1997, LEUKEMIA RES, V21, P163
[2]  
BONNE D, 1985, J BIOL CHEM, V260, P2819
[3]   Novel anticancer drug discovery [J].
Buolamwini, JK .
CURRENT OPINION IN CHEMICAL BIOLOGY, 1999, 3 (04) :500-509
[4]  
Carlson RO, 2008, EXPERT OPIN INV DRUG, V17, P707, DOI [10.1517/13543784.17.5.707, 10.1517/13543784.17.5.707 ]
[5]  
Chawla R, 2010, ACTA POL PHARM, V67, P247
[6]   Superior reactivity of thiosemicarbazides in the synthesis of 2-amino-1,3,4-oxadiazoles [J].
Dolman, Sarah J. ;
Gosselin, Francis ;
O'Shea, Paul D. ;
Davies, Ian W. .
JOURNAL OF ORGANIC CHEMISTRY, 2006, 71 (25) :9548-9551
[7]   PREPARATION AND THERMAL DECOMPOSITION OF PYRAZINOIC BENZENESULFONHYDRAZIDE [J].
FAND, TI ;
SPOERRI, PE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1952, 74 (05) :1345-1345
[8]   2-[(1-methylpropyl)dithio]-1H-imidazole inhibits tubulin polymerization through cysteine oxidation [J].
Huber, Kelly ;
Patel, Poulam ;
Zhang, Lei ;
Evans, Helen ;
Westwell, Andrew D. ;
Fischer, Peter M. ;
Chan, Stephen ;
Martin, Stewart .
MOLECULAR CANCER THERAPEUTICS, 2008, 7 (01) :143-151
[9]  
Islam M, 2008, ACTA POL PHARM, V65, P441
[10]   IMPROVED PROCESS FOR THE PREPARATION OF 2-METHYL-3-TRIFLUOROMETHYLANILINE - A VERSATILE INTERMEDIATE FOR FLUNIXIN SYNTHESIS [J].
JAOUHARI, R ;
QUINN, P .
HETEROCYCLES, 1994, 38 (10) :2243-2246