Design, synthesis and biological evaluation of a novel series of 1,3,4-oxadiazole bearing N-methyl-4-(trifluoromethyl)phenyl pyrazole moiety as cytotoxic agents

被引:104
作者
Puthiyapurayil, Pushpan [1 ,2 ]
Poojary, Boja [1 ]
Chikkanna, Chandrashekhar [3 ]
Buridipad, Sunil Kumar [4 ]
机构
[1] Mangalore Univ, Dept Chem, Mangalagangothri 574199, Karnataka, India
[2] Syngene Int Ltd, Bangalore 560099, Karnataka, India
[3] SDM Coll, Dept Med Chem, Dk 574342, Karnataka, India
[4] NET Pharm Coll, Dept Pharm Coll, Raichur 584103, Karnataka, India
关键词
N-Methyl-4(trifluoromethyl)phenyl; Pyrazole; Cytotoxic activity; MTT assay; Doxorubicin; Nuclear overhauser effect; ANTITUMOR-ACTIVITY; IN-VITRO; DERIVATIVES; INHIBITORS; IDENTIFICATION; ANALOGS; ETHERS;
D O I
10.1016/j.ejmech.2012.03.056
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
On account of the reported anticancer activity of pyrazoles and oxadiazoles, we have designed and synthesized a novel combinatorial library of S-substituted-1,3,4-oxadiazole bearing N-methyl-4-(trifluoromethyl)phenyl pyrazole moiety and tested for in-vitro cytotoxic activity by MTT assay. Amongst the tested compounds, the compound 5e was the most promising anticancer agent with IC50 value of 15.54 mu M in MCF-7 cells, compared to Doxorubicin as standard drug. The newly synthesized compounds were characterized by NOE, IR, H-1 NMR, C-13 NMR and LC-MS analysis. (C) 2012 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:203 / 210
页数:8
相关论文
共 30 条
[11]   Elucidation of fatty acid amide hydrolase inhibition by potent α-ketoheterocycle derivatives from Monte Carlo simulations [J].
Guimaraes, CRW ;
Boger, DL ;
Jorgensen, WL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (49) :17377-17384
[12]   Synthesis of some novel pyrazolo[3,4-d]pyrimidine derivatives as potential antimicrobial agents [J].
Holla, BS ;
Mahalinga, M ;
Karthikeyan, MS ;
Akberali, PM ;
Shetty, NS .
BIOORGANIC & MEDICINAL CHEMISTRY, 2006, 14 (06) :2040-2047
[13]   New potent antihyperglycemic agents in db/db mice: Synthesis and structure-activity relationship studies of (4-substituted benzyl)(trifluoromethyl)pyrazoles and -pyrazolones [J].
Kees, KL ;
Fitzgerald, JJ ;
Steiner, KE ;
Mattes, JF ;
Mihan, B ;
Tosi, T ;
Mondoro, D ;
McCaleb, ML .
JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (20) :3920-3928
[14]   Structure-activity relationships of tyrosinase inhibitory combinatorial library of 2,5-disubstituted-1,3,4-oxadiazole analogues [J].
Khan, MTH ;
Choudhary, MI ;
Khan, KM ;
Rani, M ;
Atta-ur-Rahman .
BIOORGANIC & MEDICINAL CHEMISTRY, 2005, 13 (10) :3385-3395
[15]   Antitumour 2-(4-aminophenyl)benzothiazoles generate DNA adducts in sensitive tumour cells in vitro and in vivo [J].
Leong, CO ;
Gaskell, M ;
Martin, EA ;
Heydon, RT ;
Farmer, PB ;
Bibby, MC ;
Cooper, PA ;
Double, JA ;
Bradshaw, TD ;
Stevens, MFG .
BRITISH JOURNAL OF CANCER, 2003, 88 (03) :470-477
[16]   Reversal effects of nomegestrol acetate on multidrug resistance in adriamycin-resistant MCF7 breast cancer cell line [J].
Li, J ;
Xu, LZ ;
He, KL ;
Guo, WJ ;
Zheng, YH ;
Xia, P ;
Chen, Y .
BREAST CANCER RESEARCH, 2001, 3 (04) :253-263
[17]   Stereoselective synthesis and fungicidal activities of (E)-α(methoxyimino)-benzeneacetate derivatives containing 1,3,4-oxadiazole ring [J].
Li, Y ;
Liu, H ;
Zhang, HQ ;
Yang, XP ;
Liu, ZJ .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2006, 16 (08) :2278-2282
[18]  
Manfredini S, 1996, ANTI-CANCER DRUG DES, V11, P193
[19]   omega-Dialkylaminoalkyl ethers of phenyl-(5-substituted 1-phenyl-1H-pyrazol-4-yl)methanols with analgesic and anti-inflammatory activity [J].
Menozzi, G ;
Mosti, L ;
Fossa, P ;
Mattioli, F ;
Ghia, M .
JOURNAL OF HETEROCYCLIC CHEMISTRY, 1997, 34 (03) :963-968
[20]   Mechanism of DNA damage and apoptosis induced by anticancer drugs through generation of reactive oxygen species [J].
Mizutani, Hideki .
YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN, 2007, 127 (11) :1837-1842