Synthesis, antimicrobial and anticancer activities of a novel series of diphenyl 1-(pyridin-3-yl)ethylphosphonates

被引:50
作者
Abdel-Megeed, Mohamed F. [1 ]
Badr, Badr E. [2 ]
Azaam, Mohamed M. [1 ]
El-Hiti, Gamal A. [1 ,3 ]
机构
[1] Tanta Univ, Fac Sci, Dept Chem, Tanta 31527, Egypt
[2] Tanta Univ, Dept Bot, Fac Sci, Tanta 31527, Egypt
[3] Cardiff Univ, Sch Chem, Cardiff CF10 3AT, S Glam, Wales
关键词
alpha-Aminophosphonate; Antimicrobial; Anticancer; Lethal dose; Diphenyl 1-(pyridin-3-yl)ethylphosphonates; SIDE-CHAIN SUBSTITUTION; ONE-POT SYNTHESIS; BIOLOGICAL-ACTIVITY; CONVENIENT PROCEDURE; LITHIATION; AMINOPHOSPHONATES; N'-ARYL-N; N-DIMETHYLUREAS; PHOSPHONATE; DERIVATIVES; BIOACTIVITY;
D O I
10.1016/j.bmc.2012.02.015
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 novel series of diphenyl 1-(arylamino)-1-(pyridin-3-yl)ethylphosphonates 1-5 was obtained in high yields from reactions of 3-acetyl pyridine with aromatic amines and triphenylphosphite in the presence of lithium perchlorate as a catalyst. The structures of the synthesized compounds were confirmed by IR, H-1 NMR spectral data and microanalyses. Compounds 1-5 showed high antimicrobial activities against Escherichia coli (NCIM2065) as a Gram-negative bacterium, Bacillus subtilis (PC1219) and Staphylococcus aureus (ATCC25292) as Gram-positive bacteria and Candida albicans and Saccharomyces cerevisiae as fungi, at low concentrations (10-100 mu g/mL). Also, the synthesized compounds showed significant cytotoxicity anticancer activities against liver carcinoma cell line (HepG2) and human breast adenocarcinoma cell line (MCF7). The lethal dose of the synthesized compounds was also determined and indicated that most compounds are safe to use. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2252 / 2258
页数:7
相关论文
共 41 条
[1]  
Abd El-Sattar MM., 2011, J AM SCI, V7, P357
[2]   Synthesis of tertiary α-amino phosphonate by one-pot three-component coupling mediated by LPDE [J].
Azizi, N ;
Saidi, MR .
TETRAHEDRON, 2003, 59 (28) :5329-5332
[3]   Simultaneous Quantification of Multiple Nucleic Acid Targets Using Chemiluminescent Probes [J].
Browne, Kenneth A. ;
Deheyn, Dimitri D. ;
El-Hiti, Gamal A. ;
Smith, Keith ;
Weeks, Ian .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2011, 133 (37) :14637-14648
[4]   Understanding non-enzymatic aminophospholipid glycation and its inhibition. Polar head features affect the kinetics of Schiff base formation [J].
Caldes, Catalina ;
Vilanova, Bartolome ;
Adrover, Miquel ;
Munoz, Francisco ;
Donoso, Josefa .
BIOORGANIC & MEDICINAL CHEMISTRY, 2011, 19 (15) :4536-4543
[5]   Prodrug strategies in cancer therapy [J].
Denny, WA .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2001, 36 (7-8) :577-595
[6]   A simple procedure for the side-chain substitution of 2-alkyl-3H-quinazoline-4-thiones:: Application in synthesis [J].
El-Hiti, GA .
SYNTHESIS-STUTTGART, 2004, (03) :363-368
[7]   A convenient procedure for the synthesis of novel modified 3-substituted 1H-quinoxaline-2-thiones via side-chain lithiation of 3-alkyl-1H-quinoxaline-2-thiones [J].
El-Hiti, GA .
SYNTHESIS-STUTTGART, 2003, (18) :2799-2804
[8]   Comparison of Etest and agar dilution method for antimicrobial susceptibility testing of Flavobacterium isolates [J].
Hsueh, PR ;
Chang, JC ;
Teng, LJ ;
Yang, PC ;
Ho, SW ;
Hsieh, WC ;
Luh, KT .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (04) :1021-1023
[9]   Synthesis and antiviral activities of amide derivatives containing the α-aminophosphonate moiety [J].
Hu, De-Yu ;
Wan, Qiong-Qiong ;
Yang, Song ;
Song, Bao-An ;
Bhadury, Pinaki S. ;
Jin, Lin-Hong ;
Yan, Kai ;
Liu, Fang ;
Chen, Zhuo ;
Xue, Wei .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2008, 56 (03) :998-1001
[10]  
Jing- Zi L., 2010, EUR J MED CHEM, V45, P5108