Eco-sustainable synthesis and biological evaluation of 2-phenyl 1,3-benzodioxole derivatives as anticancer, DNA binding and antibacterial agents

被引:23
作者
Gupta, Sayan Dutta [1 ]
Rao, Ganga Balaji [1 ]
Bommaka, Manish Kumar [1 ]
Raghavendra, Nulgumnalli Manjunathaiah [1 ]
Aleti, Swapna [2 ]
机构
[1] Osmania Univ, Gokaraju Rangaraju Coll Pharm, Dept Pharmaceut Chem, Hyderabad 500090, Andhra Pradesh, India
[2] Osmania Univ, Gokaraju Rangaraju Coll Pharm, Dept Biotechnol, Hyderabad, Andhra Pradesh, India
关键词
Benzodioxole; Anticancer; Antibacterial; DNA binding; Green chemistry; PALLADIUM(II) COMPLEXES; IN-VITRO; ANTITUMOR; SCAFFOLD; CANCER;
D O I
10.1016/j.arabjc.2014.08.004
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The current research and development scenario in medicinal chemistry demands small molecules synthesized in a simple, fast and effective way with enhanced activity and fewer side effects than the existing ones. Therefore, one-pot, microwave assisted green and efficient synthesis of a series of derivatives belonging to 2-phenyl 1,3-benzodioxole (1a-14a) and 2-phenyl 1,3-benzo-dioxole-4-ol (1b-14b) class were carried out and subsequently investigated for their anticancer, antibacterial and DNA binding potential. Compound 3c proved to be the most active one among the screened derivatives possessing anticancer and antibacterial potency greater than the standard reference compound (cisplatin and cinoxacin for anticancer and antibacterial activity, respectively). The most active compound in terms of DNA binding capacity was found to be 5b. A rewarding feature of the work is a facile, convenient, eco friendly one step synthesis of compounds demonstrating attenuated activity against cancer and bacterial cell with an inherent potential of binding to DNA. Subsequently, a hit molecule for further anticancer, antibacterial (compound 3c) and DNA binding studies (compound 5b) was also identified. (C) 2014 King Saud University. Production and hosting by Elsevier B.V.
引用
收藏
页码:S1875 / S1883
页数:9
相关论文
共 26 条
[1]   Antimicrobial stewardship [J].
Allerberger, F. ;
Mittermayer, H. .
CLINICAL MICROBIOLOGY AND INFECTION, 2008, 14 (03) :197-199
[2]  
Bakhite EA, 1999, PHARMAZIE, V54, P491
[3]   Exploration of in vitro time point quantitative evaluation of newly synthesized benzimidazole and benzothiazole derivatives as potential antibacterial agents [J].
Bandyopadhyay, Prabal ;
Sathe, Manisha ;
Ponmariappan, S. ;
Sharma, Arti ;
Sharma, Pratibha ;
Srivastava, A. K. ;
Kaushik, M. P. .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2011, 21 (24) :7306-7309
[4]   AN IMPROVED METHOD FOR THE SYNTHESIS OF 2,2-DISUBSTITUTED AND 2-MONOSUBSTITUTED 1,3-BENZODIOXOLES [J].
COLE, ER ;
CRANK, G ;
MINH, HTH .
AUSTRALIAN JOURNAL OF CHEMISTRY, 1980, 33 (03) :675-680
[5]   The price of innovation: new estimates of drug development costs [J].
DiMasi, JA ;
Hansen, RW ;
Grabowski, HG .
JOURNAL OF HEALTH ECONOMICS, 2003, 22 (02) :151-185
[6]   Activity of gemifloxacin, a new broad-spectrum quinolone, against 200 pneumococci by four different susceptibility testing methods [J].
Ednie, LM ;
Jacobs, MR ;
Appelbaum, PC .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2000, 45 (04) :525-528
[7]   MTT COLORIMETRIC ASSAY FOR TESTING MACROPHAGE CYTOTOXIC ACTIVITY INVITRO [J].
FERRARI, M ;
FORNASIERO, MC ;
ISETTA, AM .
JOURNAL OF IMMUNOLOGICAL METHODS, 1990, 131 (02) :165-172
[8]  
Gupta S., 2010, INT J PHARM PHARM SC, V2, P57
[9]   Microwave-assisted green synthesis of 1, 3-benzodioxole derivatives [J].
Gupta, Sayan Dutta ;
Rao, Ganga Balaji ;
Raghavendra, Nulgulmnalli Manjunathiah .
GREEN CHEMISTRY LETTERS AND REVIEWS, 2012, 5 (04) :609-620
[10]   Synthesis and antitumour evaluation of novel 2-phenylbenzimidazoles [J].
Kadri, Hachemi ;
Matthews, Charles S. ;
Bradshaw, Tracey D. ;
Stevens, Malcolm F. G. ;
Westwell, Andrew D. .
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2008, 23 (05) :641-647