

Synthesis of 3H-imidazo[4,5-b] pyridine with evaluation of their anticancer and antimicrobial activity
Rohini Narayan Shelke (1,*)






(1) Department of Chemistry, Deogiri College, Aurangabad, 431005, India
(2) Department of Chemical Technology, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad, 431004, India
(3) Department of Chemical Technology, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad, 431004, India
(4) Rao Bahadhur Narayanrao Borawake College Shrirampur, Ahmednagar, 413709, India
(5) Department of Chemistry, Deogiri College, Aurangabad, 431005, India
(6) Department of Chemistry, Deogiri College, Aurangabad, 431005, India
(*) Corresponding Author
Received: 20 Dec 2016 | Accepted: 15 Jan 2017 | Published: 31 Mar 2017 | Issue Date: March 2017
Abstract
Microwave assisted and conventional synthetic methods of new 6-bromo-2-(substituted)-3H-imidazo[4,5-b]pyridine and its derivatives are described, which were obtained in reduced reaction times, higher yields, cleaner reactions than previously described methods. All the synthesized compounds were characterized, and screened for their anticancer and antimicrobial activity. Among synthesized compounds 3b and 3k shows prominent antibacterial activity and compound 3f shows both antibacterial and antifungal activity. Compounds 3h and 3j shows prominent anticancer activity against the both breast cancer cell lines, MCF-7 and BT-474. These results suggest that the imidazo[4,5-b]pyridine moiety may serve as a new promising template for synthesis of anticancer and antimicrobial agents and further study is required for evaluation of their mechanism of action.
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DOI: 10.5155/eurjchem.8.1.25-32.1522
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Department of Chemical Technology, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad 431004, India
Citations
[1]. Sülünay Parlar, Yalçın Erzurumlu, Recep Ilhan, Petek Ballar Kırmızıbayrak, Vildan Alptüzün, Ercin Erciyas
Synthesis and evaluation of pyridinium-hydrazone derivatives as potential antitumoral agents
Chemical Biology & Drug Design 92(1), 1198, 2018
DOI: 10.1111/cbdd.13177

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