(75.101.220.230)
Users online: 156    [ij] [ij] [ij] 
Email id
 

Asian Journal of Research in Chemistry
Year : 2018, Volume : 11, Issue : 2
First page : ( 505) Last page : ( 508)
Print ISSN : 0974-4169. Online ISSN : 0974-4150.
Article DOI : 10.5958/0974-4150.2018.00090.1

Review of Heterocyclic Scaffolds for the Inhibitors of ATP synthase

Mehta Saurabh*

Department of Applied Chemistry, Delhi Technological University, Bawana Road, Delhi, 110042, India

*Corresponding Author E-mail: saurabh.mehta@dtu.ac.in; saurabh.dtu@gmail.com

Online published on 2 June, 2018.

Abstract

ATP synthase is an important enzyme and is an established drug target. The involvement of this enzyme has been attributed to various serious diseases and physiological conditions, such as cancer, obesity, neurodegenerative disorders, etc. It makes it an attractive drug target whose activity may be modulated by small molecules. A variety of inhibitors reported in the literature have been reviewed, and the important O-and Ncontaining heterocyclic scaffolds have been identified and are presented here. On examining the scaffolds, it is observed that a variety of 5-membered ring containing compounds to macrocycles inhibit ATP synthase. These include Flavones and Isoflavons, Catechins, Estrogen metabolites, Polyenic -pyrones, Amphiphilic cationic dyes, Tertiary amine local anesthetics (TALAs), N-sulfonyl tetrahydrobenzodiazepines, N-[1-Aryl-2-(1imidazolo)ethyl]-acylguanidine derivatives, O-[1-Aryl-2-(1-imidazolo)ethyl]-thiourethane derivatives and 4amino benzopyrans.

Top

Keywords

ATP synthase, Drug Discovery, Enzyme, Heterocycle, Inhibitor.

Top

  
║ Site map ║ Privacy Policy ║ Copyright ║ Terms & Conditions ║ Page Rank Tool
446,294,870 visitor(s) since 30th May, 2005.
All rights reserved. Site designed and maintained by DIVA ENTERPRISES PVT. LTD..
Note: Please use Internet Explorer (6.0 or above). Some functionalities may not work in other browsers.