| Literature DB >> 24583357 |
Imtiaz Khan1, Aliya Ibrar1, Naeem Abbas1, Aamer Saeed2.
Abstract
Drug development has been a principal driving force in the rapid maturation of the field of medicinal chemistry during the past several decades. During this period, the intriguing and challenging molecular architectures of nitrogen-containing heterocycles with potential bioactive properties have received significant attention from researchers engaged in the areas of natural product synthesis and heterocyclic methodology, and constituted a continuous stimulus for development in bio(organic) chemistry. In this perspective, the current review article is an effort to summarize recent developments in the environmentally benign synthetic methods providing access to quinazoline and quinazolinone scaffolds with promising biological potential. This article also aims to discuss potential future directions on the development of more potent and specific analogues for various biological targets.Entities:
Keywords: Biological activities; Heterocycles; Inhibitors; Quinazolines; Quinazolinones; Synthetic methods
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Year: 2014 PMID: 24583357 DOI: 10.1016/j.ejmech.2014.02.005
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514