| Literature DB >> 25438709 |
Mansi Garg1, Monika Chauhan1, Pankaj Kumar Singh1, Jimi Marin Alex1, Raj Kumar2.
Abstract
Numerous N-heterocycles are indisputably evidenced to exhibit myriad biological activities. In the recent past, attempts made to condense the various heterocycles have resulted in derivatives possessing better bioactivities. Among many such condensed heterocycles, pyrazoloquinazolines have managed to hold the attention of many researchers, owing to the broad spectrum of activities they portray. This review is the first of its kind to congregate the various pyrazoloquinazolines reported until now and categorizes these structurally isomeric classes into eleven different groups based on the fusion pattern of the ring such as [1,5-c], [5,1-b], [4,3-h], etc. Furthermore, this review is a concerted effort to highlight design, synthetic strategies as well as biological activities of each class of this condensed heterocycle. Structure-activity relationship studies and in silico approaches wherever reported have also been discussed. In addition, manuscript also offers scope for design, synthesis and generation of libraries of unreported classes of pyrazoloquinazolines for the biological evaluation.Entities:
Keywords: Biological activities; Docking; Pyrazoloquinazolines; QSAR; SAR; Synthetic strategies
Mesh:
Substances:
Year: 2014 PMID: 25438709 DOI: 10.1016/j.ejmech.2014.11.051
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514