| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1398926 | European Journal of Medicinal Chemistry | 2014 | 13 Pages |
•Natural isoxazolines medicinally gained much attention as anticancer agents.•Structural–activity relationship, isolation and synthetic pathways.•Influence of absolute configurations on anticancer potential.•Most of the compounds were cytotoxic against MCF-7 and HCT-116 cell lines.
Isoxazolines are an important class of nitrogen and oxygen containing heterocycles that belong to the azoles family which have gained much importance in the field of medicinal chemistry as the anticancer agents. Moreover, natural products are always expectedly regarded as an important hoard of a large number of potential chemotherapeutic candidates. Therefore, this review mainly focuses on the existence of isoxazoline derivatives in natural sources, their isolation and uses there of as anticancer agents besides highlighting the synthetic pathways to achieve these compounds. Structural–activity relationship and the influence of stereochemical aspects on anticancer activity of such compounds have also been discussed. It covers the literature upto 2014 and would certainly provide a great insight to scientific community to accelerate further research for the development of some novel anticancer drugs.
Graphical abstractIsoxazoline derivatives exhibit a broad spectrum of biological properties. The present review describe the existence of natural isoxazolines as anticancer agents, their isolation and synthetic pathways.Figure optionsDownload full-size imageDownload as PowerPoint slide
