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Review
. 2022 Aug;26(4):2341-2370.
doi: 10.1007/s11030-021-10332-1. Epub 2021 Oct 26.

A review on the synthesis of heteroannulated quinolones and their biological activities

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Review

A review on the synthesis of heteroannulated quinolones and their biological activities

Yaseen A M M Elshaier et al. Mol Divers. 2022 Aug.

Abstract

The quinoline scaffold has become an important construction motif for the development of new drugs. The quinolones and their heteroannulated derivatives have high importance due to their diverse spectrum of biological activities as antifungal, anti-inflammatory, anti-diabetes, anti-Alzheimer's disease, antioxidant and diuretic activities. This review summarizes the various new, efficient and convenient synthetic approaches to synthesize diverse quinolone-based scaffolds and their biological activities. We also dealt with the important mechanism, the route and type of reactions of the obtained products. The biological activities of some heteroannulated quinolones were also discussed.

Keywords: Biological activities; Furoquinolones; Heteroannulation; Oxazoloquinolones; Pyranoquinolones; Pyrroloquinolones; Thienoquinolones.

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References

    1. Akhtar MJ, Yar MS, Khan AA, Ali Z, Haider MR (2017) Recent advances in the synthesis and anticancer activity of some molecules other than nitrogen containing heterocyclic moeities. Mini-Rev Med Chem 17(17):1602–1632 - PubMed - DOI
    1. Arafa RK, Hegazy GH, Piazza GA, Abadi AH (2013) Synthesis and in vitro antiproliferative effect of novel quinoline-based potential anticancer agents. Eur J Med Chem 63:826–832 - PubMed - DOI
    1. Lee H-Y, Chang C-Y, Su C-J, Huang H-L, Mehndiratta S, Chao Y-H, Hsu C-M, Kumar S, Sung T-Y, Huang Y-Z (2016) 2-(Phenylsulfonyl) quinoline N-hydroxyacrylamides as potent anticancer agents inhibiting histone deacetylase. Eur J Med Chem 122:92–101 - PubMed - DOI
    1. Afzal O, Kumar S, Haider MR, Ali MR, Kumar R, Jaggi M, Bawa S (2015) A review on anticancer potential of bioactive heterocycle quinoline. Eur J Med Chem 97:871–910 - PubMed - DOI
    1. Ramesh M, Mohan P, Shanmugam P (1984) A convenient synthesis of flindersine, atanine and their analogues. Tetrahedron 40(20):4041–4049 - DOI

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