1,2,3-Triazole-containing hybrids as leads in medicinal chemistry: A recent overview.

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ID: 57930
2019
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Abstract
The 1,2,3-triazole ring is a major pharmacophore system among nitrogen-containing heterocycles. These five-membered heterocyclic motifs with three nitrogen heteroatoms can be prepared easily using 'click' chemistry with copper- or ruthenium-catalysed azide-alkyne cycloaddition reactions. Recently, the 'linker' property of 1,2,3-triazoles was demonstrated, and a novel class of 1,2,3-triazole-containing hybrids and conjugates was synthesised and evaluated as lead compounds for diverse biological targets. These lead compounds have been demonstrated as anticancer, antimicrobial, anti-tubercular, antiviral, antidiabetic, antimalarial, anti-leishmanial, and neuroprotective agents. The present review summarises advances in lead compounds of 1,2,3-triazole-containing hybrids, conjugates, and their related heterocycles in medicinal chemistry published in 2018. This review will be useful to scientists in research fields of organic synthesis, medicinal chemistry, phytochemistry, and pharmacology.
Reference Key
bozorov2019123triazolecontainingbioorganic Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Bozorov, Khurshed;Zhao, Jiangyu;Aisa, Haji A;
Journal bioorganic & medicinal chemistry
Year 2019
DOI
S0968-0896(19)30826-0
URL
Keywords
1,2,3-Triazole Click chemistry biological activity copper-catalysed 1,3-dipolar cycloaddition (cuaac) huisgen azide-alkyne cycloaddition lead compounds

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