| Literature DB >> 28424934 |
Andrii Lozynskyi1, Viktoria Zasidko2, Dmytro Atamanyuk1, Danylo Kaminskyy1, Halyna Derkach3, Olexandr Karpenko4, Volodymyr Ogurtsov5, Roman Kutsyk2, Roman Lesyk6.
Abstract
Here it is described the synthesis, antioxidant and antimicrobial activity determination of novel rel-([Formula: see text])-6-benzoyl-7-phenyl-2-oxo-3,5,6,7-tetrahydro-2H-thiopyrano[2,3-d]thiazole-5-carboxylic acids. The target compounds were obtained in good yields from 5-arylidene-4-thioxo-2-thiazolidinones and [Formula: see text]-aroylacrylic acids via regio- and diastereoselective hetero-Diels-Alder reaction. The stereochemistry of the cycloaddition was confirmed by NMR spectra. The antioxidant and antimicrobial activity screening identified 7 compounds (3c, 3e, 3f, 3g, 3k, 3l, 3p) with a high level of free radical scavenging (43-77% DPPH assay), and compounds with significant influence on Staphylococcus aureus, Bacillus subtilis and Candida albicans (MIC 3.13-6.25 [Formula: see text]), but slight effect on Escherichia coli.Entities:
Keywords: Antimicrobial activity; Antioxidant activity; Hetero-Diels–Alder reaction; Thiopyrano[2,3-d]thiazoles
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Year: 2017 PMID: 28424934 DOI: 10.1007/s11030-017-9737-8
Source DB: PubMed Journal: Mol Divers ISSN: 1381-1991 Impact factor: 2.943