Synthesis, antioxidant and antimicrobial activities of novel thiopyrano[2,3-d]thiazoles based on aroylacrylic acids.
Andrii LozynskyiViktoria ZasidkoDmytro AtamanyukDanylo KaminskyyHalyna DerkachOlexandr KarpenkoVolodymyr OgurtsovRoman KutsykRoman LesykPublished in: Molecular diversity (2017)
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.
Keyphrases
- candida albicans
- staphylococcus aureus
- biofilm formation
- bacillus subtilis
- oxidative stress
- escherichia coli
- anti inflammatory
- smoking cessation
- human milk
- magnetic resonance
- pseudomonas aeruginosa
- high throughput
- high resolution
- molecularly imprinted
- methicillin resistant staphylococcus aureus
- preterm infants
- low birth weight
- mass spectrometry
- solid phase extraction
- solid state
- preterm birth