ChemistrySelect · 2018 · 54 citations · 30 references
PharmacyChemistryMedicinal ChemistryDrug DesignDrug DiscoveryOrganic ChemistryAntibacterial AgentsAntibacterial PharmacologyNatural Product Drug DiscoveryAntioxidant PropertiesBacillus SubtilisFree Radical ScavengingMultistep SynthesisNovel Antibacterial AgentsNovel Antibacterial Drug DiscoveryTriazole ChemistryTriazole Synthesis
Abstract In the current study, an efficient synthesis of new triazole‐linked chalcone 3 a‐g scaffold was performed by multistep reaction sequence and was screened for their antibacterial activity against Pseudomonas aeruginosa , Escherchia coli , Staphylococcus aureus and Bacillus subtilis . The preliminary result revealed that 3 f exhibited a promising antibacterial activity. Furthermore, 3 f was modified at α, β‐ unsaturated carbonyl segment to isoxazoline 4 a , pyrimidines 5 a , 6 a‐b , pyrazoles 7 a‐c and cyanopyridine 8 a . Within the modified compounds 7 b (4‐nitro‐substituted pyrazole) turn to be more potent against all bacterial strains. In addition compounds, 5 a and 8 a showed promising free radical scavenging activity.
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Adnan A. Bekhit, Adnan A. Bekhit, Hayam M. A. Ashour et al. · European Journal of Medicinal Chemistry · 2007 · 299 citations · Full text