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Synthesis and Antifungal Activities of a Series of (1,2-Disubstituted Vinyl)imidazoles.
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1991
Year
Medicinal ChemistryAntifungal AgentBioorganic ChemistryEngineeringBiochemistryAntifungal AgentsNatural SciencesMedicinal Fungi1,2-Disubstituted VinylOrganic ChemistryVinyl GroupAntimicrobial CompoundYeast CellsPharmacologyHetero AtomPharmaceutical ChemistrySynthetic ChemistryBiomolecular Engineering
A series of vinylimidazoles containing a hetero atom such as sulfur or oxygen at a beta-position of the vinyl group was prepared and the antifungal activities were tested. It was found that sulfur-substituted derivatives such as (E)-1-[2-(methylthio)-1-[2-(pentyloxy)phenyl]ethenyl]-1H-imidazole (5a-5) and (E)-1-[1-[2-(hexyloxy)phenyl]-2-(methylthio)ethenyl]-1H-imidazole (5a-6) showed excellent antifungal activities against dermatophytes and yeast cells. The stereochemistry of the hydrochloride salt of 5a-5 was determined by X-ray crystallography. The structure-activity relationships were discussed.