| Literature DB >> 25193230 |
Ana I Ribeiro1, Carla Gabriel2, Fátima Cerqueira3, Marta Maia4, Eugénia Pinto4, João Carlos Sousa2, Rui Medeiros5, M Fernanda Proença1, Alice M Dias6.
Abstract
A mild and simple method was developed to prepare a series of fifteen 5-aminoimidazole 4-carboxamidrazones, starting from the easily accessible 5-amino-4-cyanoformimidoyl imidazoles. The antimicrobial activity of these novel amidrazones was screened against Gram positive (Staphylococcus aureus) and Gram negative (Escherichia coli, Pseudomonas aeruginosa) bacteria and Candida sp. (Candida albicans, Candida krusei, Candida parapsilosis). Only a subset of compounds displayed fair-moderate activity against S. aureus and E. coli but all exhibited activity against Candida sp. The three most potent antifungal compounds were further tested against Cryptococcus neoformans, Aspergillus fumigatus and three dermatophytes (Trichophyton rubrum, Trichophyton mentagrophytes, Microsporum gypseum). These three hit compounds strongly inhibited C. krusei and C. neoformans growth, although their activity on filamentous fungi was very weak when compared to the activity on yeasts.Entities:
Keywords: Amidrazone; Antifungal; Antimicrobial; Hydrazine; Imidazole
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Year: 2014 PMID: 25193230 DOI: 10.1016/j.bmcl.2014.08.025
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823