Your browser doesn't support javascript.
loading
Synthesis and antimicrobial activity of novel 5-aminoimidazole-4-carboxamidrazones.
Ribeiro, Ana I; Gabriel, Carla; Cerqueira, Fátima; Maia, Marta; Pinto, Eugénia; Sousa, João Carlos; Medeiros, Rui; Proença, M Fernanda; Dias, Alice M.
Afiliação
  • Ribeiro AI; Centre of Chemistry, Department of Chemistry, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal.
  • Gabriel C; FP-ENAS/CEBIMED, University Fernando Pessoa, 4200-150 Porto, Portugal.
  • Cerqueira F; FP-ENAS/CEBIMED, University Fernando Pessoa, 4200-150 Porto, Portugal; CEQUIMED/Laboratory of Microbiology, Biological Sciences Department, Faculty of Pharmacy of University of Porto, 4050-313 Porto, Portugal. Electronic address: fatimaf@ufp.edu.pt.
  • Maia M; CEQUIMED/Laboratory of Microbiology, Biological Sciences Department, Faculty of Pharmacy of University of Porto, 4050-313 Porto, Portugal; Interdisciplinary Centre of Marine and Environmental Research (CIIMAR/CIMAR), University of Porto, 4050-123 Porto, Portugal.
  • Pinto E; CEQUIMED/Laboratory of Microbiology, Biological Sciences Department, Faculty of Pharmacy of University of Porto, 4050-313 Porto, Portugal; Interdisciplinary Centre of Marine and Environmental Research (CIIMAR/CIMAR), University of Porto, 4050-123 Porto, Portugal.
  • Sousa JC; FP-ENAS/CEBIMED, University Fernando Pessoa, 4200-150 Porto, Portugal.
  • Medeiros R; FP-ENAS/CEBIMED, University Fernando Pessoa, 4200-150 Porto, Portugal; Molecular Oncology GRP and Molecular Biology Laboratory-Virology Service, Portuguese Institute of Oncology (IPO), 4200-072 Porto, Portugal.
  • Proença MF; Centre of Chemistry, Department of Chemistry, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal.
  • Dias AM; Centre of Chemistry, Department of Chemistry, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal. Electronic address: ad@quimica.uminho.pt.
Bioorg Med Chem Lett ; 24(19): 4699-4702, 2014 Oct 01.
Article em En | MEDLINE | ID: mdl-25193230
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.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Candida / Bactérias Gram-Negativas / Bactérias Gram-Positivas / Hidrazonas / Imidazóis / Antibacterianos / Antifúngicos Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Candida / Bactérias Gram-Negativas / Bactérias Gram-Positivas / Hidrazonas / Imidazóis / Antibacterianos / Antifúngicos Idioma: En Ano de publicação: 2014 Tipo de documento: Article