| Literature DB >> 24900759 |
Maurizio Sanguinetti1, Stefania Sanfilippo2, Daniele Castagnolo3, Dominique Sanglard4, Brunella Posteraro1, Giovanni Donzellini2, Maurizio Botta5.
Abstract
Novel macrocyclic amidinourea derivatives 11, 18, and 25 were synthesized and evaluated as antifungal agents against wild-type and fluconazole resistant Candida species. Macrocyclic compounds 11 and 18 were synthesized through a convergent approach using as a key step a ring-closing metathesis macrocyclization reaction, whereas compounds 25 were obtained by our previously reported synthetic pathway. All the macrocyclic amidinoureas showed antifungal activity toward different Candida species higher or comparable to fluconazole and resulted highly active against fluconazole resistant Candida strains showing in many cases minimum inhibitory concentration values lower than voriconazole.Entities:
Keywords: Antifungal; Candida species; amidinourea; antifungal drug-resistance; fluconazole; macrocyclization; ring-closing metathesis
Year: 2013 PMID: 24900759 PMCID: PMC4027461 DOI: 10.1021/ml400187w
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345