| Literature DB >> 26263912 |
Ilandari Dewage Udara Anulal Premachandra1, Kevin A Scott1, Chengtian Shen1, Fuqiang Wang2, Shelley Lane2, Haoping Liu2, David L Van Vranken3.
Abstract
A spiroindolinone, (1S,3R,3aR,6aS)-1-benzyl-6'-chloro-5-(4-fluorophenyl)-7'-methylspiro[1,2,3a,6a-tetrahydropyrrolo[3,4-c]pyrrole-3,3'-1H-indole]-2',4,6-trione, was previously reported to enhance the antifungal effect of fluconazole against Candida albicans. A diastereomer of this compound was synthesized, along with various analogues. Many of the compounds were shown to enhance the antifungal effect of fluconazole against C. albicans, some with exquisite potency. One spirocyclic piperazine derivative, which we have named synazo-1, was found to enhance the effect of fluconazole with an EC50 value of 300 pM against a susceptible strain of C. albicans and going as low as 2 nM against some resistant strains. Synazo-1 exhibits true synergy with fluconazole, with an FIC index below 0.5 in the strains tested. Synazo-1 exhibited low toxicity in mammalian cells relative to the concentrations required for antifungal synergy.Entities:
Keywords: Candida albicans; antifungal agents; fluconazole; spiro compounds; synergy
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Year: 2015 PMID: 26263912 PMCID: PMC4682886 DOI: 10.1002/cmdc.201500271
Source DB: PubMed Journal: ChemMedChem ISSN: 1860-7179 Impact factor: 3.466