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螺环吡咯烷吲哚酮与氟康唑对白色念珠菌具有强大的协同作用。

Potent Synergy between Spirocyclic Pyrrolidinoindolinones and Fluconazole against Candida albicans.

作者信息

Premachandra Ilandari Dewage Udara Anulal, Scott Kevin A, Shen Chengtian, Wang Fuqiang, Lane Shelley, Liu Haoping, Van Vranken David L

机构信息

Department of Chemistry, University of California, Irvine, 1102 Natural Sciences 2, Irvine, CA 92697-2025 (USA).

Department of Biological Chemistry, University of California, Irvine, 825 Health Sciences Road, Medical Sciences I, Irvine, CA 92697-1700 (USA).

出版信息

ChemMedChem. 2015 Oct;10(10):1672-86. doi: 10.1002/cmdc.201500271. Epub 2015 Aug 12.

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.

摘要

一种螺吲哚酮,即(1S,3R,3aR,6aS)-1-苄基-6'-氯-5-(4-氟苯基)-7'-甲基螺[1,2,3a,6a-四氢吡咯并[3,4-c]吡咯-3,3'-1H-吲哚]-2',4,6-三酮,此前有报道称其可增强氟康唑对白色念珠菌的抗真菌作用。合成了该化合物的一个非对映异构体以及各种类似物。许多化合物都显示出可增强氟康唑对白色念珠菌的抗真菌作用,有些具有极高的效力。发现一种螺环哌嗪衍生物,我们将其命名为synazo-1,它能增强氟康唑的作用,对白色念珠菌敏感菌株的EC50值为300 pM,对一些耐药菌株低至2 nM。Synazo-1与氟康唑表现出真正的协同作用,在所测试的菌株中FIC指数低于0.5。相对于抗真菌协同作用所需的浓度,Synazo-1在哺乳动物细胞中表现出低毒性。

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9
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