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1,8-取代蒽醌、蒽酮和双蒽酮作为潜在的非唑类抗真菌药物先导化合物。

1,8-Substituted anthraquinones, anthrones and bianthrones as potential non-azole leads against fungal infections.

机构信息

School of Pharmacy and Biomedical Sciences, University of Central Lancashire, Preston PR1 2HE, UK.

Chemistry, School of Physical Sciences and Computing, University of Central Lancashire, Preston PR1 2HE, UK.

出版信息

Bioorg Chem. 2019 Oct;91:103151. doi: 10.1016/j.bioorg.2019.103151. Epub 2019 Jul 24.

DOI:10.1016/j.bioorg.2019.103151
PMID:31362198
Abstract

The synthesis of a variety of 1,8-substituted anthraquinones, anthrones and bianthrones and their potential as antifungal agents is evaluated. Preliminary screening against Schizosaccharomyces pombe (S. pombe), a fission yeast, and Saccharomyces cerevisiae (S. cerevisiae), a budding yeast, is reported. Both these yeast species demonstrate close homologue to a number of pathogenic fungi.

摘要

评估了各种 1,8-取代蒽醌、蒽酮和双蒽酮的合成及其作为抗真菌剂的潜力。报道了对裂殖酵母(Schizosaccharomyces pombe,S. pombe)和酿酒酵母(Saccharomyces cerevisiae,S. cerevisiae)的初步筛选,这两种酵母与许多致病性真菌具有密切的同源性。

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