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In vitro antifungal activities (μg/mL) compounds interacting to the TRR1 target.

Figshare2015-12-03 更新2026-04-29 收录

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https://figshare.com/articles/dataset/_In_vitro_antifungal_activities_g_mL_compounds_interacting_to_the_TRR1_target_/1603741 数据链接链接失效反馈

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In vitro antifungal activities (μg/mL) compounds interacting to the TRR1 target.

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创建时间：

2015-12-03

基因组测序

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Whole genome sequencing of a clinical isolate of Trichophyton rubrum, carried out on Illumina platform with paired end reads. Samples relate to study investigating drug response of dermatophytes to an

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Crystal structure of Cryptococcus neoformans H99 Acetyl-CoA Synthetase in complex with Ac-AMS

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Crystal structure of Cryptococcus neoformans H99 Acetyl-CoA Synthetase in complex with Ac-AMS

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4‑Nitropyrazolin-5-ones as Readily Available Fungicides of the Novel Structural Type for Crop Protection: Atom-Efficient Scalable Synthesis and Key Structural Features Responsible for Activity

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The development of new types of fungicides for agriculture and medicine is highly desirable due to the uprising fungal resistance against commonly used compounds. Herein, 4-substituted-4-nitropyrazoli

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Discovery of a new chemical scaffold for the treatment of superbug Candida auris infections

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Candida auris has emerged as a serious threat of public health and caused global epidemic due to multi-drug resistance, remarkable transmissibility and high mortality. To tackle the challenging

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Candida albicans dihydrofolate reductase complexed with NADPH and 5-[3-(2,5-dimethoxy-4-phenylphenyl)but-1-yn-1-yl]-6-methylpyrimidine-2,4-diamine (UCP111E)

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抑制剂设计

Candida albicans dihydrofolate reductase complexed with NADPH and 5-[3-(2,5-dimethoxy-4-phenylphenyl)but-1-yn-1-yl]-6-methylpyrimidine-2,4-diamine (UCP111E) Descriptor: 5-[3-(2,5-dimethoxy-4-phenylphe

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In vitro antifungal activities (μg/mL) compounds interacting to the TRR1 target.

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