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首页> 外文期刊>Computational and Structural Biotechnology Journal >L1000 connectivity map interrogation identifies candidate drugs for repurposing as SARS-CoV-2 antiviral therapies
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L1000 connectivity map interrogation identifies candidate drugs for repurposing as SARS-CoV-2 antiviral therapies

机译:L1000连接地图询问识别候选药物用于重新估算SARS-COV-2抗病毒疗法

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摘要

Adaptive clinical trials are underway to determine the efficacy of potential therapies for COVID-19, with flexibility to include emerging therapies if there is sufficient preclinical evidence for their potential utility. In silico screening of connectivity maps, which link gene expression profiles to libraries of perturbagens, may facilitate the identification of such emerging therapies. The L1000 Connectivity Map is built from samples of transcripts taken from gene expression profiles of cells in various experimental conditions followed by computational inferences of the remainder of the transcriptome. Searching the L1000 Connectivity Map for modulators of a protease that facilitates coronavirus infection identifies plausible candidate drugs for repurposing as antiviral agents against SARS-CoV-2 following further investigation.
机译:正在进行自适应临床试验,以确定Covid-19的潜在疗法的功效,如果有足够的临床前诊断,可以灵活地包括新出现的疗法。在硅筛查的连接地图中,将基因表达谱链接到Perturbagens的文库,可以促进这种新出现的疗法。 L1000连接图是由在各种实验条件中从细胞的基因表达谱中取出的转录物的样本构建,然后通过转录组的其余部分的计算推论。搜索L1000连接图的蛋白酶的调节剂,促进冠状病毒感染,鉴定了在进一步调查之后对SARS-COV-2重新估算作为抗病毒剂的合理候选药物。

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