Corpus overview


MeSH Disease

HGNC Genes

SARS-CoV-2 proteins

There are no SARS-CoV-2 protein terms in the subcorpus


SARS-CoV-2 Proteins
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    Advanced Bioinformatics Rapidly Identifies Existing Therapeutics for Patients with Coronavirus Disease - 2019 ( COVID-19 MESHD)

    Authors: Jason Kim; Jenny zhang; Yoonjeong Cha; Sarah Kolitz; Jason Funt; Renan Escalante Chong; Scott Barrett; Ben Zeskind; Rebecca Kusko; Howard Kaufman

    doi:10.26434/chemrxiv.12037416.v1 Date: 2020-03-27 Source: ChemRxiv

    The recent global pandemic has placed a high priority on identifying drugs to prevent or lessen clinical infection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), caused by Coronavirus disease – 2019 ( COVID-19 MESHD). We applied two computational approaches to identify potential therapeutics. First, we sought to identify existing FDA approved drugs that could block coronaviruses from entering cells by binding to ACE2 HGNC or TMPRSS2 HGNC using a high-throughput AI-based binding affinity prediction platform. Top results included several ACE HGNC inhibitors, a beta HGNC-lactam antibiotic, two antiviral agents (Fosamprenavir and Emricasan) and glutathione. The platform also assessed specificity for ACE2 HGNC over ACE1 HGNC, important for avoiding counterregulatory effects. Further studies are needed to weigh the benefit of blocking virus entry against potential counterregulatory effects and possible protective effects of ACE2 HGNC. However, the data herein suggest readily available drugs that warrant experimental evaluation to assess potential benefit. Second, we sought to identify FDA approved drugs that could attenuate the gene expression patterns induced by coronaviruses, using our Disease Cancelling Technology (DCT) platform. DCT was run on an animal model of SARS-CoV MESHD, and ranked compounds by their ability to induce gene expression signals that counteract disease-associated signals. Top hits included Vitamin E, ruxolitinib, and glutamine. Glutathione and its precursor glutamine were highly ranked by two independent methods, suggesting both warrant further investigation for potential benefit against SARS-CoV-2. While these findings are not yet ready for clinical translation, this report highlights the potential use of two bioinformatics technologies to rapidly discover existing therapeutic agents that warrant further investigation for established and emerging disease MESHD processes.

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MeSH Disease
HGNC Genes
SARS-CoV-2 Proteins

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