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Fragment-based discovery of a new family of non-peptidic small-molecule cyclophilin inhibitors with potent antiviral activities
Cyclophilins are peptidyl-prolyl cis/trans isomerases (PPIase) that catalyse the interconversion of the peptide bond at proline residues. Several cyclophilins play a pivotal role in the life cycle of a number of viruses. The existing cyclophilin inhibitors, all derived from cyclosporine A or sanglif...
Tallennettuna:
Julkaisussa: | Nat Commun |
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Päätekijät: | , , , , , , , , , , , , |
Aineistotyyppi: | Artigo |
Kieli: | Inglês |
Julkaistu: |
Nature Publishing Group
2016
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Aiheet: | |
Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5036131/ https://ncbi.nlm.nih.gov/pubmed/27652979 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ncomms12777 |
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