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The Discovery of Aurora Kinase Inhibitor by Multi-Docking-Based Virtual Screening
We report the discovery of aurora kinase inhibitor using the fragment-based virtual screening by multi-docking strategy. Among a number of fragments collected from eMololecules, we found four fragment molecules showing potent activity (>50% at 100 μM) against aurora kinase. Based on the explored...
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| Vydáno v: | Int J Mol Sci |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
MDPI
2014
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4264174/ https://ncbi.nlm.nih.gov/pubmed/25383681 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms151120403 |
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