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Optimized S-Trityl-l-cysteine-Based Inhibitors of Kinesin Spindle Protein with Potent in Vivo Antitumor Activity in Lung Cancer Xenograft Models
[Image: see text] The mitotic kinesin Eg5 is critical for the assembly of the mitotic spindle and is a promising chemotherapy target. Previously, we identified S-trityl-l-cysteine as a selective inhibitor of Eg5 and developed triphenylbutanamine analogues with improved potency, favorable drug-like p...
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| Autors principals: | , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American
Chemical Society
2013
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| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3759169/ https://ncbi.nlm.nih.gov/pubmed/23394180 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jm3014597 |
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