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Design and synthesis of novel oridonin analogues as potent anticancer agents
To identify anticancer agents with higher potency and lower toxicity, a series of oridonin derivatives with substituted benzene moieties at the C17 position were designed, synthesised, and evaluated for their antiproliferative properties. Most of the derivatives exhibited antiproliferative effects a...
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| Veröffentlicht in: | J Enzyme Inhib Med Chem |
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| Hauptverfasser: | , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Taylor & Francis
2018
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6054517/ https://ncbi.nlm.nih.gov/pubmed/29303372 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/14756366.2017.1419219 |
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