ロード中...
Discovery of O-Alkylamino-Tethered Niclosamide Derivatives as Potent and Orally Bioavailable Anticancer Agents
[Image: see text] Niclosamide has been identified to potently inhibit the activation, nuclear translocation, and transactivation of STAT3. Nevertheless, the poor aqueous solubility and bioavailability of niclosamide have hindered its further clinical development for cancer therapy. To discover new m...
保存先:
| 主要な著者: | , , , , , , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
American
Chemical Society
2013
|
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3583367/ https://ncbi.nlm.nih.gov/pubmed/23459613 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ml3003082 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|