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Discovery of Pyridinyl Acetamide Derivatives as Potent, Selective, and Orally Bioavailable Porcupine Inhibitors
[Image: see text] Blockade of aberrant Wnt signaling is an attractive therapeutic approach in multiple cancers. We developed and performed a cellular high-throughput screen for inhibitors of Wnt secretion and pathway activation. A lead structure (GNF-1331) was identified from the screen. Further stu...
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Published in: | ACS Med Chem Lett |
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Main Authors: | , , , , , , , , , , , , , , , |
Format: | Artigo |
Language: | Inglês |
Published: |
American Chemical
Society
2016
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Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4948009/ https://ncbi.nlm.nih.gov/pubmed/27437076 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acsmedchemlett.6b00038 |
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