10 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Development of a triazole class of highly potent Porcn inhibitors.
Ut Southwestern Medical Center
Design, synthesis, and evaluation of novel porcupine inhibitors featuring a fused 3-ring system based on the 'reversed' amide scaffold.
Soochow University
The use of porcupine inhibitors to target Wnt-driven cancers.
Experimental Therapeutics Centre
Exploration of the linkage elements of porcupine antagonists led to potent Wnt signaling pathway inhibitors.
Soochow University
The development of highly potent inhibitors for porcupine.
The University of Texas Southwestern Medical Center
Discovery of Pyridinyl Acetamide Derivatives as Potent, Selective, and Orally Bioavailable Porcupine Inhibitors.
Genomics Institute of The Novartis Research Foundation
Discovery and characterization of a potent Wnt and hedgehog signaling pathways dual inhibitor.
Soochow University
Discovery of Inhibitor of Wnt Production 2 (IWP-2) and Related Compounds As Selective ATP-Competitive Inhibitors of Casein Kinase 1 (CK1) ?/?.
Ulm University Hospital