6 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
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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
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