Discovery of Pyridinyl Acetamide Derivatives as Potent, Selective, and Orally Bioavailable Porcupine Inhibitors-Reference-Cited by-同舟云学术

Discovery of Pyridinyl Acetamide Derivatives as Potent, Selective, and Orally Bioavailable Porcupine Inhibitors

Published:2016-05-11 Issue:7 Volume:7 Page:676-680
ISSN:1948-5875
Container-title:ACS Medicinal Chemistry Letters
language:en
Short-container-title:ACS Med. Chem. Lett.

Author:

Cheng Dai¹,Liu Jun¹,Han Dong¹,Zhang Guobao¹,Gao Wenqi¹,Hsieh Mindy H.¹,Ng Nicholas¹,Kasibhatla Shailaja¹,Tompkins Celin¹,Li Jie¹,Steffy Auzon¹,Sun Fangxian¹,Li Chun¹,Seidel H. Martin¹,Harris Jennifer L.¹,Pan Shifeng¹

Affiliation:

1. Genomics Institute of the Novartis Research Foundation, 10675 John Jay Hopkins Drive, San Diego, California 92121, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acsmedchemlett.6b00038

Reference22 articles.

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