| Literature DB >> 32292557 |
Peter Blomgren1, Jayaraman Chandrasekhar1, Julie A Di Paolo2, Wanchi Fung2, Guoju Geng2, Carmen Ip2, Randall Jones1, Jeffrey E Kropf1, Eric B Lansdon2, Seung Lee1, Jennifer R Lo1, Scott A Mitchell1, Bernard Murray2, Chris Pohlmeyer2, Aaron Schmitt1, Kimberly Suekawa-Pirrone2, Sarah Wise2, Jin-Ming Xiong1, Jianjun Xu1, Helen Yu2, Zhongdong Zhao1, Kevin S Currie1,2.
Abstract
Spleen tyrosine kinase (SYK) is a critical regulator of signaling in a variety of immune cell types such as B-cells, monocytes, and macrophages. Accordingly, there have been numerous efforts to identify compounds that selectively inhibit SYK as a means to treat autoimmune and inflammatory diseases. We previously disclosed GS-9973 (entospletinib) as a selective SYK inhibitor that is under clinical evaluation in hematological malignancies. However, a BID dosing regimen and drug interaction with proton pump inhibitors (PPI) prevented development of entospletinib in inflammatory diseases. Herein, we report the discovery of a second-generation SYK inhibitor, GS-9876 (lanraplenib), which has human pharmacokinetic properties suitable for once-daily administration and is devoid of any interactions with PPI. Lanraplenib is currently under clinical evaluation in multiple autoimmune indications.Entities:
Year: 2020 PMID: 32292557 PMCID: PMC7153012 DOI: 10.1021/acsmedchemlett.9b00621
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345