ACS Medicinal Chemistry Letters · 2020 · 53 citations · 19 references
MedicinePharmacokineticsPharmacologyDrug DiscoveryImmunopharmacologyMolecular PharmacologyMacrophage PharmacologyTyrosine Kinase InhibitorsProton Pump InhibitionProton Pump Inhibitor InteractionsSelective Tyrosine Kinase InhibitorsSmall Molecule Tyrosine Kinase InhibitorsSpleen Tyrosine Kinase InhibitorsSyk Kinase SignalingTherapeutic Tyrosine Kinase InhibitorsTyrosine Kinase Inhibitor Pharmacokinetics
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.
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Sylvia Braselmann, Vanessa Taylor, H. Zhao et al. · Journal of Pharmacology and Experimental Therapeutics · 2006 · 511 citations