Details

Autor(en) / Beteiligte

• Tichenor, Mark S.
• Wiener, John J. M.
• Rao, Navin L.
• Bacani, Genesis M.
• Wei, Jianmei
• Pooley Deckhut, Charlotte
• Barbay, J. Kent
• Kreutter, Kevin D.
• Chang, Leon
• Clancy, Kathleen W.
• Murrey, Heather E.
• Wang, Weixue
• Ahn, Kay
• Huber, Michael
• Rex, Elizabeth
• Coe, Kevin J.
• Wu, Jiejun
• Rui, Haopeng
• Sepassi, Kia
• Gaudiano, Marcello
• Bekkers, Mariette
• Cornelissen, Ivo
• Packman, Kathryn
• Seierstad, Mark
• Xiouras, Christos
• Bembenek, Scott D.
• Alexander, Richard
• Milligan, Cynthia
• Balasubramanian, Sriram
• Lebsack, Alec D.
• Venable, Jennifer D.
• Philippar, Ulrike
• Edwards, James P.
• Hirst, Gavin

Titel

Discovery of JNJ-64264681: A Potent and Selective Covalent Inhibitor of Bruton’s Tyrosine Kinase

Ist Teil von

• Journal of medicinal chemistry, 2022-11, Vol.65 (21), p.14326-14336

Ort / Verlag

American Chemical Society

Erscheinungsjahr

2022

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• Bruton’s tyrosine kinase (BTK) is a Tec family kinase that plays an essential role in B-cell receptor (BCR) signaling as well as Fcγ receptor signaling in leukocytes. Pharmacological inhibition of BTK has been shown to be effective in treating hematological malignancies and is hypothesized to provide an effective strategy for the treatment of autoimmune diseases such as rheumatoid arthritis and systemic lupus erythematosus. We report the discovery and preclinical properties of JNJ-64264681 (13), a covalent, irreversible BTK inhibitor with potent whole blood activity and exceptional kinome selectivity. JNJ-64264681 demonstrated excellent oral efficacy in both cancer and autoimmune models with sustained in vivo target coverage amenable to once daily dosing and has advanced into human clinical studies to investigate safety and pharmacokinetics.