3区 · 医学
Article
作者: Boriak-Sjodin, P. Ann  ; Brach, Dorothy  ; Duncan, Kenneth W.  ; Thomenius, Michael J.  ; Munchhof, Michael J.  ; Tang, Cuyue  ; Raimondi, Alejandra  ; Cosmopoulos, Kat  ; Lampe, John W.  ; Foley, Megan A.  ; Motwani, Vinny  ; Eckley, Sean T.  ; Riera, Thomas V.  ; Totman, Jennifer  ; Alford, Joshua S.  ; Harvey, Darren M.  ; Farrow, Neil A. 
SET domain-containing protein 2 (SETD2), a histone methyltransferase, has been identified as a target of interest in certain hematological malignancies, including multiple myeloma. This account details the discovery of EPZ-719, a novel and potent SETD2 inhibitor with a high selectivity over other histone methyltransferases. A screening campaign of the Epizyme proprietary histone methyltransferase-biased library identified potential leads based on a 2-amidoindole core. Structure-based drug design (SBDD) and drug metabolism/pharmacokinetics (DMPK) optimization resulted in EPZ-719, an attractive tool compound for the interrogation of SETD2 biology that enables in vivo target validation studies.