5LS6

Structure of Human Polycomb Repressive Complex 2 (PRC2) with inhibitor

5LS6 の概要

• エントリーDOI: 10.2210/pdb5ls6/pdb
• 分子名称: Histone-lysine N-methyltransferase EZH2,Histone-lysine N-methyltransferase EZH2,Histone-lysine N-methyltransferase EZH2, Polycomb protein EED, Polycomb protein SUZ12, ... (6 entities in total)
• 機能のキーワード: human prc2, inhibitor, h3k27, transferase-inhibitor complex, transferase/inhibitor
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 16
• 化学式量合計: 557894.22

構造登録者

Zhang, Y.,Justin, N.,Chen, S.,Wilson, J.,Gamblin, S. (登録日: 2016-08-22, 公開日: 2017-02-22, 最終更新日: 2024-01-17)

主引用文献

Vaswani, R.G.,Gehling, V.S.,Dakin, L.A.,Cook, A.S.,Nasveschuk, C.G.,Duplessis, M.,Iyer, P.,Balasubramanian, S.,Zhao, F.,Good, A.C.,Campbell, R.,Lee, C.,Cantone, N.,Cummings, R.T.,Normant, E.,Bellon, S.F.,Albrecht, B.K.,Harmange, J.C.,Trojer, P.,Audia, J.E.,Zhang, Y.,Justin, N.,Chen, S.,Wilson, J.R.,Gamblin, S.J.
Identification of (R)-N-((4-Methoxy-6-methyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methyl-1-(1-(1-(2,2,2-trifluoroethyl)piperidin-4-yl)ethyl)-1H-indole-3-carboxamide (CPI-1205), a Potent and Selective Inhibitor of Histone Methyltransferase EZH2, Suitable for Phase I Clinical Trials for B-Cell Lymphomas.
J. Med. Chem., 59:9928-9941, 2016

PubMed Abstract: Polycomb repressive complex 2 (PRC2) has been shown to play a major role in transcriptional silencing in part by installing methylation marks on lysine 27 of histone 3. Dysregulation of PRC2 function correlates with certain malignancies and poor prognosis. EZH2 is the catalytic engine of the PRC2 complex and thus represents a key candidate oncology target for pharmacological intervention. Here we report the optimization of our indole-based EZH2 inhibitor series that led to the identification of CPI-1205, a highly potent (biochemical IC = 0.002 μM, cellular EC = 0.032 μM) and selective inhibitor of EZH2. This compound demonstrates robust antitumor effects in a Karpas-422 xenograft model when dosed at 160 mg/kg BID and is currently in Phase I clinical trials. Additionally, we disclose the co-crystal structure of our inhibitor series bound to the human PRC2 complex.

PubMed: 27739677
DOI: 10.1021/acs.jmedchem.6b01315

実験手法

X-RAY DIFFRACTION (3.47 Å)