6BXY

Menin in complex with MI-1481

6BXY の概要

• エントリーDOI: 10.2210/pdb6bxy/pdb
• 分子名称: Menin, 4-methyl-1-{[(2S)-5-oxomorpholin-2-yl]methyl}-5-[(4-{[6-(2,2,2-trifluoroethyl)thieno[2,3-d]pyrimidin-4-yl]amino}piperidin-1-yl)methyl]-1H-indole-2-carbonitrile, DIMETHYL SULFOXIDE, ... (7 entities in total)
• 機能のキーワード: protein binding, inhibitor, transcription
• 由来する生物種: Homo sapiens (Human)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 56140.98

構造登録者

Borkin, D.,Klossowski, S.,Pollock, J.,Linhares, B.,Cierpicki, T.,Grembecka, J. (登録日: 2017-12-19, 公開日: 2018-11-28, 最終更新日: 2023-10-04)

主引用文献

Borkin, D.,Klossowski, S.,Pollock, J.,Miao, H.,Linhares, B.M.,Kempinska, K.,Jin, Z.,Purohit, T.,Wen, B.,He, M.,Sun, D.,Cierpicki, T.,Grembecka, J.
Complexity of Blocking Bivalent Protein-Protein Interactions: Development of a Highly Potent Inhibitor of the Menin-Mixed-Lineage Leukemia Interaction.
J.Med.Chem., 61:4832-4850, 2018

PubMed Abstract: The protein-protein interaction between menin and mixed-lineage leukemia 1 (MLL1) plays an important role in development of acute leukemia with translocations of the MLL1 gene and in solid tumors. Here, we report the development of a new generation of menin-MLL1 inhibitors identified by structure-based optimization of the thienopyrimidine class of compounds. This work resulted in compound 28 (MI-1481), which showed very potent inhibition of the menin-MLL1 interaction (IC = 3.6 nM), representing the most potent reversible menin-MLL1 inhibitor reported to date. The crystal structure of the menin-28 complex revealed a hydrogen bond with Glu366 and hydrophobic interactions, which contributed to strong inhibitory activity of 28. Compound 28 also demonstrates pronounced activity in MLL leukemia cells and in vivo in MLL leukemia models. Thus, 28 is a valuable menin-MLL1 inhibitor that can be used for potential therapeutic applications and in further studies regarding the role of menin in cancer.

PubMed: 29738674
DOI: 10.1021/acs.jmedchem.8b00071

実験手法

X-RAY DIFFRACTION (1.82 Å)