6B4W

TTK in Complex with Inhibitor

6B4W の概要

• エントリーDOI: 10.2210/pdb6b4w/pdb
• 分子名称: Dual specificity protein kinase TTK, 4-{[4-(cyclopentyloxy)-5-(2-methyl-1,3-benzoxazol-6-yl)-7H-pyrrolo[2,3-d]pyrimidin-2-yl]amino}-3-methoxy-N-methylbenzamide, CACODYLATE ION (3 entities in total)
• 機能のキーワード: protein kinase, signaling protein
• 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: 35522.46

構造登録者

Delker, S.,Chamberlain, P.P. (登録日: 2017-09-27, 公開日: 2017-10-25, 最終更新日: 2024-03-13)

主引用文献

Riggs, J.R.,Nagy, M.,Elsner, J.,Erdman, P.,Cashion, D.,Robinson, D.,Harris, R.,Huang, D.,Tehrani, L.,Deyanat-Yazdi, G.,Narla, R.K.,Peng, X.,Tran, T.,Barnes, L.,Miller, T.,Katz, J.,Tang, Y.,Chen, M.,Moghaddam, M.F.,Bahmanyar, S.,Pagarigan, B.,Delker, S.,LeBrun, L.,Chamberlain, P.P.,Calabrese, A.,Canan, S.S.,Leftheris, K.,Zhu, D.,Boylan, J.F.
The Discovery of a Dual TTK Protein Kinase/CDC2-Like Kinase (CLK2) Inhibitor for the Treatment of Triple Negative Breast Cancer Initiated from a Phenotypic Screen.
J. Med. Chem., 60:8989-9002, 2017

PubMed Abstract: Triple negative breast cancer (TNBC) remains a serious unmet medical need with discouragingly high relapse rates. We report here the synthesis and structure-activity relationship (SAR) of a novel series of 2,4,5-trisubstituted-7H-pyrrolo[2,3-d]pyrimidines with potent activity against TNBC tumor cell lines. These compounds were discovered from a TNBC phenotypic screen and possess a unique dual inhibition profile targeting TTK (mitotic exit) and CLK2 (mRNA splicing). Design and optimization, driven with a TNBC tumor cell assay, identified potent and selective compounds with favorable in vitro and in vivo activity profiles and good iv PK properties. This cell-based driven SAR produced compounds with strong single agent in vivo efficacy in multiple TNBC xenograft models without significant body weight loss. These data supported the nomination of CC-671 into IND-enabling studies as a single agent TNBC therapy.

PubMed: 28991472
DOI: 10.1021/acs.jmedchem.7b01223

実験手法

X-RAY DIFFRACTION (2.9 Å)