Literature DB >> 22172702

Identification of novel, potent and selective inhibitors of Polo-like kinase 1.

Shaoqing Chen1, David Bartkovitz, Jianping Cai, Yi Chen, Zhi Chen, Xin-Jie Chu, Kang Le, Nam T Le, Kin-Chun Luk, Steve Mischke, Goli Naderi-Oboodi, John F Boylan, Tom Nevins, Weiguo Qing, Yingsi Chen, Peter M Wovkulich.   

Abstract

A series of pyrimidodiazepines was identified as potent Polo-like kinase 1 (PLK1) inhibitors. The synthesis and SAR are discussed. The lead compound 7 (RO3280) has potent inhibitory activity against PLK1, good selectivity against other kinases, and excellent in vitro cellular potency. It showed strong antitumor activity in xenograft mouse models.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 22172702     DOI: 10.1016/j.bmcl.2011.11.052

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  14 in total

Review 1.  Recent Advances and New Strategies in Targeting Plk1 for Anticancer Therapy.

Authors:  Kyung S Lee; Terrence R Burke; Jung-Eun Park; Jeong K Bang; Eunhye Lee
Journal:  Trends Pharmacol Sci       Date:  2015-10-17       Impact factor: 14.819

2.  Assessing the performance of docking scoring function, FEP, MM-GBSA, and QM/MM-GBSA approaches on a series of PLK1 inhibitors.

Authors:  Chunlan Pu; Guoyi Yan; Jianyou Shi; Rui Li
Journal:  Medchemcomm       Date:  2017-05-22       Impact factor: 3.597

3.  Discovery of a Highly Selective, Brain-Penetrant Aminopyrazole LRRK2 Inhibitor.

Authors:  Bryan K Chan; Anthony A Estrada; Huifen Chen; John Atherall; Charles Baker-Glenn; Alan Beresford; Daniel J Burdick; Mark Chambers; Sara L Dominguez; Jason Drummond; Andrew Gill; Tracy Kleinheinz; Claire E Le Pichon; Andrew D Medhurst; Xingrong Liu; John G Moffat; Kevin Nash; Kimberly Scearce-Levie; Zejuan Sheng; Daniel G Shore; Hervé Van de Poël; Shuo Zhang; Haitao Zhu; Zachary K Sweeney
Journal:  ACS Med Chem Lett       Date:  2012-11-23       Impact factor: 4.345

4.  Differential BET Bromodomain Inhibition by Dihydropteridinone and Pyrimidodiazepinone Kinase Inhibitors.

Authors:  Rezaul Md Karim; Melissa J Bikowitz; Alice Chan; Jin-Yi Zhu; Dylan Grassie; Andreas Becker; Norbert Berndt; Steven Gunawan; Nicholas J Lawrence; Ernst Schönbrunn
Journal:  J Med Chem       Date:  2021-10-28       Impact factor: 8.039

5.  PLK-1 Expression is Associated with Histopathological Response to Neoadjuvant Therapy of Hepatic Metastasis of Colorectal Carcinoma.

Authors:  M J Fernández-Aceñero; D Cortés; T Gómez del Pulgar; A Cebrián; L Estrada; J Martínez-Useros; A Celdrán; J García-Foncillas; C Pastor
Journal:  Pathol Oncol Res       Date:  2015-11-17       Impact factor: 3.201

6.  1-Eth-oxy-methyl-5-methyl-9-phenyl-6,7,8,9-tetra-hydro-1H-pyrimido[4,5-b][1,4]diazepine-2,4(3H,5H)-dione.

Authors:  Gong Li; Xiaowei Wang; Zhili Zhang; Junyi Liu
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-04-18

7.  Molecular targeting of the oncoprotein PLK1 in pediatric acute myeloid leukemia: RO3280, a novel PLK1 inhibitor, induces apoptosis in leukemia cells.

Authors:  Na-Na Wang; Zhi-Heng Li; He Zhao; Yan-Fang Tao; Li-Xiao Xu; Jun Lu; Lan Cao; Xiao-Juan Du; Li-Chao Sun; Wen-Li Zhao; Pei-Fang Xiao; Fang Fang; Guang-Hao Su; Yan-Hong Li; Gang Li; Yi-Ping Li; Yun-Yun Xu; Hui-Ting Zhou; Yi Wu; Mei-Fang Jin; Lin Liu; Jian Ni; Jian Wang; Shao-Yan Hu; Xue-Ming Zhu; Xing Feng; Jian Pan
Journal:  Int J Mol Sci       Date:  2015-01-07       Impact factor: 5.923

8.  Mitotic entry: Non-genetic heterogeneity exposes the requirement for Plk1.

Authors:  Claire F Aspinall; Daniella Zheleva; Anthony Tighe; Stephen S Taylor
Journal:  Oncotarget       Date:  2015-11-03

Review 9.  PLK1, A Potential Target for Cancer Therapy.

Authors:  Zhixian Liu; Qingrong Sun; Xiaosheng Wang
Journal:  Transl Oncol       Date:  2016-11-24       Impact factor: 4.243

Review 10.  PLK-1 Targeted Inhibitors and Their Potential against Tumorigenesis.

Authors:  Shiv Kumar; Jaebong Kim
Journal:  Biomed Res Int       Date:  2015-10-18       Impact factor: 3.411

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