Characterization of a highly selective inhibitor of the Aurora kinases
- Authors
- Ferguson, Fleur M.; Doctor, Zainab M.; Chaikuad, Apirat; Sim, Taebo; Kim, Nam Doo; Knapp, Stefan; Gray, Nathanael S.
- Issue Date
- 15-9월-2017
- Publisher
- PERGAMON-ELSEVIER SCIENCE LTD
- Keywords
- Aurora kinase; Selective kinase inhibitor; Pan-Aurora inhibitor; Mitosis; Cancer
- Citation
- BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.27, no.18, pp.4405 - 4408
- Indexed
- SCIE
SCOPUS
- Journal Title
- BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
- Volume
- 27
- Number
- 18
- Start Page
- 4405
- End Page
- 4408
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/82221
- DOI
- 10.1016/j.bmcl.2017.08.016
- ISSN
- 0960-894X
- Abstract
- Aurora kinases play an essential role in mitosis and cell cycle regulation. In recent years Aurora kinases have proved popular cancer targets and many inhibitors have been developed. The majority of these clinical candidates are multi-targeted, rendering them inappropriate as tools for studying Aurora kinase mediated signaling. Here we report discovery of a highly selective inhibitor of Aurora kinases A, B and C, with potent cellular activity and minimal off-target activity (PLK4). The X-ray co-crystal structure of Aurora A in complex with compound 2 is reported, and provides insights into the structural determinants of ligand binding and selectivity. (C) 2017 Elsevier Ltd. All rights reserved.
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Collections - Graduate School > KU-KIST Graduate School of Converging Science and Technology > 1. Journal Articles
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