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4UYN

SAR156497 an exquisitely selective inhibitor of Aurora kinases

4UYN の概要
エントリーDOI10.2210/pdb4uyn/pdb
分子名称AURORA KINASE A, ethyl (9S)-9-[5-(1H-benzimidazol-2-ylsulfanyl)furan-2-yl]-8-hydroxy-5,6,7,9-tetrahydro-2H-pyrrolo[3,4-b]quinoline-3-carboxylate (3 entities in total)
機能のキーワードtransferase
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33816.71
構造登録者
主引用文献Carry, J.,Clerc, F.,Minoux, H.,Schio, L.,Mauger, J.,Nair, A.,Parmantier, E.,Le Moigne, R.,Delorme, C.,Nicolas, J.,Krick, A.,Abecassis, P.,Crocq-Stuerga, V.,Pouzieux, S.,Delarbre, L.,Maignan, S.,Bertrand, T.,Bjergarde, K.,Ma, N.,Lachaud, S.,Guizani, H.,Lebel, R.,Doerflinger, G.,Monget, S.,Perron, S.,Gasse, F.,Angouillant-Boniface, O.,Filoche-Romme, B.,Murer, M.,Gontier, S.,Prevost, C.,Monteiro, M.,Combeau, C.
Sar156497, an Exquisitely Selective Inhibitor of Aurora Kinases.
J.Med.Chem., 58:362-, 2015
Cited by
PubMed Abstract: The Aurora family of serine/threonine kinases is essential for mitosis. Their crucial role in cell cycle regulation and aberrant expression in a broad range of malignancies have been demonstrated and have prompted intensive search for small molecule Aurora inhibitors. Indeed, over 10 of them have reached the clinic as potential anticancer therapies. We report herein the discovery and optimization of a novel series of tricyclic molecules that has led to SAR156497, an exquisitely selective Aurora A, B, and C inhibitor with in vitro and in vivo efficacy. We also provide insights into its mode of binding to its target proteins, which could explain its selectivity.
PubMed: 25369539
DOI: 10.1021/JM501326K
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.9 Å)
構造検証レポート
Validation report summary of 4uyn
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-02-04に公開中

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