4C4E

Structure-based design of orally bioavailable pyrrolopyridine inhibitors of the mitotic kinase MPS1

4C4E の概要

• エントリーDOI: 10.2210/pdb4c4e/pdb
• 関連するPDBエントリー: 4C4F 4C4G 4C4H 4C4I 4C4J
• 分子名称: DUAL SPECIFICITY PROTEIN KINASE TTK, N-(3,4-dimethoxyphenyl)-2-(1H-pyrazol-4-yl)-1H-pyrrolo[3,2-c]pyridin-6-amine, PENTAETHYLENE GLYCOL, ... (5 entities in total)
• 機能のキーワード: transferase, mps1, ttk, protein kinase, mitosis, structure-based design
• 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: 38010.41

構造登録者

Naud, S.,Westwood, I.M.,Faisal, A.,Sheldrake, P.,Bavetsias, V.,Atrash, B.,Liu, M.,Hayes, A.,Schmitt, J.,Wood, A.,Choi, V.,Boxall, K.,Mak, G.,Gurden, M.,Valenti, M.,de Haven Brandon, A.,Henley, A.,Baker, R.,McAndrew, C.,Matijssen, B.,Burke, R.,Eccles, S.A.,Raynaud, F.I.,Linardopoulos, S.,van Montfort, R.,Blagg, J. (登録日: 2013-09-05, 公開日: 2013-12-04, 最終更新日: 2023-12-20)

• 主引用文献: Naud, S.,Westwood, I.M.,Faisal, A.,Sheldrake, P.W.,Bavetsias, V.,Atrash, B.,Cheung, K.J.,Liu, M.,Hayes, A.,Schmitt, J.,Wood, A.,Choi, V.,Boxall, K.,Mak, G.,Gurden, M.,Valenti, M.,De-Haven-Brandon, A.,Henley, A.,Baker, R.,Mcandrew, C.,Matijssen, B.,Burke, R.,Hoelder, S.,Eccles, S.A.,Raynaud, F.I.,Linardopoulos, S.,Van Montfort, R.L.M.,Blagg, J.; Structure-Based Design of Orally Bioavailable 1H-Pyrrolo[3, 2-C]Pyridine Inhibitors of the Mitotic Kinase Monopolar Spindle 1 (Mps1).; J.Med.Chem., 56:10045-, 2013; PubMed: 24256217; DOI: 10.1021/JM401395S

実験手法

X-RAY DIFFRACTION (2.6 Å)