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PDB: 1 件

4V0G
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BU of 4v0g by Molmil
JAK3 in complex with a covalent EGFR inhibitor
分子名称: N-[3-(2-{3-amino-6-[1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl]pyrazin-2-yl}-1H-benzimidazol-1-yl)phenyl]propanamide, TYROSINE-PROTEIN KINASE JAK3
著者Debreczeni, J.E, Hennessy, E.J, Chuaquini, C, Ashton, S, Coclough, N, Cross, D.A.E, Eberlein, C, Gingipalli, L, Klinowska, T.C.M, Orme, J.P, Sha, L, Wu, X.
登録日2014-09-16
公開日2016-01-13
実験手法X-RAY DIFFRACTION (3 Å)
主引用文献Utilisation of Structure Based Design to Identify Novel, Irreversible Inhibitors of the Epidermal Growth Factor Receptor (Egfr) Harboring the Gatekeeper T790M Mutation
To be Published

219515

件を2024-05-08に公開中

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