6HM7
CRYSTAL STRUCTURE OF SPLEEN TYROSINE KINASE (SYK) IN COMPLEX WITH A 2-(PHENOXYMETHYL)PYRIDINE INHIBITOR
6HM7 の概要
| エントリーDOI | 10.2210/pdb6hm7/pdb |
| 関連するPDBエントリー | 6HM6 |
| 分子名称 | Tyrosine-protein kinase SYK, 7-[2-methoxy-6-[(4-methylpyridin-2-yl)methoxy]phenyl]-2,3,4,5-tetrahydro-1~{H}-3-benzazepine, BROMIDE ION, ... (6 entities in total) |
| 機能のキーワード | sk363, syk, non-receptor tyrosine kinase, spleen tyrosine kinase, 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 | 32889.35 |
| 構造登録者 | |
| 主引用文献 | Barker, M.D.,Liddle, J.,Atkinson, F.L.,Wilson, D.M.,Dickson, M.C.,Ramirez-Molina, C.,Lewis, H.,Davis, R.P.,Somers, D.O.,Neu, M.,Jones, E.,Watson, R. Discovery of potent and selective Spleen Tyrosine Kinase inhibitors for the topical treatment of inflammatory skin disease. Bioorg. Med. Chem. Lett., 28:3458-3462, 2018 Cited by PubMed Abstract: The discovery and lead optimisation of a novel series of SYK inhibitors is described. These were optimised for SYK potency and selectivity against Aurora B. Compounds were profiled in a human skin penetration study to identify a suitable candidate molecule for pre-clinical development. Compound 44 (GSK2646264) was selected for progression and is currently in Phase I clinical trials. PubMed: 30249354DOI: 10.1016/j.bmcl.2018.09.022 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.64 Å) |
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