9CD7

FGFR3 Kinase Domain with Inhibitor TYRA-300

これはPDB形式変換不可エントリーです。

9CD7 の概要

• エントリーDOI: 10.2210/pdb9cd7/pdb
• 分子名称: Fibroblast growth factor receptor 3, (3P)-5-[(1R)-1-(3,5-dichloropyridin-4-yl)ethoxy]-3-{6-[6-(methanesulfonyl)-2,6-diazaspiro[3.3]heptan-2-yl]pyridin-3-yl}-1H-indazole, GLYCEROL, ... (5 entities in total)
• 機能のキーワード: kinase, transferase, inhibitor, cancer, achondroplasia, fgfr3, fgfr, transferase-transferase inhibitor complex, transferase/transferase inhibitor
• 由来する生物種: Homo sapiens (human)
• タンパク質・核酸の鎖数: 3
• 化学式量合計: 108858.23

構造登録者

Hoffman, I.H.,Nelson, K.J.,Rideout, M.C.,Nix, J.C.,Frye, C.,Bensen, D.C.,Hudkins, R.L. (登録日: 2024-06-24, 公開日: 2024-09-25)

• 主引用文献: Hudkins, R.L.,Allen, E.,Balcer, A.,Hoffman, I.D.,Iyer, S.,Neal, M.,Nelson, K.J.,Rideout, M.,Ye, Q.,Starrett, J.H.,Patel, P.,Harris, T.,Swanson, R.V.,Bensen, D.C.; Discovery of TYRA-300: First Oral Selective FGFR3 Inhibitor for the Treatment of Urothelial Cancers and Achondroplasia.; J.Med.Chem., 2024; PubMed: 39258897; DOI: 10.1021/acs.jmedchem.4c01531

実験手法

X-RAY DIFFRACTION (2.53 Å)