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PDB: 2 件

Crystal Structure of Human Cathepsin S Bound to a Non-covalent Inhibitor
分子名称:	Cathepsin S, N-[(8R)-8-(benzoylamino)-5,6,7,8-tetrahydronaphthalen-2-yl]-4-methylpiperazine-1-carboxamide, SULFATE ION
著者	Wang, Y, Jadhav, P.K, Deng, G.G.
登録日	2014-03-24
公開日	2014-10-29
最終更新日	2024-10-30
実験手法	X-RAY DIFFRACTION (1.8 Å)
主引用文献	Discovery of Cathepsin S Inhibitor LY3000328 for the Treatment of Abdominal Aortic Aneurysm. Acs Med.Chem.Lett., 5, 2014

Crystal Structure of Human Cathepsin S Bound to a Non-covalent Inhibitor.
分子名称:	(3R,4S)-4-[(4-fluorobenzoyl)amino]-6-[4-(oxetan-3-yl)piperazin-1-yl]-3,4-dihydro-2H-chromen-3-yl methylcarbamate, Cathepsin S
著者	Wang, Y, Jadhav, P.K.
登録日	2014-03-24
公開日	2014-10-29
最終更新日	2023-12-27
実験手法	X-RAY DIFFRACTION (1.58 Å)
主引用文献	Discovery of Cathepsin S Inhibitor LY3000328 for the Treatment of Abdominal Aortic Aneurysm. Acs Med.Chem.Lett., 5, 2014