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首页-抗体药物偶连体和PROTACs-PROTAC-USP7 degrader D16
USP7 degrader D16

Chemical Structure : USP7 degrader D16

CAS No.: 3056612-22-4

USP7 degrader D16

货号: PC-28661Not For Human Use, Lab Use Only.

USP7 degrader D16 is a potent and selective USP7 degrader with DC50 of 1.91 uM in TE-12 cells.

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纯度 & COA & 质检文件 纯度: >98% (HPLC)

生物&药学活性

USP7 degrader D16 is a potent and selective USP7 degrader with DC50 of 1.91 uM in TE-12 cells.
D16 degrades USP7 in KYSE-150 and MGC-803 cells with DC50 = 2.53 μM and 4.01 μM, respectively.
D16 degrades USP7 through the formation of USP7-D16-CRBN ternary complex and subsequent proteasome degradation.
D16 prevents migration of UGI cancer cells.

物理化学性质&存储条件

分子量 823.37
分子式 C42H43ClN8O6S
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

4-((5-(3-((7-(5-chloro-3-methyl-2-(piperidin-3-ylamino) phenyl) thieno [3,2-b] pyridin-2-yl) methyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl) pentyl) amino)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione

参考文献

1. Ma XB, et al. Eur J Med Chem. 2026 Feb 15;304:118488.

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