Chemical Structure : NSD2 degrader T9
Catalog No.: PC-27167Not For Human Use, Lab Use Only.
NSD2 degrader T9 is a potent, selective, FBXO22-recruiting NSD2 degrader with DC50 of 0.37 uM in in HEK293T-NSD2-HiBiT cells (4 h).
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NSD2 degrader T9 is a potent, selective, FBXO22-recruiting NSD2 degrader with DC50 of 0.37 uM in in HEK293T-NSD2-HiBiT cells (4 h).
T9 (0.1–10 uM) induces significant, dose-dependent degradation of both the long and short isoforms of NSD2.
T9 acts rapidly to induce FBXO22-mediated NSD2 elimination, acts through the ubiquitin–proteasome system (UPS).
PWWP1 engagement is required for PROTAC-mediated recruitment and subsequent proteasomal degradation.
T9 exhibits an exquisite selectivity profile, NSD2 degradation proceeds through compound-induced NSD2-FBXO22 ternary complex formation, ubiquitin transfer, and proteasome engagement, rather than by indirect or off-target effect.
Covalent engagement of FBXO22 by T9 occurs specifically through C326.
T9 (10 uM) robustly suppressed PC3 cell growth to roughly 45%, but not UNC8732.
| M.Wt | 642.71 | |
| Formula | C38H34N4O6 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Tang H, et al. J Med Chem. 2026 Jun 29. doi: 10.1021/acs.jmedchem.6c00020.

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