Chemical Structure : TNI-97
Catalog No.: PC-24898Not For Human Use, Lab Use Only.
TNI-97 is a potent, highly selective and orally bioavailable HDAC6 inhibitor with IC50 of 0.2 nM.
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TNI-97 is a potent, highly selective and orally bioavailable HDAC6 inhibitor with IC50 of 0.2 nM.
TNI-97 demonstrates minimal to no inhibition against class IIa HDACs (HDAC4, 5, 7, 9) and class IV HDAC (HDAC11), as well as HDAC10.
TNI-97 demonstrates more potent on-target activity and better selectivity over clinical candidate ACY-1215.
TNI-97 dose-dependently inhibits the MDA-MB-453 colony formation with GI50 of 0.2 uM.
TNI-97 induces apoptosis in MDA-MB-453 cells in a concentration-dependent manner.
TNI-97 also upregulated cleaved forms of GSDMD and GSDME, two biomarkers of pyroptosis, as well as phosphorylation of MLKL and RIPK3, two inducers of necroptosis.
TNI-97 (40 and 20 mg/kg, oral) demonstrated antitumor activity in the MDA-MB-453 CDX model.
M.Wt | 416.36 | |
Formula | C19H15F3N6O2 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Wang S, et al. J Med Chem. 2025 Jul 3. doi: 10.1021/acs.jmedchem.5c00278.
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