Chemical Structure : CF3CN
Catalog No.: PC-28351Not For Human Use, Lab Use Only.
CF3CN is a brain permeable, synthetic 7,8-DHF derivative and TrkB agonist, robustly binds to the LCM/CC2 motif on TrkB extracellular domain (ECD) with Kd of 80.2 nM, activates TrkB and its downstream signaling pathway.
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CF3CN is a brain permeable, synthetic 7,8-DHF derivative and TrkB agonist, robustly binds to the LCM/CC2 motif on TrkB extracellular domain (ECD) with Kd of 80.2 nM, activates TrkB and its downstream signaling pathway.
CF3CN displays a dose-dependent protection against staurosporine-induced apoptosis in T48 cells with EC50 around 26.4 nM.
CF3CN protects BR6 cells from STS-induced cell death with IC50 of 103 nM, but not TrkB-deficient SH-SY5Y cells.
CF3CN activates p-TrkB and promotes cell survival in a TrkB-dependent manner.
CF3CN dose-dependently decreases Aβ42, prevents the synaptic loss in the hippocampus in 5xFAD mouse brains.
CF3CN alleviates inflammation, inhibits delta-secretase (AEP, δ-secretase) activation, and reduces the concentrations of AEP-derived APP fragments and Tau fragments.
| M.Wt | 355.28 | |
| Formula | C18H8F3N3O2 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Chun Chen, et al. ACS Chem Neurosci. 2021 Jul 7;12(13):2448-2461.
2. Jianming Liao, et al. Neuropharmacology. 2021 Oct 1:197:108737.

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