δ-Secretase inhibitor 11 |
| Catalog No.GC66048 |
δ-L'inhibiteur de sécrétase 11 (composé 11) est un &7#948;-inhibiteur de sécrétase actif par voie orale, puissant, pénétré dans la BHE, non toxique, sélectif et spécifique, avec une IC50 de 0,7 μM. δ-l'inhibiteur de sécrétase 11 interagit À la fois avec le site actif et le site allostérique de la δ-sécrétase. δ ; - L'inhibiteur de sécrétase 11 atténue le clivage de tau et de l'APP (protéine précurseur de l'amyloÏde). δ-L'inhibiteur de sécrétase 11 améliore le dysfonctionnement synaptique et les troubles cognitifs dans les modèles de souris transgéniques tau P301S et 5XFAD. δ ; - L'inhibiteur de sécrétase 11 peut être utilisé pour la recherche sur la maladie d'Alzheimer.
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 842964-18-5
Sample solution is provided at 25 µL, 10mM.
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δ-Secretase inhibitor 11 (compound 11) is an orally active, potent, BBB-penetrated, non-toxic, selective and specific δ-secretase inhibitor, with an IC50 of 0.7 μM. δ-Secretase inhibitor 11 interacts with both the active site and allosteric site of δ-secretase. δ-Secretase inhibitor 11 attenuates tau and APP (amyloid precursor protein) cleavage. δ-Secretase inhibitor 11 ameliorates synaptic dysfunction and cognitive impairments in tau P301S and 5XFAD transgenic mouse models. δ-Secretase inhibitor 11 can be used for Alzheimer's disease research[1].
δ-Secretase inhibitor 11 (compound 11) (0-1 μM, 10 min) inhibits δ-secretase in a concentration- and time-dependent manner[1].
δ-Secretase inhibitor 11 (0-1 μM) selectively blocks tau and APP (amyloid precursor protein) fragmentation by δ-secretase[1].
δ-Secretase inhibitor 11 (compound 11) (10 mg/kg, Orally, once daily for 3 months) attenuates neuronal injury induced by OGD (oxygen-glucose deprivation), and specifically exerts neuroprotective actions[1].
δ-Secretase inhibitor 11 (0-10 mg/kg, Orally, once daily for 1.5 and 3 months) inhibits δ-secretase activity, attenuates Aβ deposition and cognitive deficits in 5XFAD mouse model[1].
| Animal Model: | Tau P301S transgenic mice (n=4 mice per group)[1] |
| Dosage: | 10 mg/kg |
| Administration: | Orally, once daily for 3 months |
| Result: | Significantly inhibited the activity of δ-secretase in both wild-type and tau P301S mice brain, increased PP2A activity, and attenuated the truncation and phosphorylation of tau in tau P301S mice. Ameliorated synaptic loss and restored synaptic dysfunction in tau P301S mice. |
| Animal Model: | 5XFAD mice[1] |
| Dosage: | 2, 5 or 10 mg kg |
| Administration: | Orally, once daily for 1.5 and 3 months |
| Result: | Attenuated the β-secretase-mediated processing of APP, significantly decreased the concentrations of Aβ 1-40 and Aβ 1-42 in the brain lysates, and attenuated Aβ deposition in a time- and dose-dependent manner. |
Average Rating: 5 (Based on Reviews and 30 reference(s) in Google Scholar.)
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