δ-Secretase inhibitor 11 |
| رقم الكتالوجGC66048 |
δ ؛ - مثبط السكريتاز 11 (المركب 11) هو فعال عن طريق الفم ، قوي ، مخترق BBB ، غير سام ، انتقائي ومحدد δ ؛ - مثبط سيكريتاز ، مع IC50 من 0.7 μ ؛ M. δ ؛ -مثبط سيكريتاز 11 يتفاعل مع كل من الموقع النشط والموقع الخيفي لـ δ ؛ -Secretase. δ ؛ - يخفف مثبط السكريتاز 11 من انقسام تاو و APP (بروتين سلائف الأميلويد). δ ؛ - يعمل مثبط السكريتاز 11 على تحسين الخلل الوظيفي المشبكي والضعف الإدراكي في نماذج الماوس المعدلة وراثيًا تاو P301S و 5 XFAD. δ ؛ -يمكن استخدام مثبطات السكريتاز 11 لأبحاث مرض الزهايمر.
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. |
| Cas No. | 842964-18-5 | SDF | |
| Formula | C10H12N4O2 | M.Wt | 220.23 |
| الذوبان | DMSO : 125 mg/mL (567.59 mM; Need ultrasonic) | Storage | Store at -20°C |
| General tips | Please select the appropriate solvent to prepare the stock solution according to the
solubility of the product in different solvents; once the solution is prepared, please store it in
separate packages to avoid product failure caused by repeated freezing and thawing.Storage method
and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored
at -20°C, please use it within 1 month. To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time. |
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| Shipping Condition | Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request. | ||
| Prepare stock solution | |||
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1 mg | 5 mg | 10 mg |
| 1 mM | 4.5407 mL | 22.7035 mL | 45.4071 mL |
| 5 mM | 0.9081 mL | 4.5407 mL | 9.0814 mL |
| 10 mM | 0.4541 mL | 2.2704 mL | 4.5407 mL |
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Quality Control & SDS
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- Purity: >98.00%
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Average Rating: 5 (Based on Reviews and 30 reference(s) in Google Scholar.)
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