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PH-002

رقم الكتالوجGC31139

PH-002 هو مثبط للتفاعل داخل الجزيئات في مجال البروتين الشحمي (apo) E4 في الخلايا العصبية التي يمكن أن تنقذ ضعف حركية الميتوكوندريا ونمو النوريت

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PH-002 التركيب الكيميائي

Cas No.: 1311174-68-1

الحجم السعر المخزون الكميّة
10mM (in 1mL DMSO)
127٫00
متوفر
5mg
117٫00
متوفر
10mg
198٫00
متوفر
25mg
432٫00
متوفر
50mg
738٫00
متوفر
100mg
836٫00
متوفر

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Sample solution is provided at 25 µL, 10mM.

Description Protocol Chemical Properties Product Documents Related Products

PH-002 is an inhibitor of apolipoprotein (apo) E4 intramolecular domain interaction in neuronal cells that could rescue impairments of mitochondrial motility and neurite outgrowth.

PH-002 is an inhibitor of apolipoprotein (apo) E4 intramolecular domain interaction in neuronal cells, with an IC50 of 116 nM in FRET[1].

PH-002 is also shown to increase COX1 levels in primary neurons from NSE-apoE4 transgenic mouse cortex and hippocampus. After 4 days of treatment with PH-002 (200 nM), COX1 levels are increased by ~60%. PH-002 (100 nM) increases dendritic spine development in primary neurons from NSE-apoE4 transgenic mice to levels comparable with those in NSE-apoE3 primary neurons (apoE3-expressing primary neurons treated with PH-002 gave results identical to untreated primary neurons)[2].

[1]. Brodbeck J, et al. Structure-dependent impairment of intracellular apolipoprotein E4 trafficking and its detrimental effects are rescued by small-molecule structure correctors. J Biol Chem. 2011 May 13;286(19):17217-26. [2]. Chen HK, et al. Small molecule structure correctors abolish detrimental effects of apolipoprotein E4 in cultured neurons. J Biol Chem. 2012 Feb 17;287(8):5253-66.

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