PH-002
CAS No. 1311174-68-1
PH-002 ( —— )
产品货号. M23470 CAS No. 1311174-68-1
PH-002 是神经元细胞中载脂蛋白 (apo) E4 分子内结构域相互作用的抑制剂。它还可以挽救线粒体运动和神经突生长的损伤。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥945 | 有现货 |
|
| 10MG | ¥1739 | 有现货 |
|
| 25MG | ¥3711 | 有现货 |
|
| 50MG | ¥5282 | 有现货 |
|
| 100MG | ¥7137 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥1074 | 有现货 |
|
生物学信息
-
产品名称PH-002
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述PH-002 是神经元细胞中载脂蛋白 (apo) E4 分子内结构域相互作用的抑制剂。它还可以挽救线粒体运动和神经突生长的损伤。
-
产品描述PH-002 is an inhibitor of apolipoprotein (apo) E4 intramolecular domain interaction in neuronal cells. It also could rescue impairments of mitochondrial motility and neurite outgrowth.
-
体外实验PH-002 is an inhibitor of apolipoprotein (apo) E4 intramolecular domain interaction in neuronal cells, with an IC50 of 116 nM in FRET.
-
体内实验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).
-
同义词——
-
通路Others
-
靶点Other Targets
-
受体Apo E4 in FRET
-
研究领域——
-
适应症——
化学信息
-
CAS Number1311174-68-1
-
分子量491.58
-
分子式C27H33N5O4
-
纯度>98% (HPLC)
-
溶解度DMSO:75 mg/mL (152.57 mM)
-
SMILESCC(C)(C)OC(N1CCN(Cc(cc2)ccc2NC(CC(c2c3cccc2)=NN(C)C3=O)=O)CC1)=O
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
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.
产品手册
关联产品
-
Eupatorin
Eupatorin 具有抗增殖和抗血管生成作用。由于 CYP1 介导的代谢,Eupatorin 对 MDA-MB-468 人乳腺癌细胞具有抗增殖和细胞抑制作用。
-
Hederasaponin B
常春藤皂苷 B 通过抑制病毒 VP2 蛋白表达并阻断病毒衣壳蛋白合成而具有抗病毒活性。
-
EG00229
EG00229 是一种神经纤维蛋白 1 受体 (NRP1) 拮抗剂。EG00229 选择性抑制 VEGF-A 与 NRP1 b1 域的结合, IC50 为 3μM,但对 VEGFA 与 VEGFR-1 和 VEGFR-2 的结合没有影响。
021-51111890
购物车()
sales@molnova.cn

