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2-Phenyl-2-(1-piperidinyl)propane 是一种具有可逆性、选择性的人 CYP2B6抑制剂,其 IC50为 5.1 μM,Ki 为 5.6。它对 CYP2D6 、CYP3A 均有抑制作用,且 IC50值分别为74 μM、200 μM。
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2-Phenyl-2-(1-piperidinyl)propane 是一种具有可逆性、选择性的人 CYP2B6抑制剂,其 IC50为 5.1 μM,Ki 为 5.6。它对 CYP2D6 、CYP3A 均有抑制作用,且 IC50值分别为74 μM、200 μM。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 179 | 现货 | |
5 mg | ¥ 395 | 现货 | |
10 mg | ¥ 663 | 现货 | |
25 mg | ¥ 1,330 | 现货 | |
50 mg | ¥ 1,950 | 现货 | |
100 mg | ¥ 2,980 | 现货 | |
200 mg | ¥ 4,320 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 393 | 现货 |
产品描述 | 2-Phenyl-2-(1-piperidinyl)propane (PPP), an analog of phencyclidine |
靶点活性 | CYP2B6:5.1 μM (IC50), CYP2C19:>300 μM (IC50), CYP2A6:>300 μM (IC50), CYP2D6:74 μM (IC50), CYP2B6:5.6 μM (Ki), CYP1A2:>300 μM (IC50), CYP2C8:>300 μM (IC50), CYP3A:200 μM (IC50), CYP2E1:>300 μM (IC50), CYP2C9:>300 μM (EC50) |
体内活性 | 2-Phenyl-2-(1-piperidinyl)propane (PPP) inactivated the 7-(benzyloxy)resorufin O-dealkylation activity of liver microsomes obtained from phenobarbital-induced rats with a K(I) of 11 microM.?The 7-ethoxy-4-(trifluoromethyl)coumarin O-deethylation activity of purified rat liver P450 2B1 and expressed human P450 2B6 was inactivated by PPP in a reconstituted system containing NADPH-cytochrome P450 reductase and lipid[1] |
分子量 | 203.32 |
分子式 | C14H21N |
CAS No. | 92321-29-4 |
Smiles | CC(C)(N1CCCCC1)c1ccccc1 |
密度 | 0.969g/cm3 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | ||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 30 mg/mL (99.8 mM) | ||||||||||||||||||||||||||||||
溶液配制表 | |||||||||||||||||||||||||||||||
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