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JNJ-42165279 是一种 FAAH 抑制剂,抑制 hFAAH 和 rFAAH,IC50分别为70 ± 8 nM 和 313 ± 28 nM。它对其他酶、离子通道、转运蛋白和受体具有高度选择性。
JNJ-42165279 是一种 FAAH 抑制剂,抑制 hFAAH 和 rFAAH,IC50分别为70 ± 8 nM 和 313 ± 28 nM。它对其他酶、离子通道、转运蛋白和受体具有高度选择性。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 179 | 现货 | |
2 mg | ¥ 257 | 现货 | |
5 mg | ¥ 413 | 现货 | |
10 mg | ¥ 678 | 现货 | |
25 mg | ¥ 1,360 | 现货 | |
50 mg | ¥ 1,980 | 现货 | |
100 mg | ¥ 2,970 | 现货 | |
200 mg | ¥ 4,170 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 598 | 现货 |
产品描述 | JNJ-42165279 covalently inactivates the FAAH enzyme but is highly selective with regard to other enzymes, ion channels, transporters, and receptors. JNJ-42165279 (10 μM) exhibits high selectivity against a panel of 50 receptors, enzymes, transporters, and ion-channels, at which concentration it does not produce >50% inhibition of binding to any of the targets. Fortunately, JNJ-42165279 (10 μM) also does not inhibit CYPs (1A2, 2C8, 2C9, 2C19, 2D6, 3A4) or hERG. |
靶点活性 | FAAH (rat):313 ± 28 nM, FAAH (human):70 ± 8 nM |
别名 | JNJ42165279 |
分子量 | 410.8 |
分子式 | C18H17ClF2N4O3 |
CAS No. | 1346528-50-4 |
Smiles | FC1(F)Oc2ccc(CN3CCN(CC3)C(=O)Nc3cnccc3Cl)cc2O1 |
密度 | 1.52 g/cm3 (Predicted) |
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: 45 mg/mL (109.54 mM) | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
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