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别名 JNJ42165279
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 | |
| 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) | ¥ 385 | 现货 |
JNJ-42165279 相关产品
| 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/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| 溶解度信息 | DMSO: 45 mg/mL (109.54 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
| 体内实验配方 | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2.5 mg/mL (6.09 mM), Sonication is recommended. 请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。 | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
DMSO
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