Powder: -20°C for 3 years | In solvent: -80°C for 1 year
MK-4409 is a novel and selective inhibitor of oxazole fatty acid amide hydrolase FAAH.MK-4409 can be used to study inflammatory and neuropathic pain.
パッケージサイズ | 在庫状況 | 単価(税別) |
---|---|---|
1 mg | 在庫あり | ¥ 67,500 |
2 mg | 在庫あり | ¥ 100,000 |
5 mg | 在庫あり | ¥ 165,000 |
10 mg | 在庫あり | ¥ 226,500 |
25 mg | 在庫あり | ¥ 342,000 |
50 mg | 在庫あり | ¥ 454,500 |
100 mg | 在庫あり | ¥ 631,500 |
説明 | MK-4409 is a novel and selective inhibitor of oxazole fatty acid amide hydrolase FAAH.MK-4409 can be used to study inflammatory and neuropathic pain. |
In vivo | MK-4409 (3, 30 and 100 mg/kg, p.o) administered to the mouse SNL model,continued to show excellent efficacy over a period of 10 days, with plasma exposures also obtained at the 3 and 24 hour time points after the 30 mg/kg dose. However a reduction in edema was observed in the animals within a few days, which may contribute to its anti-inflammatory properties. [1] |
別名 | MK4409, MK 4409 |
分子量 | 441.91 |
分子式 | C22H17ClFN3O2S |
CAS No. | 1207745-58-1 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
You can also refer to dose conversion for different animals. 詳細
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MK-4409 1207745-58-1 Metabolism Neuroscience FAAH MK4409 MK 4409 Inhibitor inhibitor inhibit