Powder: -20°C for 3 years | In solvent: -80°C for 1 year
JZP-430 is an effective, highly selective, irreversible inhibitor of α/β-hydrolase domain 6 (ABHD6) (IC50: 44 nM). It also shows ~230-fold selectivity over fatty acid amide hydrolase (FAAH) and lysosomal acid lipase (LAL).
パッケージサイズ | 在庫状況 | 単価(税別) | |||
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サンプルについてお問い合わせ | |||||
1 mg | 在庫あり | ¥ 23,500 | |||
5 mg | 在庫あり | ¥ 46,500 | |||
10 mg | 在庫あり | ¥ 70,500 | |||
25 mg | 在庫あり | ¥ 129,500 | |||
50 mg | 在庫あり | ¥ 182,000 | |||
100 mg | 在庫あり | ¥ 248,000 | |||
1 mL * 10 mM (in DMSO) | 在庫あり | ¥ 50,000 |
説明 | JZP-430 is an effective, highly selective, irreversible inhibitor of α/β-hydrolase domain 6 (ABHD6) (IC50: 44 nM). It also shows ~230-fold selectivity over fatty acid amide hydrolase (FAAH) and lysosomal acid lipase (LAL). |
ターゲット&IC50 | ABHD6:44 nM(Human) |
分子量 | 354.47 |
分子式 | C16H26N4O3S |
CAS No. | 1672691-74-5 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 90 mg/mL (253.9 mM), Sonication is recommended.
You can also refer to dose conversion for different animals. 詳細
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc.
JZP-430 1672691-74-5 Metabolism MAGL Lipase Monoacylglycerol lipase inhibit JZP430 Inhibitor JZP 430 inhibitor