SML0990

JW651

≥98% (HPLC)

• 別名: 1,1,1,3,3,3-Hexafluoropropan-2-yl 4-(bis(4-chlorophenyl)methyl)piperazine-1-carboxylate
• 実験式（ヒル表記法）: C₂₁H₁₈Cl₂F₆N₂O₂
• CAS番号: 1438416-22-8
• 分子量: 515.28
• MDL番号: MFCD28137685
• UNSPSCコード: 12352200
• PubChem Substance ID: 329825626
• NACRES: NA.77

特性

• アッセイ: ≥98% (HPLC)
• フォーム: powder
• 色: white to beige
• 溶解性: DMSO: 10 mg/mL, clear
• 保管温度: 2-8°C
• SMILES記法: ClC1=CC=C(C(C2=CC=C(Cl)C=C2)N3CCN(C(OC(C(F)(F)F)C(F)(F)F)=O)CC3)C=C1
• InChI: 1S/C21H18Cl2F6N2O2/c22-15-5-1-13(2-6-15)17(14-3-7-16(23)8-4-14)30-9-11-31(12-10-30)19(32)33-18(20(24,25)26)21(27,28)29/h1-8,17-18H,9-12H2
• InChI Key: UPIHQFKOCOKGEO-UHFFFAOYSA-N

詳細

生物化学的／生理学的作用

JW651 is a potent selective inhibitor of MAGL, the enzyme predominantly responsible for the degradation of the endocannabinoid 2-arachidonoylglycerol (2-AG). JW651 inhibited mouse MAGL with an IC₅₀ ~38 nM compared to 10,380 for ABHD6, a serine hydrolase that acts as an alternative hydrolase of 2-AG and >100,000 for FAAH, the hydrolase that degrades the endocannabinoid anandamide (AEA). JW651 was used as the MAGL inhibitor along with JW912, a fluorescent inihibitor of both MAGL and ABHD6.

JW651 is a potent selective inhibitor of MAGL; active in vivo.

特徴および利点

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安全性情報

• 保管分類コード: 11 - Combustible Solids
• WGK: WGK 3
• 引火点(°F): Not applicable
• 引火点(℃): Not applicable