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CUDA 98%

12-(3-Cyclohexylureido)dodecanoic acid

源叶(MedMol)
S23454
479413-68-8
C19H36N2O3
340.50
品牌 货号 产品规格 价格(RMB) 库存(上海) 北京 武汉 南京 购买数量
源叶(MedMol) S23454-10mg 98% ¥400.00元 10 - - -
源叶(MedMol) S23454-25mg 98% ¥580.00元 5 - - -
源叶(MedMol) S23454-50mg 98% ¥1000.00元 预计交期:2-3天 - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品

产品介绍

CUDA is a potent inhibitor of soluble epoxide hydrolase (sEH), with IC50s of 11.1 nM and 112 nM for mouse sEH and human sEH, respectively. CUDA selectively increases peroxisome proliferator-activated receptor (PPAR) alpha activity. CUDA may be valuable for the research of cardiovascular disease
产品描述: CUDA is a potent inhibitor of soluble epoxide hydrolase (sEH), with IC50s of 11.1 nM and 112 nM for mouse sEH and human sEH, respectively. CUDA selectively increases peroxisome proliferator-activated receptor (PPAR) alpha activity. CUDA may be valuable for the research of cardiovascular disease
靶点: PPARα;mouse she:11.1 nM (IC50);human she:112 nM (IC50);PPAR;EpoxideHydrolase
体外研究:
CUDA (10 μM; 18 hours) produces 6- and 3-fold increases of PPARalpha in COS-7 cells.

CUDA does not alter PPARalpha protein expression, and it competitively inhibits the binding of Wy-14643 (pirinixic acid) to the ligand binding domain of PPARalpha, suggesting that it functions as a PPARalpha ligand.
参考文献:
1. Morisseau C, et al. Structural refinement of inhibitors of urea-based soluble epoxide hydrolases. Biochem Pharmacol. 2002 May 1;63(9):1599-608.

2. Fang X, et al. Activation of peroxisome proliferator-activated receptor alpha by substituted urea-derived soluble epoxide hydrolase inhibitors. J Pharmacol Exp Ther. 2005 Jul;314(1):260-70.
溶解性: Soluble  in  DMSO
保存条件: 2-8℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.937 ml 14.684 ml 29.369 ml
5 mM 0.587 ml 2.937 ml 5.874 ml
10 mM 0.294 ml 1.468 ml 2.937 ml
50 mM 0.059 ml 0.294 ml 0.587 ml
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参考文献

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摩尔浓度计算器

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