S80346 |
IWP L6 |
源葉(MedMol) | ≥98%(HPLC) |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 2.116 ml | 10.58 ml | 21.16 ml |
5 mM | 0.423 ml | 2.116 ml | 4.232 ml |
10 mM | 0.212 ml | 1.058 ml | 2.116 ml |
50 mM | 0.042 ml | 0.212 ml | 0.423 ml |
- 提示:詳情請下載說明書。
- 產品描述: IWP L6 (Porcn Inhibitor III) is a Porcn inhibitor with an EC50 of 0.5 nM.
- 靶點: EC50 Value: 0.5 nM;Porcupine
- 體外研究:
IWP-L6 (Porcn Inhibitor III) effectively suppressed the phosphorylation of dishevelled 2 (Dvl2) in HEK293 cells, a biochemical event associated with many Wnt-dependent cellular responses. IWP-L6 inhibits Wnt mediated branching morphogenesis in cultured embryonic kidneys .
- 體內研究:
IWP-L6 (Porcn Inhibitor III) is stable in human plasma over 24 h, it was rapidly metabolized in rat plasma (t1/2 = 190 min), murine plasma (t1/2 = 2 min), and the murine liver S9 fractions (t1/2 = 26 min). The major metabolites are the amide cleavage products. Similar species-dependent metabolitic profiles due to the involvement of carboxylesterase (CES) have been reported with other drug candidates. Despite its modest metabolic stability in mouse-derived plasma, IWP-L6 was highly active in zebrafish. IWP-L6 exhibited more potent activity
- 參考文獻:
1. Wang, X., et al., The development of highly potent inhibitors for porcupine. J Med Chem, 2013. 56(6): p. 2700-4.
- 溶解性: Soluble in DMSO
- 保存條件: -20°C
- 配置溶液濃度參考:
1mg 5mg 10mg 1 mM 2.116 ml 10.58 ml 21.16 ml 5 mM 0.423 ml 2.116 ml 4.232 ml 10 mM 0.212 ml 1.058 ml 2.116 ml 50 mM 0.042 ml 0.212 ml 0.423 ml
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本計算器可幫助您計算出特定溶液中溶質的質量、溶液濃度和體積之間的關系,公式為:
質量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)