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RK-287107

RK-287107
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Purity:99.59%
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RK-287107

Catalog No. T16761Cas No. 2171386-10-8
RK-287107 is an effective and specific inhibitor of tankyrase (IC50s: 14.3 and 10.6 nM for tankyrase-1 and tankyrase-2, respectively).
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Pack SizePriceAvailabilityQuantity
1 mg$57In Stock
5 mg$118In Stock
10 mg$187In Stock
25 mg$354In Stock
50 mg$497In Stock
100 mg$687In Stock
1 mL x 10 mM (in DMSO)$135In Stock
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Product Introduction

Bioactivity
Description
RK-287107 is an effective and specific inhibitor of tankyrase (IC50s: 14.3 and 10.6 nM for tankyrase-1 and tankyrase-2, respectively).
In vitro
RK-287107 (0.03-10 μM; 16 hours) also downregulates β-catenin signaling in cultured cells. 287107 (0.03-10 μM; 16 hours) induces the accumulation of tankyrase and Axin1/2. RK-87107 (0.01-10 μM; 12 hours) displays an antiproliferative effect on colorectal cancer cells harboring short adenomatous polyposis coli mutations. The 50% growth inhibition (GI50) value of RK-287107 on COLO-320DM cells is 0.449 μM. RK- [1].
In vivo
In a mouse xenograft model, RK-287107 (100 and 300 mg/kg; i.p. administration; once per day; 5-days on/ 2-days off schedule for 2 weeks) inhibits tumor growth [1].
Chemical Properties
Molecular Weight416.46
FormulaC22H26F2N4O2
Cas No.2171386-10-8
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 120 mg/mL (288.14 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.4012 mL12.0060 mL24.0119 mL120.0595 mL
5 mM0.4802 mL2.4012 mL4.8024 mL24.0119 mL
10 mM0.2401 mL1.2006 mL2.4012 mL12.0060 mL
20 mM0.1201 mL0.6003 mL1.2006 mL6.0030 mL
50 mM0.0480 mL0.2401 mL0.4802 mL2.4012 mL
100 mM0.0240 mL0.1201 mL0.2401 mL1.2006 mL

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Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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