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XL413 xHCl

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Catalog No. T71339Cas No. 1169562-71-3
Alias XL-413 Hydrochloride, BMS-863233 HCl, BMS-863233 xHCl

XL413 HCl is an ATP-competitive Cdc7 inhibitor (IC50: 3.4 nM) that is potent and selective.XL413 HCl inhibited CK2 and PIM1 with IC50 values of 215 and 42 nM, respectively.XL413 HCl showed an EC50 value of 118 against pMCM.

XL413 xHCl

XL413 xHCl

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Purity: 99.48%
Catalog No. T71339Alias XL-413 Hydrochloride, BMS-863233 HCl, BMS-863233 xHClCas No. 1169562-71-3
XL413 HCl is an ATP-competitive Cdc7 inhibitor (IC50: 3.4 nM) that is potent and selective.XL413 HCl inhibited CK2 and PIM1 with IC50 values of 215 and 42 nM, respectively.XL413 HCl showed an EC50 value of 118 against pMCM.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$57In StockIn Stock
5 mg$122In StockIn Stock
10 mg$169In StockIn Stock
25 mg$296In StockIn Stock
50 mg$497In StockIn Stock
100 mg$723In StockIn Stock
500 mg$1,520-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.48%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
XL413 HCl is an ATP-competitive Cdc7 inhibitor (IC50: 3.4 nM) that is potent and selective.XL413 HCl inhibited CK2 and PIM1 with IC50 values of 215 and 42 nM, respectively.XL413 HCl showed an EC50 value of 118 against pMCM.
Targets&IC50
CK2:215 nM, CDC7:3.4 nM, pMCM:118 nM(EC50), Pim1:42 nM
In vitro
XL413 HCl shows cytotoxic effects on tumors, with IC50 of 22.9 µM in HCC1954 cells and 1.1 µM in Colo-205 cells.[2]
BMS-863233 HCl is an effective DDK inhibitor in vitro, with an IC50 of 22.7 nM.[2]
XL413 HCl is defective in inhibiting DDK-dependent Mcm2 phosphorylation in HCC1954 cells but is effective in Colo-205 cells.[2]
In vivo
XL413 HCl (10, 30, or 100 mg/kg; p.o.; mice) is well tolerated at all doses, with no significant body weight loss.[1]
XL413 HCl (100 mg/kg; p.o.; mice) show excellent plasma exposures in mice and possesses good PK properties.[1]
SynonymsXL-413 Hydrochloride, BMS-863233 HCl, BMS-863233 xHCl
Chemical Properties
Molecular Weight326.18
FormulaC14H12ClN3O2.xHCl
Cas No.1169562-71-3
SmilesCl.Clc1ccc2oc3c(nc([nH]c3=O)[C@@H]3CCCN3)c2c1 |lp:0:3,1:3,6:2,9:1,11:1,13:2,18:1|
Relative Density.No data available
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
H2O: 9.00 mg/mL (27.59 mM), Sonication is recommended.
DMSO: 3.10 mg/mL (9.50 mM), Sonication and heating are recommended.
Solution Preparation Table
DMSO/H2O
1mg5mg10mg50mg
1 mM3.0658 mL15.3290 mL30.6579 mL153.2896 mL
5 mM0.6132 mL3.0658 mL6.1316 mL30.6579 mL
H2O
1mg5mg10mg50mg
10 mM0.3066 mL1.5329 mL3.0658 mL15.3290 mL
20 mM0.1533 mL0.7664 mL1.5329 mL7.6645 mL

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
% DMSO
%
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