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XL413 HCl

🥰Excellent
Catalog No. T71339Cas No. 1169562-71-3
Alias XL413 hydrochloride, BMS-863233 HCl

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 HCl

XL413 HCl

🥰Excellent
Purity: 99.67%
Catalog No. T71339Alias XL413 hydrochloride, BMS-863233 HClCas 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 SizePriceAvailabilityQuantity
1 mg$57In Stock
5 mg$122In Stock
10 mg$169In Stock
25 mg$296In Stock
50 mg$497In Stock
100 mg$723In Stock
500 mg$1,520In Stock
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Purity:99.67%
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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
CDC7:3.4 nM, CK2:215 nM, Pim1:42 nM, pMCM:118 nM(EC50)
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]
AliasXL413 hydrochloride, BMS-863233 HCl
Chemical Properties
FormulaC14H12ClN3O2.xHCl
Cas No.1169562-71-3
Relative Density.No data available
Storage & Solubility Information
Storagestore at low temperature | Shipping with blue ice.
Solubility Information
H2O: 9.0 mg/mL, Sonication is recommended.
DMSO: 3.1 mg/mL, Sonication and heating are recommended.

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Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
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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