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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 Size | Price | Availability | Quantity |
---|---|---|---|
1 mg | $57 | In Stock | |
5 mg | $122 | In Stock | |
10 mg | $169 | In Stock | |
25 mg | $296 | In Stock | |
50 mg | $497 | In Stock | |
100 mg | $723 | In Stock | |
500 mg | $1,520 | In Stock |
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, Pim1:42 nM, pMCM:118 nM(EC50), CDC7:3.4 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] |
Alias | XL413 hydrochloride, BMS-863233 HCl |
Formula | C14H12ClN3O2.xHCl |
Cas No. | 1169562-71-3 |
Storage | store 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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