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HomeProduct name listXL413 (BMS-863233)

XL413 (BMS-863233)

Synonym(s):(S)-8-Chloro-2-(pyrrolidin-2-yl)benzofuro[3,2-d]pyrimidin-4(3H)-one hydrochloride;BMS-863233;XL-413

XL413 (BMS-863233) Structural

What is XL413 (BMS-863233)?

The Uses of XL413 (BMS-863233)

XL413 is a potent and selective cell division cycle 7 homolog (CDC7) kinase inhibitor.

Biological Activity

XL413 hydrochloride is a potent and selective cell division cycle 7 homolog (CDC7) kinase inhibitor with IC50 of 3.4 nM, its selectivity over CK2, Pim-1 and pMCM2 are 63-, 12- and 35-fold. Phase 1/2.

in vitro

In MDA-MB-231T and Colo-205 cell lines,XL413 hydrochloride inhibits CDC7-specific phosphorylation of MCM2. XL413 also inhibited cell proliferation in Colo-205 cells, decreased cell viability, and stimulated caspase 3/7 activity. Furthermore, XL413 resulted in altered S-phase progression and subsequent apoptosis.

in vivo

In the Colo-205 xenograft model, XL413, at a dose of 3 mg/kg, inhibited 70% of phosphorylated MCM2 and caused significant regression of tumor growth at a dose of 100 mg/kg.

storage

Store at -20°C

Properties of XL413 (BMS-863233)

storage temp.  -20°C
solubility  DMSO: Insoluble;Ethanol: Insoluble
form  powder
color  white to beige
Water Solubility  Water: 46 mg/mL (141.03 mM)
Stability: Hygroscopic

Safety information for XL413 (BMS-863233)

Signal word Danger
Pictogram(s)
ghs
Skull and Crossbones
Acute Toxicity
GHS06
GHS Hazard Statements H301:Acute toxicity,oral

Computed Descriptors for XL413 (BMS-863233)

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