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
- CAS NO.:1169562-71-3
- Empirical Formula: C14H13Cl2N3O2
- Molecular Weight: 326.18
- MDL number: MFCD28023577
- SAFETY DATA SHEET (SDS)
- Update Date: 2026-07-27 17:00:41
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) |
![]() Skull and Crossbones Acute Toxicity GHS06 |
| GHS Hazard Statements |
H301:Acute toxicity,oral |
Computed Descriptors for XL413 (BMS-863233)
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