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XL 413 hydrochloride

 - BMS 863233 hydrochloride
Axon 2268
  • Parent CAS:  1169558-38-6
Purity:  99%
  • Soluble in water and DMSO
  • MF:  C14H12ClN3O2.HCl
  • MW:  326.18

Description

XL 413 hydrochloride is a potent, selective and orally bioavailable CDC7 kinase inhibitor with an IC50 value of 3.4 nM. It inhibits tumor-cell proliferation and induces apoptosis in CDC7-overexpressing models by disrupting DNA replication initiation and S-phase progression.

CDC7 regulates origin firing and minichromosome maintenance (MCM) protein phosphorylation during DNA replication. XL 413 is valuable for studying cell-cycle dependency, replication-stress biology and CDC7-targeted oncology pharmacology.

Key Features

  • Potent CDC7 kinase inhibitor
  • IC50: 3.4 nM
  • Selective over broad kinase panels
  • Induces apoptosis in CDC7-dependent tumor-cell models

Applications

  • CDC7 pharmacology
  • DNA replication and S-phase studies
  • Cell-cycle checkpoint research
  • Oncology target-validation assays

More Information

Certificate of Analysis

Material Safety Data Sheet

Parent CAS No. 1169558-38-6
Chemical Name (S)-8-Chloro-2-(pyrrolidin-2-yl)benzofuro[3,2-d]pyrimidin-4(3H)-one hydrochloride
MFCD N.A.
Short Description CDC7 inhibitor

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