CAS 1169562-71-3
:8-Chloro-2-(2S)-2-pyrrolidinylbenzofuro[3,2-d]pyrimidin-4(3H)-one chlorhydrate (1:?)
- BMS-863233 HCl
(S)-8-Chloro-2-(pyrrolidin-2-yl)benzofuro[3,2-d]pyrimidin-4(3H)-one xhydrochloride
CAS :(S)-8-Chloro-2-(pyrrolidin-2-yl)benzofuro[3,2-d]pyrimidin-4(3H)-one xhydrochlorideDegré de pureté :98%Masse moléculaire :326.18g/molXL413
CAS :Produit contrôléStability Hygroscopic
Applications XL413 is a potent and selective cell division cycle 7 homolog (CDC7) kinase inhibitor.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Koltun, E., et al.: Bioorg. Med. Chem. Lett., 22, 3727 (2012)Formule :C14H13Cl2N3O2Couleur et forme :NeatMasse moléculaire :326.18XL413 xHCl
CAS :BMS-863233 HCl is an ATP-competitive Cdc7 inhibitor (IC50: 3.4 nM) that is potent and selective.BMS-863233 HCl inhibited CK2 and PIM1 with IC50 values of 215
Formule :C14H12ClN3O2·xHClDegré de pureté :99.37% - 99.67%Couleur et forme :SolidMasse moléculaire :326.18XL413 hydrochloride
CAS :XL413 hydrochloride is a potent small-molecule inhibitor, which is a synthetic compound specifically designed to target protein kinases. It acts as a selective inhibitor of Cdc7 kinase, a serine/threonine kinase essential for the initiation of DNA replication. This kinase is involved in the phosphorylation of MCM2 and the activation of the pre-replicative complex, a critical step in the S-phase of the cell cycle. By inhibiting Cdc7, XL413 hydrochloride effectively halts cell cycle progression, thereby impacting cellular proliferation.
Formule :C14H13Cl2N3O2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :326.18 g/mol



