ChemicalBook--->CAS DataBase List--->1353859-00-3

1353859-00-3

1353859-00-3 Structure

1353859-00-3 Structure
IdentificationBack Directory
[Name]

CX6258(HCL)
[CAS]

1353859-00-3
[Synonyms]

CX6285
CX6258(HCL)
CX6258(HCL) USP/EP/BP
CX-6258 Hydrochloride
Pim-Kinase Inhibitor X
CX6258 hydrochloride PIM inhibitor CX-6258 HCL
CX6258 hydrochloride,Pim,CX6258,CX-6258,Pim kinases,4E-BP1,CX 6258 hydrochloride,Inhibitor,CX 6258,Bad,inhibit
(E)-5-Chloro-3-((5-(3-(4-methyl-1,4-diazepane-1-carbonyl)phenyl)furan-2-yl)methylene)indolin-2-one hydrochloride
(3E)-5-chloro-3-[[5-[3-[(hexahydro-4-methyl-1H-1,4-diazepin-1-yl)carbonyl]phenyl]-2-furanyl]methylene]-1,3-dihydro-2H-Indol-2-one, hydrochloride (1:1)
CX6258(HCL) 2H-Indol-2-one, 5-chloro-3-[[5-[3-[(hexahydro-4-methyl-1H-1,4-diazepin-1-yl)carbonyl]phenyl]-2-furanyl]methylene]-1,3-dihydro-, hydro
[Molecular Formula]

C26H24ClN3O3.HCl
[MOL File]

1353859-00-3.mol
[Molecular Weight]

498.4
Chemical PropertiesBack Directory
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

DMSO:57.0(Max Conc. mg/mL);114.37(Max Conc. mM)
Ethanol:1.0(Max Conc. mg/mL);2.01(Max Conc. mM)
[form ]

Solid
[color ]

Orange to red
Hazard InformationBack Directory
[Uses]

CX-6258 HCl is a potent, orally efficacious pan-Pim kinase inhibitor.
[in vivo]

CX-6258 (50-100 mg/kg; p.o; daily; over a period of 21 days) exhibits robust in vivo efficacy in two Pim kinases driven tumor models[1].

Animal Model:Nude mice, MV-4-11 xenograft models[1]
Dosage:50 mg/kg, 100 mg/kg.
Administration:Oral administration; once daily; over a period of 21 days.
Result:Exhibitd dose dependent efficacy, with a 50 mg/kg dose producing 45% tumor growth inhibition (TGI) and a 100 mg/kg dose producing 75% TGI.
Spectrum DetailBack Directory
[Spectrum Detail]

CX6258(HCL)(1353859-00-3)1HNMR
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