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ChemicalBook--->CAS DataBase List--->1353858-99-7

1353858-99-7

1353858-99-7 Structure

1353858-99-7 Structure
IdentificationBack Directory
[Name]

CX 6258 hydrochloride hydrate
[CAS]

1353858-99-7
[Synonyms]

CX-6258 HCl hydrate
CX6258 hydrochloride hydrate
CX 6258 hydrochloride hydrate
CX-6258 (hydrochloride hydrate)
CX-6258 hydrochloride hydrate (CX6258 hydrochloride hydrate)
(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 hydrate (1:1:1)
[Molecular Formula]

C26H27Cl2N3O4
[MDL Number]

MFCD26142938
[MOL File]

1353858-99-7.mol
[Molecular Weight]

516.42
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMSO : 25 mg/mL (48.41 mM; Need ultrasonic)
[form ]

Powder
[color ]

Yellow to orange
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

CX-6258 hydrochloride hydrate is a potent and kinase selective pan-Pim kinases inhibitor, with IC50s of 5 nM, 25 nM and 16 nM for Pim-1, Pim-2 and Pim-3, respectively[1].
[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:Exhibited dose dependent efficacy, with a 50 mg/kg dose producing 45% tumor growth inhibition (TGI) and a 100 mg/kg dose producing 75% TGI.
[References]

[1] Mustapha Haddach, Jerome Michaux, Michael K, Discovery of CX-6258. A Potent, Selective, and Orally Efficacious pan-Pim Kinases Inhibitor. ACS Med. Chem. Lett., 2012, 3 (2), pp 135-139
[2] Padmanabhan A, Gosc EB, Bieberich CJ. Stabilization of the prostate-specific tumor suppressor NKX3.1 by the oncogenic protein kinase Pim-1 in prostate cancer cells. J Cell Biochem. 2013 May;114(5):1050-7. DOI:10.1002/jcb.24444
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