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1009821-06-0

1009821-06-0 Structure

1009821-06-0 Structure
IdentificationBack Directory
[Name]

PYRIMIDO[4,5-C]QUINOLINE-8-CARBOXYLIC ACID, 5-[(3-ETHYNYLPHENYL)AMINO]-
[CAS]

1009821-06-0
[Synonyms]

CX-5011
5-[(3-Ethynylphenyl)amino]-Pyrimido[4,5-c]quinoline-8-carboxylic acid
PYRIMIDO[4,5-C]QUINOLINE-8-CARBOXYLIC ACID, 5-[(3-ETHYNYLPHENYL)AMINO]-
[Molecular Formula]

C20H12N4O2
[MDL Number]

MFCD11977745
[MOL File]

1009821-06-0.mol
[Molecular Weight]

340.33
Chemical PropertiesBack Directory
[Boiling point ]

570.6±50.0 °C(Predicted)
[density ]

1.47±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

2.29±0.30(Predicted)
Hazard InformationBack Directory
[Uses]

CX-5011 free base is a potent CK2 inhibitor. CX-5011 free base also is a Rac-1 activator. CX-5011 free base induces methuosis and promotes macropinocytosis. CX-5011 free base induces apoptosis. CX-5011 free base decreases the expression of rpS6 phosphorylation[1][2].
[References]

[1] D'Amore C, et al. "Janus" efficacy of CX-5011: CK2 inhibition and methuosis induction by independent mechanisms. Biochim Biophys Acta Mol Cell Res. 2020 Nov;1867(11):118807. DOI:10.1016/j.bbamcr.2020.118807
[2] Salizzato V, et al. Inhibition of protein kinase CK2 by CX-5011 counteracts imatinib-resistance preventing rpS6 phosphorylation in chronic myeloid leukaemia cells: new combined therapeutic strategies. Oncotarget. 2016 Apr 5;7(14):18204-18. DOI:10.18632/oncotarget.7569
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