ChemicalBook--->CAS DataBase List--->2136278-38-9

2136278-38-9

2136278-38-9 Structure

2136278-38-9 Structure
IdentificationBack Directory
[Name]

2-Pyridinecarboxamide, 4-[[6-[[[[4-chloro-3-(trifluoromethyl)phenyl]amino]iminomethyl]amino]-3-pyridinyl]oxy]-N-methyl-
[CAS]

2136278-38-9
[Synonyms]

2-Pyridinecarboxamide, 4-[[6-[[[[4-chloro-3-(trifluoromethyl)phenyl]amino]iminomethyl]amino]-3-pyridinyl]oxy]-N-methyl-
[Molecular Formula]

C20H16ClF3N6O2
[MOL File]

2136278-38-9.mol
[Molecular Weight]

464.83
Chemical PropertiesBack Directory
[density ]

1.47±0.1 g/cm3(Predicted)
[form ]

Solid
[pka]

13.89±0.46(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Description]

DCZ3301 is an aryl-guanidino inhibitor that induces cell apoptosis and cell cycle arrest via suppressing the PI3K/AKT pathway in T-cell leukemia/lymphoma. DCZ3301 induces G2/M cell cycle arrest, and associates with downregulation of CDK1, cyclin B1, and cdc25C. DCZ3301 also induces cell apoptosis by decreasing MMP in T-cell leukemia/lymphoma cells.
[Uses]

DCZ3301 is a potent aryl-guanidino inhibitor. DCZ3301 inhibits cell proliferation, induces G2/M cell cycle arrest and apoptosis. DCZ3301 inhibits the activation of the PI3K/AKT pathway by downregulating the protein expression of PI3K and phosphorylation of AKT. DCZ3301 can be used in research of cancer[1].
[References]

[1] Xiao W, et, al. DCZ3301, a novel aryl-guanidino inhibitor, induces cell apoptosis and cell cycle arrest via suppressing the PI3K/AKT pathway in T-cell leukemia/lymphoma. Acta Biochim Biophys Sin (Shanghai). 2018 Jul 1;50(7):643-650. DOI:10.1093/abbs/gmy047
Spectrum DetailBack Directory
[Spectrum Detail]

2-Pyridinecarboxamide, 4-[[6-[[[[4-chloro-3-(trifluoromethyl)phenyl]amino]iminomethyl]amino]-3-pyridinyl]oxy]-N-methyl-(2136278-38-9)1HNMR
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