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1914078-41-3

1914078-41-3 Structure

1914078-41-3 Structure
IdentificationBack Directory
[Name]

eCF506
[CAS]

1914078-41-3
[Synonyms]

eCF506
ECF506; ECF-506; ECF 506.
Carbamic acid, N-[4-[4-amino-1-[2-[4-(dimethylamino)-1-piperidinyl]ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-2-methoxyphenyl]-, 1,1-dimethylethyl ester
[Molecular Formula]

C26H38N8O3
[MDL Number]

MFCD31657410
[MOL File]

1914078-41-3.mol
[Molecular Weight]

510.63
Chemical PropertiesBack Directory
[Boiling point ]

650.3±55.0 °C(Predicted)
[density ]

1.29±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO:15.0(Max Conc. mg/mL);29.38(Max Conc. mM)
Ethanol:15.0(Max Conc. mg/mL);29.38(Max Conc. mM)
[form ]

A crystalline solid
[pka]

12.60±0.70(Predicted)
[color ]

Off-white to yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS05,GHS08,GHS07
[Signal word ]

Danger
[Hazard statements ]

H315-H318-H334-H317-H341-H361-H370-H335-H413
[Precautionary statements ]

P201-P202-P260-P264-P270-P272-P273-P280-P284-P302+P352-P304+P341-P305+P351+P338-P310-P308+P313-P321-P362+P364-P333+P313-P342+P311-P363-P405-P501
Hazard InformationBack Directory
[Uses]

eCF506, induces a very potent antiproliferative effect in both MCF7 and MDA-MB-231 cells. eCF506 inhibits phosphorylation of SRC and FAK at low nanomolar levels, with complete inhibition observed at 100 nM.
[in vivo]

eCF506 shows a moderate oral bioavailability (25.3%). A significant reduction of phospho-SRCY416 is observed in the xenograft sections from mice treated with eCF506 relative to the untreated animal controls[1].

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