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911678-60-9

911678-60-9 Structure

911678-60-9 Structure
IdentificationBack Directory
[Name]

2,4-Quinazolinediamine, N4-cyclohexyl-N2-(3,4-difluorophenyl)-
[CAS]

911678-60-9
[Synonyms]

2,4-Quinazolinediamine, N4-cyclohexyl-N2-(3,4-difluorophenyl)-
[Molecular Formula]

C20H20F2N4
[MOL File]

911678-60-9.mol
[Molecular Weight]

354.4
Chemical PropertiesBack Directory
[Boiling point ]

531.6±60.0 °C(predicted)
[density ]

1.330±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)
[storage temp. ]

2-8°C
[solubility ]

DMSO: 2mg/mL, clear
[form ]

powder
[pka]

7.38±0.30(predicted)
[color ]

white to beige
Safety DataBack Directory
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Biological Activity]

Gs-biasedβ2 subtype-selective adrenergic receptor (AR) negative allosteric modulator (NAM) th at inhibits β-arrestin recruitmentbut not Gs coupling to β2AR.

DFPQ is a Gs-biasedβ2 subtype-selective adrenergic receptor (AR) negative allosteric modulator (NAM) th at inhibits β-arrestin recruitment (IC50 = 600 nM; 30-min DFPQ pretreatment prior to 12-min 1 μM ISO induction)but not Gs coupling to β2AR (30-min 10 μM DFPQ pretreatment prior to 10-min 1 μM ISO-induced cAMP production). DFPQ effectively inhibits agonist-induced β2AR phosphorylation (IC50 = 2.6 μM; 30-min DFPQ pretreatment prior to 10-min 1 μM ISO induction) and internalization (100% inhibition by 30-min 10 μM DFPQ prior to 1h 10 μM ISO) and protects against the functional desensitization of β-agonist-mediated regulation in cell and tissue models with minimal effects on β1AR.
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