ChemicalBook--->CAS DataBase List--->1357158-81-6

1357158-81-6

1357158-81-6 Structure

1357158-81-6 Structure
IdentificationBack Directory
[Name]

AZD-26
[CAS]

1357158-81-6
[Synonyms]

AZD-26
AKT-IN-1
AZD-26 ≥95%
AKT inhibitor 1
AZD-26;AZD 26;AZD26
6-(4-(1-aminocyclobutyl)phenyl)-5-phenylnicotinamide
3-PyridinecarboxaMide, 6-[4-(1-aMinocyclobutyl)phenyl]-5-pheny
6-[4-(1-Aminocyclobutyl)phenyl]-5-phenyl-3-pyridinecarboxamide
[Molecular Formula]

C22H21N3O
[MDL Number]

MFCD25977103
[MOL File]

1357158-81-6.mol
[Molecular Weight]

343.42
Chemical PropertiesBack Directory
[Boiling point ]

496.4±45.0 °C(Predicted)
[density ]

1.210±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO : 25 mg/mL (72.80 mM)
[form ]

Solid
[pka]

14.75±0.50(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

AZD-26 is an allosteric inhibitor of AKT kinase.
[in vivo]

The effects of AKT-IN-1 (Compound 26) in vivo are characterized by measuring the pharmacodynamic activity of AKT-IN-1 in a BT474c breast adenocarcinoma xenograft model. Following acute doses of 100 and 200 mg/kg, AKT-IN-1 potently inhibits the phosphorylation of its downstream substrate GSK3β as well as the phosphorylation of AKT (Ser473), with a potency consistent with its pharmacokinetic profile. The in vivo activity of AKT-IN-1 is further characterized by measuring the effects on the growth of tumor cell xenografts. Continuous (daily) oral dosing of AKT-IN-1 (100 and 200 mg/kg) to nude mice bearing BT474c breast adenocarcinoma xenografts results in inhibition of tumor growth in a dose-dependent manner. When dosed at 200 mg/kg daily, AKT-IN-1 causes significant tumor growth inhibition[1].

[storage]

Store at -20°C
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