Identification | Back 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 Properties | Back 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 Information | Back 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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Company Name: |
Lynnchem
|
Tel: |
86-(0)29-85992781 17792393971 |
Website: |
http://www.lynnchem.com/ |
Company Name: |
Novachemistry
|
Tel: |
44-20819178-90 02081917890 |
Website: |
https://www.novachemistry.com/ |
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