AZD-26
CAS No. 1357158-81-6
AZD-26( AZD-26 | AZD 26 | AZD26 )
Catalog No. M17970 CAS No. 1357158-81-6
AZD-26 is an allosteric AKT inhibitor (IC50: 1.04 μM).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 188 | In Stock |
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| 5MG | 235 | In Stock |
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| 10MG | 401 | In Stock |
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| 25MG | 653 | In Stock |
|
| 50MG | 890 | In Stock |
|
| 100MG | 1200 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameAZD-26
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NoteResearch use only, not for human use.
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Brief DescriptionAZD-26 is an allosteric AKT inhibitor (IC50: 1.04 μM).
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DescriptionAZD-26 is an inhibitor of AKT.
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In VitroAKT-IN-1 is able to potently inhibit phosphorylation of AKT in cells at both Thr308 and Ser473, with IC50s of 0.422 and 0.322 μM, respectively. AKT-IN-1 inhibits the phosphorylation of ribosomal protein S6, a downstream effector of the PI3K-AKT pathway. AKT-IN-1 potently inhibits the phosphorylation of PRAS40.
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In VivoThe 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.
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SynonymsAZD-26 | AZD 26 | AZD26
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PathwayOthers
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TargetOther Targets
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Recptorallosteric Akt
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Research Area——
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Indication——
Chemical Information
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CAS Number1357158-81-6
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Formula Weight343.42
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Molecular FormulaC22H21N3O
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Purity>98% (HPLC)
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SolubilityDMSO : 25 mg/mL 72.80 mM;
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SMILESNC1(CCC1)c2ccc(cc2)c3ncc(cc3c4ccccc4)C(N)=O
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Chemical Name6-[4-(1-Aminocyclobutyl)phenyl]-5-phenylpyridine-3-carboxamide
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Kettle JG, et al. Diverse heterocyclic scaffolds as allosteric inhibitors of AKT. J Med Chem. 2012 Feb 9;55(3):1261-73.
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