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
2MG 145 In Stock
5MG 222 In Stock
10MG 380 In Stock
25MG 618 In Stock
50MG 861 In Stock
100MG 1161 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
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Biological Information

  • Product Name
    AZD-26
  • Note
    Research use only, not for human use.
  • Brief Description
    AZD-26 is an allosteric AKT inhibitor (IC50: 1.04 μM).
  • Description
    AZD-26 is an inhibitor of AKT.
  • In Vitro
    AKT-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.
  • 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.
  • Synonyms
    AZD-26 | AZD 26 | AZD26
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    allosteric Akt
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1357158-81-6
  • Formula Weight
    343.42
  • Molecular Formula
    C22H21N3O
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : 25 mg/mL 72.80 mM;
  • SMILES
    NC1(CCC1)c2ccc(cc2)c3ncc(cc3c4ccccc4)C(N)=O
  • Chemical Name
    6-[4-(1-Aminocyclobutyl)phenyl]-5-phenylpyridine-3-carboxamide

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • 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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