A-674563

CAS No. 552325-73-2

A-674563 ( A 674563;A674563 )

Catalog No. M15000 CAS No. 552325-73-2

A-674563 is a potent, selective and orally available AKT inhibitor with Ki of 11 nM (Akt1).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 187 In Stock
5MG 124 In Stock
10MG 493 In Stock
25MG 935 In Stock
50MG 1492 In Stock
100MG 2518 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    A-674563
  • Note
    Research use only, not for human use.
  • Brief Description
    A-674563 is a potent, selective and orally available AKT inhibitor with Ki of 11 nM (Akt1).
  • Description
    A-674563 is a potent, selective and orally available AKT inhibitor with Ki of 11 nM (Akt1); increases the efficacy of paclitaxel in a PC-3 xenograft model; enhances the transcription of several chondrocyte marker genes, including Col2a1, Acan and Col11a2, in mouse primary chondrocytes by inhibiting Sox9 degradation through the ubiquitin-proteasome pathway; also suppresses FLT3-ITD positive AML both in vitro and in vivo.
  • Synonyms
    A 674563;A674563
  • Pathway
    Cytoskeleton/Cell Adhesion Molecules
  • Target
    Akt
  • Recptor
    Akt1;CDK2;ERK2;GSK-3β;PKA
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    552325-73-2
  • Formula Weight
    358.40
  • Molecular Formula
    C22H22N4O
  • Purity
    >98% (HPLC)
  • Solubility
    10 mM in DMSO
  • SMILES
    N[C@@H](CC1=CC=CC=C1)COC2=CC(C3=CC4=C(NN=C4C)C=C3)=CN=C2
  • Chemical Name
    Benzeneethanamine, a-[[[5-(3-methyl-1H-indazol-5-yl)-3-pyridinyl]oxy]methyl]-, (aS)-

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Luo Y, et al. Mol Cancer Ther. 2005 Jun;4(6):977-86.
2. Tei H, et al. Hum Cell. 2015 Jul;28(3):114-21.
3. Wang A, et al. Oncotarget. 2016 May 17;7(20):29131-42.
4. Kobayashi T, et al. Biochem Biophys Res Commun. 2018 Jan 1;495(1):1468-1475.
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