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A-674563

Chemical Structure : A-674563

CAS No.: 552325-73-2

A-674563 (A 674563;A674563)

Catalog No.: PC-43433Not For Human Use, Lab Use Only.

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

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

A-674563 is a potent, selective and orally available AKT inhibitor with Ki of 11 nM (Akt1).
A-674563 increases the efficacy of paclitaxel in a PC-3 xenograft model.
A-674563 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.
A-674563 also suppresses FLT3-ITD positive AML both in vitro and in vivo.

Physicochemical Properties

M.Wt 358.44
Formula C22H22N4O
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

Benzeneethanamine, a-[[[5-(3-methyl-1H-indazol-5-yl)-3-pyridinyl]oxy]methyl]-, (aS)-

References

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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