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AZD-8055

Chemical Structure : AZD-8055

CAS No.: 1009298-09-2

AZD-8055 (AZD8055, AZD 8055)

Catalog No.: PC-42576Not For Human Use, Lab Use Only.

AZD-8055 is a potent, selective, ATP-competitive and orally bioavailable mTOR inhibitor with IC50 of 0.8 nM.

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25 mg $98 In stock
50 mg $148 In stock
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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

AZD-8055 is a potent, selective, ATP-competitive and orally bioavailable mTOR inhibitor with IC50 of 0.8 nM.
AZD-8055 shows excellent selectivity (1,000-fold) against all class I PI3K isoforms and other PI3K-like kinases.
AZD-8055 inhibits the phosphorylation of mTORC1 substrates p70S6K and 4E-BP1, and phosphorylation of the mTORC2 substrate AKT and downstream proteins, also fully inhibits rapamycin-resistant T37/46 phosphorylation sites on 4E-BP1.
AZD-8055 potently inhibits proliferation and induces autophagy in H838 and A549 cells, exhibits tumor growth inhibition in vivo.

Physicochemical Properties

M.Wt 465.5447
Formula C25H31N5O4
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

Benzenemethanol, 5-[2,4-bis[(3S)-3-methyl-4-morpholinyl]pyrido[2,3-d]pyrimidin-7-yl]-2-methoxy-

References

1. Chresta CM, et al. Cancer Res. 2010 Jan 1;70(1):288-98.

2. Sini P, et al. Autophagy. 2010 May;6(4):553-4.

3. Jiang Q, et al. Cancer Res. 2011 Jun 15;71(12):4074-84.

4. Willems L, et al. Leukemia. 2012 Jun;26(6):1195-202.

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