A potent

AZD 8055 – 5 mg

Brand:
Cayman
CAS:
1009298-09-2
Storage:
-20
UN-No:
Non-Hazardous - /

AZD 8055 is a potent, selective ATP-competitive inhibitor of mTOR, exhibiting an IC50 value of 0.8 nM.{28008} It is ~1,000-fold selective for mTOR over all PI3K isoforms and exhibits no activity against a panel of 260 kinases at concentrations up to 10 µM. AZD 8055 inhibits proliferation of A549 and H838 cells with IC50 values of 53 and 20 nM, respectively. It inhibits growth of a variety of human tumor xenografts by at least 65% in mice at daily oral doses of 20 mg/kg.{28008}  

 

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Description

A potent, selective ATP-competitive inhibitor of mTOR (IC50 = 0.8 nM); inhibits proliferation of A549 (IC50 = 53 nM) and H838 cells (IC50 = 20 nM) as well as several human tumor xenografts (>65% at 20 mg/kg)

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

Synonyms:  CCG-168

Molecular weight: 465.5

CAS: 1009298-09-2

Purity: ≥98%

Formulation: A crystalline solid

Product Type|Biochemicals|Kinase Inhibitors|mTOR||Product Type|Biochemicals|Small Molecule Inhibitors|Kinases||Research Area|Cancer|Cell Signaling|PI3K/Akt/mTOR Signaling

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