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United States (Change Country)A66 Chemical Structure
A66 is a highly specific and selective p110α inhibitor with IC50 of 32,30 and 43 nM for p110α, p110α/E545K, p110α/H1047R, respectively. A66 S potently blocks phosphorylation of Akt/PKB in a subgroup of the cell lines tested demonstrates that some cell types are highly dependent on p110α activity. A66 is more than 100 fold less active against the other class-I PI 3-kinase isoforms and had not inhibitory activity against 200 protein kinases when tested at 10 micromolar. This makes it the most selective and specific p110alpha inhibitor available for research purposes. A66 S is more efficacious at inducing growth delay in HCT116. While A66 S did not induce tumor regression in xenograft models the ability to induce growth delay indicates p110α selective have to ability to be effective as cytostatic agents in some tumor types. [1]
| Molecular Weight (WM): | 393.53 |
|---|---|
| Formula: | C17H23N5O2S2 |
| Solubility(R.T.:25°C): | DMSO 79mg/mL |
| Water <1mg/mL | |
| Ethanol 1mg/mL |
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;GENES & DEVELOPMENT, 26, 1573–1586 A66 purchased from Selleck
;GENES & DEVELOPMENT, 26, 1573–1586 A66 purchased from Selleck
;Dr. Zhang of Tianjin Medical University A66 purchased from Selleck
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