Title : Small molecule H89 renders the phosphorylation of S6K1 and AKT resistant to mTOR inhibitors.

Pub. Date : 2020 May 29

PMID : 32347294






4 Functional Relationships(s)
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1 Small molecule H89 renders the phosphorylation of S6K1 and AKT resistant to mTOR inhibitors. N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide ribosomal protein S6 kinase B1 Homo sapiens
2 Here, we report that H89 (N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide), a well-characterized ATP-mimetic kinase inhibitor, renders the phosphorylation of S6K1 and AKT resistant to mTOR inhibitors across multiple cell lines. N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide ribosomal protein S6 kinase B1 Homo sapiens
3 Here, we report that H89 (N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide), a well-characterized ATP-mimetic kinase inhibitor, renders the phosphorylation of S6K1 and AKT resistant to mTOR inhibitors across multiple cell lines. N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide ribosomal protein S6 kinase B1 Homo sapiens
4 Moreover, H89 prevented the dephosphorylation of AKT and S6K1 under nutrient depleted conditions. N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide ribosomal protein S6 kinase B1 Homo sapiens