简介: 货 号:LC2-A-4477 名 称:(2S)-N1-[4-甲基-5-[2-(2,2,2-三氟-1,1-二甲基乙基)-4-吡啶基]-2-噻唑基]-1,2-吡咯烷二甲酰胺 别 名:Alpelisib Free Base C A S :1217486-61-7 分子量:441.47 分子式:C19H22F3N5O2S 纯 度:HPLC/TLC:>99% 说 明: 文 献:Alpelisib, also known as BYL719, is a potent and selective phosphatidylinositol-3 kinase [alpha] inhibitor. It inhibited P110[alpha], p110[beta], p110[delta], and p110[gamma] with IC50 values of 5 nM, 1.2 µM, 0.29 µM and 0.25 µM, respectively, in biochemical assays. It inhibited the Akt phosphorylation with IC50 values of 74 nM in Rat1-myr-p110[alpha] cells, 2.2 µM in Rat1-myr-p110[beta] cells, and 1.2 µM in Rat1-myr-p110[delta] cells. Furet P., et al. "Discovery of NVP-BYL719 a potent and selective phosphatidylinositol-3 kinase alpha inhibitor selected for clinical evaluation." Bioorg. Med. Chem. Lett. 23: 3741-3748 (2013).Alpelisib showed dose- and time-dependent inhibition of PI3K[alpha] signaling in vivo and demonstrated robust anti-tumor response and tolerability in PIK3CA-dependent tumor models. Fritsch C., et al. "Characterization of the novel and specific PI3Kα inhibitor NVP-BYL719 and development of the patient stratification strategy for clinical trials." Mol. Cancer Ther. 13: 1117-1129 (2014).mTORC1 inhibition is necessary for sensitivity to PI3K p110[alpha] inhibition by alpelisib in PIK3CA-mutant breast cancer. Elkabets M., et al. "mTORC1 inhibition is required for sensitivity to PI3K p110α inhibitors in PIK3CA-mutant breast cancer." Sci. Transl. Med. 5: 196ra99 (2013).