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产地 | 中国 |
品牌 | 爱必信(absin) |
货号 | abs814051 |
用途 | 见爱必信官网 |
英文名称 | 见爱必信官网 |
包装规格 | 50mg,50mg,50mg,5mg,5mg,5mg,10mg,10mg,10mg |
纯度 | >98%% |
CAS编号 | 958852-01-2 |
别名 | GSK 1059615; GSK-1059615 |
是否进口 | 否 |
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抑制剂描述: 产品名称:GSK1059615 产品别名:见爱必信官网 英文别名:GSK1059615 靶点:PI3K;mTOR CAS:958852-01-2 纯度:>98% 外观:见爱必信官网 保存方法:Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution. 描述: GSK1059615是一种PI3Kα/β/δ/γ (可逆的)和mTOR的双重抑制剂,IC50分别为0.4 nM/0.6 nM/2 nM/5 nM和12 nM。GSK1059615也抑制mTOR,IC50为12 nM。GSK1059615抑制PI3K通路,诱导细胞停滞在G1期,可观察到凋亡。GSK1059615有效作用于胸腺癌细胞。 溶解性:DMSO :2mg/ml(6 mM) 体外研究:
The pyridinylquinoline derivative GSK1059615 is a novel, ATP-competitive, and reversible inhibitor of the class I family of PI3Ks. GSK1059615 inhibits PI3K signaling, induces G1 arrest and apoptosis, especially in breast tumor cells. Data summarized in another review also shows that GSK1059615 inhibits PI3Kα, β, γ and δ, with Ki of 0.42 nM, 0.6 nM, 0.47 nM and 1.7 nM, respectively. Another report shows that GSK1059615 inhibits PI3Kα with IC50 of 2 nM. In T47D and BT474 cancer cells, GSK1059615 inhibits the phosphorylation of Akt at S473, with IC50 of 40 nM. 体内研究:In xenograft mice models of BT474 or HCC1954 breast cancer cells, GSK1059615 (25 mg/kg) effectively inhibits tumor growth.
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