中文名称: GNE-493
英文名称: GNE-493
CAS No: 1033735-94-2
分子式: C17H20N6O2S
分子量: 372.44
G11160 GNE-493 10mM in DMSO (psaitong)
密度:
1.408±0.06 g/cm3(Predicted)
包装规格:
1ml in glass bottle
产品简介:
一种泛 PI3-kinase 和 mTOR 的口服双效抑制剂,对PI3Kα、PI3Kβ、PI3Kδ、PI3Kγ和mTOR的IC50值分别为3.4 nM、12 nM、16 nM、16 nM和32 nM。
溶解性:
DMSO :45 mg/mL(120.82 mM;超声加热助溶)
储备液保存:
-80°C, 2 years
-20°C, 1 year
靶点:
PI3Kα:3.4nM (IC50);PI3Kβ:12 nM (IC50);PI3Kδ:16 nM (IC50);PI3Kγ:16 nM (IC50) ;mTOR: 30 nM (IC50)
体外研究:
GNE-493 is a low molecular weight, potent dual inhibitor of pan-PI3 kinases and mTOR. GNE-493 displays approximately equipotent inhibition of Class I PI3K isoforms, is submitted for screening in a 142 kinase panel provided by Invitrogen’s SelectScreen service. Of these kinases, only three are subject to greater than 50% inhibition by GNE-493, and none are inhibited greater than 80% when tested at 1 μM. Subsequently measured IC50s demonstrated that GNE-493 is more than 100-fold selective for PI3Kα over these three unrelated kinases (Aurora A IC50>10 μM, MLK1 IC50=591 nM and SYK IC50=371 nM).
体内研究:
To confirm and compare in vivo efficacy, GNE-493 is examined in the human MCF7.1 breast cancer xenograft model that harbors a PI3Kα activating mutation. Mice bearing xenografts are dosed orally once daily with 10 mg/kg of GNE-493 for 21 continuous days. Similar to observations made in the PC3 prostate cancer xenograft model, 10 mg/kg of GNE-493 results in 73% tumor growth inhibition at day 21 when compared to vehicle control animals. When achieving comparable levels of drug exposure, GNE-493 shows a similar suppression of the PI3K pathway and consequently, a similar efficacy profile against MCF7.1 breast tumors.
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保存条件:
-20°C
UN码:
HazardClass:
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