品牌	货号	产品规格	价格(RMB)	库存（上海）	北京	武汉	南京
源叶(MedMol)	S81768-1mg	98%	￥240.00元	10	-	-	-
源叶(MedMol)	S81768-5mg	98%	￥380.00元	6	-	-	-
源叶(MedMol)	S81768-10mg	98%	￥610.00元	6	-	-	-
源叶(MedMol)	S81768-25mg	98%	￥1070.00元	5	-	-	-

品牌

货号

产品规格

价格(RMB)

库存（上海）

北京

武汉

南京

购买数量

源叶(MedMol)

S81768-1mg

98%

￥240.00元

源叶(MedMol)

S81768-5mg

98%

￥380.00元

源叶(MedMol)

S81768-10mg

98%

￥610.00元

源叶(MedMol)

S81768-25mg

98%

￥1070.00元

产品介绍

GNE-493 is a potent, selective, and orally available dual pan-PI3-kinase/mTOR inhibitor with IC50s of 3.4 nM, 12 nM, 16 nM, 16 nM and 32 nM for PI3Kα, PI3Kβ, PI3Kδ, PI3Kγ and mTOR.

产品描述： GNE-493 is a potent, selective, and orally available dual pan-PI3-kinase/mTOR inhibitor with IC50s of 3.4 nM, 12 nM, 16 nM, 16 nM and 32 nM for PI3Kα, PI3Kβ, PI3Kδ, PI3Kγ and mTOR.

靶点： PI3Kα:3.4 nM (IC50);PI3Kβ:12 nM (IC50);PI3Kδ:16 nM (IC50);PI3Kγ:16 nM (IC50);mTOR:30 nM (IC50);PI3K; mTOR

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

参考文献：
1. Sutherlin DP, et al. Discovery of (thienopyrimidin-2-yl)aminopyrimidines as potent, selective, and orally available pan-PI3-kinase and dual pan-PI3-kinase/mTOR inhibitors for the treatment of cancer. J Med Chem. 2010 Feb 11;53(3):1086-97.

溶解性： soluble in DMSO

保存条件： -20℃

配置溶液浓度参考：

	1mg	5mg	10mg
1 mM	2.685 ml	13.425 ml	26.85 ml
5 mM	0.537 ml	2.685 ml	5.37 ml
10 mM	0.268 ml	1.342 ml	2.685 ml
50 mM	0.054 ml	0.268 ml	0.537 ml

注意：

部分产品我司仅能提供部分信息，我司不保证所提供信息的权威性，仅供客户参考交流研究之用。

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GNE-493 98%

GNE-493

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摩尔浓度计算器

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