Uprosertib
CAS No. 1047634-65-0
Uprosertib ( GSK2141795, GSK 795, Uprosertib )
产品货号. M17123 CAS No. 1047634-65-0
Uprosertib (GSK2141795) is a selective, ATP-competitive, and orally bioavailable Akt inhibitor with IC50 of 180 nM, 328 nM, and 38 nM for Akt 1, 2 and 3, respectively. Phase 2.
纯度: 97%
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥437 | 有现货 |
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5MG | ¥624 | 有现货 |
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10MG | ¥1021 | 有现货 |
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25MG | ¥1717 | 有现货 |
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50MG | ¥2754 | 有现货 |
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100MG | ¥4560 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Uprosertib
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Uprosertib (GSK2141795) is a selective, ATP-competitive, and orally bioavailable Akt inhibitor with IC50 of 180 nM, 328 nM, and 38 nM for Akt 1, 2 and 3, respectively. Phase 2.
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产品描述Uprosertib, also known as GSK2141795 and GSK795, is an orally bioavailable inhibitor of the serine/threonine protein kinase Akt (protein kinase B) with potential antineoplastic activity. Akt inhibitor GSK2141795 binds to and inhibits the activity of Akt, which may result in inhibition of the PI3K/Akt signaling pathway and tumor cell proliferation and the induction of tumor cell apoptosis. Activation of the PI3K/Akt signaling pathway is frequently associated with tumorigenesis and dysregulated PI3K/Akt signaling may contribute to tumor resistance to a variety of antineoplastic agents.
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同义词GSK2141795, GSK 795, Uprosertib
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通路Others
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靶点Other Targets
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受体Akt1; Akt2; Akt3
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研究领域Cancer
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适应症——
化学信息
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CAS Number1047634-65-0
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分子量429.25
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分子式C18H16Cl2F2N4O2
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纯度97%
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溶解度DMSO : ≥ 150 mg/mL 349.45 mM H2O : < 0.1 mg/mL
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SMILESCn1c(c(cn1)Cl)c1c(oc(c1)C(=O)N[C@@H](Cc1cc(c(cc1)F)F)CN)Cl
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化学全称N-((S)-1-amino-3-(3,4-difluorophenyl)propan-2-yl)-5-chloro-4-(4-chloro-1-methyl-1H-pyrazol-5-yl)furan-2-carboxamide
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Pachl F, et al. Characterization of a chemical affinity probe targeting Akt kinases. J Proteome Res. 2013 Aug 2;12(8):3792-800.
产品手册
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