1. PI3K/Akt/mTOR JAK/STAT Signaling Stem Cell/Wnt Epigenetics Protein Tyrosine Kinase/RTK Apoptosis NF-κB Metabolic Enzyme/Protease Immunology/Inflammation
  2. Akt mTOR JAK STAT Apoptosis Caspase Reactive Oxygen Species (ROS) NO Synthase
  3. PI3K/Akt/mTOR-IN-7

PI3K/Akt/mTOR-IN-7 是一种 AKT/mTORJAK2/STAT3 抑制剂。PI3K/Akt/mTOR-IN-7 可恢复 p-Aktp-mTORp-STAT3 的表达水平,并降低促凋亡蛋白 Caspase-3 mRNA 的表达。PI3K/Akt/mTOR-IN-7 可减少细胞内 ROS 的积累,并抑制 NO 的生成。PI3K/Akt/mTOR-IN-7 可用于中风、阿尔茨海默病和帕金森病的研究。

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PI3K/Akt/mTOR-IN-7

PI3K/Akt/mTOR-IN-7 Chemical Structure

CAS No. : 2925588-01-6

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

PI3K/Akt/mTOR-IN-7 is an AKT/mTOR and JAK2/STAT3 inhibitor. PI3K/Akt/mTOR-IN-7 restores p-Akt, p-mTOR, and p-STAT3 expression, reduces pro-apoptotic Caspase-3 mRNA expression. PI3K/Akt/mTOR-IN-7 reduces intracellular ROS accumulation and inhibits NO production. PI3K/Akt/mTOR-IN-7 can be used for research on stroke, Alzheimer's disease and Parkinson's disease[1].

IC50 & Target[1]

JAK2

 

STAT3

 

Caspase-3

 

体外研究
(In Vitro)

PI3K/Akt/mTOR-IN-7 (DG23) (10 μM;24 小时) 对 BV2 小胶质细胞无显著细胞毒性[1]
PI3K/Akt/mTOR-IN-7 (10 μM;24 小时) 可在 10 μM 浓度下使 LPS (HY-D1056) 刺激的 BV2 小胶质细胞中一氧化氮的生成量抑制 51.62%[1]
PI3K/Akt/mTOR-IN-7 (10 μM;24 小时) 对人神经母细胞瘤 SH-SY5Y 细胞在 10 μM 浓度下无明显细胞毒性[1]
PI3K/Akt/mTOR-IN-7 (10 μM;26 小时) 可在 SH-SY5Y 人神经母细胞瘤细胞中发挥神经保护作用,抵御 H2O2 诱导的氧化损伤;其在 10 μM 浓度下的细胞存活率挽救率为 42.68%,且呈现浓度依赖性的保护效应[1]
PI3K/Akt/mTOR-IN-7 (10 μM;8 小时) 对 SH-SY5Y 人神经母细胞瘤细胞中 H2O2 诱导的促凋亡 Bcl-2/BaxCaspase-3 mRNA 表达上调具有强效抑制作用[1]
PI3K/Akt/mTOR-IN-7 (2.5-10 μM;8 小时) 可剂量依赖性地抑制 H2O2 诱导的人神经母细胞瘤 SH-SY5Y 细胞中活性氧的积累,在 5 μM 和 10 μM 浓度下可观察到显著效应[1]
PI3K/Akt/mTOR-IN-7 (2.5-10 μM;8 小时) 可呈剂量依赖性降低 H2O2 诱导的 Caspase-3 蛋白表达,并在 2.5-10 μM 浓度下恢复人神经母细胞瘤 SH-SY5Y 细胞中 p-Akt、p-mTOR 和 p-STAT3 的蛋白表达,其效力高于薯蓣皂苷元[1]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Cytotoxicity Assay[1]

Cell Line: BV2 microglial cells
Concentration: 10 μM
Incubation Time: 24 h
Result: Showed no significant cytotoxicity in BV2 cells.

Cell Cytotoxicity Assay[1]

Cell Line: SH-SY5Y human neuroblastoma cells
Concentration: 10 μM
Incubation Time: 24 h
Result: Showed no obvious cytotoxicity in SH-SY5Y cells.

Real Time qPCR[1]

Cell Line: H2O2-injured SH-SY5Y human neuroblastoma cells
Concentration: 10 μM
Incubation Time: 26 h
Result: Significantly attenuated H2O2-induced upregulation of Bcl-2/Bax and Caspase-3 mRNA expression.
Reduced the Bcl-2/Bax ratio to 3.54 and Caspase-3 expression to 1.03.

Western Blot Analysis[1]

Cell Line: H2O2-injured SH-SY5Y human neuroblastoma cells
Concentration: 2.5 μM; 5 μM; 10 μM
Incubation Time: 8 h
Result: Dose-dependently decreased H2O2-induced Caspase-3 protein expression, with marked downregulation in the 10 μM group relative to the H2O2-only group.
Dose-dependently upregulated the p-Akt/Akt, p-mTOR/mTOR, and p-STAT3/STAT3 ratios, restoring phosphorylated protein expression to levels superior to diosgenin at equivalent concentrations.
分子量

605.76

Formula

C36H47NO7

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
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产品名称:
PI3K/Akt/mTOR-IN-7
目录号:
HY-183272
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