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BPS Bioscience Inc.
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A-769662
  • A-769662
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更新時間:2025-06-07 21:00:08

瀏覽次數:28

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Acetyltransferase Enzymes
Apoptosis Proteins
Bromdomain Proteins
Cell Signaling Pathway Proteins
Cholesterol Related Proteins
Coronavirus Proteins
CRISPR Proteins
Cytokine Proteins
Deacetylase Enzymes
Demethylase Enzymes
Ebola
Heat Shock Proteins
Immunotherapy Proteins
Methyltransferase Enzymes
Methyl-lysine Reader Proteins
Molecular Biology Proteins
Other Proteins
PARP Enzymes
PDE Enzymes
Phospholipase
PROTAC Proteins
Protease Enzymes
Protein Arginine Deiminase
Protein Tyrosine Phosphatase
Ras Signaling Proteins
Ubiquitination
CAR T-Cell Therapy Proteins
Acetyltransferase Assay Kits
Apoptosis Assay Kits
Bromodomain Assay Kits
Bromodomain Assay Kit Components
Cholesterol Related Assay Kits
Coronavirus Assay Kits
Cytokine Detection Assay Kits
Deacetylase Assay Kits
Demethylase Assay Kits
Demethylase Assay Kit Components
Heat Shock Protein Assay kits
Immunotherapy Assay Kits
Assay Kit Components
Metabolic Assay Kits
Methyltransferase Assay Kits
Methyltransferase Assay Kit Components
Methyl-Lysine Reader Assay Kits
Molecular Biology Assay Kits
PARP Assay Kits
PDE Assay Kits
PDE Assay Kit Components
PROTAC Assay Kits
Protease Assay Kits
Ras Signaling Assay Kits
Kinase
CAR T-Cell Therapy Cell Lines
Cell Signaling Pathway Cell Lines
Coronavirus Cell Lines
CAS9 Expressing Cells
Immunotherapy Cell Lines
Metabolic Cell Lines
PDE Cell Lines
Ion Channel Cell Lines
Inhibitors / Activators
Antibodies
細胞庫 / 細胞培養
試劑
技術服務
●Purchase●DescriptionA-769662isapotent,reversibleactivatorofAMP-activatedproteinkinase(AMPK)
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Description

A-769662 is a potent, reversible activator of AMP-activated protein kinase (AMPK). AMPK is an αβγ heterotrimer and plays an important role in regulating cellular and whole-body metabolism. A-769662 only activates AMPK heterotrimers containing the β1 subunit. A-769662 activates AMPK through the β subunit carbohydrate-binding module and the γ subunit but not the AMP-binding sites. A-769662 stimulated partially purified rat liver AMPK with an EC50 of 0.8 µM and inhibited fatty acid synthesis in primary rat hepatocytes with an IC50 of 3.2 µM.

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