STO-609

TargetMol
Product Code: TAR-T3546
Supplier: TargetMol
CodeSizePrice
TAR-T3546-1mg1mg£121.00
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Quantity:
TAR-T3546-1mL1 mL * 10 mM (in DMSO)£187.00
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Quantity:
TAR-T3546-5mg5mg£187.00
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Quantity:
TAR-T3546-10mg10mg£270.00
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Quantity:
TAR-T3546-25mg25mg£434.00
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Quantity:
TAR-T3546-50mg50mg£606.00
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Quantity:
TAR-T3546-100mg100mg£833.00
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Quantity:
TAR-T3546-500mg500mg£1,589.00
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Quantity:
Prices exclude any Taxes / VAT

Overview

Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃

Images

1 / 1

Further Information

Bioactivity:
STO-609 is a specific and cell-permeable inhibitor of the Ca2+/calmodulin-dependent protein kinase kinase (CaM-KK) for recombinant CaM-KKα/KKβ (Ki: 80/15 ng/mL).
CAS:
52029-86-4
Formula:
C19H10N2O3
Molecular Weight:
314.3
Pathway:
Chromatin/Epigenetic; Neuroscience; Autophagy; PI3K/Akt/mTOR signaling
Purity:
0.9895
SMILES:
OC(=O)c1ccc2c3nc4ccccc4n3c(=O)c3cccc1c23
Target:
CaMK; AMPK; Autophagy

References

Xu J, Xu X, Ling Y, et al.Vincamine as an agonist of G-protein-coupled receptor 40 effectively ameliorates diabetic peripheral neuropathy in mice.Acta Pharmacologica Sinica.2023: 1-16. Kukimoto-Niino M,et al. Crystal structure of the Ca??/calmodulin-dependent protein kinase kinase in complex with the inhibitor STO-609. J Biol Chem. 2011 Jun 24;286(25):22570-9. Tokumitsu H,rt al. STO-609, a specific inhibitor of the Ca(2+)/calmodulin-dependent protein kinase kinase. J Biol Chem. 2002 May 3;277(18):15813-8. Epub 2002 Feb 26. Kan J, Zhao C, Lu S, et al. S100A16, a novel lipogenesis promoting factor in livers of mice and hepatocytes in vitro[J]. Journal of cellular physiology. 2019 May 8. Kan J, Zhao C, Lu S, et al. S100A16, a novel lipogenesis promoting factor in livers of mice and hepatocytes in vitro. Journal of Cellular Physiology. 2019 May 8