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DS-6930 

Cat. No. M28026

All AbMole products are for research use only, cannot be used for human consumption.

DS-6930  Structure

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Quality Control & Documentation
Biological Activity

DS-6930 is a potent and selective agonist of PPARγ, with an EC50 of 41 nM. DS-6930 could robust reduce plasma glucose (PG), and with fewer PPARγ-related adverse effects than Rosiglitazone. DS-6930 can be used for the research of diabetes.

Chemical Information
Molecular Weight 403.43
Formula C23H21N3O4
CAS Number 1242328-82-0
Storage Please store the product under the recommended conditions in the Certificate of Analysis.
References

[1] Tsuyoshi Shinozuka, et al. ACS Med Chem Lett. Structure-Activity Relationship Studies of 3- or 4-Pyridine Derivatives of DS-6930

[2] Tsuyoshi Shinozuka, et al. Bioorg Med Chem. Discovery of DS-6930, a potent selective PPARγ modulator. Part I: Lead identification

[3] Tsuyoshi Shinozuka, et al. Bioorg Med Chem. Discovery of DS-6930, a potent selective PPARγ modulator. Part II: Lead optimization

Related PPAR Products
SR1664

SR1664 is an antidiabetic compound that binds to PPARγ and can effectively inhibit CDK5-mediated phosphorylation of PPARγ with IC50 of 80 nM and Ki of 28.67 nM.

WY 14643 (Pirinixic Acid)

WY 14643 (Pirinixic Acid) is a potent and selective, peroxisome proliferator-activated receptor-α (PPARα) agonist.

Rosiglitazone

Rosiglitazone (BRL 49653) is an orally active selective PPARγ agonist (EC50=60 nM, Kd=40 nM). Rosiglitazone is an TRPC5 activator (EC50=30 μM) and TRPM3 inhibitor.

GSK 3787

GSK3787 is an orally available selective peroxisome proliferator-activated receptor δ (PPARδ) antagonist (pIC50 = 6.6).

Rosiglitazone maleate

Rosiglitazone maleate (Avandia) is a potent and selective PPARγ ligand that binds to the PPARγ ligand-binding domain with a Kd value of 43 nM.

  Catalog
Abmole Inhibitor Catalog




Keywords: DS-6930  supplier, PPAR, inhibitors, activators

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