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PF-04957325

Chemical Structure : PF-04957325

CAS No.: 1305115-80-3

PF-04957325 (PF 04957325)

Catalog No.: PC-38701Not For Human Use, Lab Use Only.

PF-04957325 is a highly potent and selective PDE8 inhibitor with IC50 values of 0.7 nM and 0.3 nM for PDE8A and PDE8B, respectively.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

PF-04957325 is a highly potent and selective PDE8 inhibitor with IC50 values of 0.7 nM and 0.3 nM for PDE8A and PDE8B, respectively.
PF-04957325 potentiates adrenocorticotropin stimulation of steroidogenesis by increasing cAMP-dependent protein kinase activity in both primary isolated adrenocortical cells and Y-1 cells.
PF-04957325 inhibits breast cancer cell migration by activation of cAMP signaling.

Physicochemical Properties

M.Wt 400.38
Formula C14H15F3N8OS
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

3-[[(2R)-4-(2-Thiazolylmethyl)-2-morpholinyl]methyl]-5-(trifluoromethyl)-3H-1,2,3-triazolo[4,5-d]pyrimidin-7-amine

References

1. Tsai LC, et al. Mol Pharmacol. 2011 Apr;79(4):639-48.

2. Shimizu-Albergine M, et al. Mol Pharmacol. 2012 Apr;81(4):556-66.

3. Dong H, et al. Breast Cancer Res Treat. 2015 Jul;152(1):17-28.

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