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PAT-505

Chemical Structure : PAT-505

CAS No.: 1782070-85-2

PAT-505 (PAT 505;PAT505)

Catalog No.: PC-60638Not For Human Use, Lab Use Only.

PAT-505 (PAT 505, PAT505) is a potent, selective, noncompetitive, and orally active autotaxin inhibitor with IC50 of 2.0 nM against the lysoPLD activity of human ATX.

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

Biological Activity

PAT-505 (PAT 505, PAT505) is a potent, selective, noncompetitive, and orally active autotaxin inhibitor with IC50 of 2.0 nM against the lysoPLD activity of human ATX.
PAT-505 displays high selectivity over other ENPP proteins and no significant agonist or antagonist activity at PPARα and PPARγ.
PAT-505 maintains good potency for inhibition of lysoPLD activity with IC50 of 9.7 nM and 62 nM in human blood and mouse plasma, respectively.
PAT-505 robustly reduces liver fibrosis with no significant effect on steatosis, hepatocellular ballooning, or inflammation in high-fat diet model of NASH.

Physicochemical Properties

M.Wt 495.905
Formula C23H17ClF2N3NaO2S
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-((6-chloro-2-cyclopropyl-1-(1-ethyl-1H-pyrazol-4-yl)-7-fluoro-1H-indol-3-yl) thio)-2-fluorobenzoic acid sodium salt

References

1. Bain G, et al. J Pharmacol Exp Ther. 2017 Jan;360(1):1-13.

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