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GRK5-IN-2

Chemical Structure : GRK5-IN-2

CAS No.: 1642839-27-7

GRK5-IN-2 (Compound 707)

Catalog No.: PC-23911Not For Human Use, Lab Use Only.

GRK5-IN-2 (Compound 707)is a potent, selective G-protein-coupled receptor kinase 5 (GRK5) inhibitor with IC50 of 49.7 uM in luminescent ADP detection assay.

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

Biological Activity

GRK5-IN-2 (Compound 707)is a potent, selective G-protein-coupled receptor kinase 5 (GRK5) inhibitor with IC50 of 49.7 uM in luminescent ADP detection assay.
GRK5-IN-2 treatment significantly decreased TAG synthesis during 7 days of WT 3T3-L1 adipocyte differentiation in a dose-dependent manner.
GRK5-IN-2 inhibitor treatment significantly decreased the rate of TAG, cholesteryl ester (CE), and phospholipid (PL), but not free cholesterol (FC), synthesis from [14C]-acetic acid in WT 3T3-L1 adipocyte.

Physicochemical Properties

M.Wt 380.40
Formula C20H20N4O4
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

1H-Imidazo[4,5-c]pyridin-6-amine, 2-(2-furanyl)-1-methyl-N-(3,4,5-trimethoxyphenyl)-

References

1. Axel Ullrich, et al. Imidazo[4,5-c]pyridine and pyrrolo[3,2-c]pyridine compounds as G-protein-coupled receptor kinase 5 (GRK5) modulators. EP2818472A1.

2. Seramur ME, et al. Int J Obes (Lond). 2025 Jan 21. doi: 10.1038/s41366-025-01712-w.

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