Chemical Structure : GRK5-IN-2
CAS No.: 1642839-27-7
货号: 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.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
5 mg | ¥780 | In stock | |
10 mg | ¥1180 | In stock | |
25 mg | ¥2180 | In stock | |
50 mg | Get quote | ||
100 mg | Get quote |
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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.
分子量 | 380.40 | |
分子式 | C20H20N4O4 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
1H-Imidazo[4,5-c]pyridin-6-amine, 2-(2-furanyl)-1-methyl-N-(3,4,5-trimethoxyphenyl)- |
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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