Powder: -20°C for 3 years | In solvent: -80°C for 1 year
GPR40 agonist 6 (Compound 7a) is a potent and selective agonist of free fatty acid receptor 1 ( FFAR1 or GPR40 ) with an EC 50 of 0.058 μM against GPR40 [1].
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
2 mg | 5 days | $ 53.00 | |
1 mL * 10 mM (in DMSO) | 5 days | $ 130.00 |
Description | GPR40 agonist 6 (Compound 7a) is a potent and selective agonist of free fatty acid receptor 1 ( FFAR1 or GPR40 ) with an EC 50 of 0.058 μM against GPR40 [1]. |
In vitro | GPR40 agonist 6 (Compound 7a) exhibits a highly favorable ADME (Absorption, Distribution, Metabolism, and Excretion) profile, characterized by negligible inhibition of key cytochrome P450 isoforms (1A2, 2C9, 2C19, 2D6, and 3A4) at a concentration of 5 μM. Additionally, this compound demonstrates a 98.6% binding affinity to human plasma proteins and an aqueous solubility of 404 μM in PBS (pH 7.4). Its microsomal stability in mice, with a half-life of 434 minutes, and Caco-2 permeability rate of 15.2 x 10^-6 cm/s, further underscore its promising pharmacokinetic properties. These values, derived from averages of multiple experiments, highlight the compound's potential effectiveness and safety profile. |
Molecular Weight | 337.37 |
Formula | C20H19NO4 |
CAS No. | 1798751-25-3 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
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GPR40 agonist 6 1798751-25-3 inhibitor inhibit