Biological Activity
Potent FFA1 (GPR40) agonist (EC50 = 3.6 nM in an IP3 assay in GPR40 transfected A9 cells). Inhibits insulin secretion from isolated pancreatic islets. Reduces blood glucose levels following oral glucose challenge in mice. Orally bioavailable.
Technical Data
M. Wt | 488.48 |
Formula | C24H19F3O4S |
Storage | Store at -20°C |
Purity | ≥98% (HPLC) |
CAS Number | 1011531-27-3 |
PubChem ID | 24897670 |
InChI Key | BMLGZNVPWRUVNM-IBGZPJMESA-N |
Smiles | CC1=C(COC2=CC=C(C=C2)[C@H](CC(O)=O)C2=NOC=C2)SC(=N1)C1=CC=C(C=C1)C(F)(F)F |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Solubility Data
DMSO | 48.85 | 100 |
ethanol | 48.85 | 100 |
Preparing Stock Solutions
The following data is based on the product molecular weight 488.48. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
1 mM | 2.05 mL | 10.24 mL | 20.47 mL |
5 mM | 0.41 mL | 2.05 mL | 4.09 mL |
10 mM | 0.2 mL | 1.02 mL | 2.05 mL |
50 mM | 0.04 mL | 0.2 mL | 0.41 mL |
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Certificate of Analysis / Product Datasheet Safety Datasheet Select another language: English German French Spanish View SDSReferences
References are publications that support the products\' biological activity.
Liu et al (2014) Optimization of GPR40 agonists for type 2 diabetes. ACS Med.Chem.Lett. 5 517 PMID: 24900872
Keywords: AM 4668, supplier, AM4668, free, fatty, acid, receptors, FFA1, FFAR, agonists, agonism, type, 2, diabetes, potent, orally, bioavailable, Free, Fatty, Acid, Receptors, Free, Fatty, Acid, Receptors, Tocris Bioscience
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