371725 Sigma-AldrichGPR43 (FFA2) Agonist - CAS 1208552-99-1 - Calbiochem
GPR43 (FFA2) Agonist is an allosteric agonist of FFA2 (GPR43). Displays a left-shifted acetate dose response (IC50 = 0.7 µM) & 111% efficacy relative to acetate in hFFA2 forskolin-induced cAMP assays.
More>> GPR43 (FFA2) Agonist is an allosteric agonist of FFA2 (GPR43). Displays a left-shifted acetate dose response (IC50 = 0.7 µM) & 111% efficacy relative to acetate in hFFA2 forskolin-induced cAMP assays. Less<<Synonyms: (S)-2-(4-chlorophenyl)-3,3-dimethyl-N-(5-phenylthiazol-2-yl)butanamide
Recommended Products
Overview
| Replacement Information | 
|---|
Key Spec Table
| CAS # | Empirical Formula | 
|---|---|
| 1208552-99-1 | C₂₁H₂₁ClN₂OS | 
Pricing & Availability
| Catalogue Number | Availability | Packaging | Qty/Pack | Price | Quantity | |
|---|---|---|---|---|---|---|
| 371725-10MG | 
 | Glass bottle | 10 mg | 
 | — | 
| References | |
|---|---|
| References | Wang, Y., et al. 2009. Bioorg. Med. Chem. Lett. 20, 493. | 
| Product Information | |
|---|---|
| CAS number | 1208552-99-1 | 
| Form | White solid | 
| Hill Formula | C₂₁H₂₁ClN₂OS | 
| Chemical formula | C₂₁H₂₁ClN₂OS | 
| HS Code | 2934 10 90 | 
| Structure formula Image | |
| Quality Level | MQ100 | 
| Biological Information | |
|---|---|
| Purity | >98% by HPLC | 
| Physicochemical Information | 
|---|
| Dimensions | 
|---|
| Materials Information | 
|---|
| Toxicological Information | 
|---|
| Safety Information according to GHS | 
|---|
| Safety Information | 
|---|
| Product Usage Statements | 
|---|
| Packaging Information | 
|---|
| Transport Information | 
|---|
| Supplemental Information | 
|---|
| Specifications | 
|---|
| Global Trade Item Number | |
|---|---|
| Catalogue Number | GTIN | 
| 371725-10MG | 04055977213270 | 
Documentation
GPR43 (FFA2) Agonist - CAS 1208552-99-1 - Calbiochem SDS
| Title | 
|---|
GPR43 (FFA2) Agonist - CAS 1208552-99-1 - Calbiochem Certificates of Analysis
| Title | Lot Number | 
|---|---|
| 371725 | 
References
| Reference overview | 
|---|
| Wang, Y., et al. 2009. Bioorg. Med. Chem. Lett. 20, 493. | 

 


 
  

 

 
 
 
 
 
 
 
