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PX 20350
- FXR agonist Cpd 22- Soluble in DMSO
- MF: C28H22Cl2F3N3O4
- MW: 592.39
Description
PX 20350 is a potent farnesoid X receptor (FXR) agonist with enhanced affinity and efficacy compared with GW4064 in reported FXR FRET and full-length FXR reporter assays. Reported values include 12 nM in the FRET assay and 6 nM in the direct reporter assay.
FXR is a bile-acid-activated nuclear receptor that regulates bile acid synthesis, lipid metabolism, glucose metabolism and inflammatory responses. PX 20350 is relevant for metabolic disease and hepatobiliary pathway studies.
Key Features
- Potent FXR nuclear receptor agonist
- Enhanced activity compared with GW4064 in reported assays
- Modulates triglyceride and cholesterol pathways in vivo
- Useful bile-acid signaling probe
Applications
- FXR reporter assays
- Bile acid metabolism research
- Lipid and cholesterol pathway studies
- Metabolic and hepatobiliary disease models
More Information
| Parent CAS No. | 1198085-23-2 |
|---|---|
| Chemical Name | 4-(((6-((5-cyclopropyl-3-(2,6-dichlorophenyl)isoxazol-4-yl)methoxy)-2-(trifluoromethyl)pyridin-3-yl)(methyl)amino)methyl)benzoic acid |
| SMILES | C1(C(F)(F)F)N=C(OCC2=C(C3CC3)ON=C2C2C(Cl)=CC=CC=2Cl)C=CC=1N(C)CC1C=CC(C(=O)O)=CC=1 |
| MFCD | N.A. |
| InChi | InChI=1S/C28H22Cl2F3N3O4/c1-36(13-15-5-7-17(8-6-15)27(37)38)21-11-12-22(34-26(21)28(31,32)33)39-14-18-24(35-40-25(18)16-9-10-16)23-19(29)3-2-4-20(23)30/h2-8,11-12,16H,9-10,13-14H2,1H3,(H,37,38) |
| InChiKey | KNWXWQGSCZVUGX-UHFFFAOYSA-N |
| CID | 44476535 |
| Short Description | FXR agonist |
References
- U. Abel et al. Synthesis and pharmacological validation of a novel series of non-steroidal FXR agonists. Bioorg. Med. Chem. Lett. 2010, 20, 4911–4917.
- U. Deuschle et al. FXR controls the tumor suppressor NDRG2 and FXR agonists reduce liver tumor growth and metastasis in an orthotopic mouse xenograft model. PLoS One. 2012, 7, e43044.
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