HPG1860

  Cat. No.:  DC73829  
Chemical Structure
2226133-29-3
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More than 5000 active chemicals with high quality for research!
Field of application
HPG1860 is a potent, selective, nonbile acid full FXR agonist with EC50 of 5 nM and 18 nM in FR-FRET and luciferase assays, respectively.
Cas No.: 2226133-29-3
Chemical Name: HPG1860
SMILES: O=C(C1=CC(OC)=C2N=C(N3[C@H](C)CN(CC4=C(C5CC5)ON=C4C6=C(Cl)C=CC=C6Cl)CC3)SC2=C1)O
Formula: C27H26Cl2N4O4S
M.Wt: 573.49
MSDS
Cat. No. Product name Field of application
DC11547 LY-2562175 LY2562175 is a potent and selective FXR agonist, with an EC50 of 193 nM.
DC73832 PDL103 PDL103 is a potent, dual FXR/GPBAR1 antagonist with IC50 of 10 and 19 uM, respectively.
DC73831 MET409 MET409 (MET-409) is a potent, selective farnesoid X receptor (FXR) agonist with EC50 of 16 nM (human FXR).
DC73830 ID166 ID119031166 (ID166) is a novel potent, selective FXR agonist with EC50 of 3 nM and 5 nM in TR-FRET FXR co-activator assay and FXR reporter assay, respectively.
DC73829 HPG1860 HPG1860 is a potent, selective, nonbile acid full FXR agonist with EC50 of 5 nM and 18 nM in FR-FRET and luciferase assays, respectively.
DC71957 Omesdafexor Omesdafexor is a FXR agonist. Omesdafexor can be used in the research of liver disease or a metabolic inflammation-mediated disease.
DC70074 GSK-2324 GSK-2324 (GSK2324) is a potent, selective, full FXR agonist with EC50 of 120 nM in FRET assay.
DC50224 Chenodeoxycholic acid-13C Chenodeoxycholic acid-13C (CDCA-13C) is the 13C-labeled Chenodeoxycholic Acid. Chenodeoxycholic Acid is a hydrophobic primary bile acid that activates nuclear receptors (FXR) involved in cholesterol metabolism.
DC50223 Chenodeoxycholic acid-d5 Chenodeoxycholic acid-d5 (CDCA-d5) is the deuterium labeled Chenodeoxycholic Acid. Chenodeoxycholic Acid is a hydrophobic primary bile acid that activates nuclear receptors (FXR) involved in cholesterol metabolism.
DC50222 BMS-986318 BMS-986318 is a potent nonbile acid FXR agonist with EC50s of 53 and 350 nM in the FXR Gal4 and SRC-1 recruitment assays, respectively. BMS-986318 has a suitable ADME profile, and demonstrates efficacy in the mouse bile duct ligation model of liver cholestasis and fibrosis.BMS-986318 can be used for the research of nonalcoholic steatohepatitis.
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