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Fexaramine
Cat. No.:
OB0225WX-2653
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR, and HPLC.
Size:
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Product Overview
Description:
Fexaramine is a high-potency farnesoid X receptor (FXR) agonist (EC50: 25 nM) characterized by its lack of cross-reactivity with other nuclear receptors such as RXR, PPAR, or LXR.
Synonym:
574013-66-4; Methyl (E)-3-(3-(N-((4'-(dimethylamino)-[1,1'-biphenyl]-4-yl)methyl)cyclohexanecarboxamido)phenyl)acrylate; FEX; methyl (E)-3-[3-[cyclohexanecarbonyl-[[4-[4-(dimethylamino)phenyl]phenyl]methyl]amino]phenyl]prop-2-enoate; 2-Propenoic acid, 3-(3-((cyclohexylcarbonyl)((4'-(dimethylamino)(1,1'-biphenyl)-4-yl)methyl)amino]phenyl)-, methyl ester; 3-[3-[(cyclohexylcarbonyl)-[[4'-(dimethylamino)-[1,1'-biphenyl]-4-yl]methyl]amino]phenyl]-2-propenoicacidmethylester; MFCD09971007; 2-Propenoic acid, 3-[3-[(cyclohexylcarbonyl)[[4'-(dimethylamino)[1,1'-biphenyl]-4-yl]methyl]amino]phenyl]-, methyl ester; Methyl (Z)-3-[3-[cyclohexanecarbonyl-[[4-(4-dimethylaminophenyl)phenyl]methyl]amino]phenyl]prop-2-enoate
CAS No.:
574013-66-4
Compound CID:
5326713
Formula:
C32H36N2O3
Formula Weight:
496.64
Specification
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
Fexaramine is employed in metabolic research as a potent and selective FXR agonist to investigate the transcriptional regulation of bile acid, lipid, and glucose metabolism in hepatic and intestinal models.
Library Information
Target:
FXR
Receptor:
FXR
Pathways:
Metabolism
Plate Number:
L6700-07
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
99 mg/mL; 199.34 mM
ALogP:
6.87
HBA_Count:
3
HBD_Count:
0
Rotatable Bond:
9





