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FXR

FXR

货号 产品名 CAS号 信息
CSN13148 Turofexorate isopropyl 629664-81-9 WAY-362450 is an agonist of farnesoid X receptor (FXR) with EC50 of 4 nM. WAY-362450 is used to the treatment of dyslipidemia.
CSN26168 Vonafexor 1192171-69-9 Vonafexor is a farnesoid X receptor agonist.
CSN23688 Tropifexor 1383816-29-2 Tropifexor is a potent agonist of FXR with EC50 of 0.26 nM.
CSN26485 Tauro-β-muricholic acid sodium 145022-92-0 Tauro-β-muricholic Acid sodium (T-βMCA sodium), a endogenous metabolite, is a competitive and reversible farnesoid X receptor (FXR) antagonist, with an IC50 of 40 μM[1][2][3].
CSN15954 T0901317 293754-55-9 T0901317 is a selective agonist for LXR and FXR with EC50 of 50 nM and 5 μM, respectively.
CSN26448 PX20606 trans racemate 1268244-85-4 PX20606, also known as PX-102, is a FXR agonist. PX20606 induces high-density lipoprotein-mediated transhepatic cholesterol efflux in mice and monkeys and prevent atherosclerosis in cholesteryl ester transfer protein transgenic low-density lipoprotein receptor (-/-) mice. PX20606 demonstrated potent plasma cholesterol-lowering activity that affected all lipoprotein species.
CSN12883 Obeticholic acid 459789-99-2 Obeticholic acid is a selective FXR agonist with EC50 of 99 nM and it has anticholestatic activity.
CSN21073 Nidufexor 1773489-72-7 Nidufexor is a potent farnesoid X receptor (FXR) agonist for the treatment of non-alcoholic steatohepatitis (NASH) and hepatobiliary disorders.
CSN23776 LY2562175 1103500-20-4 LY2562175 is a selective and partial FXR agonist with EC50 of 193 nM.
CSN17377 INT-767 1000403-03-1 INT-767 is a potent agonist for both FXR (mean EC50, 30 nM by PerkinElmer AlphaScreen assay) and TGR5 (mean EC50, 630 nM by time resolved-fluorescence resonance energy transfer).
CSN11129 GW 4064 278779-30-9 GW4064 is a selective, non-steroidal farnesoid X receptor (FXR) agonist (EC50 = 15 nM).
CSN25374 Guggulsterone 95975-55-6 Guggulsterone is a plant sterol derived from the gum resin of the tree Commiphora wightii. Guggulsterone inhibits the growth of a wide variety of tumor cells and induces apoptosis through down regulation of antiapoptotic gene products (IAP1, xIAP, Bfl-1/A1, Bcl-2, cFLIP and survivin), modulation of cell cycle proteins (cyclin D1 and c-Myc), activation of caspases and JNK, inhibition of Akt. Guggulsterone, a farnesoid X receptor (FXR) antagonist, decreases CDCA-induced FXR activation with IC50s of 17 and 15 μM for Z- and E-Guggulsterone, respectively.
CSN15997 Fexaramine 574013-66-4 Fexaramine is a small molecule farnesoid X receptor (FXR) agonist with 100-fold increased affinity relative to natural compounds.
CSN28427 (Z)-Guggulsterone 39025-23-5 (Z)-Guggulsterone is a broad spectrum steroid receptor ligand and an antagonist of FXR with antiseptic, antirheumatic and anti-inflammatory activity in vivo.
CSN22796 DY268 1609564-75-1
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