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Search Results for " fxr "

Targets

43

Compounds

12

Natural Products

5

Recombinant Proteins

Cat No. Product Name Synonyms Targets
T6053 Turofexorate Isopropyl XL335,FXR-450,WAY-362450 FXR , Autophagy
Turofexorate Isopropyl (XL335) is a potent, selective, and orally bioavailable FXR agonist with EC50 of 4 nM
T40302 FXR/TGR5 agonist 1
FXR/TGR5 agonist 1 acts as an agonist on both FXR and TGR5 receptors and is utilized for treating fatty liver disease.
T64144 FXR antagonist 1
FXR antagonist 1 is a selective, orally active intestinal FXR antagonist with an IC50 value of 2.1 μM. FXR antagonist 1 antagonises intestinal FXR and selectively inhibits intestinal FXR signalling by feedback activation...
T74996 FXR agonist 3
FXR agonist 3, an anti-NASH (Non-Alcoholic Steatohepatitis) agent, functions by activating FXR. It demonstrates anti-fibrogenic activity by inhibiting the expression of COL1A1, TGF-β1, α-SMA, and TIMP1. Additionally, it ...
T72889 FXR agonist 4
FXR agonist 4 with an EC 50 value of 1.05 μM. FXR agonist 4 effectively improves hyperlipidemia, hepatic steatosis, insulin resistance and hepatic inflammation in DIO mice. FXR agonist 4 can be used for the research of ...
T75160 FXR agonist 5
FXR agonist 5 (compound 1), an FXR agonist, is utilized in research targeting diseases or disorders associated with metabolic inflammation [1].
T74754 FXR antagonist 2
Compound A-26, also known as FXR antagonist 2, is a diarylamide derivative that functions as a moderate FXR antagonist. It is utilized in researching hyperlipidemia and type 2 diabetes [1].
T2015 Fexaramine FXR , Autophagy
Fexaramine is a small molecule farnesoid X receptor (FXR) agonist with 100-fold increased affinity compared to natural compounds.
T7886 Nidufexor FXR , Autophagy
Nidufexor is an agonist for the farnesoid X receptor (FXR).
T2233 GW 4064 FXR , Autophagy
GW 4064 is an effective farnesoid X receptor (FXR) agonist (EC50 =65 nM).
T15806 LY2562175 FXR , Autophagy
LY2562175 is an effective and selective FXR agonist (EC50: 193 nM).
T6344 Sevelamer hydrochloride Sevelamer HCl FXR , Autophagy
Sevelamer hydrochloride (Sevelamer HCl) is a phosphate binding drug used to treat hyperphosphatemia via binding to dietary phosphate and prevents its absorption.
T31587 DY268 DY 268,DY-268 FXR
DY268 is a compound based on trisubstituted pyrazolamide without any FXR agonist activity and cytotoxicity and can be used as an effective FXR antagonist (IC50 = 7.5 nM).
T4379 Tropifexor LJN452 FXR , Autophagy
Tropifexor (LJN452) is a novel and highly potent agonist of FXR with an EC50 of 0.2 nM.
T7436 Cilofexor FXR , Autophagy
Cilofexor inhibits binding of a synthetic peptide, Cilofexor is a farnesoid X receptor (FXR) agonist.
T11428 Glyco-Obeticholic acid FXR
Glyco-Obeticholic acid is an active metabolite of Obeticholic acid. Obeticholic acid is an agonist of the farnesoid X receptor (FXR).
T2601 Vidofludimus SC12267,4sc-101 Dehydrogenase , DNA/RNA Synthesis , Interleukin
Vidofludimus (SC12267) (4SC-101, SC12267) is a novel small molecule inhibitor of dihydroorotate dehydrogenase (DHODH).
T8471 Vonafexor EYP001,PLX007,pxl007 FXR , HBV
Vonafexor (EYP001) is a farnesoid X receptor (FXR, NR1H4) agonist, with anti-HBV effects
TQ0252 BAR502 FXR , GPCR19 , Autophagy
BAR502 is a dual GPBAR1 and FXR agonist (IC50s: 0.4 μM and 2 μM).
T1789 Obeticholic Acid INT-747,6-Ethylchenodeoxycholic acid,6-ECDCA FXR , Autophagy
Obeticholic Acid (6-ECDCA) is a Farnesoid X Receptor Agonist. The mechanism of action of obeticholic acid is as a Farnesoid X Receptor Agonist.
T6690 T0901317 Apoptosis , FXR , Liver X Receptor , ROR
T0901317 is a potent and selective agonist for both LXR and FXR, with EC50 of ~50 nM and 5 μM, respectively; it inhibits nuclear factor/κB (NF/κB).
T27460 GSK2324 GSK-2324,GSK 2324 FXR
GSK2324 is a potent FXR agonist for the treatment of NAFLD by controlling hepatic lipids through reduced uptake and selective reduction of fatty acid synthesis.
T63042 NDB FXR
NDB is a selective and potent hFXRα antagonist that inhibits GW4064-stimulated FXR/RXR interactions and FXRα target gene expression in primary mouse hepatocytes.NDB is used in the study of diabetes.
T11426 Gly-β-MCA FXR
Gly-β-MCA is an orally bioactive, enteroselective and potent inhibitor of the farnesoid X receptor (FXR), a bile acid, used in the study of obesity and diabetes.
T8818 TC-G 1005 GPCR19
TC-G 1005 is a potent and selective GPBA agonist (EC50 :0.72 nM; hTGR5). Selective for TGR5 over FXR (farnesoid X receptor). Increases plasma GLP-1 levels and reduces blood glucose in mice. Orally available.
T12583 PX20606 trans racemate PX-102 trans racemate Others
PX20606 trans racemate is an agonist of FXR (EC50s of 32 and 34 nM for FXR in FRET and M1H assay, respectively).
T13093 Tauro-β-muricholic acid sodium T-βMCA sodium FXR
Tauro-β-muricholic Acid sodium is a endogenous metabolite, is a competitive and reversible antagonist of farnesoid X receptor (FXR)(IC50 of 40 μM).
T68612 DM175
DM175 is a novel partial FXR agonist, causing specific modulatory effects on FXR activity that clearly differ from classical FXR agonists.
T25417 Fexarene
Fexarene is a non-steroidal FXR agonist.
T24837 ST-1892
ST-1892 is a soluble partial FXR agonist.
T27492 GSK-8062 GSK 8062
GSK-8062 is an agonist of farnesoid X receptor (FXR).
T73414 EDP-305
EDP-305, an orally active, potent, and selective agonist of the farnesoid X receptor (FXR), exhibits EC50 values of 34 nM in chimeric FXR within CHO cells and 8 nM in full-length FXR in HEK cells. Demonstrating a potent ...
T12251 NR1H4 activator 1 Others
NR1H4 activator 1 is a potent and selective agonist of Famesoid X Receptor (FXR).
T63818 Omesdafexor
Omesdafexor is an FXR agonist that can be used to study diseases caused by liver disease or metabolic inflammation.
T70899 Vidofludimus hemicalcium 4sc-101 hemicalcium,SC12267 hemicalcium,4sc-101 hemicalcium ; SC12267 hemicalcium
Vidofludimus hemicalcium (4sc-101; SC12267) is an orally active compound that acts as a dihydroorotate dehydrogenase (DHODH) inhibitor and serves as a novel modulator of the farnesoid X receptor (FXR). This immunomodulat...
T69724 Cilofexor tromethamine
Cilofexor, also known as GS-9674, is a farnesoid X receptor (FXR) agonist. The nonsteroidal FXR agonist cilofexor (GS-9674) improves markers of cholestasis and liver injury in patients with PSC. In clinical study, cilof...
T11661 INT-767 FXR , GPCR19
INT-767 is a potent farnesoid X receptor (FXR)/TGR5 dual agonist that prevents NASH and promotes visceral adipose brown lipogenesis and mitochondrial function for the study of non-alcoholic steatohepatitis.
T37414 CAY10771
CAY10771 is a dual agonist of farnesoid X receptor (FXR) and peroxisome proliferator-activated receptor δ (PPARδ).1It activates FXR and PPARδ in reporter assays using HEK293T cells (EC50s = 0.94 and 1.5 μM, respectively)...
T69686 BMS-986318
BMS-986318 is a potent nonbile acid FXR agonist, displaying EC50 values of 53 nM and 350 nM in FXR Gal4 and SRC-1 recruitment assays, respectively. It exhibits a favorable ADME profile and shows effectiveness in mouse mo...
T78910 ZLY28 FXR
ZLY28 is a novel, first-in-class compound with specific intestinal restriction and oral activity, serving as a dual modulator of FXR and FABP1. Additionally, it is a pioneering anti-NASH agent, utilized in the study of n...
T73155 BMS-986339
BMS-986339 is an orally active, potent FXR agonist that interacts via H-bond formation with the His298 and ASN287 residues. It is utilized in research focused on primary biliary cirrhosis (PBC), primary sclerosing cholan...
T37416 Tauro-α-muricholic Acid (sodium salt)
Tauro-α-muricholic acid (TαMCA) is an antagonist of the farnesoid X receptor (FXR; IC50 = 28 μM) and a taurine-conjugated form of the murine-specific primary bile acid α-muricholic acid . TαMCA is common in rodents but h...
T83858 Tauro-Obeticholic Acid sodium Tauro-6-Ethylchenodeoxycholic Acid,Tauro-6-Ethyl-CDCA,Obeticholic Acid Taurine Conjugate,Tauro-OCA,T-ECDCA
Tauro-obeticholic acid, a farnesoid X receptor (FXR) agonist and semisynthetic derivative of chenodeoxycholic acid, is an active metabolite of obeticholic acid. This compound undergoes taurine conjugation in the liver to...

Compounds

Turofexorate Isopropyl
T6053
Synonym: XL335,FXR-450,WAY-362450
Target: FXR, Autophagy
FXR/TGR5 agonist 1
T40302
Synonym:
Target:
FXR antagonist 1
T64144
Synonym:
Target:
FXR agonist 3
T74996
Synonym:
Target:
FXR agonist 4
T72889
Synonym:
Target:
FXR agonist 5
T75160
Synonym:
Target:
FXR antagonist 2
T74754
Synonym:
Target:
Fexaramine
T2015
Synonym:
Target: FXR, Autophagy
Nidufexor
T7886
Synonym:
Target: FXR, Autophagy
GW 4064
T2233
Synonym:
Target: FXR, Autophagy
LY2562175
T15806
Synonym:
Target: FXR, Autophagy
Sevelamer hydrochloride
T6344
Synonym: Sevelamer HCl
Target: FXR, Autophagy
DY268
T31587
Synonym: DY 268,DY-268
Target: FXR
Tropifexor
T4379
Synonym: LJN452
Target: FXR, Autophagy
Cilofexor
T7436
Synonym:
Target: FXR, Autophagy
Glyco-Obeticholic acid
T11428
Synonym:
Target: FXR
Vidofludimus
T2601
Synonym: SC12267,4sc-101
Target: Dehydrogenase, DNA/RNA Synthesis, Interleukin
Vonafexor
T8471
Synonym: EYP001,PLX007,pxl007
Target: FXR, HBV
BAR502
TQ0252
Synonym:
Target: FXR, GPCR19, Autophagy
Obeticholic Acid
T1789
Synonym: INT-747,6-Ethylchenodeoxycholic acid,6-ECDCA
Target: FXR, Autophagy
T0901317
T6690
Synonym:
Target: Apoptosis, FXR, Liver X Receptor, ROR
GSK2324
T27460
Synonym: GSK-2324,GSK 2324
Target: FXR
NDB
T63042
Synonym:
Target: FXR
Gly-β-MCA
T11426
Synonym:
Target: FXR
TC-G 1005
T8818
Synonym:
Target: GPCR19
PX20606 trans racemate
T12583
Synonym: PX-102 trans racemate
Target: Others
Tauro-β-muricholic acid sodium
T13093
Synonym: T-βMCA sodium
Target: FXR
DM175
T68612
Synonym:
Target:
Fexarene
T25417
Synonym:
Target:
ST-1892
T24837
Synonym:
Target:
GSK-8062
T27492
Synonym: GSK 8062
Target:
EDP-305
T73414
Synonym:
Target:
NR1H4 activator 1
T12251
Synonym:
Target: Others
Omesdafexor
T63818
Synonym:
Target:
Vidofludimus hemicalcium
T70899
Synonym: 4sc-101 hemicalcium,SC12267 hemicalcium,4sc-101 hemicalcium ; SC12267 hemicalcium
Target:
Cilofexor tromethamine
T69724
Synonym:
Target:
INT-767
T11661
Synonym:
Target: FXR, GPCR19
CAY10771
T37414
Synonym:
Target:
BMS-986318
T69686
Synonym:
Target:
ZLY28
T78910
Synonym:
Target: FXR
BMS-986339
T73155
Synonym:
Target:
Tauro-α-muricholic Acid (sodium salt)
T37416
Synonym:
Target:
Tauro-Obeticholic Acid sodium
T83858
Synonym: Tauro-6-Ethylchenodeoxycholic Acid,Tauro-6-Ethyl-CDCA,Obeticholic Acid Taurine Conjugate,Tauro-OCA,T-ECDCA
Target:
Cat No. Product Name Synonyms Targets
T13092 Tauro-Obeticholic acid FXR
Tauro-Obeticholic acid is an active Obeticholic acid metabolite. Obeticholic acid is an orally bioavailable agonist of farnesoid-X receptor (FXR).
T0847 Chenodeoxycholic acid CDCA,Chenodiol Potassium Channel , FXR , Endogenous Metabolite , Autophagy
Chenodeoxycholic acid (CDCA) is a bile acid, usually conjugated with either glycine or taurine. It acts as a detergent to solubilize fats for intestinal absorption and is reabsorbed by the small intestine. It is used as ...
T2939 Forskolin Coleonol,Colforsin FXR , Adenylyl cyclase , AChR , Autophagy
Forskolin (Coleonol) is a natural product, an adenylate cyclase activator (EC50=0.5 μM). Forskolin increases cAMP levels, activates PXR and FXR, and induces autophagy. Forskolin produces positive inotropic effects in the...
T5574 Guggulsterone Guggulsterone E&Z Apoptosis , FXR , Akt , Caspase , JNK , Autophagy
Guggulsterone (Guggulsterone E&Z) E&Z is a 3-hydroxy steroid. It has a role as an androgen.
T0700 Ursodeoxycholic acid UDCA,Ursodiol Potassium Channel , Endogenous Metabolite
Ursodeoxycholic acid (UDCA) can be used to dissolve gallstones and reduce cholesterol absorption.
T29078 Ursodeoxycholic acid sodium UDCA Na,UDCA sodium,Sodium Ursodeoxycholate,Ursodiol sodium,Ursodeoxycholic Acid (sodium salt),Ursodeoxycholate sodium FXR , Endogenous Metabolite , GPCR19
Ursodeoxycholic acid sodium (Sodium Ursodeoxycholate) is a naturally occurring secondary bile acid with anti-inflammatory and cytoprotective activities. Ursodeoxycholic acid sodium acts as signaling molecule, exerting it...
T6S2246 Alisol B 23-acetate Alisol B Acetate,Alisol B monoacetate,23-O-Acetylalisol B,23-Acetylalismol B Others
1. Alisol B 23-acetate (Alisol B Acetate) produces protective effect against ANIT-induced hepatotoxity and cholestasis, due to FXR-mediated regulation of transporters and enzymes. 2. Alisol B 23-acetate produces promotiv...
T8895 Altenusin FXR
Altenusin is a natural nonsteroidal fungal metabolite, as a novel selective agonist of FXR with an EC50 value of 3.2 ± 0.2 μM.
T36563 (E)-Guggulsterone
Bile acids are essential for solubilization and transport of dietary lipids, are the major products of cholesterol catabolism, and are physiological ligands for farnesoid X receptor (FXR), a nuclear receptor that regulat...
T75538 Alismanol M
Alismanol M, a protostane-type triterpenoid isolated from the rhizome of Alisma orientale, functions as a farnesoid X receptor (FXR) agonist with an EC50 value of 50.25 μM. It is utilized in researching cholestasis and n...
T81030 Tauro-β-muricholic acid TβMCA FXR
Tauro-β-muricholic acid (TβMCA), a trihydroxylated bile acid, acts as a competitive and reversible FXR antagonist (IC 50 = 40 μM) and exhibits antiapoptotic effects by inhibiting bile acid-induced hepatocellular apoptosi...
TN4628 Nelumol A FXR
Nelumol A, and nelumal A show a potency comparable to the endogenous ligand, they may as a valuable potential novel lead compound in the search for FXR agonists.

Recombinant Proteins

Cat No. Product Name Species Expression System
TMPY-06756 NR1H4 Protein, Mouse, Recombinant (His) Mouse E. coli
TMPY-06768 NR1H4 Protein, Human, Recombinant (His) Human E. coli
TMPH-01355 FXR1 Protein, Human, Recombinant (His) Human E. coli
RNA-binding protein required for embryonic and postnatal development of muscle tissue. May regulate intracellular transport and local translation of certain mRNAs.
TMPY-02987 Vitamin D Receptor/VDR Protein, Mouse, Recombinant (His) Mouse Baculovirus-Insect Cells
VDR (vitamin D (1,25- dihydroxyvitamin D3) receptor), also known as NR1I1, belongs to the NR1I family, NR1 subfamily. It is composed of three domains: a modulating N-terminal domain, a DNA-binding domain and a C-terminal...
TMPY-02706 Vitamin D Receptor/VDR Protein, Human, Recombinant (His) Human Baculovirus-Insect Cells
VDR (vitamin D (1,25- dihydroxyvitamin D3) receptor), also known as NR1I1, belongs to the NR1I family, NR1 subfamily. It is composed of three domains: a modulating N-terminal domain, a DNA-binding domain and a C-terminal...
TargetMol