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ListPlate
IUPAC Name: 
sodium (4R)-4-[(1R,3aS,3bR,4R,5aS,7R,9aS,9bS,11aR)-4,7-dihydroxy-9a,11a-dimethyl-hexadecahydro-1H-cyclopenta[a]phenanthren-1-yl]pentanoate
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MedChemExpress
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10 days 30.00
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Description: Names: Chenodeoxycholic acid (sodium); CDCA (sodium); Product Description: Chenodeoxycholic acid sodium is a hydrophobic primary bile acid that activates nuclear receptors (FXR) involved in cholesterol metabolism.; Target: Autophagy;Endogenous Metabolite;FXR; CAS: 2646-38-0
MedChemExpress EU
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10 days 30.00
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Description: Names: Chenodeoxycholic acid (sodium); CDCA (sodium); Product Description: Chenodeoxycholic acid sodium is a hydrophobic primary bile acid that activates nuclear receptors (FXR) involved in cholesterol metabolism.; Target: Autophagy;Endogenous Metabolite;FXR; CAS: 2646-38-0
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IUPAC Name: 
4-[(5aR,7R,9aS,11aR)-7-hydroxy-9a,11a-dimethyl-hexadecahydro-1H-cyclopenta[a]phenanthren-1-yl]-N-(2-hydroxyethyl)pentanamide
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Specs
Ships from: Netherlands
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12 days 420.00
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Description: 4-(3-hydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)-N-(2-hydroxyethyl)pentanamide
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IUPAC Name: 
(4R)-4-[(1R,5aR,7R,9aS,11aR)-7-(formyloxy)-9a,11a-dimethyl-hexadecahydro-1H-cyclopenta[a]phenanthren-1-yl]pentanoic acid
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Specs
Ships from: Netherlands
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12 days 420.00
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Description: 4-[3-(formyloxy)-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoic acid
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IUPAC Name: 
(8S,10aS,12aS)-10a,12a-dimethyl-2-oxo-hexadecahydro-2H-phenanthro[2,1-b]pyran-8-yl acetate
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Specs
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12 days 420.00
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Description: 10a,12a-dimethyl-2-oxohexadecahydro-2H-naphtho[2,1-f]chromen-8-yl acetate
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IUPAC Name: 
(1S,2R,5aS,9aS,11aS)-1-acetyl-1,2-dihydroxy-9a,11a-dimethyl-hexadecahydro-1H-cyclopenta[a]phenanthren-7-yl acetate
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Princeton Biomolecular Research
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10 days 88.00
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IUPAC Name: 
N-{[(2R,3S,4R)-4-[(2,2-dimethylpropyl)amino]-3-hydroxyoxolan-2-yl]methyl}-3,3-dimethylbutanamide
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AnalytiCon Discovery GmbH
Ships from: Germany
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15 days 190.30
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IUPAC Name: 
sodium 2-[(4R)-4-[(1R,3aS,3bR,5aR,7R,9aS,9bS,11aR)-7-hydroxy-9a,11a-dimethyl-hexadecahydro-1H-cyclopenta[a]phenanthren-1-yl]pentanamido]ethane-1-sulfonate
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MedChemExpress
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10 days 50.00
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Description: Names: Taurolithocholic acid (sodium salt); Product Description: Taurolithocholic acid sodium salt is an orally active bile acid and antiviral agent. Taurolithocholic acid sodium salt upregulates FADS2 by activating the TGR5-PI3K/AKT-SREBP2 signaling axis, inhibits SFTSV-induced ferroptosis, viral replication and viral entry of HBV/HDV, while reducing the release of IL-1β, lipid ROS and LDH. While exerting antiviral protective effects, Taurolithocholic acid sodium salt also stimulates the recycling of hepatocellular membrane transporters, impairs canalicular bile acid secretion function, and induces hepatocyte cholestasis, apoptosis and acute hepatocellular injury. Taurolithocholic acid sodium salt serves as an experimental model compound for hepatocellular cholestasis. At concentrations ≤200 μM, Taurolithocholic acid sodium salt shows no cytotoxicity and does not activate the interferon pathway. Taurolithocholic acid sodium salt not only protects mice from lethal SFTSV infection but also is suitable for studies related to severe fever with thrombocytopenia syndrome and cholestasis; Target: Akt;Calcium Channel;Ferroptosis;HBV;PI3K;Reactive Oxygen Species (ROS); CAS: 6042-32-6
MedChemExpress EU
Ships from: Sweden
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10 days 50.00
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Description: Names: Taurolithocholic acid (sodium salt); Product Description: Taurolithocholic acid sodium salt is an orally active bile acid and antiviral agent. Taurolithocholic acid sodium salt upregulates FADS2 by activating the TGR5-PI3K/AKT-SREBP2 signaling axis, inhibits SFTSV-induced ferroptosis, viral replication and viral entry of HBV/HDV, while reducing the release of IL-1β, lipid ROS and LDH. While exerting antiviral protective effects, Taurolithocholic acid sodium salt also stimulates the recycling of hepatocellular membrane transporters, impairs canalicular bile acid secretion function, and induces hepatocyte cholestasis, apoptosis and acute hepatocellular injury. Taurolithocholic acid sodium salt serves as an experimental model compound for hepatocellular cholestasis. At concentrations ≤200 μM, Taurolithocholic acid sodium salt shows no cytotoxicity and does not activate the interferon pathway. Taurolithocholic acid sodium salt not only protects mice from lethal SFTSV infection but also is suitable for studies related to severe fever with thrombocytopenia syndrome and cholestasis; Target: Akt;Calcium Channel;Ferroptosis;HBV;PI3K;Reactive Oxygen Species (ROS); CAS: 6042-32-6
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IUPAC Name: 
2-{2-[4-phenyl-2-(propan-2-yl)oxan-4-yl]ethyl}-2,3-dihydro-1H-isoindole-1,3-dione
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Princeton Biomolecular Research
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10 days 88.00
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ChemBridge Corp.
Ships from: United States
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14 days 68.20
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Description: Name: 2-[2-(2-isopropyl-4-phenyltetrahydro-2H-pyran-4-yl)ethyl]-1H-isoindole-1,3(2H)-dione; Stereochemistry: unknown; Compound state: liquid
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IUPAC Name: 
3-[(3S,3aR,4R,6S,7S,9aR,9bR)-3-[(2S,4E)-2,6-dihydroxy-6-methylhept-4-en-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-4-{[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}-dodecahydro-1H-cyclopenta[a]naphthalen-6-yl]propanoic acid
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AnalytiCon Discovery GmbH
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15 days 339.90
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Description: CAS: 168146-27-8
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IUPAC Name: 
(2S,3S,4S,5R,6R)-6-{[(1R,3aS,3bR,4R,5aR,7R,9aS,9bS,11aR)-1-[(2R)-4-carboxybutan-2-yl]-4-hydroxy-9a,11a-dimethyl-hexadecahydro-1H-cyclopenta[a]phenanthren-7-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic acid
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MedChemExpress
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10 days 97.00
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Description: Names: Chenodeoxycholic acid 3-glucuronide; Product Description: Chenodeoxycholic acid 3-glucuronide is a metabolite of Chenodeoxycholic acid that can activate the key nuclear receptor (FXR), with an EC50 of 8 μM, and in HEK293T cells, the EC50 for activating FXR is 11 μM; Target: FXR; CAS: 58814-71-4
MedChemExpress EU
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Description: Names: Chenodeoxycholic acid 3-glucuronide; Product Description: Chenodeoxycholic acid 3-glucuronide is a metabolite of Chenodeoxycholic acid that can activate the key nuclear receptor (FXR), with an EC50 of 8 μM, and in HEK293T cells, the EC50 for activating FXR is 11 μM; Target: FXR; CAS: 58814-71-4
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IUPAC Name: 
(1R,3aS,3bS,7S,9aR,9bS,11aR)-1-[(2R,5R)-5-hydroxy-6-methylheptan-2-yl]-9a,11a-dimethyl-1H,2H,3H,3aH,3bH,4H,6H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-7-ol
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Apexbio Technology LLC
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10 days 277.20
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Description: Name: 24(R)-hydroxy Cholesterol; LXRα and LXRβ nuclear receptors activator; Format: a crystalline solid; CAS: 27460-26-0
MedChemExpress
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Description: Names: 24(R)-Hydroxycholesterol; 24R-OHC; 24R-HC; 24(R)-Cerebrosterol; Product Description: 24(R)-Hydroxycholesterol (24R-OHC) is a key intermediate of Tacalcitol (HY-32337); Target: Drug Intermediate; CAS: 27460-26-0
MedChemExpress EU
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Description: Names: 24(R)-Hydroxycholesterol; 24R-OHC; 24R-HC; 24(R)-Cerebrosterol; Product Description: 24(R)-Hydroxycholesterol (24R-OHC) is a key intermediate of Tacalcitol (HY-32337); Target: Drug Intermediate; CAS: 27460-26-0
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IUPAC Name: 
sodium (4R)-4-[(1R,3aS,3bR,4S,5aS,7R,9aS,9bS,11aR)-4,7-dihydroxy-9a,11a-dimethyl-hexadecahydro-1H-cyclopenta[a]phenanthren-1-yl]pentanoate
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MedChemExpress
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10 days 25.00
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Description: Names: Ursodeoxycholic acid (sodium); Ursodeoxycholate (sodium); Ursodiol (sodium); UCDA (sodium); Product Description: Ursodeoxycholic acid (Ursodeoxycholate) sodium is a secondary bile acid issued from the transformation of (cheno)deoxycholic acid by intestinal bacteria, acting as a key regulator of the intestinal barrier integrity and essential for lipid metabolism. Ursodeoxycholic acid sodium acts as signaling molecule, exerting its effects by interacting with bile acid activated receptors, including G-protein coupled bile acid receptor 5 (TGR5, GPCR19) and the farnesoid X receptor (FXR). Ursodeoxycholic acid sodium can be used for the research of a variety of hepatic and gastrointestinal diseases. Orally active; Target: Endogenous Metabolite;FXR;G protein-coupled Bile Acid Receptor 1; CAS: 2898-95-5
MedChemExpress EU
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10 days 25.00
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Description: Names: Ursodeoxycholic acid (sodium); Ursodeoxycholate (sodium); Ursodiol (sodium); UCDA (sodium); Product Description: Ursodeoxycholic acid (Ursodeoxycholate) sodium is a secondary bile acid issued from the transformation of (cheno)deoxycholic acid by intestinal bacteria, acting as a key regulator of the intestinal barrier integrity and essential for lipid metabolism. Ursodeoxycholic acid sodium acts as signaling molecule, exerting its effects by interacting with bile acid activated receptors, including G-protein coupled bile acid receptor 5 (TGR5, GPCR19) and the farnesoid X receptor (FXR). Ursodeoxycholic acid sodium can be used for the research of a variety of hepatic and gastrointestinal diseases. Orally active; Target: Endogenous Metabolite;FXR;G protein-coupled Bile Acid Receptor 1; CAS: 2898-95-5
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