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CAS: 335196-25-3
IUPAC Name: 
2-oxooxolan-3-yl adamantane-1-carboxylate
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Enamine Ltd.
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5 days 83.00
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Zoom the structure CSSS00026098601 Add to cart
IUPAC Name: 
methyl 7-hydroxy-9a,11a-dimethyl-1H,2H,3H,3aH,3bH,4H,6H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthrene-1-carboxylate
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Enamine Ltd.
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5 days 74.00
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UORSY
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5 days 74.00
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Zoom the structure CSSS00026705790 Add to cart
IUPAC Name: 
3-[6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-3-(2,4,5-trihydroxy-6-methylhept-6-en-2-yl)-4-[(3,4,5-trihydroxy-6-methyloxan-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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Zoom the structure CSSS03437843615 Add to cart
IUPAC Name: 
3-[6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-3-(2,4,5-trihydroxy-6-methylhept-6-en-2-yl)-4-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-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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Zoom the structure CSSS20621634852 Add to cart
IUPAC Name: 
7-{[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-1-[1-(6-methoxy-5-methyloxan-2-yl)ethyl]-9a,11a-dimethyl-hexadecahydro-1H-cyclopenta[a]phenanthren-5-one
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AnalytiCon Discovery GmbH
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IUPAC Name: 
(7S,9aR,11aS)-7-{[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-1-[1-(6-methoxy-5-methyloxan-2-yl)ethyl]-9a,11a-dimethyl-hexadecahydro-1H-cyclopenta[a]phenanthren-5-one
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AnalytiCon Discovery GmbH
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Zoom the structure CSSS20621634877 Add to cart
IUPAC Name: 
methyl (4R)-4-[(1R,3aS,3bR,4R,5aR,9aS,9bS,11aR)-4-hydroxy-9a,11a-dimethyl-7-oxo-hexadecahydro-1H-cyclopenta[a]phenanthren-1-yl]pentanoate
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MedChemExpress
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10 days 70.00
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Description: Names: Methyl 7α-hydroxy-3-ketocholanoate; Product Description: Methyl 7α-hydroxy-3-ketocholanoate is a bile acid compound that can be used in neurological disease research; Target: Biochemical Assay Reagents; CAS: 14773-00-3
MedChemExpress EU
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Description: Names: Methyl 7α-hydroxy-3-ketocholanoate; Product Description: Methyl 7α-hydroxy-3-ketocholanoate is a bile acid compound that can be used in neurological disease research; Target: Biochemical Assay Reagents; CAS: 14773-00-3
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Zoom the structure CSSS00020664658 Add to cart
IUPAC Name: 
(2S,3R,4S,5S,6R)-2-{[(2R,3R,4S,5S,6R)-2-{[(1S,3aR,3bR,5S,5aR,7S,9aR,9bR,11R,11aR)-7,11-dihydroxy-1-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-3a,3b,6,6,9a-pentamethyl-hexadecahydro-1H-cyclopenta[a]phenanthren-5-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol
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MedChemExpress
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10 days 56.00
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Description: Names: Ginsenoside Rf; Panaxoside Rf; Product Description: Ginsenoside Rf is a trace component of ginseng root. Ginsenoside Rf inhibits N-type Ca2 channel.; Target: Calcium Channel;Endogenous Metabolite; CAS: 52286-58-5
MedChemExpress EU
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Description: Names: Ginsenoside Rf; Panaxoside Rf; Product Description: Ginsenoside Rf is a trace component of ginseng root. Ginsenoside Rf inhibits N-type Ca2 channel.; Target: Calcium Channel;Endogenous Metabolite; CAS: 52286-58-5
ChemFaces
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12 days
24.00
1 mg
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Targetmol Chemicals Inc
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30 days 44.00
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Description: Ginsenoside Rf (Panaxoside Rf) is a trace component of ginseng root. Ginsenoside Rf inhibits N-type Ca2 channel.; CAS: 52286-58-5
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Zoom the structure CSSS00159261226 Add to cart
IUPAC Name: 
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-sulfonic acid
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BLD PHARMATECH LTD CN
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7 days 55.00
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Description: Name:2-((R)-4-((3R,5R,8R,9S,10S,13R,14S,17R)-3-Hydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanamido)ethane-1-sulfonic acid; Hazard statement: 8; CAS: 516-90-5
MedChemExpress
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10 days 60.00
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Description: Names: Taurolithocholic acid; Product Description: Taurolithocholic acid is an orally active bile acid and antiviral agent. Taurolithocholic acid upregulates FADS2 by activating the TGR5-PI3K/AKT-SREBP2 signaling axis, inhibits SFTSV-induced ferroptosis (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 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 serves as an experimental model compound for hepatocellular cholestasis. At concentrations ≤200 μM, Taurolithocholic acid shows no cytotoxicity and does not activate the interferon pathway. Taurolithocholic acid 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: 516-90-5
MedChemExpress EU
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10 days 60.00
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Description: Names: Taurolithocholic acid; Product Description: Taurolithocholic acid is an orally active bile acid and antiviral agent. Taurolithocholic acid upregulates FADS2 by activating the TGR5-PI3K/AKT-SREBP2 signaling axis, inhibits SFTSV-induced ferroptosis (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 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 serves as an experimental model compound for hepatocellular cholestasis. At concentrations ≤200 μM, Taurolithocholic acid shows no cytotoxicity and does not activate the interferon pathway. Taurolithocholic acid 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: 516-90-5
Apexbio Technology LLC
Ships from: United States
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10 days
143.00
100 ug
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Description: Name: Taurolithocholic Acid MaxSpec® Standard; Taurolithocholic acid is a quantitative analytical standard guaranteed to meet MaxSpec identity, purity, stability, and concentration specifications.; CAS: 516-90-5
Targetmol Chemicals Inc
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30 days 30.00
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Description: Taurolithocholic acid 3-sulfate (TLC-S) induces Ca²⁺ signaling in isolated murine pancreatic acinar cells (PACs). Ca²⁺ oscillations occur at concentrations as low as 25 μM and are triggered in nearly all cells at 200 μM. At 300–500 μM, Taurolithocholic produces prolonged Ca²⁺ elevations that begin with intracellular Ca²⁺ release and are sustained by extracellular Ca²⁺ influx. Other bile salts, including taurodeoxycholate (TDC) and taurocholate (TC), can also stimulate local and global Ca²⁺ oscillations but only at much higher concentrations (approximately 1 mM and 5 mM). Taurolithocholic is a potent Ca²⁺-releasing bile acid tested in PACs and is uniquely effective at inducing Ca²⁺-independent ionic currents even at low micromolar levels. Therefore implicating Taurolithocholic as a strong canidate for researches in gut metabolism.; CAS: 516-90-5
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Zoom the structure CSSS00102595833 Add to cart
IUPAC Name: 
2-[(4R)-4-[(1R,3aS,3bS,5S,5aR,7R,9aR,9bS,11aR)-5,7-dihydroxy-9a,11a-dimethyl-hexadecahydro-1H-cyclopenta[a]phenanthren-1-yl]pentanamido]ethane-1-sulfonic acid
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BLD Pharmatech Co., Limited
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1 day 80.00
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Description: Name:2-((R)-4-((3R,5R,6S,8S,9S,10R,13R,14S,17R)-3,6-Dihydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanamido)ethane-1-sulfonic acid; Hazard statement: 8; CAS: 2958-04-5
BLD PHARMATECH LTD CN
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7 days 80.00
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Description: Name:2-((R)-4-((3R,5R,6S,8S,9S,10R,13R,14S,17R)-3,6-Dihydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanamido)ethane-1-sulfonic acid; Hazard statement: 8; CAS: 2958-04-5
MedChemExpress
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10 days 120.00
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Description: Names: Taurohyodeoxycholic acid; Product Description: Taurohyodeoxycholic acid is an orally active 6 alpha-hydroxylated bile acid. Taurohyodeoxycholic acid decreases colonic MPO activity, TNF-α, lL-6 serum levels and the expression of COX-2. Taurohyodeoxycholic acid alleviates trinitrobenzene sulfonic acid induced ulcerative colitis via regulating Th1/Th2 and Th17/Treg cells balance. Taurohyodeoxycholic acid ameliorates high-fat diet-induced nonalcoholic fatty liver disease in mice. Taurohyodeoxycholic acid prevents Taurochenodeoxycholic acid (HY-N2027)-induced hepatotoxicity in bile fistula rats. Taurohyodeoxycholic acid can be used for the study of nonalcoholic fatty liver disease (NAFLD), colitis and biliary fistula; Target: COX;Endogenous Metabolite;Glutathione Peroxidase;Interleukin Related;TNF Receptor; CAS: 2958-04-5
MedChemExpress EU
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10 days 120.00
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Description: Names: Taurohyodeoxycholic acid; Product Description: Taurohyodeoxycholic acid is an orally active 6 alpha-hydroxylated bile acid. Taurohyodeoxycholic acid decreases colonic MPO activity, TNF-α, lL-6 serum levels and the expression of COX-2. Taurohyodeoxycholic acid alleviates trinitrobenzene sulfonic acid induced ulcerative colitis via regulating Th1/Th2 and Th17/Treg cells balance. Taurohyodeoxycholic acid ameliorates high-fat diet-induced nonalcoholic fatty liver disease in mice. Taurohyodeoxycholic acid prevents Taurochenodeoxycholic acid (HY-N2027)-induced hepatotoxicity in bile fistula rats. Taurohyodeoxycholic acid can be used for the study of nonalcoholic fatty liver disease (NAFLD), colitis and biliary fistula; Target: COX;Endogenous Metabolite;Glutathione Peroxidase;Interleukin Related;TNF Receptor; CAS: 2958-04-5
Targetmol Chemicals Inc
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30 days 42.00
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Description: Taurohyodeoxycholic acid (THDCA) is a bile acid that plays a key role in regulating the hepatic inflammatory microenvironment.THDCA reduces the expression of TNF-α and IL-6 and inhibits the development of hepatocellular carcinoma (HCC). It is able to inhibit non-alcoholic fatty liver disease and regulate bile acid metabolism in combination with astragalus polysaccharides: it reduces CD36 expression in the liver and decreases hepatic lipid accumulation by up-regulating CYP7B1 and down-regulating CYP7A1.; CAS: 2958-04-5
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Zoom the structure CSSS00020618952 Add to cart
IUPAC Name: 
(1R,3aS,5aR,7R,8S,9aR,9bR,11aR)-1-[(2S,3R)-3,6-dihydroxy-6-methylheptan-2-yl]-3a,7,8-trihydroxy-9a,11a-dimethyl-1H,2H,3H,3aH,5H,5aH,6H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-5-one
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MedChemExpress
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10 days 127.00
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Description: Names: Ecdysone; α-Ecdysone; Product Description: Ecdysone (α-Ecdysone), a major steroid hormone in insects and herbs, triggers mineralocorticoid receptor (MR) activation and induces cellular apoptosis. Ecdysone plays essential roles in coordinating developmental transitions and homeostatic sleep regulation through its active metabolite 20-hydroxyecdysone (Crustecdysone; 20E; HY-N6979); Target: Apoptosis;Endogenous Metabolite; CAS: 3604-87-3
MedChemExpress EU
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10 days 127.00
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Description: Names: Ecdysone; α-Ecdysone; Product Description: Ecdysone (α-Ecdysone), a major steroid hormone in insects and herbs, triggers mineralocorticoid receptor (MR) activation and induces cellular apoptosis. Ecdysone plays essential roles in coordinating developmental transitions and homeostatic sleep regulation through its active metabolite 20-hydroxyecdysone (Crustecdysone; 20E; HY-N6979); Target: Apoptosis;Endogenous Metabolite; CAS: 3604-87-3
ChemFaces
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12 days
257.00
1 mg
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Zoom the structure CSSS00000052408 Add to cart
IUPAC Name: 
(3R,3aS,6R,6aS,9R,10R,10aS)-9,10-dihydroxy-3,6,9-trimethyl-decahydro-2H-naphtho[4a,4-b]furan-2-one
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ChemFaces
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12 days
243.00
1 mg
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Zoom the structure CSSS00159260781 Add to cart
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