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ListPlate
IUPAC Name: 
(1R,3aS,3bS,5R,7S,9aR,9bS,11aR)-1-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1H,2H,3H,3aH,3bH,4H,5H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthrene-5,7-diol
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ChemFaces
Ships from: China
To:
12 days
204.00
1 mg
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CAS: 70389-88-7
IUPAC Name: 
(1S,2S,4aR,5R,8aS)-4a-methyl-8-methylidene-2-(propan-2-yl)-decahydronaphthalene-1,5-diol
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ChemFaces
Ships from: China
To:
12 days
204.00
1 mg
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IUPAC Name: 
[(2S,3R,4R,5R)-3,4-dihydroxy-5-({1-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-3a,3b,6,6,9a-pentamethyl-11-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-hexadecahydro-1H-cyclopenta[a]phenanthren-7-yl}oxy)oxolan-2-yl]methyl acetate
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AnalytiCon Discovery GmbH
Ships from: Germany
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15 days 339.90
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Description: CAS: 1403937-87-0
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IUPAC Name: 
(1R,2R,4S,7S,8R,9R,10S,11R,12S,13S,14R,17R,18R,19R)-8-(acetyloxy)-10,19-dihydroxy-1,9,18-trimethyl-15-oxo-16,20-dioxahexacyclo[15.3.2.0²,¹³.0⁴,¹².0⁷,¹¹.0¹⁴,¹⁹]docos-5-ene-5-carboxylic acid
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AnalytiCon Discovery GmbH
Ships from: Germany
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15 days 408.10
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IUPAC Name: 
(3S,4S,5R)-4-[(2R,3R)-3-[(1S,5aR,7R,8S,9aR,9bR,11aR)-3a,7,8-trihydroxy-9a,11a-dimethyl-5-oxo-1H,2H,3H,3aH,5H,5aH,6H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-1-yl]-2,3-dihydroxybutyl]-5-hydroxy-3-methyloxan-2-one
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Targetmol Chemicals Inc
Ships from: United States
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30 days 30.00
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Description: Cyasterone (Cyasteron), a natural EGFR inhibitor, can inhibit the growth of A549 and MGC823 cells, via regulating EGFR signaling pathway, it may be a promising anti-cancer agent. Cyasterone has antifeeding activity.; CAS: 17086-76-9
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IUPAC Name: 
N-[7-(2,4-difluoro-5-methylbenzoyl)-1-oxa-7-azaspiro[4.4]nonan-3-yl]-3,3-dimethylbutanamide
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Enamine Ltd.
Ships from: Ukraine
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TBD 104.00
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IUPAC Name: 
(4S,5S)-9-[(4-fluoro-3-methylphenyl)methyl]-1-oxa-9-azaspiro[5.5]undecane-4,5-diol
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ChemBridge Corp.
Ships from: United States
To:
14 days
68.20
1 mg
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Description: Name: rel-(4S,5S)-9-(4-fluoro-3-methylbenzyl)-1-oxa-9-azaspiro[5.5]undecane-4,5-diol; Stereochemistry: racemic; Compound state: dry film
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IUPAC Name: 
1-{1,7-dihydroxy-2,9a,11a-trimethyl-hexadecahydro-1H-cyclopenta[a]phenanthren-1-yl}ethan-1-one
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ChemBridge Corp.
Ships from: United States
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14 days 68.20
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Description: Name: 3,17-dihydroxy-16-methylpregnan-20-one; Stereochemistry: unknown; Compound state: solid
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IUPAC Name: 
sodium 2-[(4R)-4-[(1R,3aS,3bR,5aR,7R,9aS,9bS,11aR)-7-hydroxy-9a,11a-dimethyl-hexadecahydro(6,6,8,8-²H₄)-1H-cyclopenta[a]phenanthren-1-yl]pentanamido]ethane-1-sulfonate
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MedChemExpress
Ships from: United States
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10 days 430.00
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Description: Names: Taurolithocholic acid-d4 (sodium); Product Description: Taurolithocholic acid-d4 (sodium) is the deuterium labeled Taurolithocholic acid (sodium salt). Taurolithocholic acid sodium is an orally active bile acid and antiviral agent. Taurolithocholic acid sodium 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 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 serves as an experimental model compound for hepatocellular cholestasis. At concentrations ≤200 μM, Taurolithocholic acid sodium shows no cytotoxicity and does not activate the interferon pathway. Taurolithocholic acid sodium 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;Isotope-Labeled Compounds;PI3K;Reactive Oxygen Species (ROS); CAS: 2410279-97-7
MedChemExpress EU
Ships from: Sweden
To:
10 days 430.00
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Description: Names: Taurolithocholic acid-d4 (sodium); Product Description: Taurolithocholic acid-d4 (sodium) is the deuterium labeled Taurolithocholic acid (sodium salt). Taurolithocholic acid sodium is an orally active bile acid and antiviral agent. Taurolithocholic acid sodium 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 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 serves as an experimental model compound for hepatocellular cholestasis. At concentrations ≤200 μM, Taurolithocholic acid sodium shows no cytotoxicity and does not activate the interferon pathway. Taurolithocholic acid sodium 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;Isotope-Labeled Compounds;PI3K;Reactive Oxygen Species (ROS); CAS: 2410279-97-7
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CAS: 64936-83-0
IUPAC Name: 
sodium 2-[(4R)-4-[(1R,3aS,3bR,5aR,7R,9aS,9bS,11aR)-9a,11a-dimethyl-7-{[(sodiooxy)sulfonyl]oxy}-hexadecahydro-1H-cyclopenta[a]phenanthren-1-yl]pentanamido]ethane-1-sulfonate
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MedChemExpress
Ships from: United States
To:
10 days 78.00
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Description: Names: Taurolithocholic acid 3-sulfate (disodium); 3-Sulfotaurolithocholic acid (disodium); Product Description: Taurolithocholic acid 3-sulfate disodium is a GPR39 agonist with EC50s of 71.6 and 69.4 (absence of Zn2 ) and 9 and 9.6 μM (presence of Zn2 ) in M39-20 and hGPR39-2 cells, respectively. Taurolithocholic acid 3-sulfate disodium stimulates GPR39 receptors to initiate intracellular calcium signaling, independent of Zn2 binding sites H17 and H19. Taurolithocholic acid 3-sulfate disodium can be used for the research of gallbladder disease; Target: GPR39; CAS: 64936-83-0
MedChemExpress EU
Ships from: Sweden
To:
10 days 78.00
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Description: Names: Taurolithocholic acid 3-sulfate (disodium); 3-Sulfotaurolithocholic acid (disodium); Product Description: Taurolithocholic acid 3-sulfate disodium is a GPR39 agonist with EC50s of 71.6 and 69.4 (absence of Zn2 ) and 9 and 9.6 μM (presence of Zn2 ) in M39-20 and hGPR39-2 cells, respectively. Taurolithocholic acid 3-sulfate disodium stimulates GPR39 receptors to initiate intracellular calcium signaling, independent of Zn2 binding sites H17 and H19. Taurolithocholic acid 3-sulfate disodium can be used for the research of gallbladder disease; Target: GPR39; CAS: 64936-83-0
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IUPAC Name: 
sodium (2S,3S,4S,5R,6R)-6-{[(1R,3aS,3bR,4R,5aR,7R,9aS,9bS,11S,11aR)-4,11-dihydroxy-9a,11a-dimethyl-1-[(2R)-5-oxo-5-(sodiooxy)pentan-2-yl]-hexadecahydro-1H-cyclopenta[a]phenanthren-7-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylate
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MedChemExpress
Ships from: United States
To:
10 days
325.00
1 mg
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Description: Names: Cholic acid 3-O-glucuronide (disodium); OCA-3-glucuronide (disodium); Product Description: Cholic acid 3-O-glucuronide (OCA-3-glucuronide) disodium is a farnesoid X receptor (FXR) agonist with an EC50 value of 91.5 μM. Cholic acid 3-O-glucuronide is promising for research of bile acid metabolism and detoxification; Target: FXR; CAS: 59274-69-0
MedChemExpress EU
Ships from: Sweden
To:
10 days
325.00
1 mg
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Description: Names: Cholic acid 3-O-glucuronide (disodium); OCA-3-glucuronide (disodium); Product Description: Cholic acid 3-O-glucuronide (OCA-3-glucuronide) disodium is a farnesoid X receptor (FXR) agonist with an EC50 value of 91.5 μM. Cholic acid 3-O-glucuronide is promising for research of bile acid metabolism and detoxification; Target: FXR; CAS: 59274-69-0
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IUPAC Name: 
N-{[(2R,3S,4R)-4-{[(2-fluorophenyl)methyl]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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