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(20S)-Protopanaxatriol - 10mM in DMSO, high purity , CAS No.34080-08-5
Ginsenoside Rg1, Re, Rf and Rg2 analog
Basic Description Synonyms (20S)-Protopanaxatriol | 34080-08-5 | Protopanaxatriol | Protopanaxtriol | 20(S)-protopanaxatriol | 20S-Protopanaxatriol | g-PPT | ZMK19P3WMP | 20(S)-APPT | CHEBI:75951 | dammar-24-ene-3beta,6alpha,12beta,20-tetrol | (3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-17-[(2S)-2-hydroxy-6-me Specifications & Purity 10mM in DMSO Biochemical and Physiological Mechanisms Ginsenoside Rg1 , Re, Rf and Rg2 analog. Increases intracellular Ca 2+ levels. Induces eNOS activation and NO production. Functional GR and ERβ receptor ligand. Active in vivo. Storage Temp Store at -80°C Shipped In Ice chest + Ice pads
Associated Targets(Human) Associated Targets(non-human) Names and Identifiers IUPAC Name (3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-17-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,6,12-triol INCHI InChI=1S/C30H52O4/c1-18(2)10-9-13-30(8,34)19-11-15-28(6)24(19)20(31)16-22-27(5)14-12-23(33)26(3,4)25(27)21(32)17-29(22,28)7/h10,19-25,31-34H,9,11-17H2,1-8H3/t19-,20+,21-,22+,23-,24-,25-,27+,28+,29+,30-/m0/s1 InChi Key SHCBCKBYTHZQGZ-CJPZEJHVSA-N Canonical SMILES CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CC(C4C3(CCC(C4(C)C)O)C)O)C)O)C)O)C Isomeric SMILES CC(=CCC[C@@](C)([C@H]1CC[C@@]2([C@@H]1[C@@H](C[C@H]3[C@]2(C[C@@H]([C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)O)C)O)C)O)C PubChem CID 11468733 Molecular Weight 476.73
Chemical and Physical Properties Sensitivity light sensitive
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