1.0 2010-04-08 22:12:58 UTC 2019-11-26 03:14:29 UTC FDB017224 Ginsenoside Rh5 Constituent of Panax vietnamensis (Vietnamese ginseng). Ginsenoside Rh5 is found in tea. Ginsenoside Rh5 C37H64O9 652.8987 652.455033646 2-{[5,16-dihydroxy-14-(2-methoxy-6-methylhept-5-en-2-yl)-2,6,6,10,11-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-8-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol 2-{[5,16-dihydroxy-14-(2-methoxy-6-methylhept-5-en-2-yl)-2,6,6,10,11-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-8-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol 340270-88-4 COC(C)(CCC=C(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(CC21C)OC1OC(CO)C(O)C(O)C1O InChI=1S/C37H64O9/c1-20(2)11-10-14-37(8,44-9)21-12-16-35(6)27(21)22(39)17-25-34(5)15-13-26(40)33(3,4)31(34)23(18-36(25,35)7)45-32-30(43)29(42)28(41)24(19-38)46-32/h11,21-32,38-43H,10,12-19H2,1-9H3 WTSNEXSNFSFTFK-UHFFFAOYSA-N belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Triterpenoids Organic compounds Lipids and lipid-like molecules Prenol lipids Triterpenoids Aliphatic heteropolycyclic compounds 12-hydroxysteroids 3-hydroxysteroids Acetals Cyclic alcohols and derivatives Dialkyl ethers Hexoses Hydrocarbon derivatives O-glycosyl compounds Oxacyclic compounds Oxanes Polyols Primary alcohols Secondary alcohols 12-hydroxysteroid 3-hydroxysteroid Acetal Alcohol Aliphatic heteropolycyclic compound Cyclic alcohol Dialkyl ether Ether Glycosyl compound Hexose monosaccharide Hydrocarbon derivative Hydroxysteroid Monosaccharide O-glycosyl compound Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Oxane Polyol Primary alcohol Secondary alcohol Steroid Triterpenoid logp 3.34 ALOGPS logs -4.50 ALOGPS solubility 2.05e-02 g/l ALOGPS logp 3.1 ChemAxon pka_strongest_acidic 12.21 ChemAxon pka_strongest_basic -2.8 ChemAxon iupac 2-{[5,16-dihydroxy-14-(2-methoxy-6-methylhept-5-en-2-yl)-2,6,6,10,11-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-8-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol ChemAxon average_mass 652.8987 ChemAxon mono_mass 652.455033646 ChemAxon smiles COC(C)(CCC=C(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(CC21C)OC1OC(CO)C(O)C(O)C1O ChemAxon formula C37H64O9 ChemAxon inchi InChI=1S/C37H64O9/c1-20(2)11-10-14-37(8,44-9)21-12-16-35(6)27(21)22(39)17-25-34(5)15-13-26(40)33(3,4)31(34)23(18-36(25,35)7)45-32-30(43)29(42)28(41)24(19-38)46-32/h11,21-32,38-43H,10,12-19H2,1-9H3 ChemAxon inchikey WTSNEXSNFSFTFK-UHFFFAOYSA-N ChemAxon polar_surface_area 149.07 ChemAxon refractivity 175.99 ChemAxon polarizability 74.43 ChemAxon rotatable_bond_count 8 ChemAxon acceptor_count 9 ChemAxon donor_count 6 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 96477 Specdb::MsMs 96478 Specdb::MsMs 96479 Specdb::MsMs 160959 Specdb::MsMs 160960 Specdb::MsMs 160961 Specdb::MsMs 2438455 Specdb::MsMs 2438456 Specdb::MsMs 2438457 Specdb::MsMs 2523324 Specdb::MsMs 2523325 Specdb::MsMs 2523326 Specdb::CMs 646682 Specdb::CMs 646683 Specdb::CMs 646684 Specdb::CMs 646685 Specdb::CMs 646686 Specdb::CMs 646687 Specdb::CMs 646688 Specdb::CMs 646689 Specdb::CMs 646690 Specdb::CMs 646691 Specdb::CMs 646692 Specdb::CMs 646693 Specdb::CMs 646694 Specdb::CMs 646695 Specdb::CMs 646696 Specdb::CMs 646697 Specdb::CMs 646698 Specdb::CMs 646699 Specdb::CMs 646700 Specdb::CMs 646701 Specdb::CMs 646702 Specdb::CMs 646703 Specdb::CMs 646704 Specdb::CMs 646705 Specdb::CMs 646706 HMDB38016 #<Reference:0x000055ce335db9c8> Black tea Type 1 Green tea Type 1 Herbal tea Type 1 Red tea Type 1 Tea Type 1 specific Camellia sinensis 4442