1.0 2010-04-08 22:08:07 UTC 2019-11-26 03:02:40 UTC FDB008508 Ginsenoside Rg5 Isolated from ginseng. Ginsenoside Rg5 is found in tea. G-Rg5 Ginsenoside Rg5 Ginsenoside-Rg5 C42H70O12 766.998 766.486727704 2-{[4,5-dihydroxy-2-({16-hydroxy-2,6,6,10,11-pentamethyl-14-[(2Z)-6-methylhepta-2,5-dien-2-yl]tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-yl}oxy)-6-(hydroxymethyl)oxan-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol 2-{[4,5-dihydroxy-2-({16-hydroxy-2,6,6,10,11-pentamethyl-14-[(2Z)-6-methylhepta-2,5-dien-2-yl]tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-yl}oxy)-6-(hydroxymethyl)oxan-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol 74964-14-0 CC(C)=CC\C=C(\C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC21C InChI=1S/C42H70O12/c1-21(2)10-9-11-22(3)23-12-16-42(8)30(23)24(45)18-28-40(6)15-14-29(39(4,5)27(40)13-17-41(28,42)7)53-38-36(34(49)32(47)26(20-44)52-38)54-37-35(50)33(48)31(46)25(19-43)51-37/h10-11,23-38,43-50H,9,12-20H2,1-8H3/b22-11- NJUXRKMKOFXMRX-JJFYIABZSA-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 Acetals Cyclic alcohols and derivatives Disaccharides Hydrocarbon derivatives O-glycosyl compounds Oxacyclic compounds Oxanes Polyols Primary alcohols Secondary alcohols Steroidal glycosides 12-hydroxysteroid Acetal Alcohol Aliphatic heteropolycyclic compound Cyclic alcohol Disaccharide Glycosyl compound Hydrocarbon derivative Hydroxysteroid O-glycosyl compound Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Oxane Polyol Primary alcohol Secondary alcohol Steroid Steroidal glycoside Triterpenoid logp 2.83 ALOGPS logs -4.00 ALOGPS solubility 7.59e-02 g/l ALOGPS logp 2.9 ChemAxon pka_strongest_acidic 12.09 ChemAxon pka_strongest_basic -0.45 ChemAxon iupac 2-{[4,5-dihydroxy-2-({16-hydroxy-2,6,6,10,11-pentamethyl-14-[(2Z)-6-methylhepta-2,5-dien-2-yl]tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-yl}oxy)-6-(hydroxymethyl)oxan-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol ChemAxon average_mass 766.998 ChemAxon mono_mass 766.486727704 ChemAxon smiles CC(C)=CC\C=C(\C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC21C ChemAxon formula C42H70O12 ChemAxon inchi InChI=1S/C42H70O12/c1-21(2)10-9-11-22(3)23-12-16-42(8)30(23)24(45)18-28-40(6)15-14-29(39(4,5)27(40)13-17-41(28,42)7)53-38-36(34(49)32(47)26(20-44)52-38)54-37-35(50)33(48)31(46)25(19-43)51-37/h10-11,23-38,43-50H,9,12-20H2,1-8H3/b22-11- ChemAxon inchikey NJUXRKMKOFXMRX-JJFYIABZSA-N ChemAxon polar_surface_area 198.76 ChemAxon refractivity 201.23 ChemAxon polarizability 86.71 ChemAxon rotatable_bond_count 9 ChemAxon acceptor_count 12 ChemAxon donor_count 8 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 782247 Specdb::CMs 782248 Specdb::CMs 782249 Specdb::CMs 782250 Specdb::CMs 782251 Specdb::CMs 782252 Specdb::CMs 782253 Specdb::CMs 782254 Specdb::CMs 782255 Specdb::CMs 782256 Specdb::CMs 782257 Specdb::CMs 782258 Specdb::CMs 782259 Specdb::CMs 782260 Specdb::CMs 782261 Specdb::CMs 782262 Specdb::MsMs 106812 Specdb::MsMs 106813 Specdb::MsMs 106814 Specdb::MsMs 173646 Specdb::MsMs 173647 Specdb::MsMs 173648 Specdb::MsMs 3058087 Specdb::MsMs 3058088 Specdb::MsMs 3058089 Specdb::MsMs 3112577 Specdb::MsMs 3112578 Specdb::MsMs 3112579 HMDB31830 #<Reference:0x000055ce32c17c20> Black tea Type 1 Green tea Type 1 Herbal tea Type 1 Red tea Type 1 Tea Type 1 specific Camellia sinensis 4442