1.0 2010-04-08 22:11:04 UTC 2019-11-26 03:09:28 UTC FDB014070 Ginsenoside C Constituent of Panax ginseng (ginseng). Ginsenoside C is found in tea. Chikusetsusaponin I Ginsenoside C Ginsenoside Rg2 Ginsenoside-rg2 ginsenoside-Rg2, (3beta,6alpha,12beta,20R)-isomer Panaxoside Rg2 Prosapogenin C2 C42H72O13 785.0133 784.49729239 2-[(2-{[5,16-dihydroxy-14-(2-hydroxy-6-methylhept-5-en-2-yl)-2,6,6,10,11-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-8-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol 2-[(2-{[5,16-dihydroxy-14-(2-hydroxy-6-methylhept-5-en-2-yl)-2,6,6,10,11-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-8-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol 52286-74-5 CC1OC(OC2C(O)C(O)C(CO)OC2OC2CC3(C)C(CC(O)C4C(CCC34C)C(C)(O)CCC=C(C)C)C3(C)CCC(O)C(C)(C)C23)C(O)C(O)C1O InChI=1S/C42H72O13/c1-20(2)11-10-14-42(9,51)22-12-16-40(7)28(22)23(44)17-26-39(6)15-13-27(45)38(4,5)35(39)24(18-41(26,40)8)53-37-34(32(49)30(47)25(19-43)54-37)55-36-33(50)31(48)29(46)21(3)52-36/h11,21-37,43-51H,10,12-19H2,1-9H3 AGBCLJAHARWNLA-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 Disaccharides Hydrocarbon derivatives O-glycosyl compounds Oxacyclic compounds Oxanes Polyols Primary alcohols Secondary alcohols Tertiary alcohols 12-hydroxysteroid 20-hydroxysteroid 3-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 Tertiary alcohol Triterpenoid logp 1.88 ALOGPS logs -3.66 ALOGPS solubility 1.73e-01 g/l ALOGPS melting_point Mp 187-189° logp 1.73 ChemAxon pka_strongest_acidic 12.1 ChemAxon pka_strongest_basic -2.9 ChemAxon iupac 2-[(2-{[5,16-dihydroxy-14-(2-hydroxy-6-methylhept-5-en-2-yl)-2,6,6,10,11-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-8-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol ChemAxon average_mass 785.0133 ChemAxon mono_mass 784.49729239 ChemAxon smiles CC1OC(OC2C(O)C(O)C(CO)OC2OC2CC3(C)C(CC(O)C4C(CCC34C)C(C)(O)CCC=C(C)C)C3(C)CCC(O)C(C)(C)C23)C(O)C(O)C1O ChemAxon formula C42H72O13 ChemAxon inchi InChI=1S/C42H72O13/c1-20(2)11-10-14-42(9,51)22-12-16-40(7)28(22)23(44)17-26-39(6)15-13-27(45)38(4,5)35(39)24(18-41(26,40)8)53-37-34(32(49)30(47)25(19-43)54-37)55-36-33(50)31(48)29(46)21(3)52-36/h11,21-37,43-51H,10,12-19H2,1-9H3 ChemAxon inchikey AGBCLJAHARWNLA-UHFFFAOYSA-N ChemAxon polar_surface_area 218.99 ChemAxon refractivity 202.11 ChemAxon polarizability 87.55 ChemAxon rotatable_bond_count 9 ChemAxon acceptor_count 13 ChemAxon donor_count 9 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 785889 Specdb::CMs 785890 Specdb::CMs 785891 Specdb::CMs 785892 Specdb::CMs 785893 Specdb::CMs 785894 Specdb::CMs 785895 Specdb::CMs 785896 Specdb::CMs 785897 Specdb::CMs 785898 Specdb::CMs 785899 Specdb::CMs 785900 Specdb::CMs 785901 Specdb::CMs 785902 Specdb::CMs 785903 Specdb::CMs 785904 Specdb::CMs 785905 Specdb::CMs 785906 Specdb::MsMs 10388 Specdb::MsMs 10389 Specdb::MsMs 10390 Specdb::MsMs 17060 Specdb::MsMs 17061 Specdb::MsMs 17062 Specdb::MsMs 2231611 Specdb::MsMs 2232602 Specdb::MsMs 2250559 Specdb::MsMs 2251813 Specdb::MsMs 2252781 Specdb::MsMs 2253684 Specdb::MsMs 2255693 Specdb::MsMs 2256825 Specdb::MsMs 2257759 Specdb::MsMs 2258791 Specdb::MsMs 2259799 Specdb::MsMs 3055358 Specdb::MsMs 3055359 Specdb::MsMs 3055360 Specdb::MsMs 3111608 Specdb::MsMs 3111609 Specdb::MsMs 3111610 HMDB35395 #<Reference:0x000055ce32594ba0> #<Reference:0x000055ce325949e8> Black tea Type 1 Green tea Type 1 Herbal tea Type 1 Red tea Type 1 Tea Type 1 specific Camellia sinensis 4442