1.0 2010-04-08 22:12:15 UTC 2025-11-19 01:44:10 UTC FDB016118 Goyaglycoside f Constituent of Momordica charantia (bitter melon). Goyaglycoside f is found in fruits. Goyaglycoside f C42H68O13 780.9815 780.465992262 2-(hydroxymethyl)-6-{[2-methyl-6-(5,9,17,17-tetramethyl-16-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-18-oxapentacyclo[10.5.2.0¹,¹³.0⁴,¹².0⁵,⁹]nonadec-2-en-8-yl)hept-2-en-4-yl]oxy}oxane-3,4,5-triol 2-(hydroxymethyl)-6-{[2-methyl-6-(5,9,17,17-tetramethyl-16-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-18-oxapentacyclo[10.5.2.0¹,¹³.0⁴,¹².0⁵,⁹]nonadec-2-en-8-yl)hept-2-en-4-yl]oxy}oxane-3,4,5-triol 333333-13-4 CC(CC(OC1OC(CO)C(O)C(O)C1O)C=C(C)C)C1CCC2(C)C3C=CC45OCC3(CCC12C)C4CCC(OC1OC(CO)C(O)C(O)C1O)C5(C)C InChI=1S/C42H68O13/c1-21(2)16-23(52-36-34(49)32(47)30(45)25(18-43)53-36)17-22(3)24-10-12-40(7)27-11-13-42-28(41(27,20-51-42)15-14-39(24,40)6)8-9-29(38(42,4)5)55-37-35(50)33(48)31(46)26(19-44)54-37/h11,13,16,22-37,43-50H,8-10,12,14-15,17-20H2,1-7H3 ABQUGMVYQWOOLF-UHFFFAOYSA-N belongs to the class of organic compounds known as cucurbitacin glycosides. These are polycyclic compounds containing a carbohydrate derivative glycosidically linked to a curcubitane nucleus. Cucurbitacin glycosides Organic compounds Lipids and lipid-like molecules Steroids and steroid derivatives Steroidal glycosides Aliphatic heteropolycyclic compounds Acetals Alkyl glycosides Cucurbitacins Dialkyl ethers Fatty acyl glycosides of mono- and disaccharides Hydrocarbon derivatives Monosaccharides O-glycosyl compounds Oxacyclic compounds Oxanes Polyols Primary alcohols Secondary alcohols Tetrahydrofurans Triterpenoids Acetal Alcohol Aliphatic heteropolycyclic compound Alkyl glycoside Cucurbitacin glycoside skeleton Cucurbitacin skeleton Dialkyl ether Ether Fatty acyl Fatty acyl glycoside Fatty acyl glycoside of mono- or disaccharide Glycosyl compound Hydrocarbon derivative Monosaccharide O-glycosyl compound Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Oxane Polyol Primary alcohol Secondary alcohol Tetrahydrofuran Triterpenoid logp 2.09 ALOGPS logs -4.24 ALOGPS solubility 4.51e-02 g/l ALOGPS logp 1.98 ChemAxon pka_strongest_acidic 11.91 ChemAxon pka_strongest_basic -3 ChemAxon iupac 2-(hydroxymethyl)-6-{[2-methyl-6-(5,9,17,17-tetramethyl-16-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-18-oxapentacyclo[10.5.2.0¹,¹³.0⁴,¹².0⁵,⁹]nonadec-2-en-8-yl)hept-2-en-4-yl]oxy}oxane-3,4,5-triol ChemAxon average_mass 780.9815 ChemAxon mono_mass 780.465992262 ChemAxon smiles CC(CC(OC1OC(CO)C(O)C(O)C1O)C=C(C)C)C1CCC2(C)C3C=CC45OCC3(CCC12C)C4CCC(OC1OC(CO)C(O)C(O)C1O)C5(C)C ChemAxon formula C42H68O13 ChemAxon inchi InChI=1S/C42H68O13/c1-21(2)16-23(52-36-34(49)32(47)30(45)25(18-43)53-36)17-22(3)24-10-12-40(7)27-11-13-42-28(41(27,20-51-42)15-14-39(24,40)6)8-9-29(38(42,4)5)55-37-35(50)33(48)31(46)26(19-44)54-37/h11,13,16,22-37,43-50H,8-10,12,14-15,17-20H2,1-7H3 ChemAxon inchikey ABQUGMVYQWOOLF-UHFFFAOYSA-N ChemAxon polar_surface_area 207.99 ChemAxon refractivity 200.98 ChemAxon polarizability 86.59 ChemAxon rotatable_bond_count 10 ChemAxon acceptor_count 13 ChemAxon donor_count 8 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 106905 Specdb::MsMs 106906 Specdb::MsMs 106907 Specdb::MsMs 173754 Specdb::MsMs 173755 Specdb::MsMs 173756 Specdb::MsMs 2813252 Specdb::MsMs 2813253 Specdb::MsMs 2813254 Specdb::MsMs 2896266 Specdb::MsMs 2896267 Specdb::MsMs 2896268 Specdb::CMs 785047 Specdb::CMs 785048 Specdb::CMs 785049 Specdb::CMs 785050 Specdb::CMs 785051 Specdb::CMs 785052 Specdb::CMs 785053 Specdb::CMs 785054 Specdb::CMs 785055 Specdb::CMs 785056 Specdb::CMs 785057 Specdb::CMs 785058 Specdb::CMs 785059 Specdb::CMs 785060 Specdb::CMs 785061 Specdb::CMs 785062 HMDB37124 #<Reference:0x000055ce326d2e90> Fruits Unknown generic