1.0 2010-04-08 22:13:24 UTC 2019-11-26 03:15:27 UTC FDB017925 Goshonoside F1 Constituent of Rubus foliolosus (Ceylon raspberry). Goshonoside F1 is found in fruits. Goshonoside F1 C26H44O8 484.6228 484.303618384 2-{[(2E)-5-[6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-decahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol 2-{[(2E)-5-[6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-en-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol 90851-24-4 C\C(CCC1C(=C)CCC2C(C)(CO)C(O)CCC12C)=C/COC1OC(CO)C(O)C(O)C1O InChI=1S/C26H44O8/c1-15(10-12-33-24-23(32)22(31)21(30)18(13-27)34-24)5-7-17-16(2)6-8-19-25(17,3)11-9-20(29)26(19,4)14-28/h10,17-24,27-32H,2,5-9,11-14H2,1,3-4H3/b15-10+ JAFZKPLEKRHFFD-XNTDXEJSSA-N belongs to the class of organic compounds known as diterpene glycosides. These are diterpenoids in which an isoprene unit is glycosylated. Diterpene glycosides Organic compounds Lipids and lipid-like molecules Prenol lipids Terpene glycosides Aliphatic heteropolycyclic compounds Acetals Alkyl glycosides Cyclic alcohols and derivatives Diterpenoids Fatty acyl glycosides of mono- and disaccharides Hexoses Hydrocarbon derivatives O-glycosyl compounds Oxacyclic compounds Oxanes Polyols Primary alcohols Secondary alcohols Acetal Alcohol Aliphatic heteropolycyclic compound Alkyl glycoside Cyclic alcohol Diterpene glycoside Diterpenoid Fatty acyl Fatty acyl glycoside Fatty acyl glycoside of mono- or disaccharide Glycosyl compound Hexose monosaccharide Hydrocarbon derivative Labdane diterpenoid Monosaccharide O-glycosyl compound Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Oxane Polyol Primary alcohol Secondary alcohol logp 0.82 ALOGPS logs -3.08 ALOGPS solubility 4.05e-01 g/l ALOGPS melting_point Mp 95-98° logp 0.88 ChemAxon pka_strongest_acidic 12.21 ChemAxon pka_strongest_basic -2.8 ChemAxon iupac 2-{[(2E)-5-[6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-decahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol ChemAxon average_mass 484.6228 ChemAxon mono_mass 484.303618384 ChemAxon smiles C\C(CCC1C(=C)CCC2C(C)(CO)C(O)CCC12C)=C/COC1OC(CO)C(O)C(O)C1O ChemAxon formula C26H44O8 ChemAxon inchi InChI=1S/C26H44O8/c1-15(10-12-33-24-23(32)22(31)21(30)18(13-27)34-24)5-7-17-16(2)6-8-19-25(17,3)11-9-20(29)26(19,4)14-28/h10,17-24,27-32H,2,5-9,11-14H2,1,3-4H3/b15-10+ ChemAxon inchikey JAFZKPLEKRHFFD-XNTDXEJSSA-N ChemAxon polar_surface_area 139.84 ChemAxon refractivity 127.76 ChemAxon polarizability 54.35 ChemAxon rotatable_bond_count 8 ChemAxon acceptor_count 8 ChemAxon donor_count 6 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 14172 Specdb::CMs 45899 Specdb::CMs 170448 Specdb::MsMs 98394 Specdb::MsMs 98395 Specdb::MsMs 98396 Specdb::MsMs 163308 Specdb::MsMs 163309 Specdb::MsMs 163310 Specdb::MsMs 2434288 Specdb::MsMs 2434289 Specdb::MsMs 2434290 Specdb::MsMs 2503874 Specdb::MsMs 2503875 Specdb::MsMs 2503876 HMDB38539 #<Reference:0x000055ce315e1398> Fruits Unknown generic