1.0 2010-04-08 22:12:58 UTC 2025-11-19 01:52:44 UTC FDB017226 Cryptomeridiol 11-rhamnoside Constituent of fruits of Cananga odorata (ylang ylang) (4a,5a)-4,11-Eudesmanediol 11-O-a-L-rhamnopyranoside Cryptomeridiol 11-O-a-L-rhamnopyranoside Cryptomeridiol 11-O-a-L-rhamnoside Cryptomeridiol 11-rhamnoside C21H38O6 386.5228 386.266838948 2-{[2-(8-hydroxy-4a,8-dimethyl-decahydronaphthalen-2-yl)propan-2-yl]oxy}-6-methyloxane-3,4,5-triol 2-{[2-(8-hydroxy-4a,8-dimethyl-octahydronaphthalen-2-yl)propan-2-yl]oxy}-6-methyloxane-3,4,5-triol 349112-30-7 CC1OC(OC(C)(C)C2CCC3(C)CCCC(C)(O)C3C2)C(O)C(O)C1O InChI=1S/C21H38O6/c1-12-15(22)16(23)17(24)18(26-12)27-19(2,3)13-7-10-20(4)8-6-9-21(5,25)14(20)11-13/h12-18,22-25H,6-11H2,1-5H3 HUSBLOAZNQURFJ-UHFFFAOYSA-N belongs to the class of organic compounds known as eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids. These are sesquiterpenoids with a structure based on the eudesmane skeleton. Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids Organic compounds Lipids and lipid-like molecules Prenol lipids Sesquiterpenoids Aliphatic heteropolycyclic compounds Acetals Cyclic alcohols and derivatives Hexoses Hydrocarbon derivatives O-glycosyl compounds Oxacyclic compounds Oxanes Polyols Secondary alcohols Tertiary alcohols Acetal Alcohol Aliphatic heteropolycyclic compound Cyclic alcohol Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoid Glycosyl compound Hexose monosaccharide Hydrocarbon derivative Monosaccharide O-glycosyl compound Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Oxane Polyol Secondary alcohol Tertiary alcohol logp 1.98 ALOGPS logs -2.88 ALOGPS solubility 5.06e-01 g/l ALOGPS melting_point Mp 189-190° logp 1.84 ChemAxon pka_strongest_acidic 12.22 ChemAxon pka_strongest_basic -0.49 ChemAxon iupac 2-{[2-(8-hydroxy-4a,8-dimethyl-decahydronaphthalen-2-yl)propan-2-yl]oxy}-6-methyloxane-3,4,5-triol ChemAxon average_mass 386.5228 ChemAxon mono_mass 386.266838948 ChemAxon smiles CC1OC(OC(C)(C)C2CCC3(C)CCCC(C)(O)C3C2)C(O)C(O)C1O ChemAxon formula C21H38O6 ChemAxon inchi InChI=1S/C21H38O6/c1-12-15(22)16(23)17(24)18(26-12)27-19(2,3)13-7-10-20(4)8-6-9-21(5,25)14(20)11-13/h12-18,22-25H,6-11H2,1-5H3 ChemAxon inchikey HUSBLOAZNQURFJ-UHFFFAOYSA-N ChemAxon polar_surface_area 99.38 ChemAxon refractivity 101.14 ChemAxon polarizability 43.01 ChemAxon rotatable_bond_count 3 ChemAxon acceptor_count 6 ChemAxon donor_count 4 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 10605 Specdb::CMs 45646 Specdb::CMs 172657 Specdb::MsMs 95331 Specdb::MsMs 95332 Specdb::MsMs 95333 Specdb::MsMs 159579 Specdb::MsMs 159580 Specdb::MsMs 159581 Specdb::MsMs 2809604 Specdb::MsMs 2809605 Specdb::MsMs 2809606 Specdb::MsMs 2899095 Specdb::MsMs 2899096 Specdb::MsMs 2899097 HMDB38018 #<Reference:0x000055ce320777f8>