1.0 2010-04-08 22:10:09 UTC 2019-11-26 03:06:41 UTC FDB012391 Lusitanicoside Isolated from cherries (Prunus lusitanica). Lusitanicoside is found in sweet marjoram and fruits. Lusitanicoside C21H30O10 442.4569 442.18389718 2-methyl-6-({3,4,5-trihydroxy-6-[4-(prop-2-en-1-yl)phenoxy]oxan-2-yl}methoxy)oxane-3,4,5-triol 2-methyl-6-({3,4,5-trihydroxy-6-[4-(prop-2-en-1-yl)phenoxy]oxan-2-yl}methoxy)oxane-3,4,5-triol 499-35-4 CC1OC(OCC2OC(OC3=CC=C(CC=C)C=C3)C(O)C(O)C2O)C(O)C(O)C1O InChI=1S/C21H30O10/c1-3-4-11-5-7-12(8-6-11)30-21-19(27)17(25)15(23)13(31-21)9-28-20-18(26)16(24)14(22)10(2)29-20/h3,5-8,10,13-27H,1,4,9H2,2H3 DAELTTGCCPRYTP-UHFFFAOYSA-N belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. Phenolic glycosides Organic compounds Organic oxygen compounds Organooxygen compounds Carbohydrates and carbohydrate conjugates Aromatic heteromonocyclic compounds Acetals Disaccharides Hydrocarbon derivatives O-glycosyl compounds Oxacyclic compounds Oxanes Phenol ethers Phenoxy compounds Polyols Secondary alcohols Acetal Alcohol Aromatic heteromonocyclic compound Benzenoid Disaccharide Hydrocarbon derivative Monocyclic benzene moiety O-glycosyl compound Organoheterocyclic compound Oxacycle Oxane Phenol ether Phenolic glycoside Phenoxy compound Polyol Secondary alcohol logp -0.18 ALOGPS logs -1.70 ALOGPS solubility 8.87e+00 g/l ALOGPS melting_point Mp 187-188.5° logp -0.22 ChemAxon pka_strongest_acidic 11.91 ChemAxon pka_strongest_basic -3.6 ChemAxon iupac 2-methyl-6-({3,4,5-trihydroxy-6-[4-(prop-2-en-1-yl)phenoxy]oxan-2-yl}methoxy)oxane-3,4,5-triol ChemAxon average_mass 442.4569 ChemAxon mono_mass 442.18389718 ChemAxon smiles CC1OC(OCC2OC(OC3=CC=C(CC=C)C=C3)C(O)C(O)C2O)C(O)C(O)C1O ChemAxon formula C21H30O10 ChemAxon inchi InChI=1S/C21H30O10/c1-3-4-11-5-7-12(8-6-11)30-21-19(27)17(25)15(23)13(31-21)9-28-20-18(26)16(24)14(22)10(2)29-20/h3,5-8,10,13-27H,1,4,9H2,2H3 ChemAxon inchikey DAELTTGCCPRYTP-UHFFFAOYSA-N ChemAxon polar_surface_area 158.3 ChemAxon refractivity 105.34 ChemAxon polarizability 44.9 ChemAxon rotatable_bond_count 7 ChemAxon acceptor_count 10 ChemAxon donor_count 6 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::NmrOneD 124518 Specdb::NmrOneD 124519 Specdb::NmrOneD 124520 Specdb::NmrOneD 124521 Specdb::NmrOneD 124522 Specdb::NmrOneD 124523 Specdb::NmrOneD 124524 Specdb::NmrOneD 124525 Specdb::NmrOneD 124526 Specdb::NmrOneD 124527 Specdb::NmrOneD 124528 Specdb::NmrOneD 124529 Specdb::NmrOneD 124530 Specdb::NmrOneD 124531 Specdb::NmrOneD 124532 Specdb::NmrOneD 124533 Specdb::NmrOneD 124534 Specdb::NmrOneD 124535 Specdb::NmrOneD 124536 Specdb::NmrOneD 124537 Specdb::CMs 24631 Specdb::CMs 43722 Specdb::CMs 149403 Specdb::CMs 155856 Specdb::CMs 280064 Specdb::MsMs 84360 Specdb::MsMs 84361 Specdb::MsMs 84362 Specdb::MsMs 146190 Specdb::MsMs 146191 Specdb::MsMs 146192 Specdb::MsMs 2339421 Specdb::MsMs 2339422 Specdb::MsMs 2339423 Specdb::MsMs 2626082 Specdb::MsMs 2626083 Specdb::MsMs 2626084 HMDB34120 #<Reference:0x000055ce32afeb90> Fruits Unknown generic Sweet marjoram Type 1 specific Origanum majorana 268884