1.0 2010-04-08 22:15:43 UTC 2019-11-26 03:20:26 UTC FDB021480 Marmesin galactoside Constituent of Murraya koenigii (curry leaf tree). Marmesin galactoside is found in herbs and spices. Marmesin galactoside C20H24O9 408.3992 408.142032366 2-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl)-2H,3H,7H-furo[3,2-g]chromen-7-one 2-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl)-2H,3H-furo[3,2-g]chromen-7-one 156363-69-8 CC(C)(OC1OC(CO)C(O)C(O)C1O)C1CC2=C(O1)C=C1OC(=O)C=CC1=C2 InChI=1S/C20H24O9/c1-20(2,29-19-18(25)17(24)16(23)13(8-21)28-19)14-6-10-5-9-3-4-15(22)27-11(9)7-12(10)26-14/h3-5,7,13-14,16-19,21,23-25H,6,8H2,1-2H3 HXCGUCZXPFBNRD-UHFFFAOYSA-N belongs to the class of organic compounds known as psoralens. These are organic compounds containing a psoralen moiety, which consists of a furan fused to a chromenone to for 7H-furo[3,2-g]chromen-7-one. Psoralens Organic compounds Phenylpropanoids and polyketides Coumarins and derivatives Furanocoumarins Aromatic heteropolycyclic compounds 1-benzopyrans Acetals Alkyl aryl ethers Benzenoids Coumarans Heteroaromatic compounds Hexoses Hydrocarbon derivatives Lactones O-glycosyl compounds Organic oxides Oxacyclic compounds Oxanes Polyols Primary alcohols Pyranones and derivatives Secondary alcohols 1-benzopyran Acetal Alcohol Alkyl aryl ether Aromatic heteropolycyclic compound Benzenoid Benzopyran Coumaran Ether Glycosyl compound Heteroaromatic compound Hexose monosaccharide Hydrocarbon derivative Lactone Monosaccharide O-glycosyl compound Organic oxide Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Oxane Polyol Primary alcohol Psoralen Pyran Pyranone Secondary alcohol logp 0.18 ALOGPS logs -2.38 ALOGPS solubility 1.71e+00 g/l ALOGPS logp -0.038 ChemAxon pka_strongest_acidic 12.21 ChemAxon pka_strongest_basic -3 ChemAxon iupac 2-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl)-2H,3H,7H-furo[3,2-g]chromen-7-one ChemAxon average_mass 408.3992 ChemAxon mono_mass 408.142032366 ChemAxon smiles CC(C)(OC1OC(CO)C(O)C(O)C1O)C1CC2=C(O1)C=C1OC(=O)C=CC1=C2 ChemAxon formula C20H24O9 ChemAxon inchi InChI=1S/C20H24O9/c1-20(2,29-19-18(25)17(24)16(23)13(8-21)28-19)14-6-10-5-9-3-4-15(22)27-11(9)7-12(10)26-14/h3-5,7,13-14,16-19,21,23-25H,6,8H2,1-2H3 ChemAxon inchikey HXCGUCZXPFBNRD-UHFFFAOYSA-N ChemAxon polar_surface_area 134.91 ChemAxon refractivity 98.75 ChemAxon polarizability 41.12 ChemAxon rotatable_bond_count 4 ChemAxon acceptor_count 8 ChemAxon donor_count 4 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 10703 Specdb::MsMs 10704 Specdb::MsMs 10705 Specdb::MsMs 12560 Specdb::MsMs 12561 Specdb::MsMs 12562 Specdb::MsMs 17375 Specdb::MsMs 17376 Specdb::MsMs 17377 Specdb::MsMs 19232 Specdb::MsMs 19233 Specdb::MsMs 19234 Specdb::MsMs 2798459 Specdb::MsMs 2798460 Specdb::MsMs 2798461 Specdb::MsMs 2883086 Specdb::MsMs 2883087 Specdb::MsMs 2883088 Specdb::NmrOneD 47102 Specdb::NmrOneD 47103 Specdb::NmrOneD 47104 Specdb::NmrOneD 47105 Specdb::NmrOneD 47106 Specdb::NmrOneD 47107 Specdb::NmrOneD 47108 Specdb::NmrOneD 47109 Specdb::NmrOneD 47110 Specdb::NmrOneD 47111 Specdb::NmrOneD 47112 Specdb::NmrOneD 47113 Specdb::NmrOneD 47114 Specdb::NmrOneD 47115 Specdb::NmrOneD 47116 Specdb::NmrOneD 47117 Specdb::NmrOneD 47118 Specdb::NmrOneD 47119 Specdb::NmrOneD 47120 Specdb::NmrOneD 47121 Specdb::CMs 26508 Specdb::CMs 47354 Specdb::CMs 117506 Specdb::CMs 165192 Specdb::CMs 950824 Specdb::CMs 950825 Specdb::CMs 950826 Specdb::CMs 950827 Specdb::CMs 950828 Specdb::CMs 950829 Specdb::CMs 950830 Specdb::CMs 950831 Specdb::CMs 950832 Specdb::CMs 950833 Specdb::CMs 950834 Specdb::CMs 950835 Specdb::CMs 950836 Specdb::CMs 950837 Specdb::CMs 950838 Specdb::CMs 950839 Specdb::CMs 950840 Specdb::CMs 950841 Specdb::CMs 950842 Specdb::CMs 950843 Specdb::CMs 950844 HMDB41508 #<Reference:0x000055ce32ae93d0> Herbs and Spices Unknown generic