1.0 2010-04-08 22:14:07 UTC 2025-11-19 02:16:44 UTC FDB019073 (1S,2S,4R)-p-Menth-8-ene-1,2,10-triol 2-glucoside Isolated from caraway fruit. (1S,2S,4R)-p-Menth-8-ene-1,2,10-triol 2-glucoside is found in herbs and spices. (1S,2S,4R)-p-Menth-8-ene-1,2,10-triol 2-glucoside (1S,2S,4R)-p-Menth-8-ene-1,2,10-triol 2-O-b-D-glucopyranoside C16H28O8 348.3887 348.178417872 2-{[2-hydroxy-5-(3-hydroxyprop-1-en-2-yl)-2-methylcyclohexyl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol 2-{[2-hydroxy-5-(3-hydroxyprop-1-en-2-yl)-2-methylcyclohexyl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol 378254-11-6 CC1(O)CCC(CC1OC1OC(CO)C(O)C(O)C1O)C(=C)CO InChI=1S/C16H28O8/c1-8(6-17)9-3-4-16(2,22)11(5-9)24-15-14(21)13(20)12(19)10(7-18)23-15/h9-15,17-22H,1,3-7H2,2H3 DDQFHDNWZKJNLC-UHFFFAOYSA-N belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone. Terpene glycosides Organic compounds Lipids and lipid-like molecules Prenol lipids Terpene glycosides Aliphatic heteromonocyclic compounds Acetals Cyclic alcohols and derivatives Cyclohexanols Hexoses Hydrocarbon derivatives Menthane monoterpenoids Monocyclic monoterpenoids O-glycosyl compounds Oxacyclic compounds Oxanes Polyols Primary alcohols Tertiary alcohols Acetal Alcohol Aliphatic heteromonocyclic compound Cyclic alcohol Cyclohexanol Glycosyl compound Hexose monosaccharide Hydrocarbon derivative Monocyclic monoterpenoid Monosaccharide Monoterpenoid O-glycosyl compound Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Oxane P-menthane monoterpenoid Polyol Primary alcohol Secondary alcohol Terpene glycoside Tertiary alcohol logp -1.54 ALOGPS logs -1.11 ALOGPS solubility 2.69e+01 g/l ALOGPS logp -1.9 ChemAxon pka_strongest_acidic 12.2 ChemAxon pka_strongest_basic -2 ChemAxon iupac 2-{[2-hydroxy-5-(3-hydroxyprop-1-en-2-yl)-2-methylcyclohexyl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol ChemAxon average_mass 348.3887 ChemAxon mono_mass 348.178417872 ChemAxon smiles CC1(O)CCC(CC1OC1OC(CO)C(O)C(O)C1O)C(=C)CO ChemAxon formula C16H28O8 ChemAxon inchi InChI=1S/C16H28O8/c1-8(6-17)9-3-4-16(2,22)11(5-9)24-15-14(21)13(20)12(19)10(7-18)23-15/h9-15,17-22H,1,3-7H2,2H3 ChemAxon inchikey DDQFHDNWZKJNLC-UHFFFAOYSA-N ChemAxon polar_surface_area 139.84 ChemAxon refractivity 82.94 ChemAxon polarizability 35.98 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 8 ChemAxon donor_count 6 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 11202 Specdb::CMs 46418 Specdb::CMs 132615 Specdb::CMs 140349 Specdb::CMs 149368 Specdb::CMs 279720 Specdb::NmrOneD 33162 Specdb::NmrOneD 33163 Specdb::NmrOneD 33164 Specdb::NmrOneD 33165 Specdb::NmrOneD 33166 Specdb::NmrOneD 33167 Specdb::NmrOneD 33168 Specdb::NmrOneD 33169 Specdb::NmrOneD 33170 Specdb::NmrOneD 33171 Specdb::NmrOneD 33172 Specdb::NmrOneD 33173 Specdb::NmrOneD 33174 Specdb::NmrOneD 33175 Specdb::NmrOneD 33176 Specdb::NmrOneD 33177 Specdb::NmrOneD 33178 Specdb::NmrOneD 33179 Specdb::NmrOneD 33180 Specdb::NmrOneD 33181 Specdb::MsMs 103281 Specdb::MsMs 103282 Specdb::MsMs 103283 Specdb::MsMs 169281 Specdb::MsMs 169282 Specdb::MsMs 169283 Specdb::MsMs 2827836 Specdb::MsMs 2827837 Specdb::MsMs 2827838 Specdb::MsMs 2850535 Specdb::MsMs 2850536 Specdb::MsMs 2850537 HMDB39469 #<Reference:0x00007f093c0d0150> Herbs and Spices Unknown generic