1.0 2010-04-08 22:14:19 UTC 2025-11-19 02:19:23 UTC FDB019394 3''-O-Acetylafzelin Constituent of Zingiber zerumbet (wild ginger). 3''-O-Acetylafzelin is found in herbs and spices. 3''-O-Acetylafzelin Kaempferol 3-O-(3'-O-acetyl-alpha-L-rhamnopyranoside) C23H22O11 474.4142 474.116211546 2-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-3-yl]oxy}-3,5-dihydroxy-6-methyloxan-4-yl acetate 2-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy}-3,5-dihydroxy-6-methyloxan-4-yl acetate 135618-16-5 CC1OC(OC2=C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC=C(O)C=C2)C(O)C(OC(C)=O)C1O InChI=1S/C23H22O11/c1-9-17(28)21(32-10(2)24)19(30)23(31-9)34-22-18(29)16-14(27)7-13(26)8-15(16)33-20(22)11-3-5-12(25)6-4-11/h3-9,17,19,21,23,25-28,30H,1-2H3 APRVHMRKRPHQLM-UHFFFAOYSA-N belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds. Oligosaccharides Organic compounds Organic oxygen compounds Organooxygen compounds Carbohydrates and carbohydrate conjugates Aliphatic heteromonocyclic compounds Acetals Beta hydroxy acids and derivatives Carbonyl compounds Carboxylic acids Hemiacetals Hydrocarbon derivatives O-glucuronides O-glycosyl compounds Organic oxides Oxacyclic compounds Oxanes Polyols Pyrans Secondary alcohols Tricarboxylic acids and derivatives 1-o-glucuronide Acetal Alcohol Aliphatic heteromonocyclic compound Beta-hydroxy acid Carbonyl group Carboxylic acid Carboxylic acid derivative Glucuronic acid or derivatives Glycosyl compound Hemiacetal Hydrocarbon derivative Hydroxy acid O-glucuronide O-glycosyl compound Oligosaccharide Organic oxide Organoheterocyclic compound Oxacycle Oxane Polyol Pyran Secondary alcohol Tricarboxylic acid or derivatives logp 2.45 ALOGPS logs -2.74 ALOGPS solubility 8.66e-01 g/l ALOGPS melting_point Mp 117° logp 1.65 ChemAxon pka_strongest_acidic 6.43 ChemAxon pka_strongest_basic -3.6 ChemAxon iupac 2-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-3-yl]oxy}-3,5-dihydroxy-6-methyloxan-4-yl acetate ChemAxon average_mass 474.4142 ChemAxon mono_mass 474.116211546 ChemAxon smiles CC1OC(OC2=C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC=C(O)C=C2)C(O)C(OC(C)=O)C1O ChemAxon formula C23H22O11 ChemAxon inchi InChI=1S/C23H22O11/c1-9-17(28)21(32-10(2)24)19(30)23(31-9)34-22-18(29)16-14(27)7-13(26)8-15(16)33-20(22)11-3-5-12(25)6-4-11/h3-9,17,19,21,23,25-28,30H,1-2H3 ChemAxon inchikey APRVHMRKRPHQLM-UHFFFAOYSA-N ChemAxon polar_surface_area 172.21 ChemAxon refractivity 114.9 ChemAxon polarizability 45.58 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 10 ChemAxon donor_count 5 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 15368 Specdb::CMs 46554 Specdb::CMs 148153 Specdb::MsMs 8426 Specdb::MsMs 8427 Specdb::MsMs 8428 Specdb::MsMs 9911 Specdb::MsMs 9912 Specdb::MsMs 9913 Specdb::MsMs 15098 Specdb::MsMs 15099 Specdb::MsMs 15100 Specdb::MsMs 16583 Specdb::MsMs 16584 Specdb::MsMs 16585 Specdb::MsMs 2426923 Specdb::MsMs 2426924 Specdb::MsMs 2426925 Specdb::MsMs 2512191 Specdb::MsMs 2512192 Specdb::MsMs 2512193 HMDB39747 #<Reference:0x000055ce32d074a0> Herbs and Spices Unknown generic