1.0 2010-04-08 22:12:03 UTC 2025-11-19 00:59:37 UTC FDB015799 Colubrinic acid Constituent of Zizyphus jujuba (Chinese date). Colubrinic acid is found in fruits. Zizyberanalic acid C30H46O4 470.6838 470.33960996 15-formyl-16-hydroxy-1,2,14,17,17-pentamethyl-8-(prop-1-en-2-yl)pentacyclo[11.7.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁸]icosane-5-carboxylic acid 15-formyl-16-hydroxy-1,2,14,17,17-pentamethyl-8-(prop-1-en-2-yl)pentacyclo[11.7.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁸]icosane-5-carboxylic acid 67594-73-4 CC(=C)C1CCC2(CCC3(C)C(CCC4C5(C)C(C=O)C(O)C(C)(C)C5CCC34C)C12)C(O)=O InChI=1S/C30H46O4/c1-17(2)18-10-13-30(25(33)34)15-14-27(5)19(23(18)30)8-9-22-28(27,6)12-11-21-26(3,4)24(32)20(16-31)29(21,22)7/h16,18-24,32H,1,8-15H2,2-7H3,(H,33,34) SLWJVQQNDGLXTK-UHFFFAOYSA-N belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Triterpenoids Organic compounds Lipids and lipid-like molecules Prenol lipids Triterpenoids Aliphatic homopolycyclic compounds 16-hydroxysteroids 18-hydroxysteroids 3-carboxy steroids Aldehydes Carboxylic acids Cyclic alcohols and derivatives Hydrocarbon derivatives Monocarboxylic acids and derivatives Organic oxides Oxosteroids Secondary alcohols 16-hydroxysteroid 18-hydroxysteroid 18-oxosteroid 3-carboxy steroid Alcohol Aldehyde Aliphatic homopolycyclic compound Carbonyl group Carboxylic acid Carboxylic acid derivative Cyclic alcohol Hydrocarbon derivative Hydroxysteroid Monocarboxylic acid or derivatives Organic oxide Organic oxygen compound Organooxygen compound Oxosteroid Secondary alcohol Steroid Steroid acid Triterpenoid logp 5.08 ALOGPS logs -5.90 ALOGPS solubility 5.96e-04 g/l ALOGPS melting_point Mp 282-284° (263-265°) logp 5.42 ChemAxon pka_strongest_acidic 4.68 ChemAxon pka_strongest_basic -3.1 ChemAxon iupac 15-formyl-16-hydroxy-1,2,14,17,17-pentamethyl-8-(prop-1-en-2-yl)pentacyclo[11.7.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁸]icosane-5-carboxylic acid ChemAxon average_mass 470.6838 ChemAxon mono_mass 470.33960996 ChemAxon smiles CC(=C)C1CCC2(CCC3(C)C(CCC4C5(C)C(C=O)C(O)C(C)(C)C5CCC34C)C12)C(O)=O ChemAxon formula C30H46O4 ChemAxon inchi InChI=1S/C30H46O4/c1-17(2)18-10-13-30(25(33)34)15-14-27(5)19(23(18)30)8-9-22-28(27,6)12-11-21-26(3,4)24(32)20(16-31)29(21,22)7/h16,18-24,32H,1,8-15H2,2-7H3,(H,33,34) ChemAxon inchikey SLWJVQQNDGLXTK-UHFFFAOYSA-N ChemAxon polar_surface_area 74.6 ChemAxon refractivity 133.18 ChemAxon polarizability 54.68 ChemAxon rotatable_bond_count 3 ChemAxon acceptor_count 4 ChemAxon donor_count 2 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 19417 Specdb::CMs 45073 Specdb::CMs 160762 Specdb::MsMs 7145 Specdb::MsMs 7146 Specdb::MsMs 7147 Specdb::MsMs 13817 Specdb::MsMs 13818 Specdb::MsMs 13819 Specdb::MsMs 2248792 Specdb::MsMs 2249609 Specdb::MsMs 2251626 Specdb::MsMs 2426695 Specdb::MsMs 2426696 Specdb::MsMs 2426697 Specdb::MsMs 2511933 Specdb::MsMs 2511934 Specdb::MsMs 2511935 HMDB36847 #<Reference:0x000055ce326d61a8> Fruits Unknown generic Jujube Type 1 specific Ziziphus zizyphus 48393