1.0 2010-04-08 22:11:47 UTC 2019-11-26 03:11:27 UTC FDB015329 3beta,15alpha-Diacetoxylanosta-8,24-dien-26-oic acid Constituent of Ganoderma lucidum (reishi). 3beta,15alpha-Diacetoxylanosta-8,24-dien-26-oic acid is found in mushrooms. 3b,15a-Diacetoxylanosta-8,24-dien-26-oic acid C34H52O6 556.7731 556.376389396 (2Z)-6-[5,12-bis(acetyloxy)-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl]-2-methylhept-2-enoic acid (2Z)-6-[5,12-bis(acetyloxy)-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl]-2-methylhept-2-enoic acid 117842-20-3 CC(CC\C=C(\C)C(O)=O)C1CC(OC(C)=O)C2(C)C3=C(CCC12C)C1(C)CCC(OC(C)=O)C(C)(C)C1CC3 InChI=1S/C34H52O6/c1-20(11-10-12-21(2)30(37)38)26-19-29(40-23(4)36)34(9)25-13-14-27-31(5,6)28(39-22(3)35)16-17-32(27,7)24(25)15-18-33(26,34)8/h12,20,26-29H,10-11,13-19H2,1-9H3,(H,37,38)/b21-12- FFHZCNIREJAVOS-MTJSOVHGSA-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 Bile acids, alcohols and derivatives Carbonyl compounds Carboxylic acid esters Carboxylic acids Hydrocarbon derivatives Organic oxides Steroid acids Steroid esters Tricarboxylic acids and derivatives Aliphatic homopolycyclic compound Bile acid, alcohol, or derivatives Carbonyl group Carboxylic acid Carboxylic acid derivative Carboxylic acid ester Hydrocarbon derivative Organic oxide Organic oxygen compound Organooxygen compound Steroid Steroid acid Steroid ester Tricarboxylic acid or derivatives Triterpenoid logp 6.91 ALOGPS logs -6.11 ALOGPS solubility 4.28e-04 g/l ALOGPS logp 6.55 ChemAxon pka_strongest_acidic 4.62 ChemAxon pka_strongest_basic -6.7 ChemAxon iupac (2Z)-6-[5,12-bis(acetyloxy)-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl]-2-methylhept-2-enoic acid ChemAxon average_mass 556.7731 ChemAxon mono_mass 556.376389396 ChemAxon smiles CC(CC\C=C(\C)C(O)=O)C1CC(OC(C)=O)C2(C)C3=C(CCC12C)C1(C)CCC(OC(C)=O)C(C)(C)C1CC3 ChemAxon formula C34H52O6 ChemAxon inchi InChI=1S/C34H52O6/c1-20(11-10-12-21(2)30(37)38)26-19-29(40-23(4)36)34(9)25-13-14-27-31(5,6)28(39-22(3)35)16-17-32(27,7)24(25)15-18-33(26,34)8/h12,20,26-29H,10-11,13-19H2,1-9H3,(H,37,38)/b21-12- ChemAxon inchikey FFHZCNIREJAVOS-MTJSOVHGSA-N ChemAxon polar_surface_area 89.9 ChemAxon refractivity 156.08 ChemAxon polarizability 64.78 ChemAxon rotatable_bond_count 9 ChemAxon acceptor_count 4 ChemAxon donor_count 1 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 18943 Specdb::CMs 44874 Specdb::CMs 281941 Specdb::CMs 340788 Specdb::MsMs 50457 Specdb::MsMs 50458 Specdb::MsMs 50459 Specdb::MsMs 147201 Specdb::MsMs 147202 Specdb::MsMs 147203 Specdb::MsMs 2413969 Specdb::MsMs 2413970 Specdb::MsMs 2413971 Specdb::MsMs 2551154 Specdb::MsMs 2551155 Specdb::MsMs 2551156 HMDB36442 #<Reference:0x000055ce30539c70> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322