1.0 2010-04-08 22:12:44 UTC 2019-11-26 03:13:57 UTC FDB016920 Ganoderiol I Metabolite of Ganoderma lucidum (reishi). Ganoderiol I is found in mushrooms. 15a,26,27-Trihydroxy-7a-methoxy-8,24-lanostadien-3-one Ganoderiol I C31H50O5 502.7257 502.36582471 12-hydroxy-14-[7-hydroxy-6-(hydroxymethyl)hept-5-en-2-yl]-9-methoxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-5-one 12-hydroxy-14-[7-hydroxy-6-(hydroxymethyl)hept-5-en-2-yl]-9-methoxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-5-one 114567-49-6 COC1CC2C(C)(C)C(=O)CCC2(C)C2=C1C1(C)C(O)CC(C(C)CCC=C(CO)CO)C1(C)CC2 InChI=1S/C31H50O5/c1-19(9-8-10-20(17-32)18-33)22-15-26(35)31(6)27-21(11-14-30(22,31)5)29(4)13-12-25(34)28(2,3)24(29)16-23(27)36-7/h10,19,22-24,26,32-33,35H,8-9,11-18H2,1-7H3 SQJBJGSQYVYNPM-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 3-oxosteroids Cyclic alcohols and derivatives Cyclic ketones Dialkyl ethers Dihydroxy bile acids, alcohols and derivatives Fatty alcohols Hydrocarbon derivatives Hydroxysteroids Organic oxides Primary alcohols Secondary alcohols 15-hydroxysteroid 26-hydroxysteroid 3-oxosteroid Alcohol Aliphatic homopolycyclic compound Bile acid, alcohol, or derivatives Carbonyl group Cyclic alcohol Cyclic ketone Dialkyl ether Dihydroxy bile acid, alcohol, or derivatives Ether Fatty acyl Fatty alcohol Hydrocarbon derivative Hydroxy bile acid, alcohol, or derivatives Hydroxysteroid Ketone Organic oxide Organic oxygen compound Organooxygen compound Oxosteroid Primary alcohol Secondary alcohol Steroid Triterpenoid logp 4.88 ALOGPS logs -5.16 ALOGPS solubility 3.52e-03 g/l ALOGPS logp 3.89 ChemAxon pka_strongest_acidic 14.4 ChemAxon pka_strongest_basic -2.8 ChemAxon iupac 12-hydroxy-14-[7-hydroxy-6-(hydroxymethyl)hept-5-en-2-yl]-9-methoxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-5-one ChemAxon average_mass 502.7257 ChemAxon mono_mass 502.36582471 ChemAxon smiles COC1CC2C(C)(C)C(=O)CCC2(C)C2=C1C1(C)C(O)CC(C(C)CCC=C(CO)CO)C1(C)CC2 ChemAxon formula C31H50O5 ChemAxon inchi InChI=1S/C31H50O5/c1-19(9-8-10-20(17-32)18-33)22-15-26(35)31(6)27-21(11-14-30(22,31)5)29(4)13-12-25(34)28(2,3)24(29)16-23(27)36-7/h10,19,22-24,26,32-33,35H,8-9,11-18H2,1-7H3 ChemAxon inchikey SQJBJGSQYVYNPM-UHFFFAOYSA-N ChemAxon polar_surface_area 86.99 ChemAxon refractivity 145.05 ChemAxon polarizability 59.04 ChemAxon rotatable_bond_count 7 ChemAxon acceptor_count 5 ChemAxon donor_count 3 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 15530 Specdb::CMs 45543 Specdb::MsMs 43179 Specdb::MsMs 43180 Specdb::MsMs 43181 Specdb::MsMs 137361 Specdb::MsMs 137362 Specdb::MsMs 137363 Specdb::MsMs 2347391 Specdb::MsMs 2347392 Specdb::MsMs 2347393 Specdb::MsMs 2592178 Specdb::MsMs 2592179 Specdb::MsMs 2592180 HMDB37778 #<Reference:0x000055ce300d99a0> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322