1.0 2010-04-08 22:11:28 UTC 2025-11-19 00:49:36 UTC FDB014781 Ganodermanontriol Constituent of Ganoderma lucidum (reishi). Ganodermanontriol is found in mushrooms. 24,25,26-Trihydroxylanosta-7,9(11)-dien-3-one 24(S),25,26-Trihydroxy-5alpha-lanosta-7,9(11)-dien-3-one Ganodermanontriol C30H48O4 472.6997 472.355260024 2,6,6,11,15-pentamethyl-14-(5,6,7-trihydroxy-6-methylheptan-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),9-dien-5-one 2,6,6,11,15-pentamethyl-14-(5,6,7-trihydroxy-6-methylheptan-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),9-dien-5-one 106518-63-2 CC(CCC(O)C(C)(O)CO)C1CCC2(C)C3=CCC4C(C)(C)C(=O)CCC4(C)C3=CCC12C InChI=1S/C30H48O4/c1-19(8-11-25(33)30(7,34)18-31)20-12-16-29(6)22-9-10-23-26(2,3)24(32)14-15-27(23,4)21(22)13-17-28(20,29)5/h9,13,19-20,23,25,31,33-34H,8,10-12,14-18H2,1-7H3 KASALCUNLBTNAA-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-oxo delta-7-steroids Cyclic ketones Delta-7-steroids Fatty alcohols Hydrocarbon derivatives Hydroxysteroids Organic oxides Polyols Primary alcohols Secondary alcohols Tertiary alcohols Trihydroxy bile acids, alcohols and derivatives 24-hydroxysteroid 25-hydroxysteroid 26-hydroxysteroid 3-oxo-delta-7-steroid 3-oxosteroid Alcohol Aliphatic homopolycyclic compound Bile acid, alcohol, or derivatives Carbonyl group Cholane-skeleton Cyclic ketone Delta-7-steroid Fatty acyl Fatty alcohol Hydrocarbon derivative Hydroxy bile acid, alcohol, or derivatives Ketone Organic oxide Organic oxygen compound Organooxygen compound Oxosteroid Polyol Primary alcohol Secondary alcohol Steroid Tertiary alcohol Trihydroxy bile acid, alcohol, or derivatives Triterpenoid logp 6.22 ALOGPS logs -5.17 ALOGPS solubility 3.22e-03 g/l ALOGPS melting_point Mp 168-170° logp 4.72 ChemAxon pka_strongest_acidic 13.19 ChemAxon pka_strongest_basic -3.1 ChemAxon iupac 2,6,6,11,15-pentamethyl-14-(5,6,7-trihydroxy-6-methylheptan-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),9-dien-5-one ChemAxon average_mass 472.6997 ChemAxon mono_mass 472.355260024 ChemAxon smiles CC(CCC(O)C(C)(O)CO)C1CCC2(C)C3=CCC4C(C)(C)C(=O)CCC4(C)C3=CCC12C ChemAxon formula C30H48O4 ChemAxon inchi InChI=1S/C30H48O4/c1-19(8-11-25(33)30(7,34)18-31)20-12-16-29(6)22-9-10-23-26(2,3)24(32)14-15-27(23,4)21(22)13-17-28(20,29)5/h9,13,19-20,23,25,31,33-34H,8,10-12,14-18H2,1-7H3 ChemAxon inchikey KASALCUNLBTNAA-UHFFFAOYSA-N ChemAxon polar_surface_area 77.76 ChemAxon refractivity 138.73 ChemAxon polarizability 56.14 ChemAxon rotatable_bond_count 6 ChemAxon acceptor_count 4 ChemAxon donor_count 3 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 24306 Specdb::CMs 44667 Specdb::CMs 136641 Specdb::CMs 144375 Specdb::MsMs 98490 Specdb::MsMs 98491 Specdb::MsMs 98492 Specdb::MsMs 163419 Specdb::MsMs 163420 Specdb::MsMs 163421 Specdb::MsMs 2420604 Specdb::MsMs 2420605 Specdb::MsMs 2420606 Specdb::MsMs 2545857 Specdb::MsMs 2545858 Specdb::MsMs 2545859 HMDB35977 #<Reference:0x000055ce31954f48> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322