1.0 2010-04-08 22:11:28 UTC 2019-11-26 03:10:45 UTC FDB014788 Ganoderal A Constituent of Ganoderma lucidum (reishi). Ganoderal A is found in mushrooms. (+)-Ganoderal A 3-Oxolanosta-7,9(11),24E-trien-26-al Ganoderal A C30H44O2 436.6692 436.334130652 (2E)-2-methyl-6-{2,6,6,11,15-pentamethyl-5-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),9-dien-14-yl}hept-2-enal (2E)-2-methyl-6-{2,6,6,11,15-pentamethyl-5-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),9-dien-14-yl}hept-2-enal 104700-98-3 CC(CC\C=C(/C)C=O)C1CCC2(C)C3=CCC4C(C)(C)C(=O)CCC4(C)C3=CCC12C InChI=1S/C30H44O2/c1-20(19-31)9-8-10-21(2)22-13-17-30(7)24-11-12-25-27(3,4)26(32)15-16-28(25,5)23(24)14-18-29(22,30)6/h9,11,14,19,21-22,25H,8,10,12-13,15-18H2,1-7H3/b20-9+ RHNFCIPJKSUUES-AWQFTUOYSA-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 Aldehydes Bile acids, alcohols and derivatives Cyclic ketones Delta-7-steroids Enals Hydrocarbon derivatives Organic oxides 26-oxosteroid 27-oxosteroid 3-oxo-delta-7-steroid 3-oxosteroid Aldehyde Aliphatic homopolycyclic compound Alpha,beta-unsaturated aldehyde Bile acid, alcohol, or derivatives Carbonyl group Cholane-skeleton Cyclic ketone Delta-7-steroid Enal Hydrocarbon derivative Ketone Organic oxide Organic oxygen compound Organooxygen compound Oxosteroid Steroid Triterpenoid logp 7.77 ALOGPS logs -5.94 ALOGPS solubility 5.05e-04 g/l ALOGPS melting_point Mp 127-128° logp 6.94 ChemAxon pka_strongest_acidic 19.64 ChemAxon pka_strongest_basic -4.1 ChemAxon iupac (2E)-2-methyl-6-{2,6,6,11,15-pentamethyl-5-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),9-dien-14-yl}hept-2-enal ChemAxon average_mass 436.6692 ChemAxon mono_mass 436.334130652 ChemAxon smiles CC(CC\C=C(/C)C=O)C1CCC2(C)C3=CCC4C(C)(C)C(=O)CCC4(C)C3=CCC12C ChemAxon formula C30H44O2 ChemAxon inchi InChI=1S/C30H44O2/c1-20(19-31)9-8-10-21(2)22-13-17-30(7)24-11-12-25-27(3,4)26(32)15-16-28(25,5)23(24)14-18-29(22,30)6/h9,11,14,19,21-22,25H,8,10,12-13,15-18H2,1-7H3/b20-9+ ChemAxon inchikey RHNFCIPJKSUUES-AWQFTUOYSA-N ChemAxon polar_surface_area 34.14 ChemAxon refractivity 135.63 ChemAxon polarizability 53 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 2 ChemAxon donor_count 0 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 21492 Specdb::CMs 149756 Specdb::MsMs 43665 Specdb::MsMs 43666 Specdb::MsMs 43667 Specdb::MsMs 160083 Specdb::MsMs 160084 Specdb::MsMs 160085 Specdb::MsMs 2727319 Specdb::MsMs 2727320 Specdb::MsMs 2727321 Specdb::MsMs 2978099 Specdb::MsMs 2978100 Specdb::MsMs 2978101 HMDB35983 #<Reference:0x00007f093c112ca8> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322