1.0 2010-04-08 22:13:22 UTC 2019-11-26 03:15:22 UTC FDB017872 Polyporusterone F Constituent of Polyporus umbellatus (zhu ling). Polyporusterone F is found in mushrooms. Polyporusterone F C28H46O5 462.6618 462.334524582 4,5,11-trihydroxy-14-(3-hydroxy-5,6-dimethylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-9-en-8-one 4,5,11-trihydroxy-14-(3-hydroxy-5,6-dimethylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-9-en-8-one 141360-93-2 CC(C)C(C)CC(O)C(C)C1CCC2(O)C3=CC(=O)C4CC(O)C(O)CC4(C)C3CCC12C InChI=1S/C28H46O5/c1-15(2)16(3)11-22(29)17(4)18-8-10-28(33)20-12-23(30)21-13-24(31)25(32)14-26(21,5)19(20)7-9-27(18,28)6/h12,15-19,21-22,24-25,29,31-33H,7-11,13-14H2,1-6H3 UPQHDDLJIDVNJE-UHFFFAOYSA-N belongs to the class of organic compounds known as tetrahydroxy bile acids, alcohols and derivatives. These are prenol lipids structurally characterized by a bile acid or alcohol which bears four hydroxyl groups. Tetrahydroxy bile acids, alcohols and derivatives Organic compounds Lipids and lipid-like molecules Steroids and steroid derivatives Bile acids, alcohols and derivatives Aliphatic homopolycyclic compounds 14-hydroxysteroids 3-hydroxy delta-7-steroids 6-oxosteroids Cyclic alcohols and derivatives Cyclohexenones Delta-7-steroids Ecdysteroids Ergosterols and derivatives Hydrocarbon derivatives Organic oxides Polyols Secondary alcohols Tertiary alcohols 14-hydroxysteroid 2-hydroxysteroid 22-hydroxysteroid 3-hydroxy-delta-7-steroid 3-hydroxysteroid 6-oxosteroid Alcohol Aliphatic homopolycyclic compound Carbonyl group Cyclic alcohol Cyclohexenone Delta-7-steroid Ecdysteroid Ergostane-skeleton Ergosterol-skeleton Hydrocarbon derivative Hydroxysteroid Ketone Organic oxide Organic oxygen compound Organooxygen compound Oxosteroid Polyol Secondary alcohol Tertiary alcohol Tetrahydroxy bile acid, alcohol, or derivatives logp 3.09 ALOGPS logs -4.15 ALOGPS solubility 3.29e-02 g/l ALOGPS melting_point Mp 251° logp 3.45 ChemAxon pka_strongest_acidic 13.53 ChemAxon pka_strongest_basic -0.68 ChemAxon iupac 4,5,11-trihydroxy-14-(3-hydroxy-5,6-dimethylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-9-en-8-one ChemAxon average_mass 462.6618 ChemAxon mono_mass 462.334524582 ChemAxon smiles CC(C)C(C)CC(O)C(C)C1CCC2(O)C3=CC(=O)C4CC(O)C(O)CC4(C)C3CCC12C ChemAxon formula C28H46O5 ChemAxon inchi InChI=1S/C28H46O5/c1-15(2)16(3)11-22(29)17(4)18-8-10-28(33)20-12-23(30)21-13-24(31)25(32)14-26(21,5)19(20)7-9-27(18,28)6/h12,15-19,21-22,24-25,29,31-33H,7-11,13-14H2,1-6H3 ChemAxon inchikey UPQHDDLJIDVNJE-UHFFFAOYSA-N ChemAxon polar_surface_area 97.99 ChemAxon refractivity 130.14 ChemAxon polarizability 53.52 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 5 ChemAxon donor_count 4 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 24369 Specdb::CMs 45865 Specdb::CMs 130991 Specdb::CMs 138725 Specdb::MsMs 89607 Specdb::MsMs 89608 Specdb::MsMs 89609 Specdb::MsMs 152568 Specdb::MsMs 152569 Specdb::MsMs 152570 Specdb::MsMs 2306004 Specdb::MsMs 2306005 Specdb::MsMs 2306006 Specdb::MsMs 3063184 Specdb::MsMs 3063185 Specdb::MsMs 3063186 HMDB38499 #<Reference:0x000055ce32c2a230> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322