1.0 2010-04-08 22:07:02 UTC 2019-11-26 03:01:01 UTC FDB006228 24-Methylene-31-nor-5alpha-lanost-9(11)-3beta-ol 24-methylene-31-nor-5alpha-lanost-9(11)-3beta-ol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). 24-methylene-31-nor-5alpha-lanost-9(11)-3beta-ol can be found in french plantain, which makes 24-methylene-31-nor-5alpha-lanost-9(11)-3beta-ol a potential biomarker for the consumption of this food product. C30H50O 426.7174 426.386166222 (2S,5S,7S,11S,14R,15R)-2,6,11,15-tetramethyl-14-[(2R)-6-methyl-5-methylideneheptan-2-yl]tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(17)-en-5-ol (2S,5S,7S,11S,14R,15R)-2,6,11,15-tetramethyl-14-[(2R)-6-methyl-5-methylideneheptan-2-yl]tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(17)-en-5-ol CC(C)C(=C)CC[C@@H](C)[C@H]1CC[C@@]2(C)C3CC[C@H]4C(C)[C@@H](O)CC[C@]4(C)C3=CC[C@]12C InChI=1S/C30H50O/c1-19(2)20(3)9-10-21(4)23-13-17-30(8)26-12-11-24-22(5)27(31)15-16-28(24,6)25(26)14-18-29(23,30)7/h14,19,21-24,26-27,31H,3,9-13,15-18H2,1-2,4-8H3/t21-,22?,23-,24+,26?,27+,28+,29-,30+/m1/s1 FPGXQODNUNHTTC-JEUQCIQHSA-N belongs to the class of organic compounds known as ergosterols and derivatives. These are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton. Ergosterols and derivatives Organic compounds Lipids and lipid-like molecules Steroids and steroid derivatives Ergostane steroids Aliphatic homopolycyclic compounds 14-alpha-methylsteroids 3-beta-hydroxysteroids Cyclic alcohols and derivatives Hydrocarbon derivatives Secondary alcohols 14-alpha-methylsteroid 3-beta-hydroxysteroid 3-hydroxysteroid Alcohol Aliphatic homopolycyclic compound Cyclic alcohol Ergosterol-skeleton Hydrocarbon derivative Hydroxysteroid Organic oxygen compound Organooxygen compound Secondary alcohol logp 7.67 ALOGPS logs -6.50 ALOGPS solubility 1.35e-04 g/l ALOGPS logp 7.72 ChemAxon pka_strongest_acidic 18.96 ChemAxon pka_strongest_basic -1.1 ChemAxon iupac (2S,5S,7S,11S,14R,15R)-2,6,11,15-tetramethyl-14-[(2R)-6-methyl-5-methylideneheptan-2-yl]tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(17)-en-5-ol ChemAxon average_mass 426.7174 ChemAxon mono_mass 426.386166222 ChemAxon smiles CC(C)C(=C)CC[C@@H](C)[C@H]1CC[C@@]2(C)C3CC[C@H]4C(C)[C@@H](O)CC[C@]4(C)C3=CC[C@]12C ChemAxon formula C30H50O ChemAxon inchi InChI=1S/C30H50O/c1-19(2)20(3)9-10-21(4)23-13-17-30(8)26-12-11-24-22(5)27(31)15-16-28(24,6)25(26)14-18-29(23,30)7/h14,19,21-24,26-27,31H,3,9-13,15-18H2,1-2,4-8H3/t21-,22?,23-,24+,26?,27+,28+,29-,30+/m1/s1 ChemAxon inchikey FPGXQODNUNHTTC-JEUQCIQHSA-N ChemAxon polar_surface_area 20.23 ChemAxon refractivity 133.89 ChemAxon polarizability 55.11 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 1 ChemAxon donor_count 1 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 68949 Specdb::MsMs 68950 Specdb::MsMs 68951 Specdb::MsMs 127110 Specdb::MsMs 127111 Specdb::MsMs 127112 Specdb::MsMs 3602681 Specdb::MsMs 3602682 Specdb::MsMs 3602683 Specdb::MsMs 3602684 Specdb::MsMs 3602685 Specdb::MsMs 3602686 French plantain Type 1 specific Musa X paradisiaca 89151