1.0 2010-04-08 22:14:13 UTC 2019-11-26 03:17:15 UTC FDB019219 Hericenone F Constituent of the edible lion's mane mushroom Hericium erinaceum. Hericenone F is found in mushrooms. 8-Formyl-5-methoxy-2-methyl-2-(4'-methyl-2'-oxo-3'-pentenyl)-7-chromanylmethylplamitate C35H54O6 570.7997 570.39203946 [8-formyl-5-methoxy-2-methyl-2-(4-methyl-2-oxopent-3-en-1-yl)-3,4-dihydro-2H-1-benzopyran-7-yl]methyl hexadecanoate [8-formyl-5-methoxy-2-methyl-2-(4-methyl-2-oxopent-3-en-1-yl)-3,4-dihydro-1-benzopyran-7-yl]methyl hexadecanoate 141996-36-3 CCCCCCCCCCCCCCCC(=O)OCC1=CC(OC)=C2CCC(C)(CC(=O)C=C(C)C)OC2=C1C=O InChI=1S/C35H54O6/c1-6-7-8-9-10-11-12-13-14-15-16-17-18-19-33(38)40-26-28-23-32(39-5)30-20-21-35(4,24-29(37)22-27(2)3)41-34(30)31(28)25-36/h22-23,25H,6-21,24,26H2,1-5H3 ACYSSVIUKOTZQD-UHFFFAOYSA-N belongs to the class of organic compounds known as 1-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 1-position. 1-benzopyrans Organic compounds Organoheterocyclic compounds Benzopyrans 1-benzopyrans Aromatic heteropolycyclic compounds Acryloyl compounds Alkyl aryl ethers Anisoles Aryl-aldehydes Carboxylic acid esters Enones Fatty acid esters Hydrocarbon derivatives Ketones Monocarboxylic acids and derivatives Organic oxides Oxacyclic compounds 1-benzopyran Acryloyl-group Aldehyde Alkyl aryl ether Alpha,beta-unsaturated ketone Anisole Aromatic heteropolycyclic compound Aryl-aldehyde Benzenoid Carbonyl group Carboxylic acid derivative Carboxylic acid ester Enone Ether Fatty acid ester Fatty acyl Hydrocarbon derivative Ketone Monocarboxylic acid or derivatives Organic oxide Organic oxygen compound Organooxygen compound Oxacycle logp 8.00 ALOGPS logs -7.10 ALOGPS solubility 4.52e-05 g/l ALOGPS logp 9.78 ChemAxon pka_strongest_acidic 19.15 ChemAxon pka_strongest_basic -4.2 ChemAxon iupac [8-formyl-5-methoxy-2-methyl-2-(4-methyl-2-oxopent-3-en-1-yl)-3,4-dihydro-2H-1-benzopyran-7-yl]methyl hexadecanoate ChemAxon average_mass 570.7997 ChemAxon mono_mass 570.39203946 ChemAxon smiles CCCCCCCCCCCCCCCC(=O)OCC1=CC(OC)=C2CCC(C)(CC(=O)C=C(C)C)OC2=C1C=O ChemAxon formula C35H54O6 ChemAxon inchi InChI=1S/C35H54O6/c1-6-7-8-9-10-11-12-13-14-15-16-17-18-19-33(38)40-26-28-23-32(39-5)30-20-21-35(4,24-29(37)22-27(2)3)41-34(30)31(28)25-36/h22-23,25H,6-21,24,26H2,1-5H3 ChemAxon inchikey ACYSSVIUKOTZQD-UHFFFAOYSA-N ChemAxon polar_surface_area 78.9 ChemAxon refractivity 167.13 ChemAxon polarizability 70 ChemAxon rotatable_bond_count 22 ChemAxon acceptor_count 5 ChemAxon donor_count 0 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 21114 Specdb::MsMs 9212 Specdb::MsMs 9213 Specdb::MsMs 9214 Specdb::MsMs 15884 Specdb::MsMs 15885 Specdb::MsMs 15886 Specdb::MsMs 2749618 Specdb::MsMs 2749619 Specdb::MsMs 2749620 Specdb::MsMs 2928535 Specdb::MsMs 2928536 Specdb::MsMs 2928537 HMDB39593 #<Reference:0x000055ce31ccff88> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322