1.0 2010-04-08 22:13:48 UTC 2019-11-26 03:16:21 UTC FDB018577 Lactariamide B Isolated from the fungus Lactarius volemus (tawny milkcap mushroom). Lactariamide B is found in mushrooms. Lactariamide B C37H71NO4 593.9639 593.538309765 (2R)-N-[(2S,3R,4E,8E)-1,3-dihydroxy-9-methyloctadeca-4,8-dien-2-yl]-2-hydroxyoctadecanimidic acid (2R)-N-[(2S,3R,4E,8E)-1,3-dihydroxy-9-methyloctadeca-4,8-dien-2-yl]-2-hydroxyoctadecanimidic acid CCCCCCCCCCCCCCCC[C@@H](O)C(=O)N[C@@H](CO)[C@H](O)\C=C\CC\C=C(/C)CCCCCCCCC InChI=1S/C37H71NO4/c1-4-6-8-10-12-13-14-15-16-17-18-20-22-26-31-36(41)37(42)38-34(32-39)35(40)30-27-23-25-29-33(3)28-24-21-19-11-9-7-5-2/h27,29-30,34-36,39-41H,4-26,28,31-32H2,1-3H3,(H,38,42)/b30-27+,33-29+/t34-,35+,36+/m0/s1 SFUUTBQJLKKRBN-ZLUXHSFOSA-N belongs to the class of organic compounds known as ceramides. These are lipid molecules containing a sphingosine in which the amine group is linked to a fatty acid. Ceramides Organic compounds Lipids and lipid-like molecules Sphingolipids Ceramides Aliphatic acyclic compounds Carbonyl compounds Hydrocarbon derivatives Monosaccharides N-acyl amines Organic oxides Organonitrogen compounds Organopnictogen compounds Primary alcohols Secondary alcohols Secondary carboxylic acid amides Alcohol Aliphatic acyclic compound Carbonyl group Carboxamide group Carboxylic acid derivative Ceramide Fatty acyl Fatty amide Hydrocarbon derivative Monosaccharide N-acyl-amine Organic nitrogen compound Organic oxide Organic oxygen compound Organonitrogen compound Organooxygen compound Organopnictogen compound Primary alcohol Secondary alcohol Secondary carboxylic acid amide logp 9.14 ALOGPS logs -6.47 ALOGPS solubility 2.00e-04 g/l ALOGPS logp 11.58 ChemAxon pka_strongest_acidic 4.29 ChemAxon pka_strongest_basic 2.05 ChemAxon iupac (2R)-N-[(2S,3R,4E,8E)-1,3-dihydroxy-9-methyloctadeca-4,8-dien-2-yl]-2-hydroxyoctadecanimidic acid ChemAxon average_mass 593.9639 ChemAxon mono_mass 593.538309765 ChemAxon smiles CCCCCCCCCCCCCCCC[C@@H](O)C(=O)N[C@@H](CO)[C@H](O)\C=C\CC\C=C(/C)CCCCCCCCC ChemAxon formula C37H71NO4 ChemAxon inchi InChI=1S/C37H71NO4/c1-4-6-8-10-12-13-14-15-16-17-18-20-22-26-31-36(41)37(42)38-34(32-39)35(40)30-27-23-25-29-33(3)28-24-21-19-11-9-7-5-2/h27,29-30,34-36,39-41H,4-26,28,31-32H2,1-3H3,(H,38,42)/b30-27+,33-29+/t34-,35+,36+/m0/s1 ChemAxon inchikey SFUUTBQJLKKRBN-ZLUXHSFOSA-N ChemAxon polar_surface_area 93.28 ChemAxon refractivity 182.39 ChemAxon polarizability 78.4 ChemAxon rotatable_bond_count 31 ChemAxon acceptor_count 5 ChemAxon donor_count 4 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 100482 Specdb::MsMs 100483 Specdb::MsMs 100484 Specdb::MsMs 165819 Specdb::MsMs 165820 Specdb::MsMs 165821 HMDB39077 #<Reference:0x000055ce31eda0a8> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322