1.0 2010-04-08 22:11:07 UTC 2019-11-26 03:09:36 UTC FDB014166 N-[(4E,8E)-1,3-dihydroxyoctadeca-4,8-dien-2-yl]hexadecanamide Isolated from Vigna angularis (azuki bean). N-[(4E,8E)-1,3-dihydroxyoctadeca-4,8-dien-2-yl]hexadecanamide is found in pulses. N-[(4E,8E)-1,3-dihydroxyoctadeca-4,8-dien-2-yl]hexadecanamide N-Hexadecanoyl-(2S,3R,4E,8E)-2-amino-4,8-octadecadiene-1,3-diol C34H65NO3 535.8848 535.496444951 N-[(4Z,8Z)-1,3-dihydroxyoctadeca-4,8-dien-2-yl]hexadecanamide N-[(4Z,8Z)-1,3-dihydroxyoctadeca-4,8-dien-2-yl]hexadecanamide 141980-53-2 CCCCCCCCCCCCCCCC(=O)NC(CO)C(O)\C=C/CC\C=C/CCCCCCCCC InChI=1S/C34H65NO3/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-33(37)32(31-36)35-34(38)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h19,21,27,29,32-33,36-37H,3-18,20,22-26,28,30-31H2,1-2H3,(H,35,38)/b21-19-,29-27- GMWIWVUTMCBDSP-RTXSCNSFSA-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 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 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 9.51 ALOGPS logs -7.23 ALOGPS solubility 3.18e-05 g/l ALOGPS melting_point Mp 82-83° logp 10.5 ChemAxon pka_strongest_acidic 13.6 ChemAxon pka_strongest_basic 0.02 ChemAxon iupac N-[(4Z,8Z)-1,3-dihydroxyoctadeca-4,8-dien-2-yl]hexadecanamide ChemAxon average_mass 535.8848 ChemAxon mono_mass 535.496444951 ChemAxon smiles CCCCCCCCCCCCCCCC(=O)NC(CO)C(O)\C=C/CC\C=C/CCCCCCCCC ChemAxon formula C34H65NO3 ChemAxon inchi InChI=1S/C34H65NO3/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-33(37)32(31-36)35-34(38)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h19,21,27,29,32-33,36-37H,3-18,20,22-26,28,30-31H2,1-2H3,(H,35,38)/b21-19-,29-27- ChemAxon inchikey GMWIWVUTMCBDSP-RTXSCNSFSA-N ChemAxon polar_surface_area 69.56 ChemAxon refractivity 166.89 ChemAxon polarizability 70.83 ChemAxon rotatable_bond_count 29 ChemAxon acceptor_count 3 ChemAxon donor_count 3 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 44408 Specdb::CMs 250045 Specdb::CMs 250046 Specdb::CMs 250047 Specdb::CMs 250048 Specdb::CMs 250049 Specdb::CMs 250050 Specdb::CMs 250051 Specdb::CMs 250052 Specdb::CMs 250053 Specdb::CMs 250054 Specdb::CMs 250055 Specdb::CMs 281199 Specdb::MsMs 56976 Specdb::MsMs 56977 Specdb::MsMs 56978 Specdb::MsMs 112512 Specdb::MsMs 112513 Specdb::MsMs 112514 Specdb::MsMs 2290407 Specdb::MsMs 2290408 Specdb::MsMs 2290409 Specdb::MsMs 2644395 Specdb::MsMs 2644396 Specdb::MsMs 2644397 HMDB35480 #<Reference:0x000055ce32178df0> Pulses Unknown generic