1.0 2010-04-08 22:13:55 UTC 2019-11-26 03:16:38 UTC FDB018754 N-(gamma-Glutamyl)ethanolamine Constituent of the fruiting body of Agaricus bisporus (button mushroom). N-(gamma-Glutamyl)ethanolamine is found in mushrooms. N-(g-Glutamyl)ethanolamine, 8CI C7H14N2O4 190.1971 190.095356946 (2S)-2-amino-4-[(2-hydroxyethyl)-C-hydroxycarbonimidoyl]butanoic acid (2S)-2-amino-4-[(2-hydroxyethyl)-C-hydroxycarbonimidoyl]butanoic acid 2650-74-0 [H][C@](N)(CCC(=O)NCCO)C(O)=O InChI=1S/C7H14N2O4/c8-5(7(12)13)1-2-6(11)9-3-4-10/h5,10H,1-4,8H2,(H,9,11)(H,12,13)/t5-/m0/s1 DGBJQQBLTDLFMF-YFKPBYRVSA-N belongs to the class of organic compounds known as glutamine and derivatives. Glutamine and derivatives are compounds containing glutamine or a derivative thereof resulting from reaction of glutamine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. Glutamine and derivatives Organic compounds Organic acids and derivatives Carboxylic acids and derivatives Amino acids, peptides, and analogues Aliphatic acyclic compounds Amino acids Carbonyl compounds Carboxylic acids Fatty acids and conjugates Hydrocarbon derivatives L-alpha-amino acids Monoalkylamines Monocarboxylic acids and derivatives N-acyl amines N-acylethanolamines Organic oxides Organopnictogen compounds Primary alcohols Secondary carboxylic acid amides Alcohol Aliphatic acyclic compound Alkanolamine Alpha-amino acid Amine Amino acid Carbonyl group Carboxamide group Carboxylic acid Fatty acid Fatty acyl Fatty amide Glutamine or derivatives Hydrocarbon derivative L-alpha-amino acid Monocarboxylic acid or derivatives N-acyl-amine N-acylethanolamine Organic nitrogen compound Organic oxide Organic oxygen compound Organonitrogen compound Organooxygen compound Organopnictogen compound Primary alcohol Primary aliphatic amine Primary amine Secondary carboxylic acid amide logp -3.22 ALOGPS logs -1.49 ALOGPS solubility 6.21e+00 g/l ALOGPS melting_point Mp 188.5-191° logp -3.8 ChemAxon pka_strongest_acidic 2.26 ChemAxon pka_strongest_basic 9.54 ChemAxon iupac (2S)-2-amino-4-[(2-hydroxyethyl)-C-hydroxycarbonimidoyl]butanoic acid ChemAxon average_mass 190.1971 ChemAxon mono_mass 190.095356946 ChemAxon smiles [H][C@](N)(CCC(=O)NCCO)C(O)=O ChemAxon formula C7H14N2O4 ChemAxon inchi InChI=1S/C7H14N2O4/c8-5(7(12)13)1-2-6(11)9-3-4-10/h5,10H,1-4,8H2,(H,9,11)(H,12,13)/t5-/m0/s1 ChemAxon inchikey DGBJQQBLTDLFMF-YFKPBYRVSA-N ChemAxon polar_surface_area 116.14 ChemAxon refractivity 44.82 ChemAxon polarizability 19.12 ChemAxon rotatable_bond_count 6 ChemAxon acceptor_count 6 ChemAxon donor_count 4 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 104511 Specdb::MsMs 104512 Specdb::MsMs 104513 Specdb::MsMs 170817 Specdb::MsMs 170818 Specdb::MsMs 170819 HMDB39222 #<Reference:0x000055ce331072a8> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322