1.0 2010-04-08 22:13:22 UTC 2019-11-26 03:15:24 UTC FDB017896 Linatine Isolated from Linum usitatissimum (flax). Linatine is found in tea and fats and oils. 1-((4-amino-4-Carboxy-1-oxobutyl)amino)-(S)-D-proline 1-((N-gamma-L-Glutamyl)amino)-D-proline 1-[N-(g-L-Glutamyl)amino]-D-proline D-Proline, 1-((4-amino-4-carboxy-1-oxobutyl)amino)-, (S)- Glutamine, N-(D-2-carboxy-1-pyrrolidinyl)-, L- Linatine N-(D-2-Carboxy-1-pyrrolidinyl)-L-glutamine N-(gamma-l-glutamyl)amino-d-proline NN-[(2R)-2-carboxypyrrolidin-1-yl]-L-glutamine C10H17N3O5 259.2591 259.116820669 (2R)-1-{[(4S)-4-amino-4-carboxy-1-hydroxybutylidene]amino}pyrrolidine-2-carboxylic acid (2R)-1-{[(4S)-4-amino-4-carboxy-1-hydroxybutylidene]amino}pyrrolidine-2-carboxylic acid 10139-06-7 N[C@@H](CCC(=O)NN1CCC[C@@H]1C(O)=O)C(O)=O InChI=1S/C10H17N3O5/c11-6(9(15)16)3-4-8(14)12-13-5-1-2-7(13)10(17)18/h6-7H,1-5,11H2,(H,12,14)(H,15,16)(H,17,18)/t6-,7+/m0/s1 KWWHDNLMGLRNRN-NKWVEPMBSA-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 heteromonocyclic compounds Amino acids Azacyclic compounds Carbonyl compounds Carboxylic acid hydrazides Carboxylic acids Dicarboxylic acids and derivatives Heterocyclic fatty acids Hydrocarbon derivatives L-alpha-amino acids Monoalkylamines Organic oxides Organopnictogen compounds Proline and derivatives Pyrrolidine carboxylic acids Aliphatic heteromonocyclic compound Alpha-amino acid Amine Amino acid Azacycle Carbonyl group Carboxylic acid Carboxylic acid hydrazide Dicarboxylic acid or derivatives Fatty acid Fatty acyl Glutamine or derivatives Heterocyclic fatty acid Hydrocarbon derivative L-alpha-amino acid Organic nitrogen compound Organic oxide Organic oxygen compound Organoheterocyclic compound Organonitrogen compound Organooxygen compound Organopnictogen compound Primary aliphatic amine Primary amine Proline or derivatives Pyrrolidine Pyrrolidine carboxylic acid Pyrrolidine carboxylic acid or derivatives D-proline derivative carbohydrazide pyrrolidinemonocarboxylic acid logp -3.24 ALOGPS logs -1.71 ALOGPS solubility 5.02e+00 g/l ALOGPS logp -3.3 ChemAxon pka_strongest_acidic 2.06 ChemAxon pka_strongest_basic 9.54 ChemAxon iupac (2R)-1-{[(4S)-4-amino-4-carboxy-1-hydroxybutylidene]amino}pyrrolidine-2-carboxylic acid ChemAxon average_mass 259.2591 ChemAxon mono_mass 259.116820669 ChemAxon smiles N[C@@H](CCC(=O)NN1CCC[C@@H]1C(O)=O)C(O)=O ChemAxon formula C10H17N3O5 ChemAxon inchi InChI=1S/C10H17N3O5/c11-6(9(15)16)3-4-8(14)12-13-5-1-2-7(13)10(17)18/h6-7H,1-5,11H2,(H,12,14)(H,15,16)(H,17,18)/t6-,7+/m0/s1 ChemAxon inchikey KWWHDNLMGLRNRN-NKWVEPMBSA-N ChemAxon polar_surface_area 136.45 ChemAxon refractivity 60.1 ChemAxon polarizability 25.31 ChemAxon rotatable_bond_count 6 ChemAxon acceptor_count 8 ChemAxon donor_count 4 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 56586 Specdb::MsMs 56587 Specdb::MsMs 56588 Specdb::MsMs 112035 Specdb::MsMs 112036 Specdb::MsMs 112037 HMDB38516 28004 #<Reference:0x000055ce333a1dd8> Black tea Type 1 Fats and oils Unknown generic Green tea Type 1 Herbal tea Type 1 Red tea Type 1 Tea Type 1 specific Camellia sinensis 4442