1.0 2010-04-08 22:14:08 UTC 2019-11-26 03:17:07 UTC FDB019111 gamma-Glutamyl-S-methylcysteinyl-beta-alanine Constituent of the seeds of the mung bean (Vigna radiata). gamma-Glutamyl-S-methylcysteinyl-beta-alanine is found in pulses. g-Glutamyl-S-methylcysteinyl-b-alanine S-Methylhomoglutathione C12H21N3O6S 335.377 335.115106109 (2R)-2-amino-4-{[(1R)-1-[(2-carboxyethyl)-C-hydroxycarbonimidoyl]-2-(methylsulfanyl)ethyl]-C-hydroxycarbonimidoyl}butanoic acid (2R)-2-amino-4-{[(1R)-1-[(2-carboxyethyl)-C-hydroxycarbonimidoyl]-2-(methylsulfanyl)ethyl]-C-hydroxycarbonimidoyl}butanoic acid 102148-91-4 CSC[C@H](NC(=O)CC[C@@H](N)C(O)=O)C(=O)NCCC(O)=O InChI=1S/C12H21N3O6S/c1-22-6-8(11(19)14-5-4-10(17)18)15-9(16)3-2-7(13)12(20)21/h7-8H,2-6,13H2,1H3,(H,14,19)(H,15,16)(H,17,18)(H,20,21)/t7-,8+/m1/s1 MSEXKIKRSMQHDG-SFYZADRCSA-N belongs to the class of organic compounds known as hybrid peptides. Hybrid peptides are compounds containing at least two different types of amino acids (alpha, beta, gamma, delta) linked to each other through a peptide bond. Hybrid peptides Organic compounds Organic acids and derivatives Peptidomimetics Hybrid peptides Aliphatic acyclic compounds Alpha amino acid amides Amino acids Beta amino acids and derivatives Carbonyl compounds Carboxylic acids Cysteine and derivatives D-alpha-amino acids Dialkylthioethers Dicarboxylic acids and derivatives Dipeptides Fatty acids and conjugates Glutamine and derivatives Hydrocarbon derivatives Monoalkylamines N-acyl amines N-acyl-alpha amino acids and derivatives Organic oxides Organopnictogen compounds Secondary carboxylic acid amides Sulfenyl compounds Aliphatic acyclic compound Alpha-amino acid Alpha-amino acid amide Alpha-amino acid or derivatives Alpha-dipeptide Amine Amino acid Amino acid or derivatives Beta amino acid or derivatives Carbonyl group Carboxamide group Carboxylic acid Carboxylic acid derivative Cysteine or derivatives D-alpha-amino acid Dialkylthioether Dicarboxylic acid or derivatives Fatty acid Fatty acyl Fatty amide Glutamine or derivatives Hybrid peptide Hydrocarbon derivative N-acyl-alpha amino acid or derivatives N-acyl-amine N-substituted-alpha-amino acid Organic nitrogen compound Organic oxide Organic oxygen compound Organonitrogen compound Organooxygen compound Organopnictogen compound Organosulfur compound Primary aliphatic amine Primary amine Secondary carboxylic acid amide Sulfenyl compound Thioether logp -2.59 ALOGPS logs -3.09 ALOGPS solubility 2.73e-01 g/l ALOGPS logp -3.8 ChemAxon pka_strongest_acidic 1.75 ChemAxon pka_strongest_basic 9.54 ChemAxon iupac (2R)-2-amino-4-{[(1R)-1-[(2-carboxyethyl)-C-hydroxycarbonimidoyl]-2-(methylsulfanyl)ethyl]-C-hydroxycarbonimidoyl}butanoic acid ChemAxon average_mass 335.377 ChemAxon mono_mass 335.115106109 ChemAxon smiles CSC[C@H](NC(=O)CC[C@@H](N)C(O)=O)C(=O)NCCC(O)=O ChemAxon formula C12H21N3O6S ChemAxon inchi InChI=1S/C12H21N3O6S/c1-22-6-8(11(19)14-5-4-10(17)18)15-9(16)3-2-7(13)12(20)21/h7-8H,2-6,13H2,1H3,(H,14,19)(H,15,16)(H,17,18)(H,20,21)/t7-,8+/m1/s1 ChemAxon inchikey MSEXKIKRSMQHDG-SFYZADRCSA-N ChemAxon polar_surface_area 165.8 ChemAxon refractivity 79.51 ChemAxon polarizability 33.69 ChemAxon rotatable_bond_count 11 ChemAxon acceptor_count 9 ChemAxon donor_count 5 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon HMDB39504 #<Reference:0x000055ce32f61d68> Pulses Unknown generic