1.0 2011-09-21 01:32:23 UTC 2015-07-21 06:59:17 UTC FDB027945 L-Glycyl-L-hydroxyproline A dipeptide found in urine (PMID: 3782411). This is a proteolytic breakdown product of collagen. [HMDB] g-HP Dipeptide GHP dipeptide Glu-Hyp Gly-hpro Glycine hydroxyproline dipeptide Glycine-hydroxyproline dipeptide Glycylhydroxyproline C7H12N2O4 188.1812 188.079706882 1-(2-aminoacetyl)-4-hydroxypyrrolidine-2-carboxylic acid 1-(2-aminoacetyl)-4-hydroxypyrrolidine-2-carboxylic acid NCC(=O)N1CC(O)CC1C(O)=O InChI=1S/C7H12N2O4/c8-2-6(11)9-3-4(10)1-5(9)7(12)13/h4-5,10H,1-3,8H2,(H,12,13) ZJQXGJBINIMBOY-UHFFFAOYSA-N belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond. Dipeptides Organic compounds Organic acids and derivatives Carboxylic acids and derivatives Amino acids, peptides, and analogues Aliphatic heteromonocyclic compounds Alpha amino acid amides Amino acids Azacyclic compounds Carbonyl compounds Carboxylic acids Hydrocarbon derivatives Monoalkylamines Monocarboxylic acids and derivatives N-acyl-alpha amino acids N-acylpyrrolidines Organic oxides Organopnictogen compounds Proline and derivatives Pyrrolidine carboxylic acids Secondary alcohols Tertiary carboxylic acid amides Alcohol Aliphatic heteromonocyclic compound Alpha-amino acid amide Alpha-amino acid or derivatives Alpha-dipeptide Amine Amino acid Amino acid or derivatives Azacycle Carbonyl group Carboxamide group Carboxylic acid Hydrocarbon derivative Monocarboxylic acid or derivatives N-acyl-alpha amino acid or derivatives N-acyl-alpha-amino acid N-acylpyrrolidine 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 Secondary alcohol Tertiary carboxylic acid amide Solid logp -3.14 ALOGPS logs 0.24 ALOGPS solubility 3.25e+02 g/l ALOGPS logp -4.8 ChemAxon pka_strongest_acidic 3.42 ChemAxon pka_strongest_basic 8.13 ChemAxon iupac 1-(2-aminoacetyl)-4-hydroxypyrrolidine-2-carboxylic acid ChemAxon average_mass 188.1812 ChemAxon mono_mass 188.079706882 ChemAxon smiles NCC(=O)N1CC(O)CC1C(O)=O ChemAxon formula C7H12N2O4 ChemAxon inchi InChI=1S/C7H12N2O4/c8-2-6(11)9-3-4(10)1-5(9)7(12)13/h4-5,10H,1-3,8H2,(H,12,13) ChemAxon inchikey ZJQXGJBINIMBOY-UHFFFAOYSA-N ChemAxon polar_surface_area 103.86 ChemAxon refractivity 42.31 ChemAxon polarizability 17.53 ChemAxon rotatable_bond_count 2 ChemAxon acceptor_count 5 ChemAxon donor_count 3 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 16879 Specdb::CMs 39583 Specdb::MsMs 303298 Specdb::MsMs 303299 Specdb::MsMs 303300 Specdb::MsMs 346216 Specdb::MsMs 346217 Specdb::MsMs 346218 HMDB28842 #<Reference:0x000055ce32c4e2e8>