1.0 2016-09-30 22:44:50 UTC 2020-05-21 16:28:29 UTC BMDB0001369 BMDB01369 Pyrroline hydroxycarboxylic acid Pyrroline hydroxycarboxylate 3-Hydroxy-L-1-pyrroline-5-carboxylate L-1-Pyrroline 3-hydroxy-5-carboxylate L-1-Pyrroline-3-hydroxy-5-carboxylate L-Delta1-Pyrroline 3-hydroxy-5-carboxylate Pyrroline-hydroxy-carboxylate 3,4-Dihydro-3-hydroxy-2H-pyrrole-5-carboxylic acid 3-Hydroxy delta 1-pyrroline-5-carboxylic acid 3-Hydroxy delta 1-pyrroline-5-carboxylic acid, anion C5H7NO3 129.114 129.042593095 4-hydroxy-3,4-dihydro-2H-pyrrole-2-carboxylic acid pyrroline-hydroxy-carboxylate 22573-88-2 OC1CC(N=C1)C(O)=O InChI=1S/C5H7NO3/c7-3-1-4(5(8)9)6-2-3/h2-4,7H,1H2,(H,8,9) WFOFKRKDDKGRIK-UHFFFAOYSA-N belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof. Organic compounds Organic acids and derivatives Carboxylic acids and derivatives Amino acids, peptides, and analogues Alpha amino acids and derivatives Azacyclic compounds Carbonyl compounds Carboxylic acids Hydrocarbon derivatives Imines Monocarboxylic acids and derivatives Organic oxides Organopnictogen compounds Propargyl-type 1,3-dipolar organic compounds Pyrroline carboxylic acids Secondary alcohols Alcohol Aliphatic heteromonocyclic compound Alpha-amino acid or derivatives Azacycle Carbonyl group Carboxylic acid Hydrocarbon derivative Imine Monocarboxylic acid or derivatives Organic 1,3-dipolar compound Organic nitrogen compound Organic oxide Organic oxygen compound Organoheterocyclic compound Organonitrogen compound Organooxygen compound Organopnictogen compound Propargyl-type 1,3-dipolar organic compound Pyrroline Pyrroline carboxylic acid Pyrroline carboxylic acid or derivatives Secondary alcohol Aliphatic heteromonocyclic compounds 1-pyrrolinecarboxylic acid Solid logp -1.10 ALOGPS logs -0.58 ALOGPS logp -1.5 ChemAxon pka_strongest_acidic 3.72 ChemAxon pka_strongest_basic 2.59 ChemAxon iupac 4-hydroxy-3,4-dihydro-2H-pyrrole-2-carboxylic acid ChemAxon average_mass 129.114 ChemAxon mono_mass 129.042593095 ChemAxon smiles OC1CC(N=C1)C(O)=O ChemAxon formula C5H7NO3 ChemAxon inchi InChI=1S/C5H7NO3/c7-3-1-4(5(8)9)6-2-3/h2-4,7H,1H2,(H,8,9) ChemAxon inchikey WFOFKRKDDKGRIK-UHFFFAOYSA-N ChemAxon polar_surface_area 69.89 ChemAxon refractivity 28.85 ChemAxon polarizability 11.6 ChemAxon rotatable_bond_count 1 ChemAxon acceptor_count 4 ChemAxon donor_count 2 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon number_of_rings 1 ChemAxon bioavailability 1 ChemAxon rule_of_five Yes ChemAxon ghose_filter Yes ChemAxon veber_rule Yes ChemAxon mddr_like_rule Yes ChemAxon Arginine and Proline Metabolism SMP0087178 Specdb::CMs 2714 Specdb::CMs 38042 Specdb::CMs 165574 Specdb::NmrOneD 147570 Specdb::NmrOneD 147571 Specdb::NmrOneD 147572 Specdb::NmrOneD 147573 Specdb::NmrOneD 147574 Specdb::NmrOneD 147575 Specdb::NmrOneD 147576 Specdb::NmrOneD 147577 Specdb::NmrOneD 147578 Specdb::NmrOneD 147579 Specdb::NmrOneD 147580 Specdb::NmrOneD 147581 Specdb::NmrOneD 147582 Specdb::NmrOneD 147583 Specdb::NmrOneD 147584 Specdb::NmrOneD 147585 Specdb::NmrOneD 147586 Specdb::NmrOneD 147587 Specdb::NmrOneD 147588 Specdb::NmrOneD 147589 Specdb::MsMs 1537 Specdb::MsMs 178719 Specdb::MsMs 178720 Specdb::MsMs 178721 Specdb::MsMs 181038 Specdb::MsMs 181039 Specdb::MsMs 181040 Specdb::MsMs 2398137 Specdb::MsMs 2398138 Specdb::MsMs 2398139 Specdb::MsMs 2536784 Specdb::MsMs 2536785 Specdb::MsMs 2536786 C04281 FDB022582 1030 1059 27391 43511 6196 BMDBP01018 Pyrroline-5-carboxylate reductase 2 Q17QJ7 PYCR2 Enzyme BMDBP02872 Proline dehydrogenase 1, mitochondrial Q148G5 PRODH Enzyme