1.0 2016-09-30 22:36:53 UTC 2020-05-05 18:37:24 UTC BMDB0000808 BMDB00808 N-Butyrylglycine 2-Butanamidoacetic acid 2-Butyramidoacetic acid Butanamidoacetic acid Butyramidoacetic acid N-(1-Oxobutyl)glycine N-Butyryl-glycine 2-Butanamidoacetate 2-Butyramidoacetate Butanamidoacetate Butyramidoacetate N-Butanoylglycine Butyrylglycine N-Butyrylglycine C6H11NO3 145.1564 145.073893223 2-butanamidoacetic acid butyrylglycine 20208-73-5 CCCC(=O)NCC(O)=O InChI=1S/C6H11NO3/c1-2-3-5(8)7-4-6(9)10/h2-4H2,1H3,(H,7,8)(H,9,10) WPSSBBPLVMTKRN-UHFFFAOYSA-N belongs to the class of organic compounds known as n-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. Organic compounds Organic acids and derivatives Carboxylic acids and derivatives Amino acids, peptides, and analogues N-acyl-alpha amino acids Carbonyl compounds Carboximidic acids Carboxylic acids Hydrocarbon derivatives Monocarboxylic acids and derivatives Organic oxides Organonitrogen compounds Organopnictogen compounds Propargyl-type 1,3-dipolar organic compounds Aliphatic acyclic compound Carbonyl group Carboximidic acid Carboximidic acid derivative Carboxylic acid Hydrocarbon derivative Monocarboxylic acid or derivatives N-acyl-alpha-amino acid Organic 1,3-dipolar compound Organic nitrogen compound Organic oxide Organic oxygen compound Organonitrogen compound Organooxygen compound Organopnictogen compound Propargyl-type 1,3-dipolar organic compound Aliphatic acyclic compounds Solid logp 0.03 ALOGPS logs -0.92 ALOGPS logp -0.18 ChemAxon pka_strongest_acidic 4.06 ChemAxon pka_strongest_basic -1.9 ChemAxon iupac 2-butanamidoacetic acid ChemAxon average_mass 145.1564 ChemAxon mono_mass 145.073893223 ChemAxon smiles CCCC(=O)NCC(O)=O ChemAxon formula C6H11NO3 ChemAxon inchi InChI=1S/C6H11NO3/c1-2-3-5(8)7-4-6(9)10/h2-4H2,1H3,(H,7,8)(H,9,10) ChemAxon inchikey WPSSBBPLVMTKRN-UHFFFAOYSA-N ChemAxon polar_surface_area 66.4 ChemAxon refractivity 34.68 ChemAxon polarizability 14.64 ChemAxon rotatable_bond_count 4 ChemAxon acceptor_count 3 ChemAxon donor_count 2 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon number_of_rings 0 ChemAxon bioavailability 1 ChemAxon rule_of_five Yes ChemAxon ghose_filter Yes ChemAxon veber_rule Yes ChemAxon mddr_like_rule Yes ChemAxon Specdb::NmrOneD 1551 Specdb::CMs 14490 Specdb::CMs 37778 Specdb::CMs 133342 Specdb::CMs 141076 Specdb::CMs 1077427 Specdb::CMs 1077429 Specdb::CMs 1077431 Specdb::MsMs 1155 Specdb::MsMs 1156 Specdb::MsMs 1157 Specdb::MsMs 297982 Specdb::MsMs 297983 Specdb::MsMs 297984 Specdb::MsMs 339649 Specdb::MsMs 339650 Specdb::MsMs 339651 Specdb::MsMs 2228765 Specdb::MsMs 2230659 Specdb::MsMs 2232081 Specdb::MsMs 2232099 Specdb::MsMs 2234439 Specdb::MsMs 2234512 Specdb::MsMs 2252363 Specdb::MsMs 2254110 Specdb::MsMs 2254471 Specdb::MsMs 2256116 Specdb::MsMs 2256531 Specdb::MsMs 2258045 Specdb::MsMs 2258507 Specdb::MsMs 2260087 Specdb::MsMs 2269351 Specdb::MsMs 2269352 Specdb::MsIr 872 Specdb::MsIr 873 Specdb::MsIr 874 Liver Metabolomics analysis was performed using GC-MS/LC-MS in multiparous Holstein dairy cows Shahzad K, Lopreiato V, Liang Y, Trevisi E, Osorio JS, Xu C, Loor JJ: Hepatic metabolomics and transcriptomics to study susceptibility to ketosis in response to prepartal nutritional management. J Anim Sci Biotechnol. 2019 Dec 18;10:96. doi: 10.1186/s40104-019-0404-z. eCollection 2019. 31867104 FDB022256 79766 88412 89963 5772 Bondi, S.; Eissler, F. Lipoproteins and the Fatty Degeneration of Cells. Biochemische Zeitschrift (1910), 23 499-513.