1.0 2020-05-05 15:49:58 UTC 2020-05-05 18:39:09 UTC BMDB0109689 N5-Acetylornithine N(delta)-Acetylornithine N(Δ)-acetylornithine N(delta)-Acetylornithine, (DL)-isomer N-Acetylornithine delta-N-Acetylornithine (2S)-2-Acetamido-5-aminopentanoic acid (2S)-2-Amino-5-acetamidopentanoic acid (2S)-5-Amino-2-acetamidopentanoic acid N(delta)-Acetyl-L-ornithine N(Δ)-acetyl-L-ornithine N-Acetyl-L-ornithine N-delta-Acetylornithine N-Δ-acetylornithine N5-Acetyl-L-ornithine Ndelta-acetyl-L-ornithine Ndelta-acetylornithine Nδ-acetyl-L-ornithine Nδ-acetylornithine delta-Acetyl-L-ornithine Omega-N-acetylornithine Δ-acetyl-L-ornithine Ω-N-acetylornithine N5-Acetylornithine C7H14N2O3 174.1977 174.100442324 (2S)-2-amino-5-acetamidopentanoic acid N(delta)-acetylornithine 2185-16-2 CC(=O)NCCC[C@H](N)C(O)=O InChI=1S/C7H14N2O3/c1-5(10)9-4-2-3-6(8)7(11)12/h6H,2-4,8H2,1H3,(H,9,10)(H,11,12)/t6-/m0/s1 SRXKAYJJGAAOBP-LURJTMIESA-N belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom. Organic compounds Organic acids and derivatives Carboxylic acids and derivatives Amino acids, peptides, and analogues L-alpha-amino acids Acetamides Amino acids Carbonyl compounds Carboxylic acids Fatty acids and conjugates Hydrocarbon derivatives Monoalkylamines Monocarboxylic acids and derivatives Organic oxides Organopnictogen compounds Secondary carboxylic acid amides Acetamide Aliphatic acyclic compound Amine Amino acid Carbonyl group Carboxamide group Carboxylic acid Fatty acid Hydrocarbon derivative L-alpha-amino acid Monocarboxylic acid or derivatives Organic nitrogen compound Organic oxide Organic oxygen compound Organonitrogen compound Organooxygen compound Organopnictogen compound Primary aliphatic amine Primary amine Secondary carboxylic acid amide Aliphatic acyclic compounds N(5)-acyl-L-ornithine acetylornithine logp -2.75 ALOGPS logs -0.65 ALOGPS logp -3.6 ChemAxon pka_strongest_acidic 2.35 ChemAxon pka_strongest_basic 9.23 ChemAxon iupac (2S)-2-amino-5-acetamidopentanoic acid ChemAxon average_mass 174.1977 ChemAxon mono_mass 174.100442324 ChemAxon smiles CC(=O)NCCC[C@H](N)C(O)=O ChemAxon formula C7H14N2O3 ChemAxon inchi InChI=1S/C7H14N2O3/c1-5(10)9-4-2-3-6(8)7(11)12/h6H,2-4,8H2,1H3,(H,9,10)(H,11,12)/t6-/m0/s1 ChemAxon inchikey SRXKAYJJGAAOBP-LURJTMIESA-N ChemAxon polar_surface_area 92.42 ChemAxon refractivity 42.65 ChemAxon polarizability 18.09 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 4 ChemAxon donor_count 3 ChemAxon physiological_charge 0 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::CMs 133637 Specdb::CMs 141371 Specdb::MsMs 1452599 Specdb::MsMs 1452600 Specdb::MsMs 1452601 Specdb::MsMs 1463570 Specdb::MsMs 1463571 Specdb::MsMs 1463572 Specdb::MsMs 2720712 Specdb::MsMs 2720713 Specdb::MsMs 2720714 Specdb::MsMs 2958231 Specdb::MsMs 2958232 Specdb::MsMs 2958233 Specdb::NmrOneD 75832 Specdb::NmrOneD 75833 Specdb::NmrOneD 75834 Specdb::NmrOneD 75835 Specdb::NmrOneD 75836 Specdb::NmrOneD 75837 Specdb::NmrOneD 75838 Specdb::NmrOneD 75839 Specdb::NmrOneD 75840 Specdb::NmrOneD 75841 Specdb::NmrOneD 75842 Specdb::NmrOneD 75843 Specdb::NmrOneD 75844 Specdb::NmrOneD 75845 Specdb::NmrOneD 75846 Specdb::NmrOneD 75847 Specdb::NmrOneD 75848 Specdb::NmrOneD 75849 Specdb::NmrOneD 75850 Specdb::NmrOneD 75851 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 167777 193343 44673 FDB112403 CPD-13644