Ornithine oxoglurateProduct ingredient for Ornithine
- Name
- Ornithine oxoglurate
- Drug Entry
- Ornithine
Produced during the urea cycle, ornithine is an amino acid produced from the splitting off of urea from arginine. L-Ornithine allows for the disposal of excess nitrogen and acts as a precursor of citrulline and arginine.
- Accession Number
- DBSALT002529
- Structure
Structure for Ornithine oxoglurate (DBSALT002529)
- Synonyms
- Ornithine alpha-ketoglutarate / Ornithine monoxoglurate / Ornithine oxoglutarate
- UNII
- 4FEN49K96W
- CAS Number
- 5191-97-9
- Weight
- Average: 278.261
Monoisotopic: 278.111400928 - Chemical Formula
- C10H18N2O7
- InChI Key
- SLPUVFBNQHVEEU-WCCKRBBISA-N
- InChI
- InChI=1S/C5H12N2O2.C5H6O5/c6-3-1-2-4(7)5(8)9;6-3(5(9)10)1-2-4(7)8/h4H,1-3,6-7H2,(H,8,9);1-2H2,(H,7,8)(H,9,10)/t4-;/m0./s1
- IUPAC Name
- (2S)-2,5-diaminopentanoic acid; 2-oxopentanedioic acid
- SMILES
- NCCC[C@H](N)C(O)=O.OC(=O)CCC(=O)C(O)=O
- External Links
- ChemSpider
- 71201
- ChEMBL
- CHEMBL3138616
- Wikipedia
- Ornithine_oxoglutarate
- Predicted Properties
Property Value Source Water Solubility 53.1 mg/mL ALOGPS logP -0.6 ALOGPS logP -0.11 Chemaxon logS -0.44 ALOGPS pKa (Strongest Acidic) 2.66 Chemaxon pKa (Strongest Basic) -9.7 Chemaxon Physiological Charge -2 Chemaxon Hydrogen Acceptor Count 5 Chemaxon Hydrogen Donor Count 2 Chemaxon Polar Surface Area 91.67 Å2 Chemaxon Rotatable Bond Count 8 Chemaxon Refractivity 28.88 m3·mol-1 Chemaxon Polarizability 12.14 Å3 Chemaxon Number of Rings 0 Chemaxon Bioavailability 1 Chemaxon Rule of Five Yes Chemaxon Ghose Filter No Chemaxon Veber's Rule No Chemaxon MDDR-like Rule No Chemaxon