Ornithine aspartateProduct ingredient for Ornithine
- Name
- Ornithine aspartate
- 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
- DBSALT002898 (DB15577)
- Structure
- Synonyms
- Ornithine L-form aspartate
- UNII
- JA08T3B97O
- CAS Number
- 3230-94-2
- Weight
- Average: 265.266
Monoisotopic: 265.127385344 - Chemical Formula
- C9H19N3O6
- InChI Key
- IXUZXIMQZIMPSQ-ZBRNBAAYSA-N
- InChI
- InChI=1S/C5H12N2O2.C4H7NO4/c6-3-1-2-4(7)5(8)9;5-2(4(8)9)1-3(6)7/h4H,1-3,6-7H2,(H,8,9);2H,1,5H2,(H,6,7)(H,8,9)/t4-;2-/m00/s1
- IUPAC Name
- (4S)-4-amino-4-carboxybutan-1-aminium (2S)-2-amino-3-carboxypropanoate
- SMILES
- N[C@@H](CCC[NH3+])C(O)=O.N[C@@H](CC(O)=O)C([O-])=O
- External Links
- ChemSpider
- 17566
- Predicted Properties
Property Value Source Water Solubility 4.97 mg/mL ALOGPS logP -3.9 ALOGPS logP -3.7 Chemaxon logS -1.7 ALOGPS pKa (Strongest Acidic) 2.67 Chemaxon pKa (Strongest Basic) 10.29 Chemaxon Physiological Charge 1 Chemaxon Hydrogen Acceptor Count 3 Chemaxon Hydrogen Donor Count 3 Chemaxon Polar Surface Area 90.96 Å2 Chemaxon Rotatable Bond Count 7 Chemaxon Refractivity 44.5 m3·mol-1 Chemaxon Polarizability 14.28 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