Ornithine hydrochlorideProduct ingredient for Ornithine
- Name
- Ornithine hydrochloride
- 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
- DBSALT002530
- Structure
Structure for Ornithine hydrochloride (DBSALT002530)
- Synonyms
- Ornithine HCl / Ornithine monohydrochloride
- UNII
- HBK84K66XH
- CAS Number
- 3184-13-2
- Weight
- Average: 168.62
Monoisotopic: 168.0665554 - Chemical Formula
- C5H13ClN2O2
- InChI Key
- GGTYBZJRPHEQDG-WCCKRBBISA-N
- InChI
- InChI=1S/C5H12N2O2.ClH/c6-3-1-2-4(7)5(8)9;/h4H,1-3,6-7H2,(H,8,9);1H/t4-;/m0./s1
- IUPAC Name
- (2S)-2,5-diaminopentanoic acid hydrochloride
- SMILES
- Cl.NCCC[C@H](N)C(O)=O
- External Links
- ChemSpider
- 69117
- ChEMBL
- CHEMBL3184113
- Predicted Properties
Property Value Source Water Solubility 172.0 mg/mL ALOGPS logP -3.6 ALOGPS logP -3.7 Chemaxon logS 0.11 ALOGPS pKa (Strongest Acidic) 2.67 Chemaxon pKa (Strongest Basic) 10.29 Chemaxon Physiological Charge 1 Chemaxon Hydrogen Acceptor Count 4 Chemaxon Hydrogen Donor Count 3 Chemaxon Polar Surface Area 89.34 Å2 Chemaxon Rotatable Bond Count 4 Chemaxon Refractivity 33.21 m3·mol-1 Chemaxon Polarizability 13.77 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