Ornithine dihydrochlorideProduct ingredient for Ornithine
- Name
- Ornithine dihydrochloride
- 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
- DBSALT001925
- Structure
Structure for Ornithine dihydrochloride (DBSALT001925)
- Synonyms
- L-ornithine dihydrochloride / L-ornithine, hydrochloride (1:2) / Ornithine L-form dihydrochloride
- UNII
- 8N284L2VLC
- CAS Number
- 6211-16-1
- Weight
- Average: 205.08
Monoisotopic: 204.0432331 - Chemical Formula
- C5H14Cl2N2O2
- InChI Key
- HGBAVEGDXFHRQP-FHNDMYTFSA-N
- InChI
- InChI=1S/C5H12N2O2.2ClH/c6-3-1-2-4(7)5(8)9;;/h4H,1-3,6-7H2,(H,8,9);2*1H/t4-;;/m0../s1
- IUPAC Name
- (2S)-2,5-diaminopentanoic acid dihydrochloride
- SMILES
- Cl.Cl.[H][C@](N)(CCCN)C(O)=O
- External Links
- ChemSpider
- 72574
- 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 13.82 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