Lysine monohydrateProduct ingredient for Lysine
- Name
- Lysine monohydrate
- Drug Entry
- Lysine
Lysine (abbreviated as Lys or K) is an α-amino acid with the chemical formula HO2CCH(NH2)(CH2)4NH2. This amino acid is an essential amino acid, which means that humans cannot synthesize it. Its codons are AAA and AAG. Lysine is a base, as are arginine and histidine. The ε-amino group acts as a site for hydrogen binding and a general base in catalysis. Common posttranslational modifications include methylation of the ε-amino group, giving methyl-, dimethyl-, and trimethyllysine. The latter occurs in calmodulin. Other posttranslational modifications include acetylation. Collagen contains hydroxylysine which is derived from lysine by lysyl hydroxylase. O-Glycosylation of lysine residues in the endoplasmic reticulum or Golgi apparatus is used to mark certain proteins for secretion from the cell.
- Accession Number
- DBSALT003003
- Structure
- Synonyms
- L-Lysine monohydrate / L-Lysine, monohydrate / Lysine monohydrate
- UNII
- F7625B974U
- CAS Number
- 39665-12-8
- Weight
- Average: 164.205
Monoisotopic: 164.116092383 - Chemical Formula
- C6H16N2O3
- InChI Key
- HZRUTVAFDWTKGD-JEDNCBNOSA-N
- InChI
- InChI=1S/C6H14N2O2.H2O/c7-4-2-1-3-5(8)6(9)10;/h5H,1-4,7-8H2,(H,9,10);1H2/t5-;/m0./s1
- IUPAC Name
- (2S)-2,6-diaminohexanoic acid hydrate
- SMILES
- O.NCCCC[C@H](N)C(O)=O
- External Links
- ChemSpider
- 17339755
- Predicted Properties
Property Value Source Water Solubility 105.0 mg/mL ALOGPS logP -3.8 ALOGPS logP -3.2 Chemaxon logS -0.14 ALOGPS pKa (Strongest Acidic) 2.74 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 5 Chemaxon Refractivity 37.81 m3·mol-1 Chemaxon Polarizability 15.84 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