Weight | 146.19 g/mol |
---|---|
Formula | C6H14N2O2 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 3 |
Aromatic Rings | 0 |
Rotatable Bonds | 5 |
DL-Lysine (70-54-2)
Score:
#1879 in Physics
,
#2310 in Biochemistry
,
#4613 in Biology
,
#5849 in Chemistry
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- N-EPSILON-(DL-2-AMINO-2-CARBOXYETHYL)-L-LYSINE, A NEW AMINO ACID FORMED ON ALKALINE TREATMENT OF PROTEINS. (Journal of Biological Chemistry, 1964)
- Enhancement of certain biological activities of muramyl dipeptide derivatives after conjugation to a multi-poly(DL-alanine)--poly(L-lysine) carrier. (Proceedings of the National Academy of Sciences of the United States of America, 1979)
- Estimation of the true ileal digestible lysine and sulfur amino acid requirement and comparison of the bioefficacy of 2-hydroxy-4-(methylthio)butanoic acid and dl-methionine in eleven- to twenty-six-kilogram nursery pigs (Journal of Animal Science, 2006)
- Conversion of D- and DL--Amino--caprolactam into L-Lysine Using Both Yeast Cells and Bacterial Cells (Agricultural and biological chemistry, 1977)
- The availability of -acetyl-d-lysine and -methyl-dl-lysine for growth (Biochemical Journal, 1944)
- Renal toxicity of n-(dl-2-amino-2-carboxyethyl)-l-lysine (lysinoalanine) in rats (Food and Cosmetics Toxicology, 1977)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(CCN)CC(C(=O)O)N
-
InChIKeyKDXKERNSBIXSRK-UHFFFAOYSA-N
- Pubchem - DL-Lysine
- Wikipedia - DL-lysine
Lysine (abbreviated as Lys or K), encoded by the codons AAA and AAG, is an -amino acid that is used in the biosynthesis of proteins. It contains an -amino group (which is in the protonated NH3+ form under biological conditions), an -carboxylic acid group (which is in the deprotonated COO form under biological conditions), and a side chain lysyl ((CH2)4NH2), classifying it as a charged (at physiological pH), aliphatic amino acid. It is essential in humans, meaning the body cannot synthesize it and thus it must be obtained from the diet.
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