| Weight | 146.19 g/mol |
|---|---|
| Formula | C6H14N2O2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 5 |
L-lysine
Lysine · Lysine Hydrochloride · L Lysine
20166-34-1, 56-87-1, 12798-06-0, 25104-18-1, 923-27-3, 26714-32-9
Score:
#196 in Biochemistry
,
#795 in Biology
,
#874 in Chemistry
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- Sigma-Aldrich - L-lysine16.20 - 900.00 USD
- Fisher Scientific - Search for L-lysine
- TCI - L-lysine35.00 - 93.00 USD
- PERIODATE-LYSINE-PARAFORMALDEHYDE FIXATIVE A NEW FIXATIVE FOR IMMUNOELECTRON MICROSCOPY (Journal of Histochemistry and Cytochemistry, 1974)
- Lysine acetylation targets protein complexes and co-regulates major cellular functions. (Science, 2009)
- Role of Histone H3 Lysine 27 Methylation in Polycomb-Group Silencing (Science, 2002)
- Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins (Nature, 2001)
- Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain (Nature, 2001)
- Regulation of Heterochromatic Silencing and Histone H3 Lysine-9 Methylation by RNAi (Science, 2002)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Lysine
- Lysine Hydrochloride
- L Lysine
- Lysine Acetate
- Enisyl
-
SMILESC(CCN)CC(C(=O)O)N
-
InChIKeyKDXKERNSBIXSRK-UHFFFAOYSA-N
- Pubchem - L-lysine
- Wikipedia - L-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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Similar Compounds
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L-lysine
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