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Details

Stereochemistry ABSOLUTE
Molecular Formula C8H16N2O3.2ClH
Molecular Weight 261.146
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N6-Acetyl-L-lysine dihydrochloride

SMILES

Cl.Cl.CC(=O)NCCCC[C@H](N)C(O)=O

InChI

InChIKey=DJZSLFLQVHLNPD-KLXURFKVSA-N
InChI=1S/C8H16N2O3.2ClH/c1-6(11)10-5-3-2-4-7(9)8(12)13;;/h7H,2-5,9H2,1H3,(H,10,11)(H,12,13);2*1H/t7-;;/m0../s1

HIDE SMILES / InChI

Molecular Formula C8H16N2O3
Molecular Weight 188.2242
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Nε-lysine acetylation of a bacterial transcription factor inhibits Its DNA-binding activity.
2010-12-31
Transition state of ADP-ribosylation of acetyllysine catalyzed by Archaeoglobus fulgidus Sir2 determined by kinetic isotope effects and computational approaches.
2010-09-08
N(epsilon)-Modified lysine containing inhibitors for SIRT1 and SIRT2.
2010-08-01
Synthetic biology approaches in drug discovery and pharmaceutical biotechnology.
2010-06
Degradation of 1-deoxy-D-erythro-hexo-2,3-diulose in the presence of lysine leads to formation of carboxylic acid amides.
2010-05-26
A convenient method for genetic incorporation of multiple noncanonical amino acids into one protein in Escherichia coli.
2010-04
Substrate specificity of SIRT1-catalyzed lysine Nepsilon-deacetylation reaction probed with the side chain modified Nepsilon-acetyl-lysine analogs.
2010-02
A method for genetically installing site-specific acetylation in recombinant histones defines the effects of H3 K56 acetylation.
2009-10-09
Plasmodium falciparum Sir2 is an NAD+-dependent deacetylase and an acetyllysine-dependent and acetyllysine-independent NAD+ glycohydrolase.
2008-09-23
Adding l-lysine derivatives to the genetic code of mammalian cells with engineered pyrrolysyl-tRNA synthetases.
2008-07-11
Utility of immonium ions for assignment of epsilon-N-acetyllysine-containing peptides by tandem mass spectrometry.
2008-05-01
Genetically encoding N(epsilon)-acetyllysine in recombinant proteins.
2008-04
A spectrophotometric assay for histone deacetylase 8.
2008-01-01
Substituting N(epsilon)-thioacetyl-lysine for N(epsilon)-acetyl-lysine in peptide substrates as a general approach to inhibiting human NAD(+)-dependent protein deacetylases.
2008-01
Characterization of Nalpha-benzyloxycarbonyl-L-lysine oxidizing enzyme from Rhodococcus sp. AIU Z-35-1.
2007-09
N(epsilon)-methanesulfonyl-lysine as a non-hydrolyzable functional surrogate for N(epsilon)-acetyl-lysine.
2007-03-21
Nepsilon-thioacetyl-lysine: a multi-facet functional probe for enzymatic protein lysine Nepsilon-deacetylation.
2006-07-15
Proteomic analysis of organ-specific post-translational lysine-acetylation and -methylation in mice by use of anti-acetyllysine and -methyllysine mouse monoclonal antibodies.
2005-12
Purification and characterization of a novel aminoacylase from Streptomyces mobaraensis.
2005-10
Kinetics and comparative reactivity of human class I and class IIb histone deacetylases.
2004-08-31
Four different clones of mouse anti-acetyllysine monoclonal antibodies having different recognition properties share a common immunoglobulin framework structure.
2003-01-15
Switching osmolyte strategies: response of Methanococcus thermolithotrophicus to changes in external NaCl.
2001-11-15
A case of hyperlysinemia: biochemical and clinical observations.
1967-04
Substance Class Chemical
Created
by admin
on Wed Apr 02 15:08:32 GMT 2025
Edited
by admin
on Wed Apr 02 15:08:32 GMT 2025
Record UNII
5F28VMW9DT
Record Status Validated (UNII)
Record Version
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Name Type Language
L-Lysine, N<SUP>6</SUP>-acetyl-, hydrochloride (1:2)
Preferred Name English
N6-Acetyl-L-lysine dihydrochloride
Common Name English
(2S)-2-Amino-6-acetamidohexanoic acid dihydrochloride
Systematic Name English
Code System Code Type Description
PUBCHEM
163342557
Created by admin on Wed Apr 02 15:08:32 GMT 2025 , Edited by admin on Wed Apr 02 15:08:32 GMT 2025
PRIMARY
FDA UNII
5F28VMW9DT
Created by admin on Wed Apr 02 15:08:32 GMT 2025 , Edited by admin on Wed Apr 02 15:08:32 GMT 2025
PRIMARY
CAS
2408937-00-6
Created by admin on Wed Apr 02 15:08:32 GMT 2025 , Edited by admin on Wed Apr 02 15:08:32 GMT 2025
PRIMARY
Related Record Type Details
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