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Details

Stereochemistry ABSOLUTE
Molecular Formula C8H16N2O3
Molecular Weight 188.2242
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N6-ACETYLLYSINE

SMILES

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

InChI

InChIKey=DTERQYGMUDWYAZ-ZETCQYMHSA-N
InChI=1S/C8H16N2O3/c1-6(11)10-5-3-2-4-7(9)8(12)13/h7H,2-5,9H2,1H3,(H,10,11)(H,12,13)/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

Approval Year

PubMed

PubMed

TitleDatePubMed
Kinetics and comparative reactivity of human class I and class IIb histone deacetylases.
2004 Aug 31
Nepsilon-thioacetyl-lysine: a multi-facet functional probe for enzymatic protein lysine Nepsilon-deacetylation.
2006 Jul 15
N(epsilon)-methanesulfonyl-lysine as a non-hydrolyzable functional surrogate for N(epsilon)-acetyl-lysine.
2007 Mar 21
Genetically encoding N(epsilon)-acetyllysine in recombinant proteins.
2008 Apr
Adding l-lysine derivatives to the genetic code of mammalian cells with engineered pyrrolysyl-tRNA synthetases.
2008 Jul 11
Utility of immonium ions for assignment of epsilon-N-acetyllysine-containing peptides by tandem mass spectrometry.
2008 May 1
Plasmodium falciparum Sir2 is an NAD+-dependent deacetylase and an acetyllysine-dependent and acetyllysine-independent NAD+ glycohydrolase.
2008 Sep 23
A convenient method for genetic incorporation of multiple noncanonical amino acids into one protein in Escherichia coli.
2010 Apr
Substrate specificity of SIRT1-catalyzed lysine Nepsilon-deacetylation reaction probed with the side chain modified Nepsilon-acetyl-lysine analogs.
2010 Feb
Synthetic biology approaches in drug discovery and pharmaceutical biotechnology.
2010 Jun
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:51:36 GMT 2023
Edited
by admin
on Sat Dec 16 08:51:36 GMT 2023
Record UNII
470AD5VY1X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N6-ACETYLLYSINE
Systematic Name English
N.EPSILON.-ACETYL-L-LYSINE
Systematic Name English
N6-ACETYL-L-LYSINE
Systematic Name English
NSC-102777
Code English
.EPSILON.-N-ACETYLLYSINE
Common Name English
LYSINE, N6-ACETYL-
Systematic Name English
Classification Tree Code System Code
LOINC 79578-1
Created by admin on Sat Dec 16 08:51:36 GMT 2023 , Edited by admin on Sat Dec 16 08:51:36 GMT 2023
LOINC 79634-2
Created by admin on Sat Dec 16 08:51:36 GMT 2023 , Edited by admin on Sat Dec 16 08:51:36 GMT 2023
Code System Code Type Description
CAS
692-04-6
Created by admin on Sat Dec 16 08:51:36 GMT 2023 , Edited by admin on Sat Dec 16 08:51:36 GMT 2023
PRIMARY
PUBCHEM
92832
Created by admin on Sat Dec 16 08:51:36 GMT 2023 , Edited by admin on Sat Dec 16 08:51:36 GMT 2023
PRIMARY
WIKIPEDIA
Acetyllysine
Created by admin on Sat Dec 16 08:51:36 GMT 2023 , Edited by admin on Sat Dec 16 08:51:36 GMT 2023
PRIMARY
EPA CompTox
DTXSID90862371
Created by admin on Sat Dec 16 08:51:36 GMT 2023 , Edited by admin on Sat Dec 16 08:51:36 GMT 2023
PRIMARY
FDA UNII
470AD5VY1X
Created by admin on Sat Dec 16 08:51:36 GMT 2023 , Edited by admin on Sat Dec 16 08:51:36 GMT 2023
PRIMARY
CHEBI
17752
Created by admin on Sat Dec 16 08:51:36 GMT 2023 , Edited by admin on Sat Dec 16 08:51:36 GMT 2023
PRIMARY
ECHA (EC/EINECS)
211-725-9
Created by admin on Sat Dec 16 08:51:36 GMT 2023 , Edited by admin on Sat Dec 16 08:51:36 GMT 2023
PRIMARY
NSC
102777
Created by admin on Sat Dec 16 08:51:36 GMT 2023 , Edited by admin on Sat Dec 16 08:51:36 GMT 2023
PRIMARY