Jump to content
 







Main menu
   


Navigation  



Main page
Contents
Current events
Random article
About Wikipedia
Contact us
Donate
 




Contribute  



Help
Learn to edit
Community portal
Recent changes
Upload file
 








Search  

































Create account

Log in
 









Create account
 Log in
 




Pages for logged out editors learn more  



Contributions
Talk
 



















Contents

   



(Top)
 


1 References  














N(6)-Carboxymethyllysine






تۆرکجه
فارسی

Русский
Српски / srpski
Srpskohrvatski / српскохрватски
 

Edit links
 









Article
Talk
 

















Read
Edit
View history
 








Tools
   


Actions  



Read
Edit
View history
 




General  



What links here
Related changes
Upload file
Special pages
Permanent link
Page information
Cite this page
Get shortened URL
Download QR code
Wikidata item
 




Print/export  



Download as PDF
Printable version
 
















Appearance
   

 






From Wikipedia, the free encyclopedia
 


N(6)-Carboxymethyllysine
Stereo, skeletal formula of N(6)-carboxymethyllysine (S)
Names
IUPAC name

N6-(Carboxymethyl)-L-lysine

Systematic IUPAC name

(2S)-2-Amino-6-[(carboxymethyl)amino]hexanoic acid

Identifiers

CAS Number

3D model (JSmol)

Beilstein Reference

4989963 S
ChEBI
ChemSpider
  • 110350 S ☒N
  • 21467765 R ☒N
  • MeSH N(6)-carboxymethyllysine

    PubChem CID

  • 26175690 R
  • 123800 S
  • UNII

    CompTox Dashboard (EPA)

    • InChI=1S/C8H16N2O4/c9-6(8(13)14)3-1-2-4-10-5-7(11)12/h6,10H,1-5,9H2,(H,11,12)(H,13,14) ☒N

      Key: NUXSIDPKKIEIMI-UHFFFAOYSA-N ☒N

    • NC(CCCCNCC(=O)O)C(=O)O

    Properties

    Chemical formula

    C8H16N2O4
    Molar mass 204.226 g·mol−1
    Related compounds

    Related alkanoic acids

    gamma-Glutamylcysteine

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    ☒N verify (what is checkY☒N ?)

    Infobox references

    N(6)-Carboxymethyllysine (CML), also known as Nε-(carboxymethyl)lysine, is an advanced glycation endproduct (AGE). CML has been the most used marker for AGEs in food analysis.[1]

    Recently, it has been demonstrated that gut microbiota mediates an aging-associated decline in gut barrier function, allowing AGEs to leak into the bloodstream from the gut and impairing microglial function in the brain. It is suggested that the amount of CML in human blood samples may correlated with age.[2]

    A humanized monoclonal antibody which binds to N6 – carboxymethyl lysine shows considerable promise as a possible therapeutic agent for treating pancreatic cancer.[3]

    References

    [edit]
    1. ^ Semba RD, Nicklett EJ, Ferrucci L (2010). "Does accumulation of advanced glycation end products contribute to the aging phenotype?". The Journals of Gerontology. 65A (9): 963–975. doi:10.1093/gerona/glq074. PMC 2920582. PMID 20478906.
  • ^ O. Mossad, B. Batut, B. Yilmaz, N. Dokalis, C. Mezö, E. Nent, L. S. Nabavi, M. Mayer, F. J. M. Maron, J. M. Buescher, M. G. de Agüero, A. Szalay, T. Lämmermann, A. J. Macpherson, S. C. Ganal-Vonarburg, R. Backofen, D. Erny, M. Prinz, T. Blank (2022). "Gut microbiota drives age-related oxidative stress and mitochondrial damage in microglia via the metabolite N6-carboxymethyllysine". Nat. Neurosci. 25 (3): 295–305. doi:10.1038/s41593-022-01027-3. PMID 35241804. S2CID 247228807.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  • ^ Rossi, Gabriela R.; Jensen, Ashley; Ng, Serina; Yin, Zhirong; Li, Aimin; Misra, Anjan; Von Hoff, Daniel D.; Gruber, Lewis; Gruber, Misty; Han, Haiyong (7 October 2023). "Advanced glycation end product (AGE) targeting antibody SIWA318H is efficacious in preclinical models for pancreatic cancer". Scientific Reports. 13 (1): 16953. Bibcode:2023NatSR..1316953R. doi:10.1038/s41598-023-44211-6. PMC 10560265. PMID 37805542.

  • t
  • e

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=N(6)-Carboxymethyllysine&oldid=1182859133"

    Categories: 
    Alpha-Amino acids
    Amino acid derivatives
    Advanced glycation end-products
    Biochemistry stubs
    Hidden categories: 
    CS1 maint: multiple names: authors list
    Chemical articles with multiple compound IDs
    Multiple chemicals in an infobox that need indexing
    Chemical articles with multiple PubChem CIDs
    Articles without InChI source
    Articles without KEGG source
    Articles with changed EBI identifier
    Articles with changed ChemSpider identifier
    Articles with changed FDA identifier
    Articles with changed InChI identifier
    Articles containing unverified chemical infoboxes
    Articles with short description
    Short description matches Wikidata
    All stub articles
     



    This page was last edited on 31 October 2023, at 20:23 (UTC).

    Text is available under the Creative Commons Attribution-ShareAlike License 4.0; additional terms may apply. By using this site, you agree to the Terms of Use and Privacy Policy. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc., a non-profit organization.



    Privacy policy

    About Wikipedia

    Disclaimers

    Contact Wikipedia

    Code of Conduct

    Developers

    Statistics

    Cookie statement

    Mobile view



    Wikimedia Foundation
    Powered by MediaWiki