Literature DB >> 28091667

Selective recognition of the di/trimethylammonium motif by an artificial carboxycalixarene receptor.

Thomas Hanauer1, Richard J Hopkinson2, Kamal Patel3, Yu Li3, Danilo Correddu3, Akane Kawamura2, Vijayalekshmi Sarojini3, Ivanhoe K H Leung3, Tobias Gruber1.   

Abstract

Chemical tools that recognise post-translational modifications have promising applications in biochemistry and in therapy. We report a simple carboxycalixarene that selectively binds molecules containing di/trimethylammonium moieties in isolation, in cell lysates and when incorporated in histone peptides. Our findings reveal the potential of using carboxycalixarene-based receptors to study epigenetic regulation.

Entities:  

Year:  2017        PMID: 28091667     DOI: 10.1039/c6ob02616h

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  p-tert-Butylthiacalix[4]arenes functionalized by N-(4'-nitrophenyl)acetamide and N,N-diethylacetamide fragments: synthesis and binding of anionic guests.

Authors:  Alena A Vavilova; Ivan I Stoikov
Journal:  Beilstein J Org Chem       Date:  2017-09-13       Impact factor: 2.883

  1 in total

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