Literature DB >> 24710000

Cyclo-oligo-(1 → 6)-β-D-glucosamine based artificial channels for tunable transmembrane ion transport.

Tanmoy Saha1, Arundhati Roy, Marina L Gening, Denis V Titov, Alexey G Gerbst, Yury E Tsvetkov, Nikolay E Nifantiev, Pinaki Talukdar.   

Abstract

Unimolecular ion channels were designed by functionalization of a new type of cyclic oligosaccharides, cyclo-oligo-(1 → 6)-β-d-glucosamines, with pentabutylene glycol chains. Their ion transporting activity was tuned by varying oligomericity. A halide selectivity sequence, Cl(-) > Br(-) > I(-) was observed.

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Year:  2014        PMID: 24710000     DOI: 10.1039/c3cc49490j

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Apoptosis-inducing activity of a fluorescent barrel-rosette M+/Cl- channel.

Authors:  Javid Ahmad Malla; Rintu M Umesh; Amal Vijay; Arnab Mukherjee; Mayurika Lahiri; Pinaki Talukdar
Journal:  Chem Sci       Date:  2020-01-29       Impact factor: 9.825

2.  Tandem Electrospray Mass Spectrometry of Cyclic N-Substituted Oligo-β-(1→6)-D-glucosamines.

Authors:  Alexander O Chizhov; Marina L Gening; Yury E Tsvetkov; Nikolay E Nifantiev
Journal:  Int J Mol Sci       Date:  2020-11-05       Impact factor: 5.923

  2 in total

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