Literature DB >> 25572650

The first 2(IB),3(IA)-heterodifunctionalized β-cyclodextrin derivatives as artificial enzymes.

S Letort1, D Mathiron, T Grel, C Albaret, S Daulon, F Djedaïni-Pilard, G Gouhier, F Estour.   

Abstract

Novel 2,3-heterodisubstituted β-cyclodextrin derivatives were designed as artificial enzymes to degrade chemical warfare agents. One of them reduced the acetylcholinesterase inhibitory potential by soman faster than its monosubstituted analog.

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Year:  2015        PMID： 25572650     DOI： 10.1039/c4cc09189b

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


  3 in total

Review 1.  Current and emerging strategies for organophosphate decontamination: special focus on hyperstable enzymes.

Authors:  Pauline Jacquet; David Daudé; Janek Bzdrenga; Patrick Masson; Mikael Elias; Eric Chabrière
Journal:  Environ Sci Pollut Res Int       Date:  2016-02-02       Impact factor: 4.223

2.  Structure-efficiency relationships of cyclodextrin scavengers in the hydrolytic degradation of organophosphorus compounds.

Authors:  Sophie Letort; Michaël Bosco; Benedetta Cornelio; Frédérique Brégier; Sébastien Daulon; Géraldine Gouhier; François Estour
Journal:  Beilstein J Org Chem       Date:  2017-03-06       Impact factor: 2.883

3.  Enhanced single-isomer separation and pseudoenantiomer resolution of new primary rim heterobifunctionalized α-cyclodextrin derivatives.

Authors:  Iveta Tichá; Gábor Benkovics; Milo Malanga; Jindřich Jindřich
Journal:  Beilstein J Org Chem       Date:  2018-11-13       Impact factor: 2.883
  3 in total

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