Literature DB >> 26264193

Stable analogues of nojirimycin--synthesis and biological evaluation of nojiristegine and manno-nojiristegine.

Agnete H Viuff1, Louise M Besenbacher, Akiko Kamori, Mikkel T Jensen, Mogens Kilian, Atsushi Kato, Henrik H Jensen.   

Abstract

Two novel iminosugars called nojiristegines, being structural hybrids between nor-tropane alkaloid calystegine and nojirimycins, have been synthesised and found to be stable molecules despite the presence of a hemiaminal functionality. The synthesised iminosugars were evaluated against a panel of glycosidases and the best inhibition (IC50), found against α-glucosidases, was in the micromolar region. The compounds were also evaluated as potential antibiotics but no useful level of activity was observed.

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Year:  2015        PMID: 26264193     DOI: 10.1039/c5ob01281c

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


  2 in total

1.  1,3-Dibromo-5,5-dimethylhydantoin as promoter for glycosylations using thioglycosides.

Authors:  Fei-Fei Xu; Claney L Pereira; Peter H Seeberger
Journal:  Beilstein J Org Chem       Date:  2017-09-22       Impact factor: 2.883

2.  Carbohydrate-Based Chiral Iodoarene Catalysts: A Survey through the Development of an Improved Catalyst Design.

Authors:  Michael R Imrich; Linda E Biehler; Cäcilia Maichle-Mössmer; Thomas Ziegler
Journal:  Molecules       Date:  2019-10-28       Impact factor: 4.411

  2 in total

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