Literature DB >> 25621897

Synthesis and glycosidase inhibition of australine and its fluorinated derivatives.

Yi-Xian Li1, Yousuke Shimada, Kasumi Sato, Atsushi Kato, Wei Zhang, Yue-Mei Jia, George W J Fleet, Min Xiao, Chu-Yi Yu.   

Abstract

Australine (1), 7-epi-australine (2), and their C-7-fluorinated derivatives 4 and 5 have been synthesized efficiently from D-arabinose-derived cyclic nitrone 11. Fluorination at the C-7 position enhanced the inhibition against A. niger α-glucosidase, and this constitutes the first example of fluorination substitution for a hydroxyl increasing the inhibition of any glycosidases. The enantiomers synthesized from nitrone ent-11 showed no inhibition of the corresponding enzymes.

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Year:  2015        PMID: 25621897     DOI: 10.1021/ol503728e

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  1 in total

1.  Enantioselective synthesis of anti-3-alkenyl-2-amido-3-hydroxy esters: application to the total synthesis of (+)-alexine.

Authors:  Lu Yu; Peter Somfai
Journal:  RSC Adv       Date:  2019-01-21       Impact factor: 4.036

  1 in total

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