Literature DB >> 2867936

Castanospermine: a potent inhibitor of sucrase from the human enterocyte-like cell line Caco-2.

G Trugnan, M Rousset, A Zweibaum.   

Abstract

The addition of castanospermine (5-50 microM) to a culture medium of Caco-2 cells results in a specific suppression of sucrase activity without modification of the biosynthesis of the enzyme. This effect is due to a direct inhibiting effect of castanospermine on Caco-2 sucrase activity. This inhibition is time-dependent (half-maximum efficiency at 10 min for 100 nM), enhanced by preincubation (suggesting a strong interaction with the enzyme), dose-dependent (ED50 at 4 nM after 1 h preincubation period) and of the fully non-competitive type. The calculated Ki (2.6 nM) suggests that castanospermine is the most potent inhibitor of sucrase so far reported.

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Year:  1986        PMID: 2867936     DOI: 10.1016/0014-5793(86)80123-5

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  3 in total

1.  Diastereoselective nitrenium ion-mediated cyclofunctionalization: total synthesis of (+)-castanospermine.

Authors:  Edward G Bowen; Duncan J Wardrop
Journal:  Org Lett       Date:  2010-10-21       Impact factor: 6.005

2.  Differential inhibition by castanospermine of various insect disaccharidases.

Authors:  B C Campbell; R J Molyneux; K C Jones
Journal:  J Chem Ecol       Date:  1987-07       Impact factor: 2.626

3.  The posttranslational processing of sucrase-isomaltase in HT-29 cells is a function of their state of enterocytic differentiation.

Authors:  G Trugnan; M Rousset; I Chantret; A Barbat; A Zweibaum
Journal:  J Cell Biol       Date:  1987-05       Impact factor: 10.539

  3 in total

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