Literature DB >> 6693987

Metabolism of orally administered alkyl beta-glycosides in the mouse.

N Weber, H Benning.   

Abstract

The metabolism of octyl beta-D-[U-14C]glucoside, ]1-14C]dodecyl beta-D-maltoside and [1-14C]hexadecyl beta-D-glucoside was studied after oral administration to mice. The beta-glycosidic bond was rapidly hydrolyzed in intestine and liver. The cleavage products, sugars and long-chain alcohols, entered the pathways of lipid and carbohydrate metabolism. It appears that alkyl beta-glycosides are suitable as additives in food and feed.

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Year:  1984        PMID: 6693987     DOI: 10.1093/jn/114.2.247

Source DB:  PubMed          Journal:  J Nutr        ISSN: 0022-3166            Impact factor:   4.798


  3 in total

1.  n-Dodecyl-β-D-maltoside inhibits aggregation of human interferon-β-1b and reduces its immunogenicity.

Authors:  Robert A Rifkin; Edward T Maggio; Sonny Dike; Douglas A Kerr; Michael Levy
Journal:  J Neuroimmune Pharmacol       Date:  2010-06-08       Impact factor: 4.147

2.  Metabolism of sitosteryl beta-D-glucoside and its nutritional effects in rats.

Authors:  N Weber
Journal:  Lipids       Date:  1988-01       Impact factor: 1.880

3.  Effect of Nonionic Surfactants (Dodecyl Maltoside and Polysorbate 20) on Prevention of Aggregation and Conformational Changes of Recombinant Human IFNβ_1b Induced by Light.

Authors:  Najmeh Mahjoubi; Ahmad Fazeli; Rassoul Dinarvand; Mohammad Reza Khoshayand; Maryam Shekarchi; Mohammad Reza Fazeli
Journal:  Iran J Pharm Res       Date:  2017       Impact factor: 1.696

  3 in total

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