Results 201 to 210 of about 18,333 (256)
Culmorin inhibits detoxification of the mycotoxin deoxynivalenol by plant UDP-glucosyltransferases
Michlmayr H +11 more
europepmc +1 more source
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Phytochemistry, 2008
beta- and gamma-Hydroxynitrile glucosides are structurally related to cyanogenic glucosides (alpha-hydroxynitrile glucosides) but do not give rise to hydrogen cyanide release upon hydrolysis. Structural similarities and frequent co-occurrence suggest that the biosynthetic pathways for these compounds share common features. Based on available literature
Nanna Bjarnholt +1 more
exaly +4 more sources
beta- and gamma-Hydroxynitrile glucosides are structurally related to cyanogenic glucosides (alpha-hydroxynitrile glucosides) but do not give rise to hydrogen cyanide release upon hydrolysis. Structural similarities and frequent co-occurrence suggest that the biosynthetic pathways for these compounds share common features. Based on available literature
Nanna Bjarnholt +1 more
exaly +4 more sources
Dermatitis®, 2017
Alkyl glucosides are surfactants synthesized through the condensation of long-chain fatty alcohols and glucose, extracted from vegetal, renewable sources. Although available for more than 4 decades, they have been rediscovered in recent years because of their eco-friendly character.
Maisa, Alfalah +2 more
openaire +2 more sources
Alkyl glucosides are surfactants synthesized through the condensation of long-chain fatty alcohols and glucose, extracted from vegetal, renewable sources. Although available for more than 4 decades, they have been rediscovered in recent years because of their eco-friendly character.
Maisa, Alfalah +2 more
openaire +2 more sources
Production of zearalenone-4-glucoside, a-zearalenol-4-glucoside and ß-zearalenol-4-glucoside
Mycotoxin Research, 2007The work at hand describes the production of the zearalenone (ZON) metabolites zearalenone-4-glucoside (ZON-4G), a-zearalenol-4-glucoside (oc-ZOL-4G) and ß-zearalenol-4-glucoside (ß-ZOL-4G). In a first step a genetically modified yeast strain, expressing theArabidopsis thaliana UDP-glu-cosyltransferase UGT73C6, was treated with ZON to produce ZON-4G ...
P, Krenn +7 more
openaire +2 more sources
Microbial glucosidation of dihydroxyanthraquinones. General properties of the glucosidation system
Folia Microbiologica, 1974Corresponding mono-β-d-glucosides were obtained by fermentation ofStreptomyces aureofaciens B 96 with four isomeric dihydroxyanthraquinones (alizarin, quinizarin, chrysazin and anthraflavin). The effect of some factors (sugar source, concentration of substrates, pH) on biosynthesis of 1-hydroxy-2-(β-d-glucopyranosyloxy)anthraquinone was studied and ...
J, Matĕjů +4 more
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Generation of primary amide glucosides from cyanogenic glucosides
Phytochemistry, 2009The cyanogenic glucoside-related compound prunasinamide, (2R)-beta-d-glucopyranosyloxyacetamide, has been detected in dried, but not in fresh leaves of the prunasin-containing species Olinia ventosa, Prunus laurocerasus, Pteridium aquilinium and Holocalyx balansae. Experiments with leaves of O.
Jandirk, Sendker, Adolf, Nahrstedt
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Pharmacology & Therapeutics, 1990
A number of studies have shown that drug glucosidation occurs in vertebrates. This review summarizes information on the chemical, physical and biological properties of eleven drug glucosides. Three out of two hundred individuals exhibited a complete lack of amobarbital-N-glucoside formation. The data from a pair of identical twins who were deficient in
openaire +2 more sources
A number of studies have shown that drug glucosidation occurs in vertebrates. This review summarizes information on the chemical, physical and biological properties of eleven drug glucosides. Three out of two hundred individuals exhibited a complete lack of amobarbital-N-glucoside formation. The data from a pair of identical twins who were deficient in
openaire +2 more sources