Results 201 to 210 of about 17,776 (241)
β-Glucosidase Activity of <i>Lactiplantibacillus plantarum</i>: A Key Player in Food Fermentation and Human Health. [PDF]
FoodsPaventi G +4 more
europepmc +1 more source
Add-on effects of total glucosides of paeony on conventional therapies for psoriasis: a systematic review and meta-analysis of randomized controlled trials. [PDF]
Front PharmacolLi Z, Lu J, Guan K, Liang H, Lu C, Yu J.
europepmc +1 more source
Nemophilosides A-I, nine meroterpenoid glucosides isolated from Nemophila menziesii. [PDF]
J Nat MedKurosawa N +6 more
europepmc +1 more source
Effects of plant active substances in rheumatoid arthritis-a systematic review and network meta-analysis. [PDF]
Front PharmacolPeng Q +8 more
europepmc +1 more source
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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
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
Bjarnholt, Nanna +1 more
openaire +3 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
Bjarnholt, Nanna +1 more
openaire +3 more sources
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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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
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Pyrimidinylmethylphenyl glucoside as novel C-aryl glucoside SGLT2 inhibitors
Bioorganic & Medicinal Chemistry Letters, 2010Novel C-aryl glucoside SGLT2 inhibitors containing pyrimidine motif were designed and synthesized for biological evaluation. Among the compounds assayed, pyrimidine containing methylthio moiety 11 g demonstrated the best in vitro inhibitory activity against SGLT2 in this series to date (IC(50)=10.7 nM).
Junwon, Lee +5 more
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