Results 61 to 70 of about 2,579 (147)

Dietary Consumption of Type 2 Resistant Starch and d‐Fagomine Delays Progression of Metabolic Disturbances in Male Rats on High‐Fat Diet

open access: yesMolecular Nutrition &Food Research, Volume 69, Issue 22, November 2025.
This study compared the preventive effects of dietary resistant starch (RS2) from maize and d‐fagomine (FG) from buckwheat on cardiometabolic risk factors in high‐fat (HF) diet‐fed rats. Wistar‐Kyoto rats (n = 11–12/group) received STD, HF, HF + RS, or HF + FG diets for 10 weeks.
Bernat Miralles‐Pérez   +10 more
wiley   +1 more source

Intramolecular [3+2] cycloaddition of azido-unsaturated esters derived of monosaccharides [PDF]

open access: yes, 2013
Iminosugars have been shown to be very potent inhibitors of glycosidases and glycolsyltransferases. Due to their ability to resemble the transition states of the sugars involved in these processes, a variety of m onocyclic and bicyclic iminosugars have
Calvo-Losada, Saturnino   +3 more
core  

Developments in Carbohydrate-Based Metzincin Inhibitors

open access: yesPharmaceuticals, 2020
Matrix metalloproteinases (MMPs) and A disintegrin and Metalloproteinase (ADAMs) are zinc-dependent endopeptidases belonging to the metzincin superfamily.
Doretta Cuffaro   +3 more
doaj   +1 more source

Synthesis of Novel 3-Amino(Hydroxy)methyl-l-fuco-Azafagomines as Leads for Selective Inhibitors of α-l-Fucosidases [PDF]

open access: yes, 2010
The synthesis of 3-substituted l-fuco-azafagomines from d-lyxose is reported. They represent the first example of aza-C-glycosides having a biimino (-NH-NH-) moiety.
Carmona Asenjo, Ana Teresa   +4 more
core   +1 more source

A Fullerene‐Based Selenosugar Ball

open access: yesEuropean Journal of Organic Chemistry, Volume 28, Issue 36, September 29, 2025.
A fullerene hexakis‐adduct decorated with 12 peripheral seleno‐d‐talitol moieties is synthesized efficiently with a Th‐symmetry from a hexakis‐adduct of [60]fullerene prepared by a cycloaddition reaction and subsequent copper‐catalyzed azide‐alkyne cycloaddition click chemistry.
Reinier Lemos   +8 more
wiley   +1 more source

An Efficient Synthesis of Aldohexose-Derived Piperidine Nitrones: Precursors of Piperidine Iminosugars

open access: yesMolecules, 2013
D-Glucopyranose-derived and L-idopyranose-derived piperidine nitrones were synthesized in good overall yields through six-step reaction sequence starting from readily available 2,3,4,6-tetra-O-benzyl-D-glucopyranose.
Chu-Yi Yu   +4 more
doaj   +1 more source

Synthesis of “All-Cis” Trihydroxypiperidines from a Carbohydrate-Derived Ketone: Hints for the Design of New β-Gal and GCase Inhibitors

open access: yesMolecules, 2020
Pharmacological chaperones (PCs) are small compounds able to rescue the activity of mutated lysosomal enzymes when used at subinhibitory concentrations.
Maria Giulia Davighi   +6 more
doaj   +1 more source

Effectiveness of Cucumis sativus L. Supplementation on Mood, Anxiety, and Sleep Quality: A Randomized Double‐Blind Placebo‐Controlled Study

open access: yesHealth Science Reports, Volume 8, Issue 7, July 2025.
ABSTRACT Background and Aims Despite widespread use, more research is needed to assess the health effects of herbal plants. Preliminary research indicates that cucumber extract (Cucumis sativus L.) is safe and may exhibit analgesic properties for joint pain, but studies on its impact on other health‐related outcomes—including mood, sleep, and health ...
Heather A. Hausenblas   +2 more
wiley   +1 more source

A Biocatalytic Cascade for the Valorization of Sugars

open access: yesChemCatChem, Volume 17, Issue 12, June 23, 2025.
We report a one‐pot, three‐step biocatalytic cascade to synthesize trihydroxy‐piperidine and ‐azepane iminosugars directly from monosaccharides, employing transaminase (ATA) and galactose oxidase (GOase) enzymes. Abstract Biocatalytic cascades offer products of multistep synthesis without the use of protecting groups or isolation of intermediates. This
Kathryn Yeow   +4 more
wiley   +1 more source

Synthesis of lipophilic 1-deoxygalactonojirimycin derivatives as D-galactosidase inhibitors

open access: yesBeilstein Journal of Organic Chemistry, 2010
N-Alkylation at the ring nitrogen of the D-galactosidase inhibitor 1-deoxygalactonojirimycin with a functionalised C6 alkyl chain followed by modification with different aromatic substituents provided lipophilic 1-deoxygalactonojirimycin derivatives ...
Georg Schitter   +13 more
doaj   +1 more source

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