Results 101 to 110 of about 665,601 (180)

Targeting Selectivity: Improving Golgi α-Mannosidase II (GMII) Inhibitors Through In Silico Studies

open access: yesBiomolecules
Aberrant glycosylation is a recognized hallmark of cancer, establishing Golgi α-mannosidase II (GMII) as strategic therapeutic target. While the natural alkaloid swainsonine demonstrated potent anticancer activity, its clinical use is hampered by ...
Nieves G. Ledesma   +4 more
doaj   +1 more source

Synthesis and evaluation of hydroxymethylaminocyclitols as glycosidase inhibitors [PDF]

open access: yes, 2015
Four series of C7N aminocyclitol analogues of glucose were synthesized by stereocontrolled epoxide opening of hydroxyl protected forms of the cyclohexane epoxides cyclophellitol and 1,6-epi-cyclophellitol.
Egido-Gabás, Meritxell   +11 more
core   +1 more source

Molecular modeling studies of pseudouridine isoxazolidinyl nucleoside analogues as potential inhibitors of the pseudouridine 5ʹ-monophosphate glycosidase

open access: yes, 2018
In this paper, we investigated the hypothesis that pseudouridine isoxazolidinyl nucleoside analogues could act as potential inhibitors of the pseudouridine 5ʹ-monophosphate glycosidase. This purpose was pursued using molecular modeling and in silico ADME-
Damigella Arcangelo   +8 more
core   +1 more source

Acarbose versus trans-chalcone: comparing the effect of two glycosidase inhibitors on obese mice

open access: yesArchives of Endocrinology and Metabolism
Objective Acarbose and trans-chalcone are glucosidase inhibitors whose beneficial effects have been demonstrated in diabetes. The present study aimed at investigating their potential effects in obesity.Materials and methods NMRI male mice (n = 48) were ...
Fatemeh Jalalvand   +4 more
doaj   +1 more source

Inhibition of a prokaryotic GH78 α-l-rhamnosidase by synthetic pyrrolidines compared to a eukaryotic α-l-rhamnosidase from Penicillium decumbens

open access: yesResults in Chemistry
This study presents the first evaluation of diverse iminosugars as inhibitors of a prokaryotic GH78 α-l-rhamnosidase. The pyrrolidine derivatives acted as enzyme competitive inhibitors.
Vladimír Puchart   +2 more
doaj   +1 more source

Facing Glycoscience

open access: yesCHIMIA, 2001
This essay describes an approach facing some of the challenges of glycoscience, concentrating on the relation between structure and reactivity. This has resulted in new methods, precursors of carbohydrate-derived reactive intermediates, analysis
Andrea Vaselia
doaj  

A formal total synthesis of deoxynojirimycin from D-glucitol

open access: yesJournal of the Brazilian Chemical Society, 2003
This report deals with the formal synthesis of deoxynojirimycin using D-glucitol as an inexpensive starting material. Through a sequence of several selective protection/deprotection and nucleophilic substitution reactions, many isopropylidene derivatives
Braga Raquel M., Kato Lucilia
doaj  

N-Alkyl Isofagomine Lactams: Synthesis, Glycosidase Inhibition, and Antimicrobial Assessments [PDF]

open access: yes
A series of six N-alkyl isofagomine lactam derivatives were synthesized over ten steps from D-arabinose. The compounds were evaluated as glycosidase inhibitors.
Sydnes, Magne O.   +9 more
core   +1 more source

Total Synthesis of a Lactam Glycosidase Inhibitor Precursor

open access: yes, 2008
A total synthesis of an α,β-unsaturated γ-lactam is presented. This heterocycle is a precursor to a glycosidase inhibitor. Glycosidases function in the breakage of complex carbohydrates, yielding smaller sugars for cellular metabolism.
Eliasen, Anders
core  

Back to (non-)Basics: An Update on Neutral and Charge-Balanced Glycosidase Inhibitors

open access: yes, 2018
Glycosidases have important anti-cancer, anti-viral and anti-diabetic properties. This review covers the literature in the past 15 years since our initial review in this journal on “neutral” glycosidase inhibitors lacking a basic nitrogen found in ...
Laura J. Mares   +13 more
core   +1 more source

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