Results 91 to 100 of about 2,579 (147)

UDP-GlcNAc Analogues as Inhibitors of O-GlcNAc Transferase (OGT):Spectroscopic, Computational, and Biological Studies [PDF]

open access: yes, 2018
A series of glycomimetics of UDP-GlcNAc, in which the β-phosphate has been replaced by either an alkyl chain or a triazolyl ring and the sugar moiety has been replaced by a pyrrolidine ring, has been synthesized by the application of different click ...
Ardèvol   +67 more
core   +4 more sources

Synthesis of the first examples of iminosugar clusters based on cyclopeptoid cores

open access: yesBeilstein Journal of Organic Chemistry, 2014
Cyclic N-propargyl α-peptoids of various sizes were prepared by way of macrocyclizations of linear N-substituted oligoglycines. These compounds were used as molecular platforms to synthesize a series of iminosugar clusters with different valency and ...
Mathieu L. Lepage   +6 more
doaj   +1 more source

Functionalization of Glycals Leading to 2-Deoxy-O-glycosides, Aminosugars, Nitrosugars and Glycosidase Inhibitors: Our Experience

open access: yesCHIMIA, 2012
Glycals have been transformed into a variety of functionalized substrates which have been found to be useful in synthesizing some aminosugars, N-glycopeptides, nitrosugars and some iminosugars which are potential glycosidase inhibitors.
Rima Lahiri   +2 more
doaj   +1 more source

Inhibiting influenza virus replication using novel and established antiviral compounds

open access: yes, 2011
Circulating influenza viruses have the potential to cause pandemics, as seen in 2009 with the emergence of a novel H1N1 virus that rapidly disseminated worldwide.
Brookes, Daniel William   +1 more
core   +1 more source

Synthesis and evaluation of hepatitis C antivirals : viral E2 glycoprotein / human CD81 receptor interaction inhibitors [PDF]

open access: yes, 2008
The aim of the present work was to prepare compounds which inhibit the CD81-LEL—HCV-E2 interaction by binding to CD81-LEL. Starting point was a virtual screening using the open conformation of the LEL followed by synthesis and biological validation by ...
Holzer, Marcel
core  

[[alternative]]Syntheses of 2-(Hydroxymethyl)Azepan-(4,5,6)-Triols Derivatives and the Skeleton of (-)-Stenine Alkaloid [PDF]

open access: yes
計畫編號:NSC94-2113-M032-006研究期間:200508~200607研究經費:1,589,000[[abstract]]當類似醣類分子中,氮原子取代了原來環內的氧原子時,這類分子被統稱為 iminosugars 或azasugars 。而它們的生物活性, 主要是抑制glycosidases 及 glycosyltranstransterase,特別針對了代謝方面的疾病,如:糖尿病、抗病毒及抗不正 當增生,已具潛在的療效。也因此,合成化學家對於合成各式樣之glycosidase 抑制 ...
施增廉
core  

Monosaccharide and Disaccharide Mimics: New Molecular Tools for Biology and Medicine

open access: yesCHIMIA, 2001
Intercellular communication is governed by interactions between surface oligosaccharides and glycoproteins. The biosynthesis of these molecules involves glycosidations catalyzed by glycosyltransferases and hydrolysis of O-glycosyl linkages ...
Pierre Vogel
doaj  

<i>N</i>-Alkyl Derivatives of Deoxynojirimycin (DNJ) as Antiviral Agents: Overview and Update. [PDF]

open access: yesMolecules
Checconi P   +10 more
europepmc   +1 more source

Stereoselective Synthesis of Heavily Hydroxylated Azepane Iminosugars via Osmium-Catalyzed Tethered Aminohydroxylation. [PDF]

open access: yesOrg Lett, 2023
Martínez-Bailén M   +5 more
europepmc   +1 more source

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