Results 11 to 20 of about 665,601 (180)
Azasugar Glycosidase Inhibitors: Useful Tools for Glycobiologists [PDF]
Glycosidase inhibitors are moving increasingly as potential agents for the treatment of diseases by altering glycosylation or catabolism of glycoconjugates.
Sylviane Picasso
doaj +4 more sources
Functionalization of Glycals Leading to 2-Deoxy-O-glycosides, Aminosugars, Nitrosugars and Glycosidase Inhibitors: Our Experience [PDF]
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 +2 more sources
This review covers the literature in the past 15 years on glycosidase inhibitors lacking a basic nitrogen (for example iminosugars/azasugars) with a focus on natural terpenoids, and mono- and polycyclic aromatic hydrocarbons.
Campkin, David +9 more
core +1 more source
An efficient and general synthetic route to all eight stereoisomeric d-glycono-δ-lactams has been developed. The strategy involves, as a key step, a stereodivergent δ-lactam formation with configurational retention or inversion at C-4 of a starting γ ...
Hayamitsu Adachi (1666837) +6 more
core +3 more sources
Biosynthetic Pathways to Glycosidase Inhibitors [PDF]
Glycosidase inhibitors are important compounds that can interfere with several biosynthetic processes including N-linked glycosylation and the biosynthesis of several glycoproteins.
Delso, J. Ignacio +3 more
core +1 more source
Synephrine and phenylephrine act as -amylase, -glycosidase, acetylcholinesterase, butyrylcholinesterase, and carbonic anhydrase enzymes inhibitors [PDF]
In this paper, synephrine and phenylephrine compounds showed excellent inhibitory effects against human carbonic anhydrase (hCA) isoforms I and II, -amylase, -glycosidase, acetylcholinesterase (AChE), and butyrylcholinesterase (BChE).
Taslimi, Parham +6 more
core +1 more source
Potent and specific inhibition of glycosidases by small artificial binding proteins (affitins).
Glycosidases are associated with various human diseases. The development of efficient and specific inhibitors may provide powerful tools to modulate their activity.
Agustín Correa +8 more
doaj +1 more source
IOOC Route to Substituted Chiral Pyrrolidines. Potential Glycosidase Inhibitors
Branched-chain five-membered ring aza-sugar analogues, synthesized from amino acids by an intramolecular oxime−olefin cycloaddition reaction, the IOOC route, were found to be selective glycosidase inhibitors.
Yosi Bechor (3046173) +5 more
core +2 more sources
?-Trimethylsilylmethylamine Radical Cation in the Synthesis of Cyclic Amines and Beyond
The evolution of chemistry associated with the photoinduced electron transfer (PET)-generated ?-trimethylsilylmethylamine radical cation cyclization to a tethered olefin to synthesize cyclic amine structural frame works is presented in ...
Ganesh Pandey +2 more
doaj +1 more source
Stabilizing Functional Nucleic Acids for Real‐Sample Diagnostics
Functional nucleic acids enable programmable real‐sample diagnostics, but often lose function in complex biological matrices. This review highlights four stabilization levers—chemical, topological, architectural, and microenvironment/interface engineering—that preserve aptamer and DNAzyme performance in saliva, serum, urine, and stool, reframing ...
Soyeon Lee +4 more
wiley +2 more sources

