Iminosugars past, present and future: medicines for tomorrow

G Horne, FX Wilson, J Tinsley, DH Williams… - Drug discovery today, 2011 - Elsevier
Iminosugars comprise the most attractive class of carbohydrate mimetics reported to date
and are ideally positioned to take advantage of our increasing understanding of …

Iminosugars as glycosyltransferase inhibitors

I Conforti, A Marra - Organic & biomolecular chemistry, 2021 - pubs.rsc.org
Iminosugars are naturally occurring carbohydrate analogues known since 1967. These
natural compounds and hundreds of their synthetic derivatives prepared over five decades …

Therapeutic applications of iminosugars: current perspectives and future opportunities

G Horne, FX Wilson - Progress in Medicinal Chemistry, 2011 - Elsevier
Publisher Summary The understanding of the role of carbohydrates, their receptors, and
their handling processes in the functioning of biological systems is an area in which major …

Glycomimetics at the mirror: Medicinal chemistry of L-iminosugars

D D'Alonzo, A Guaragna… - Current medicinal …, 2009 - ingentaconnect.com
Inhibition of carbohydrate processing enzymes is a topic of great interest, as these enzymes
are involved in a plethora of key biochemical events, such as digestion, lysosomal …

Recent results from non-basic glycosidase inhibitors: How structural diversity can inform general strategies for improving inhibition potency

MI Simone, A Wood, D Campkin, MJ Kiefel… - European Journal of …, 2022 - Elsevier
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 …

[HTML][HTML] Combination of tunicamycin with anticancer drugs synergistically enhances their toxicity in multidrug-resistant human ovarian cystadenocarcinoma cells

DC Hiss, GA Gabriels, PI Folb - Cancer cell international, 2007 - Springer
Background The pharmacologic modulatory effects of the antibiotic, tunicamycin (TM), on
multidrug-resistant human UWOV2 ovarian cancer cells are reported. The UWOV2 cell line …

Dihydroxyacetone phosphate aldolase catalyzed synthesis of structurally diverse polyhydroxylated pyrrolidine derivatives and evaluation of their glycosidase …

J Calveras, M Egido‐Gabás, L Gómez… - … A European Journal, 2009 - Wiley Online Library
The chemoenzymatic synthesis of a collection of pyrrolidine‐type iminosugars generated by
the aldol addition of dihydroxyacetone phosphate (DHAP) to C‐α‐substituted N‐Cbz‐2 …

Carbohydrate-based bioactive compounds for medicinal chemistry applications

L Cipolla, F Peri - Mini reviews in medicinal chemistry, 2011 - ingentaconnect.com
In this article we review our work over the years on carbohydrates and carbohydrate
mimetics and their applications in medicinal chemistry. In the first part of the review …

[HTML][HTML] D (−) lentiginosine-induced apoptosis involves the intrinsic pathway and is p53-independent

A Minutolo, S Grelli, F Marino-Merlo, FM Cordero… - Cell Death & …, 2012 - nature.com
We have recently found that D (−) lentiginosine, a synthetic iminosugar exerting glucosidase
inhibitory activity, but not its natural enantiomer lentiginosine, is endowed with an …

Straightforward synthesis of thiodisaccharides by ring-opening of sugar epoxides

VE Manzano, ML Uhrig, O Varela - The Journal of Organic …, 2008 - ACS Publications
3, 4-Anhydro hexopyranosides have been prepared by diastereoselective epoxidation of
derivatives of 2-propyl 3, 4-dideoxy-α-d-erythro-hex-3-enopyranoside (5), selectively …