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 …
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 …
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 …
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 …
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
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 …
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 …
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 …
the aldol addition of dihydroxyacetone phosphate (DHAP) to C‐α‐substituted N‐Cbz‐2 …
Carbohydrate-based bioactive compounds for medicinal chemistry applications
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 …
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
We have recently found that D (−) lentiginosine, a synthetic iminosugar exerting glucosidase
inhibitory activity, but not its natural enantiomer lentiginosine, is endowed with an …
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 …
derivatives of 2-propyl 3, 4-dideoxy-α-d-erythro-hex-3-enopyranoside (5), selectively …