Glycosidase inhibitors: update and perspectives on practical use

N Asano - Glycobiology, 2003 - academic.oup.com
About 40 years have passed since the classical glycosidase inhibitor nojirimycin was
discovered from the cultured broth of the Streptomyces species. Since then, over 100 …

Targeting ceramide metabolism—a strategy for overcoming drug resistance

A Senchenkov, DA Litvak… - Journal of the National …, 2001 - academic.oup.com
Inherent or acquired drug resistance, which frequently characterizes cancer cells, is caused
by multiple mechanisms, including dysfunctional metabolism of the lipid second messenger …

N-butyldeoxynojirimycin is a novel inhibitor of glycolipid biosynthesis.

FM Platt, GR Neises, RA Dwek, TD Butters - Journal of Biological Chemistry, 1994 - ASBMB
The imino sugar deoxynojirimycin and its alkylated derivatives are inhibitors of the N-linked
oligosaccharide processing enzymes alpha-glucosidase I and II. These compounds are …

Targeting macrophage TFEB-14-3-3 epsilon Interface by naringenin inhibits abdominal aortic aneurysm

Y Jia, L Zhang, Z Liu, C Mao, Z Ma, W Li, F Yu, Y Wang… - Cell Discovery, 2022 - nature.com
Abdominal aortic aneurysm (AAA) is a lethal cardiovascular disease, and there is no proven
drug treatment for this condition. In this study, by using the Connectivity Map (CMap) …

Accumulation of glucosylceramides in multidrug-resistant cancer cells

Y Lavie, H Cao, SL Bursten, AE Giuliano… - Journal of Biological …, 1996 - ASBMB
Multidrug-resistant (MDR) tumors and cancer cell lines demonstrate a wide variety of
biochemical changes. In this study we used drug-sensitive wild-type (wt) cancer cell lines …

Targeting of Shiga toxin B-subunit to retrograde transport route in association with detergent-resistant membranes

T Falguieres, F Mallard, C Baron, D Hanau… - Molecular biology of …, 2001 - Am Soc Cell Biol
In HeLa cells, Shiga toxin B-subunit is transported from the plasma membrane to the
endoplasmic reticulum, via early endosomes and the Golgi apparatus, circumventing the …

Inhibition of glucosylceramide accumulation results in effective blockade of polycystic kidney disease in mouse models

TA Natoli, LA Smith, KA Rogers, B Wang… - Nature medicine, 2010 - nature.com
Polycystic kidney disease (PKD) represents a family of genetic disorders characterized by
renal cystic growth and progression to kidney failure. No treatment is currently available for …

Improved inhibitors of glucosylceramide synthase

L Lee, A Abe, JA Shayman - Journal of Biological Chemistry, 1999 - ASBMB
Previous work has led to the identification of inhibitors of glucosylceramide synthase, the
enzyme catalyzing the first glycosylation step in the synthesis of glucosylceramide-based …

(1S, 2R)-D-erythro-2-(N-Myristoylamino)-1-phenyl-1-propanol as an Inhibitor of Ceramidase (∗)

A Bielawska, MS Greenberg, D Perry, S Jayadev… - Journal of Biological …, 1996 - ASBMB
In this study, we have examined the cellular and biochemical activities of the ceramide
analog (1S, 2R)-Derythro-2-(N-myristoylamino)-1-phenyl-1-propanol (Derythro-MAPP) …

A specific and potent inhibitor of glucosylceramide synthase for substrate inhibition therapy of Gaucher disease

KA McEachern, J Fung, S Komarnitsky… - Molecular genetics and …, 2007 - Elsevier
An approach to treating Gaucher disease is substrate inhibition therapy which seeks to
abate the aberrant lysosomal accumulation of glucosylceramide. We have identified a novel …