The lipophilic bullet hits the targets: medicinal chemistry of adamantane derivatives

L Wanka, K Iqbal, PR Schreiner - Chemical reviews, 2013 - ACS Publications
A simple, primary amine bearing a C10H15 alkyl residue was found to display potent anti-
Influenza A properties in 1964. 1 Soon thereafter, antiviral activity of this amine was found …

A review on synthesis, mechanism of action, and structure-activity relationships of 1, 2, 3-triazole-based α-glucosidase inhibitors as promising anti-diabetic agents

Z Fallah, M Tajbakhsh, M Alikhani, B Larijani… - Journal of Molecular …, 2022 - Elsevier
Abstract α-Glucosidase is a key enzyme in hydrolysis of carbohydrates to glucose and
located in the small intestine brush border. Inhibition of this enzyme delay the release of …

Re-exploring promising α-glucosidase inhibitors for potential development into oral anti-diabetic drugs: Finding needle in the haystack

U Ghani - European journal of medicinal chemistry, 2015 - Elsevier
Abstract Treatment of diabetes mellitus by oral α-glucosidase inhibitors is currently confined
to acarbose, miglitol and voglibose marred by efficacy problems and unwanted side effects …

[HTML][HTML] Carbohydrate CuAAC click chemistry for therapy and diagnosis

XP He, YL Zeng, Y Zang, J Li, RA Field… - Carbohydrate Research, 2016 - Elsevier
Carbohydrates are important as signaling molecules and for cellular recognition events,
therefore offering scope for the development of carbohydrate-mimetic diagnostics and drug …

Synthesis and biological properties of multivalent iminosugars

R Zelli, JF Longevial, P Dumy, A Marra - New Journal of Chemistry, 2015 - pubs.rsc.org
Glycosidases are extremely widespread enzymes responsible for the cleavage of glycosidic
bonds in glycoconjugates found in living organisms. Although it was well-known that the …

β-Glucosidase 2 (GBA2) activity and imino sugar pharmacology

CM Ridley, KE Thur, J Shanahan… - Journal of Biological …, 2013 - ASBMB
β-Glucosidase 2 (GBA2) is an enzyme that cleaves the membrane lipid glucosylceramide
into glucose and ceramide. The GBA2 gene is mutated in genetic neurological diseases …

5-C-Branched Deoxynojirimycin: Strategy for Designing a 1-Deoxynojirimycin-Based Pharmacological Chaperone with a Nanomolar Affinity for Pompe Disease

A Kato, I Nakagome, U Kanekiyo, TT Lu… - Journal of Medicinal …, 2022 - ACS Publications
In recent years, the function of pharmacological chaperones as a “thermodynamic stabilizer”
has been attracting attention in combination therapy. The coadministration of a …

Synthesis and therapeutic applications of iminosugars in cystic fibrosis

A Esposito, D D'Alonzo, M De Fenza… - International Journal of …, 2020 - mdpi.com
Iminosugars are sugar analogues endowed with a high pharmacological potential. The wide
range of biological activities exhibited by these glycomimetics associated with their excellent …

Rapid assembly of a library of lipophilic iminosugars via the thiol–ene reaction yields promising pharmacological chaperones for the treatment of Gaucher disease

ED Goddard-Borger, MB Tropak… - Journal of medicinal …, 2012 - ACS Publications
A highly divergent route to lipophilic iminosugars that utilizes the thiol–ene reaction was
developed to enable the rapid synthesis of a collection of 16 dideoxyiminoxylitols bearing …

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 …