20 articles for SG Withers
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Cmpds
Data
Article Title
Organization
5
Synthesis of C-5a-chain extended derivatives of 4-epi-isofagomine: Powerfulß-galactosidase inhibitors and low concentration activators of GM1-gangliosidosis-related human lysosomalß-galactosidase.

Graz University of Technology
7
Concise synthesis of C-1-cyano-iminosugars via a new Staudinger/aza Wittig/Strecker multicomponent reaction strategy.

Technical University Graz
19
Rapid assembly of a library of lipophilic iminosugars via the thiol-ene reaction yields promising pharmacological chaperones for the treatment of Gaucher disease.

University of British Columbia
2
Synthesis and biological evaluation of novel biotin-iminoalditol conjugates.

Technische Universit£T Graz
7
N-Acetylhexosaminidase inhibitory properties of C-1 homologated GlcNAc- and GalNAc-thiazolines.

The State University of New Jersey
3
Glycosidase profiling with immobilised glycosidase-inhibiting iminoalditols--a proof-of-concept study.

Technische Universit£T Graz
4
A fluorescent probe for GM1 gangliosidosis relatedß-galactosidase: N-(dansylamino)hexylaminocarbonylpentyl-1,5-dideoxy-1,5-imino-D-galactitol.

Industrial Research
2
OGA inhibition by GlcNAc-selenazoline.

Daegu University
6
β-Glucosidase inhibitors incorporating pyridinium as a glucosyl mimic

TBA
1
1-Deoxygalactonojirimycin-lysine hybrids as potent D-galactosidase inhibitors.

Technische UniversitäT Graz
16
Fluorescent glycosidase inhibiting 1,5-dideoxy-1,5-iminoalditols.

Technische UniversitäT Graz
5
Powerful probes for glycosidases: novel, fluorescently tagged glycosidase inhibitors.

Institut FüR Biochemie Der Technischen UniversitäT Graz
7
Novel, lipophilic derivatives of 2,5-dideoxy-2,5-imino-D-mannitol (DMDP) are powerful beta-glucosidase inhibitors.

Technische UniversitäT Graz
7
A new type of pharmacological chaperone for G

Graz University of Technology
22
Substituted indazoles, methods for the production thereof, pharmaceutical preparations that contain said new substituted indazoles, and use of said new substituted indazoles to produce drugs

Bayer Pharma Aktiengesellschaft
15
Kinase inhibitors

Topivert Pharma
12
Microwave-assisted synthesis and tyrosinase inhibitory activity of chalcone derivatives.

Shaoyang University
8
Differences in agonist/antagonist binding affinity and receptor transduction using recombinant human gamma-aminobutyric acid type A receptors.

Merck Sharp and Dohme Research Laboratories
5
Inhibition of adenosine deaminase by analogues of adenosine and inosine, incorporating a common heterocyclic base, 4(7)-amino-6(5)H-imidazo[4,5-d]pyridazin-7(4)one.

University of Maryland Baltimore County