Adrianus H. Van Den Nieuwendijk

Leiden, ZH 2333CC, Netherlands

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 15 publications

A 16 × 8 Focused Compound Library Comprising All Configurational Isomers of the Archetypal Iminosugar, 1-Deoxynojirimycin.

A 16 × 8 Focused Compound Library Comprising All Configurational Isomers of the Archetypal Iminosugar, 1-Deoxynojirimycin.

Journal: Journal of medicinal chemistry

Published: April 15, 2026

Epi-Cyclophellitol Cyclosulfate, a Mechanism-Based Endoplasmic Reticulum α-Glucosidase II Inhibitor, Blocks Replication of SARS-CoV-2 and Other Coronaviruses.

Epi-Cyclophellitol Cyclosulfate, a Mechanism-Based Endoplasmic Reticulum α-Glucosidase II Inhibitor, Blocks Replication of SARS-CoV-2 and Other Coronaviruses.

Journal: ACS central science

Published: March 28, 2024

The development of a broad-spectrum retaining β-exo-galactosidase activity-based probe.

The development of a broad-spectrum retaining β-exo-galactosidase activity-based probe.

Journal: Organic & biomolecular chemistry

Published: September 19, 2023

Design, Synthesis and Structural Analysis of Glucocerebrosidase Imaging Agents.

Design, Synthesis and Structural Analysis of Glucocerebrosidase Imaging Agents.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)

Published: June 30, 2021

Direct Stereoselective Aziridination of Cyclohexenols with 3-Amino-2-(trifluoromethyl)quinazolin-4(3H)-one in the Synthesis of Cyclitol Aziridine Glycosidase Inhibitors.

Direct Stereoselective Aziridination of Cyclohexenols with 3-Amino-2-(trifluoromethyl)quinazolin-4(3H)-one in the Synthesis of Cyclitol Aziridine Glycosidase Inhibitors.

Journal: European journal of organic chemistry

Published: December 15, 2018

Comprehensive structure-activity-relationship of azaindoles as highly potent FLT3 inhibitors.

Comprehensive structure-activity-relationship of azaindoles as highly potent FLT3 inhibitors.

Journal: Bioorganic & medicinal chemistry

Published: November 25, 2018

Design and Synthesis of Quenched Activity-based Probes for Diacylglycerol Lipase and α,β-Hydrolase Domain Containing Protein 6.

Design and Synthesis of Quenched Activity-based Probes for Diacylglycerol Lipase and α,β-Hydrolase Domain Containing Protein 6.

Journal: Chemistry, an Asian journal

Published: March 26, 2018

Chiral disubstituted piperidinyl ureas: a class of dual diacylglycerol lipase-α and ABHD6 inhibitors.

Chiral disubstituted piperidinyl ureas: a class of dual diacylglycerol lipase-α and ABHD6 inhibitors.

Journal: MedChemComm

Published: January 16, 2017

Triazole Ureas Act as Diacylglycerol Lipase Inhibitors and Prevent Fasting-Induced Refeeding.

Triazole Ureas Act as Diacylglycerol Lipase Inhibitors and Prevent Fasting-Induced Refeeding.

Journal: Journal of medicinal chemistry

Published: December 20, 2016

Photo-crosslinking of clinically relevant kinases using H89-derived photo-affinity probes.

Photo-crosslinking of clinically relevant kinases using H89-derived photo-affinity probes.

Journal: Molecular bioSystems

Published: May 04, 2016

Enantioselective synthesis of adamantylalanine and carboranylalanine and their incorporation into the proteasome inhibitor bortezomib.

Enantioselective synthesis of adamantylalanine and carboranylalanine and their incorporation into the proteasome inhibitor bortezomib.

Journal: Chemical communications (Cambridge, England)

Published: February 20, 2016

Rapid and profound rewiring of brain lipid signaling networks by acute diacylglycerol lipase inhibition.

Rapid and profound rewiring of brain lipid signaling networks by acute diacylglycerol lipase inhibition.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: December 16, 2015

Showing 1-12 of 15

Last Updated: 09/26/2026