Marta E. Artola

Leiden, ZH 2333CC, Netherlands

Last Updated: 09/26/2026

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Found 43 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

Oseltamivir aziridines are potent influenza neuraminidase inhibitors and imaging agents.

Oseltamivir aziridines are potent influenza neuraminidase inhibitors and imaging agents.

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

Published: March 23, 2026

Unraveling A4GALT Mechanism and Its Modulation With Adamantyl-Galactosylceramide Analogues: Advancing Fabry Disease Therapeutic Strategies.

Unraveling A4GALT Mechanism and Its Modulation With Adamantyl-Galactosylceramide Analogues: Advancing Fabry Disease Therapeutic Strategies.

Journal: Angewandte Chemie (International ed. in English)

Published: December 10, 2025

C-Branched Iminosugars as Selective Pharmacological Chaperones of Lysosomal α-Glucosidase for the Treatment of Pompe Disease.

C-Branched Iminosugars as Selective Pharmacological Chaperones of Lysosomal α-Glucosidase for the Treatment of Pompe Disease.

Journal: Journal of medicinal chemistry

Published: September 15, 2025

Glucosylated cholesterol accumulates in atherosclerotic lesions and impacts macrophage immune response.

Glucosylated cholesterol accumulates in atherosclerotic lesions and impacts macrophage immune response.

Journal: Journal of lipid research

Published: March 12, 2025

Cultured Macrophage Models for the Investigation of Lysosomal Glucocerebrosidase and Gaucher Disease.

Cultured Macrophage Models for the Investigation of Lysosomal Glucocerebrosidase and Gaucher Disease.

Journal: International journal of molecular sciences

Published: January 27, 2025

Structure-guided design of C3-branched swainsonine as potent and selective human Golgi α-mannosidase (GMII) inhibitor.

Structure-guided design of C3-branched swainsonine as potent and selective human Golgi α-mannosidase (GMII) inhibitor.

Journal: Chemical communications (Cambridge, England)

Published: September 25, 2024

Development of selective nanomolar cyclic peptide ligands as GBA1 enzyme stabilisers.

Development of selective nanomolar cyclic peptide ligands as GBA1 enzyme stabilisers.

Journal: RSC chemical biology

Published: September 12, 2024

Precision Activity-Based α-Amylase Probes for Dissection and Annotation of Linear and Branched-Chain Starch-Degrading Enzymes.

Precision Activity-Based α-Amylase Probes for Dissection and Annotation of Linear and Branched-Chain Starch-Degrading Enzymes.

Journal: Angewandte Chemie (International ed. in English)

Published: August 09, 2024

Synthesis and Biological Evaluation of Deoxycyclophellitols as Human Retaining β-Glucosidase Inhibitors.

Synthesis and Biological Evaluation of Deoxycyclophellitols as Human Retaining β-Glucosidase Inhibitors.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)

Published: August 08, 2024

6-O-alkyl 4-methylumbelliferyl-β-D-glucosides as selective substrates for GBA1 in the discovery of glycosylated sterols.

6-O-alkyl 4-methylumbelliferyl-β-D-glucosides as selective substrates for GBA1 in the discovery of glycosylated sterols.

Journal: Journal of lipid research

Published: June 28, 2024

High-throughput competitive binding assay for targeting RNA tertiary structures with small molecules: application to pseudoknots and G-quadruplexes.

High-throughput competitive binding assay for targeting RNA tertiary structures with small molecules: application to pseudoknots and G-quadruplexes.

Journal: Nucleic acids research

Published: April 18, 2024

Showing 1-12 of 43

Last Updated: 09/26/2026