Anders D. Poulsen
10 Biopolis Road #05-01 Chromos
138670, Singapore
138670, Singapore
Last Updated: 09/26/2026
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Found 53 publications
Testing the large genome constraint hypothesis in tropical rhizomatous herbs: life strategies, plant traits and habitat preferences in gingers.
Journal: The Plant journal : for cell and molecular biology
Published: February 08, 2023
Fragment-based lead discovery of indazole-based compounds as AXL kinase inhibitors.
Journal: Bioorganic & medicinal chemistry
Published: July 16, 2021
Strategic Design of Catalytic Lysine-Targeting Reversible Covalent BCR-ABL Inhibitors*.
Journal: Angewandte Chemie (International ed. in English)
Published: April 20, 2021
Discovery of a Novel Mycobacterial F-ATP Synthase Inhibitor and its Potency in Combination with Diarylquinolines.
Journal: Angewandte Chemie (International ed. in English)
Published: February 20, 2020
Stepwise Evolution of Fragment Hits against MAPK Interacting Kinases 1 and 2.
Journal: Journal of medicinal chemistry
Published: January 08, 2020
Correction to "Discovery of Irreversible Inhibitors Targeting Histone Methyltransferase, SMYD3".
Journal: ACS medicinal chemistry letters
Published: August 16, 2019
Discovery of Irreversible Inhibitors Targeting Histone Methyltransferase, SMYD3.
Journal: ACS medicinal chemistry letters
Published: April 15, 2019
Targeting the Bacterial Epitranscriptome for Antibiotic Development: Discovery of Novel tRNA-(N1G37) Methyltransferase (TrmD) Inhibitors.
Journal: ACS infectious diseases
Published: January 26, 2019
Fragment-based Discovery of a Small-Molecule Protein Kinase C-iota Inhibitor Binding Post-kinase Domain Residues.
Journal: ACS medicinal chemistry letters
Published: November 12, 2018
Intranasal administration of a stapled relaxin-3 mimetic has anxiolytic- and antidepressant-like activity in rats.
Journal: British journal of pharmacology
Published: September 24, 2018
Novel Acetamide Indirectly Targets Mycobacterial Transporter MmpL3 by Proton Motive Force Disruption.
Journal: Frontiers in microbiology
Published: September 12, 2018
Design and synthesis of potent dual inhibitors of JAK2 and HDAC based on fusing the pharmacophores of XL019 and vorinostat.
Journal: European journal of medicinal chemistry
Published: July 11, 2018
Last Updated: 09/26/2026