Anna Aagaard
BioPharmaceuticals R&D, AstraZeneca
Goeteborg, O, Sweden
Goeteborg, O, Sweden
Last Updated: 09/26/2026
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Found 20 publications
Mineralocorticoid Receptor Antagonists With an Acylurea as a Key Polar Interaction Motif.
Journal: ChemMedChem
Published: November 19, 2025
Discovery and Validation of a Novel Class of Necroptosis Inhibitors Targeting RIPK1.
Journal: ACS chemical biology
Published: June 20, 2025
Generation of a potent & selective series of IRAK4 inhibitors based on a structure based, hybridization approach.
Journal: Bioorganic & medicinal chemistry
Published: June 11, 2025
Thermostable ancestors enabled evolutionary diversification of promiscuous chemical defence enzymes.
Thermostable ancestors enabled evolutionary diversification of promiscuous chemical defence enzymes.
Journal: The EMBO journal
Published: February 06, 2025
Identification and optimisation of a pyrimidopyridone series of IRAK4 inhibitors.
Journal: Bioorganic & medicinal chemistry
Published: January 13, 2022
AZD0284, a Potent, Selective, and Orally Bioavailable Inverse Agonist of Retinoic Acid Receptor-Related Orphan Receptor C2.
Journal: Journal of medicinal chemistry
Published: August 31, 2021
Fragment-Based Discovery of Novel Allosteric MEK1 Binders.
Journal: ACS medicinal chemistry letters
Published: October 20, 2020
Improving metabolic stability and removing aldehyde oxidase liability in a 5-azaquinazoline series of IRAK4 inhibitors.
Journal: Bioorganic & medicinal chemistry
Published: September 01, 2020
Discovery of Potent and Orally Bioavailable Inverse Agonists of the Retinoic Acid Receptor-Related Orphan Receptor C2.
Journal: ACS medicinal chemistry letters
Published: April 05, 2019
Identification of Mineralocorticoid Receptor Modulators with Low Impact on Electrolyte Homeostasis but Maintained Organ Protection.
Journal: Journal of medicinal chemistry
Published: January 01, 2019
Molecular tuning of farnesoid X receptor partial agonism.
Journal: Nature communications
Published: October 18, 2018
Potent and Orally Bioavailable Inverse Agonists of RORγt Resulting from Structure-Based Design.
Journal: Journal of medicinal chemistry
Published: August 11, 2018
Last Updated: 09/26/2026