K. Granberg

发表

Mineralocorticoid Receptor Antagonists.

Anneli Nordqvist, K. Granberg, 2019, Vitamins and hormones.

Structure‐Based Drug Design of Mineralocorticoid Receptor Antagonists to Explore Oxosteroid Receptor Selectivity

Yafeng Xue, A. Gunnarsson, A. Hogner, 2017, ChemMedChem.

Signals Generated by Neutrophil Receptors for Danger Molecules Transactivate Allosterically Modulated FFA2R: Distinct response patterns are mediated by modulators recognized by different allosteric receptor sites

C. Dahlgren, H. Forsman, Simon Lind, 2022, bioRxiv.

Preclinical pharmacology of AZD9977: A novel mineralocorticoid receptor modulator separating organ protection from effects on electrolyte excretion

U. Johansson, F. Jaisser, S. Geschwindner, 2018, PloS one.

On the Mechanism of Palladium(0)-Catalyzed Reactions of Allylic Substrates with Nucleophiles. Origin of the Loss of Stereospecificity

J. Bäckvall, K. Granberg, A. Heumann, 1991 .

Targeting thrombin and factor VIIa: design, synthesis, and inhibitory activity of functionally relevant indolizidinones.

Eric Therrien, S. Hanessian, I. Nilsson, 2002, Bioorganic & medicinal chemistry letters.

Targeting thrombin and factor VIIa: design, synthesis, and inhibitory activity of functionally relevant indolizidinones.

Stephen Hanessian, Ingemar Nilsson, Eric Therrien, 2002, Bioorganic & medicinal chemistry letters.

A strategy for generalization of the regiospecific synthesis of substituted quinones from cyclobutenediones

L. S. Liebeskind, K. Granberg, J. Zhang, 1992 .

Correction. Isomerization of (π-Allyl)Palladium Complexes via Nucleophilic Displacement by Palladium(0). A Common Mechanism in Palladium(0)-Catalyzed Allylic Substitution

J. Bäckvall, K. Granberg, 1992 .

Retro-aldol cleavage of bafilomycin derivatives

K. Nilsson, K. Edvinsson, K. Granberg, 1999 .

Palladium-catalyzed cis- and trans-annulations to 1,3-cyclohexadiene and 1,3-cycloheptadiene1

J. Bäckvall, K. Granberg, Jan O. V»gberg, 1989 .

Multiple ligand recognition sites in free fatty acid receptor 2 (FFA2R) direct distinct neutrophil activation patterns.

C. Dahlgren, H. Forsman, Simon Lind, 2021, Biochemical pharmacology.

Multiple ligand recognition sites in free fatty acid receptor 2 (FFAR2) direct distinct neutrophil activation patterns

C. Dahlgren, H. Forsman, Simon Lind, 2020, bioRxiv.

Discovery and Early Clinical Development of an Inhibitor of 5-Lipoxygenase Activating Protein (AZD5718) for Treatment of Coronary Artery Disease.

A. Plowright, J. Ulander, Malin Lemurell, 2019, Journal of medicinal chemistry.

A high-content, in vitro cardiac fibrosis assay for high-throughput, phenotypic identification of compounds with anti-fibrotic activity.

A. Sabirsh, G. Palano, S. Martinsson, 2020, Journal of molecular and cellular cardiology.

Identification of Mineralocorticoid Receptor Modulators with Low Impact on Electrolyte Homeostasis but Maintained Organ Protection.

U. Johansson, N. Selmi, A. Hogner, 2018, Journal of medicinal chemistry.

Improved Palladium-Catalyzed 1,4-Haloacyloxylation and 1,4-Diacyloxylation of Cyclic Conjugated Dienes.

D. Aksnes, G. Francis, J. Bäckvall, 1990 .

Predicting the relative binding affinity of mineralocorticoid receptor antagonists by density functional methods

Anders Hogner, Eva Hansson, Martin J. Packer, 2015, Journal of Computer-Aided Molecular Design.

The allosterically modulated FFAR2 is transactivated by signals generated by other neutrophil GPCRs

C. Dahlgren, H. Forsman, Simon Lind, 2023, PloS one.

A remarkably facile and stereochemically controlled fragmentation reaction in the hygrolide group of macrolide antibiotics

S. Hanessian, Q. Meng, K. Granberg, 1996 .

AZ2158 is a more potent formyl peptide receptor 1 inhibitor than the commonly used peptide antagonists in abolishing neutrophil chemotaxis.

C. Dahlgren, H. Forsman, L. Björkman, 2023, Biochemical pharmacology.

Identification of Novel Series of Potent and Selective Relaxin Family Peptide Receptor 1 (RXFP1) Agonists.

K. Granberg, Ryuichi Fuchigami, Shigeki Sakamaki, 2024, Journal of medicinal chemistry.