Michael Worch Boesgaard
Postdoc
Experimental Pharmacology
byg 18, 2100 København Ø
- 2019
- Published
Structure–Activity Relationship Studies of the Natural Product G q/11 Protein Inhibitor YM-254890. / Xiong, Xiao Feng; Zhang, Hang; Boesgaard, Michael W.; Underwood, Christina R.; Bräuner-Osborne, Hans; Strømgaard, Kristian.
In: ChemMedChem, Vol. 14, No. 8, 04.2019, p. 865-870.Research output: Contribution to journal › Journal article › Research › peer-review
- 2018
- Published
Structure–activity relationship and conformational studies of the natural product cyclic depsipeptides YM-254890 and FR900359. / Zhang, Hang; Nielsen, Alexander L.; Boesgaard, Michael W.; Harpsøe, Kasper; Daly, Norelle L.; Xiong, Xiao-feng; Underwood, Christina R.; Haugaard-kedström, Linda M.; Bräuner-osborne, Hans; Gloriam, David E.; Strømgaard, Kristian.
In: European Journal of Medicinal Chemistry, Vol. 156, 05.08.2018, p. 847-860.Research output: Contribution to journal › Journal article › Research › peer-review
- 2017
- Published
Identification of Histamine H3 Receptor Ligands Using a New Crystal Structure Fragment-based Method. / Frandsen, Ida Osborn; Boesgaard, Michael W; Fidom, Kimberley; Hauser, Alexander S; Isberg, Vignir; Bräuner-Osborne, Hans; Wellendorph, Petrine; Gloriam, David E.
In: Scientific Reports, Vol. 7, No. 1, 4829, 06.07.2017.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Structure-Activity Relationship Studies of the Cyclic Depsipeptide Natural Product YM-254890, Targeting the Gq Protein. / Zhang, Hang; Xiong, Xiao-feng; Boesgaard, Michael W; Underwood, Christina R; Bräuner-Osborne, Hans; Strømgaard, Kristian.
In: ChemMedChem, Vol. 12, No. 11, 07.06.2017, p. 830-834.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Structural insight to mutation effects uncover a common allosteric site in class C GPCRs. / Harpsøe, Kasper; Boesgaard, Michael W; Munk, Christian; Bräuner-Osborne, Hans; Gloriam, David E.
In: Bioinformatics (Oxford, England), Vol. 33, No. 8, btw784, 2017, p. 1116-1120.Research output: Contribution to journal › Journal article › Research › peer-review
- 2015
- Published
Selective Allosteric Antagonists for the G Protein-Coupled Receptor GPRC6A Based on the 2-Phenylindole Privileged Structure Scaffold. / Johansson, Henrik; Boesgaard, Michael Worch; Nørskov-Lauritsen, Lenea; Larsen, Inna; Kuhne, Sebastiaan; Gloriam, David E; Bräuner-Osborne, Hans; Sejer Pedersen, Daniel.
In: Journal of Medicinal Chemistry, Vol. 58, No. 22, 25.11.2015, p. 8938-51.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 156726754
Most downloads
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Identification of Histamine H3 Receptor Ligands Using a New Crystal Structure Fragment-based Method
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
76
downloads
Structural insight to mutation effects uncover a common allosteric site in class C GPCRs
Research output: Contribution to journal › Journal article › Research › peer-review
Published