Petrine Wellendorph
Professor
Molecular and Cellular Pharmacology
Universitetsparken 2
2100 København Ø
- 2006
- Published
Activity of L-alpha-amino acids at the promiscuous goldfish odorant receptor 5.24
Christiansen, B., Wellendorph, Petrine & Bräuner, Hans, 24 Apr 2006, In: European Journal of Pharmacology. 536, 1-2, p. 98-101Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Known regulators of nitric oxide synthase and arginase are agonists at the human G-protein-coupled receptor GPRC6A
Christiansen, B., Wellendorph, Petrine & Bräuner, Hans, Apr 2006, In: British Journal of Pharmacology. 147, 8, p. 855-63Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Hydroxy-1,2,5-oxadiazolyl moiety as bioisoster of the carboxy function.Synthesis, ionization constants and pharmacological characterization of gamma-aminobutyric acid (GABA) related compounds
Lolli, M. L., Hansen, S. L., Rolando, B., Nielsen, Birgitte, Wellendorph, Petrine, Madsen, K., Larsen, O. M., Kristiansen, Uffe, Fruttero, R., Gasco, A. & Johansen, Tommy Nørskov, 2006, In: J. Med. Chem.. 49, p. 4442-4446 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Tuning wasp toxin structure for nicotinic receptor antagonism: cyclohexylalanine-containing analogues as potent and voltage-dependent blockers
Olsen, Christian Adam, Mellor, I. R., Wellendorph, Petrine, Usherwood, P. N. R., Witt, M., Franzyk, Henrik & Jaroszewski, J. W., 2006, In: ChemMedChem. 1, 3, p. 303-5 3 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2005
- Published
Novel cyclic gamma-hydroxybutyrate (GHB) analogs with high affinity and stereoselectivity of binding to GHB sites in rat brain
Wellendorph, Petrine, Høg, S., Greenwood, J. R., de Lichtenberg, A., Nielsen, Birgitte, Frølund, Bente, Brehm, L., Clausen, Rasmus Prætorius & Bräuner, Hans, Oct 2005, In: Journal of Pharmacology and Experimental Therapeutics. 315, 1, p. 346-51Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Deorphanization of GPRC6A: a promiscuous L-alpha-amino acid receptor with preference for basic amino acids
Wellendorph, Petrine, Hansen, K. B., Balsgaard, A., Greenwood, J. R., Egebjerg, J. & Bräuner, Hans, Mar 2005, In: Molecular Pharmacology. 67, 3, p. 589-97Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Hvordan virker Fantasy i hjernen?
Høg, S., Wellendorph, Petrine, Greenwood, J. & Clausen, Rasmus Prætorius, 2005, In: Lægemiddelforskning. 2005, p. 16-17Research output: Contribution to journal › Journal article › Communication
- 2004
- Published
Molecular cloning, expression, and sequence analysis of GPRC6A, a novel family C G-protein-coupled receptor
Wellendorph, Petrine & Bräuner, Hans, 23 Jun 2004, In: Gene. 335, p. 37-46Research output: Contribution to journal › Journal article › Research › peer-review
- 2003
- Published
Specific gamma-hydroxybutyrate-binding sites but loss of pharmacological effects of gamma-hydroxybutyrate in GABA-B1-deficient mice
Kaupmann, K., Cryan, J. F., Wellendorph, Petrine, Mombereau, C., Sansig, G., Klebs, K., Schmutz, M., Froestl, W., van der Putten, H., Mosbacher, J., Bräuner, Hans, Waldmeier, P. & Bettler, B., Nov 2003, In: European Journal of Neuroscience. 18, 10, p. 2722-30Research output: Contribution to journal › Journal article › Research › peer-review
- Published
A sequential high-yielding large-scale solution-method for synthesis of philanthotoxin analogues
Wellendorph, Petrine, Jaroszewski, J. W., Hansen, S. H. & Franzyk, Henrik, 2003, In: European Journal of Medicinal Chemistry. 38, 1, p. 117-22 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 1301791
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Kemogenomik: Receptoren set fra lægemiddelstoffets synspunkt
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Published -
352
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Chemogenomic discovery of allosteric antagonists at the GPRC6A receptor
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
244
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Identification of Histamine H3 Receptor Ligands Using a New Crystal Structure Fragment-based Method
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Published