Trond Ulven
Professor
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Phenoxyacetic acid derivatives as CRTH2 receptor ligands, their preparation, pharmaceutical compositions, and use in therapy
Ulven, Trond, Frimurer, Thomas Michael, Rist, Ø., Kostenis, E., Högberg, T., Receveur, J. & Grimstrup, M., 2007, Patent No. WO 2007/062678 A1Research output: Patent
Phenanthroline-2,9-bistriazoles as selective G-quadruplex ligands
Nielsen, M. C., Larsen, A. F., Abdikadir, F. H. & Ulven, Trond, 2014, In: European Journal of Medicinal Chemistry. 72, p. 119-126 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
Pharmacological Tool Compounds for the Free Fatty Acid Receptor 4 (FFA4/GPR120)
Hansen, S. V. F. & Ulven, Trond, 2017, Free Fatty Acid Receptors. Springer Science+Business Media, p. 33-56 24 p.Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Research › peer-review
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Pathophysiological regulation of lung function by the free fatty acid receptor FFA4
Prihandoko, R., Kaur, D., Wiegman, C. H., Alvarez-Curto, E., Donovan, C., Chachi, L., Ulven, Trond, Tyas, M. R., Euston, E., Dong, Z., Alharbi, A. G. M., Kim, R. Y., Lowe, J. G., Hansbro, P. M., Chung, K. F., Brightling, C. E., Milligan, G. & Tobin, A. B., 2020, In: Science Translational Medicine. 12, 557, 13 p., 9009.Research output: Contribution to journal › Journal article › Research › peer-review
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PGH1, the precursor for the anti-inflammatory prostaglandins of the 1-series, is a potent activator of the pro-inflammatory receptor CRTH2/DP2
Schröder, R., Xue, L., Konya, V., Martini, L., Kampitsch, N., Whistler, J. L., Ulven, Trond, Heinemann, A., Pettipher, R. & Kostenis, E., 2012, In: P L o S One. 7, 3, p. e33329Research output: Contribution to journal › Journal article › Research › peer-review
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Oxalyl chloride as a practical carbon monoxide source for carbonylation reactions
Hansen, S. V. F. & Ulven, Trond, 5 Jun 2015, In: Organic Letters. 17, 11, p. 2832-2835 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
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One-Pot Synthesis of Xanthone by Carbonylative Suzuki Coupling Reaction
Loureiro, D. R. P., Soares, J. X., Maia, A., Silva, A. M. N., Rangel, M., Azevedo, C. M. G., Hansen, S., Ulven, Trond, Pinto, M. M. M., Reis, S. & Afonso, C. M. M., 2021, In: ChemistrySelect. 6, 18, p. 4511-4514 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
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On the mechanism of interaction of potent, surmountable and insurmountable antagonists with the prostaglandin D2 receptor CRTH2
Mathiesen, Jesper M., Christopoulos, A., Ulven, Trond, Royer, J. F., Campillo, M., Heinemann, A., Pardo, L. & Kostenis, E., 2006, In: Molecular Pharmacology. 69, 4, p. 1441-1453 13 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Novel selective thiazoleacetic acids as CRTH2 antagonists developed from in silico derived hits. Part 2
Grimstrup, M., Rist, Ø., Receveur, J., Frimurer, Thomas Michael, Ulven, Trond, Mathiesen, Jesper M., Kostenis, E. & Högberg, T., 1 Feb 2010, In: Bioorganic & Medicinal Chemistry Letters. 20, 3, p. 1181-1185 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Novel selective thiazoleacetic acids as CRTH2 antagonists developed from in silico derived hits. Part 1
Rist, O., Grimstrup, M., Receveur, J., Frimurer, Thomas Michael, Ulven, Trond, Kostenis, E. & Högberg, T., 4 Dec 2009, In: Bioorganic & Medicinal Chemistry Letters. 20, 3, p. 1177-1180 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 187375453
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278
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Discovery of a Potent Thiazolidine Free Fatty Acid Receptor 2 Agonist with Favorable Pharmacokinetic Properties
Research output: Contribution to journal › Journal article › Research › peer-review
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109
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Butyrate ameliorates allergic airway inflammation by limiting eosinophil trafficking and survival
Research output: Contribution to journal › Journal article › Research › peer-review
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109
downloads
Dihydropyridine Fluorophores Allow for Specific Detection of Human Antibodies in Serum
Research output: Contribution to journal › Journal article › Research › peer-review
Published