- Klein, M. ; Dinér, P. ; Dorin-Semblat, D. ; Doerig, C. ; Grøtli, M. Synthesis of 3-(1,2,3-triazol-1-yl)- and 3-(1,2,3-triazol-4-yl)-substituted pyrazolo[3,4-d]pyrimidin-4-amines via click chemistry: potential inhibitors of the Plasmodium falciparum PfPK7 protein kinase. Org. Biomol. Chem. 2009, 7, 3421-3429
- Dyrager, C. ; Friberg, A. ; Dahlén, K. ; Fridén-Saxin, M. ; Börjesson, K. ; Wilhelmsson, L. M. ; Smedh, M. ; Grøtli, M. ; Luthman, K. 2,6,8-Trisubstituted 3-hydroxychromone derivatives as fluorophores for live-cell imaging.Chem. Eur.J. 2009, 15, 9417-9423
- Lehmann, F. ; Currier, E. A. ; Clemons, B. ; Hansen, L. K. ; Olsson, R. ; Hacksell, U. ; Luthman, K. Novel and potent small-molecule urotensin II receptor agonists. Bioorg. Med. Chem. 2009, 17, 4657-4665
- Flaten, G. E. ; Awoyemi, O. ; Luthman, K. ; Brandl, M. ; Massing, U. The Phospholipid Vesicle-Based Drug Permeability Assay: 5. Development Toward an Automated Procedure for High-Throughput Permeability Screening. Journal of the Association for Laboratory Automation. 2009, 14, 12-21
- Lehmann, F. ; Currier, E. A. ; Clemons, B. ; Hansen, L. K. ; Olsson, R. ; Hacksell, U. ; Luthman, K. Novel and potent small-molecule urotensin II receptor agonists. Bioorg. Med. Chem. 2009, 17, 4657-4665
- Andersson, H. ; Gustafsson, M. ; Bostrom, D. ; Olsson, R. ; Almqvist, F. The Regio- and Stereoselective Synthesis of trans-2,3-Dihydropyridine N-oxides and Piperidines. Angew. Chem. Int. Ed. 2009, 48, 3288-3291
- Berggren, K. ; Johansson, B. ; Fex, T. ; Kihlberg, J. ; Bjorck, L. ; Luthman, K. Synthesis and biological evaluation of reversible inhibitors of IdeS, a bacterial cysteine protease and virulence determinant.. Bioorg. Med. Chem. 2009, 17, 3463-3470
- Pettersson, H. ; Bulow, A. ; Ek, F. ; Jensen, J. ; Ottesen, L. K. ; Fejzic, A. ; Ma, J. ; Del Tredici, A. L. ; Currier, E. A. ; Gardell, L. R. ; Tabatabaei, A. ; Craig, D. ; McFarland, K. ; Ott, T. R. ; Piu, F. ; Burstein, E. S. ; Olsson, R. Synthesis and evaluation of dibenzothiazepines: a novel class of selective cannabinoid-1 receptor inverse agonists. J. Med. Chem. 2009, 52, 1975-1982
- Dinér, P.; Andersson, T.; Kjellén, J.;Elbing, K.; Hohmann, S; Grøtli, M. Short cut to 1,2,3-triazole-based p38 MAP kinase inhibitors via [3+2]-cycloaddition chemistry. New J. Chem. 2009, 33, 1010-1016
- Dyrager, C. ; Börjesson, K. ; Dinér, P. ; Elf, A. ; Albinsson, B. ; Wilhelmsson, L. M. ; Grotli, M. Synthesis and Photophysical Characterisation of Fluorescent 8-(1H-1,2,3-Triazol-4-yl)adenosine Derivatives. Eur. J. Org. Chem. 2009, 1515-1521
- Friden-Saxin, M. ; Pemberton, N. ; Andersson, K. d. S. ; Dyrager, C. ; Friberg, A. ; Grotli, M. ; Luthman, K. Synthesis of 2-alkyl-substituted chromone derivatives using microwave irradiation.J. Org. Chem. 2009, 74, 2755-2759
- Lund, B. W. ; Knapp, A. E. ; Piu, F. ; Gauthier, N. K. ; Begtrup, M. ; Hacksell, U. ; Olsson, R. Design, synthesis, and structure-activity analysis of isoform-selective retinoic acid receptor beta ligands. J. Med. Chem. 2009, 52, 1540-1545
- Malik, L. ; Kelly, N. M. ; Ma, J. ; Currier, E. A. ; Burstein, E. S. ; Olsson, R. Discovery of non-peptidergic MrgX1 and MrgX2 receptor agonists and exploration of an initial SAR using solid-phase synthesis.. Bioorg. Med. Chem. Lett. 2009, 19, 1729-1732
- Galanis, A. S. ; Albericio, F. ; Grotli, M. Enhanced microwave-assisted method for on-bead disulfide bond formation: synthesis of alpha-conotoxin MII. Biopolymers. 2009, 92, 23-34
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