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Jump to: 2007 | 2006 | 2003 | 2002
Number of items: 4.

2007

Mahboobi, Siavosh and Uecker, A. and Cénac, C. and Sellmer, A. and Eichhorn, E. and Elz, Sigurd and Böhmer, F.-D. and Dove, Stefan (2007) Inhibition of FLT3 and PDGFR tyrosine kinase activity by bis(benzo[b]furan-2-yl)methanones. Bioorganic & medicinal chemistry 15 (5), pp. 2187-2197.

2006

Mahboobi, Siavosh and Uecker, A. and Sellmer, A. and Cénac, C. and Höcher, H. and Pongratz, H. and Hufsky, H. and Trümpler, A. and Sicker, M. and Heidel, F. and Fischer, T. and Stocking, C. and Elz, Sigurd and Böhmer, F.-D. and Dove, Stefan (2006) Novel bis-(1H-indol-2-yl)-methanones as potent inhibitors of FLT3 and platelet-derived growth factor receptor tyrosine kinase. Journal of Medicinal Chemistry 49 (11), pp. 3101-3115.

2003

Böhmer, F.D. and Karagyozov, L. and Uecker, A. and Serve, H. and Botzki, A. and Mahboobi, Siavosh and Dove, Stefan (2003) A single amino acid exchange inverts susceptibility of related receptor tyrosine kinases for the ATP-site inhibitor STI-571. The Journal of Biological Chemistry 278 (7), pp. 5148-5155.

2002

Mahboobi, Siavosh and Teller, S. and Pongratz, H. and Hufsky, H. and Sellmer, A. and Botzki, Alexander and Uecker, A. and Beckers, T. and Baasner, S. and Schächtele, C. and Überall, F. and Kassack, M. U. and Dove, Stefan and Böhmer, F.-D. (2002) Bis(1H-2-indolyl)methanones as a novel class of inhibitors of the platelet-derived growth factor receptor kinase. Journal of Medicinal Chemistry 45 (5), pp. 1002-1018.

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