Number of items: 4.
2007
Mahboobi, Siavosh,
Uecker, A.,
Cénac, C.,
Sellmer, A.,
Eichhorn, E.,
Elz, Sigurd,
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.
Fulltext not available.
2006
Mahboobi, Siavosh,
Uecker, A.,
Sellmer, A.,
Cénac, C.,
Höcher, H.,
Pongratz, H.,
Hufsky, H.,
Trümpler, A.,
Sicker, M.,
Heidel, F.,
Fischer, T.,
Stocking, C.,
Elz, Sigurd,
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.
Fulltext not available.
2003
Böhmer, F. D.,
Karagyozov, L.,
Uecker, A.,
Serve, H.,
Botzki, A.,
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.
Fulltext not available.
2002
Mahboobi, Siavosh,
Teller, S.,
Pongratz, H.,
Hufsky, H.,
Sellmer, A.,
Botzki, Alexander,
Uecker, A.,
Beckers, T.,
Baasner, S.,
Schächtele, C.,
Überall, F.,
Kassack, M. U.,
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.
Fulltext not available.
This list was generated on Fri Oct 11 21:57:14 2024 CEST.