Kissau, L., P. Stahl, R. Mazitschek, A. Giannis and H. Waldmann: Development of natural product-derived receptor tyrosine kinase inhibitors based on conservation of protein domain fold. In: Journal of Medicinal Chemistry 46, 14, 2917-2931, Seq. No.: 1 (2003).
url: http://dx.doi.org/10.1021/jm0307943
Stieber, F., U. Grether, R. Mazitschek, N. Soric, A. Giannis and H. Waldmann: Multistep solid-phase synthesis of an antibiotic and receptor tyrosine kinase inhibitors using the traceless phenylhydrazide linker. In: Chemistry-A European Journal 9, 14, 3282-3291, Seq. No.: 1 (2003).
url: http://dx.doi.org/10.1002/chem.200304821
Stieber, F., R. Mazitschek, N. Soric, A. Giannis and H. Waldmann: Traceless solid-phase synthesis of 2-aminothiazoles: Receptor tyrosine kinase inhibitors with dual selectivity for tie-2 and VEGFR-2. In: Angewandte Chemie - International Edition 41, 24, 4757-4761, Seq. No.: 1 (2002).
url: http://dx.doi.org/10.1002/anie.200290040
Stieber, F., R. Mazitschek, N. Soric, A. Giannis and H. Waldmann: Festphasensynthese von 2-Aminothiazolen unter Verwendung des spurlosen Hydrazid-Ankers: Rezeptortyrosinkinase-Inhibitoren mit dualer Selektivität für Tie-2 und VEGFR-2. In: Angewandte Chemie 114, 24, 4951-4955, Seq. No.: 1 (2002).
url: http://dx.doi.org/10.1002/ange.200290039
Stahl, P., L. Kissau, R. Mazitschek, A. Giannis and H. Waldmann: Natural product derived receptor tyrosine kinase inhibitors: Identification of IGF1R, Tie-2, and VEGFR-3 inhibitors. In: Angewandte Chemie - International Edition 41, 7, 1174-1178, Seq. No.: 1 (2002).
url: http://dx.doi.org/10.1002/1521-3773(20020402)41:7<1174::AID-ANIE1174>3.0.CO;2-V
Stahl, P., L. Kissau, R. Mazitschek, A. Giannis and H. Waldmann: Naturstoffanaloga als Tyrosinkinaseinhibitoren: Identifikation von IGF1R-, Tie-2- und VEGFR-3-Inhibitoren. In: Angewandte Chemie 114, 7, 1222-1226, Seq. No.: 1 (2002).
url: http://dx.doi.org/10.1002/1521-3757(20020402)114:7<1222::AID-ANGE1222>3.0.CO;2-R
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