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Results: 1-3 |
Results: 3
Highly selective glycosylated prodrugs of cytostatic CC-1065 analogues forantibody-directed enzyme tumor therapy
Authors: Tietze, LF Herzig, T Fecher, A Haunert, F Schuberth, I
Citation: Lf. Tietze et al., Highly selective glycosylated prodrugs of cytostatic CC-1065 analogues forantibody-directed enzyme tumor therapy, CHEMBIOCHEM, 2(10), 2001, pp. 758-765
Regioselective reduction and ring cleavage of polycyclic barbituric acid analogues derived from intramolecular hetero-Diels-Alder reactions
Authors: Tietze, LF Ott, C Geissler, H Haunert, F
Citation: Lf. Tietze et al., Regioselective reduction and ring cleavage of polycyclic barbituric acid analogues derived from intramolecular hetero-Diels-Alder reactions, EUR J ORG C, (9), 2001, pp. 1625-1630
A strategy for tumor-selective chemotherapy by enzymatic liberation of seco-duocarmycin SA-derivatives from nontoxic prodrugs
Authors: Tietze, LF Lieb, M Herzig, T Haunert, F Schuberth, I
Citation: Lf. Tietze et al., A strategy for tumor-selective chemotherapy by enzymatic liberation of seco-duocarmycin SA-derivatives from nontoxic prodrugs, BIO MED CH, 9(7), 2001, pp. 1929-1939
Risultati: 1-3 |