Cargando…
Synthesis and Biological Evaluation of a Novel Pentagastrin-Toxin Conjugate Designed for a Targeted Prodrug Mono-therapy of Cancer
A novel carbamate prodrug 2 containing a pentagastrin moiety was synthesized. 2 was designed as a detoxified analogue of the highly cytotoxic natural antibiotic duocarmycin SA (1) for the use in a targeted prodrug monotherapy of cancers expressing cholecystokinin (CCK-B)/gastrin receptors. The synth...
Autores principales: | Tietze, Lutz F., Panknin, Olaf, Krewer, Birgit, Major, Felix, Schuberth, Ingrid |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2635707/ https://www.ncbi.nlm.nih.gov/pubmed/19325786 http://dx.doi.org/10.3390/ijms9050821 |
Ejemplares similares
-
Determination of the Biological Activity and Structure Activity Relationships of Drugs Based on the Highly Cytotoxic Duocarmycins and CC-1065
por: Tietze, Lutz F., et al.
Publicado: (2009) -
Histamine dependence of pentagastrin-stimulated gastric acid secretion in rats.
por: Shankley, N. P., et al.
Publicado: (1992) -
TSPO Ligand-Methotrexate Prodrug Conjugates: Design, Synthesis, and Biological Evaluation
por: Laquintana, Valentino, et al.
Publicado: (2016) -
Synthesis and Biological Evaluation of Liguzinediol Mono- and Dual Ester Prodrugs as Promising Inotropic Agents
por: Zhang, Jing, et al.
Publicado: (2014) -
Investigation of the transformations of a novel anti-cancer agent combining HPLC, HPLC–MS and direct ESI–HRMS analyses
por: Tietze, Lutz F., et al.
Publicado: (2009)