Cargando…
The Aza-Analogous Benzo[c]phenanthridine P8-D6 Acts as a Dual Topoisomerase I and II Poison, thus Exhibiting Potent Genotoxic Properties
The benzo[c]phenanthridine P8-D6 was recently found to suppress the catalytic activity of both human topoisomerase (Topo) I and II. Concomitantly, potent cytotoxic activity was observed in different human tumor cell lines, raising questions about the underlying mechanisms in vitro. In the present st...
Autores principales: | Aichinger, Georg, Lichtenberger, Falk-Bach, Steinhauer, Tamara N., Flörkemeier, Inken, Del Favero, Giorgia, Clement, Bernd, Marko, Doris |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7180443/ https://www.ncbi.nlm.nih.gov/pubmed/32230817 http://dx.doi.org/10.3390/molecules25071524 |
Ejemplares similares
-
QSAR Modeling on Benzo[c]phenanthridine Analogues as Topoisomerase I Inhibitors and Anti-cancer Agents
por: Thai, Khac-Minh, et al.
Publicado: (2012) -
“Golden” Cascade Cyclization to Benzo[c]‐Phenanthridines
por: Hendrich, Christoph M., et al.
Publicado: (2021) -
Synthesis, Bacteriostatic and Anticancer Activity of Novel Phenanthridines Structurally Similar to Benzo[c]phenanthridine Alkaloids
por: Lasák, Pavel, et al.
Publicado: (2018) -
Newly developed dual topoisomerase inhibitor P8-D6 is highly active
in ovarian cancer
por: Flörkemeier, Inken, et al.
Publicado: (2021) -
Oxidative Photocyclization of Aromatic Schiff Bases in Synthesis of Phenanthridines and Other Aza-PAHs †
por: Kos, Martin, et al.
Publicado: (2020)