| PDF (1MB) |
- URN zum Zitieren dieses Dokuments:
- urn:nbn:de:bvb:355-epub-156968
- DOI zum Zitieren dieses Dokuments:
- 10.5283/epub.15696
Zusammenfassung
Methoxysubstituted 5,6-dihydro-indolo[2,1-a]isoquinolines with a methyl (2b-f) or a formyl group at C-12 (4a-f) and 12,12-dimethylisoquinolinium salts (3b-f) were synthesized and tested for cytostatic activity in vitro. The tetramethoxy-indoloisoquinoline 4f was the most active derivative in the P 388 D1 leukemia cell line, whereas compounds with two methoxy groups (4a, 4b) were more potent ...
![plus plus](/style/images/plus.png)
Nur für Besitzer und Autoren: Kontrollseite des Eintrags