11H-Pyrido[3',2':4,5]pyrrolo[2,3-g]isoquinoléines (aza-7 ellipticines) substituées sur leur position 6 |
| |
Authors: | C Rivalle C Ducrocq J-M Lhoste F Wendling E Bisagni J-C Chermann |
| |
Institution: | Institut Curie, Section de Biologie, Bâtiments 110-112, 15 rue Georges Clémenceau, 91405 Orsay, France;Unité d''Oncologie Virale, Institut Pasteur, 28 rue du Dr Roux, 75024 Paris Cedex 15, France |
| |
Abstract: | 6-Dialkylaminoalkylamino substituted 11H-pyrido3',2':4,5]pyrrolo2,3-g]isoquinolines (7-aza ellipti-cines) were obtained by a six step synthesis starting from 2-chloro-3-nitro pyridine and 6-amino-5-methyl (and 5,8-dimethyl) isoquinoline-1-2H-ones already described. A brief survey of biological results shows that derivatives of this new heterocyclic ring system are less interesting than their 5H-pyrido(3',4':4,5]pyrrolo2,3-g]isoquinolines (9-aza ellipticines) and pyrido4,3-b]carbazoles (ellipticines) analogues. |
| |
Keywords: | |
本文献已被 ScienceDirect 等数据库收录! |
|