An expeditious synthesis of cytotoxic pyrroloisoquinoline derivatives. Structure-activity comparative studies with isomeric pyrroloquinolines
MetadataShow full item record
A number of pyrroloisoquinolines have been prepared by reaction of 5-nitroisoquinoline with vinylmagnesium bromide followed by N-alkylation with the appropriate 2-chloro-N,N-dialkylethylamine. Their cytotoxicity was evaluated in a number of ovarian cell lines and compared to their analogous isomeric pyrroloquinolines. Two of the new compounds, 7c and 7d, are selective toward the A2780 cisplatin-resistant line. (C) 2002 Elsevier Science B.V. All rights reserved.
Version of record
License start date
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2002, 17 pp. 139 - 143
ELSEVIER SCIENCE BV