| Literature DB >> 20570510 |
Julien Debray1, Walid Zeghida, Brigitte Baldeyrou, Christine Mahieu, Amélie Lansiaux, Martine Demeunynck.
Abstract
Two new heterocycles, pyrimido[4,5-c]carbazole and pyrimido[5,4-b]indole, were prepared in three steps from 3-aminocarbazole and 3-aminoindole, respectively. The key Friedel-Crafts intramolecular cyclization was realized under microwave irradiation using montmorillonite K-10 clay as a catalyst. The pyrimido[4,5-c]carbazole derivative shows significant micromolar IC(50) against cancer cell lines. Unlike similar carbazole and indolocarbazole compounds, the molecule does not interfere with topoisomerase activity. 2010 Elsevier Ltd. All rights reserved.Entities:
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Year: 2010 PMID: 20570510 DOI: 10.1016/j.bmcl.2010.05.028
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823