The cytotoxicities of 6,7-modified-5,8-quinoxalinedione derivatives and heterocyclic quinoxaline derivatives containing nitrogen, sulfur, and oxygen on human lung adenocarcinoma cell (PC 14), human gastric adenocarcinoma cell (MKN 45), and human colon adenocarcinoma cell (colon 205) were examined in vitro using MTT assay. Pyrido[1,2-a]imidazo[4,5-g]quinoxaline-6,11-dione (10) was markedly cytotoxic against MKN 45 compared with adriamycin and cis- platin used as anticancer drugs. The IC50 value of compound 10 was 0.073 μM while those of adriamycin and cis-platin were 0.12 μM and 2.67 μM, respectively.
|Number of pages||3|
|Journal||Archiv der Pharmazie|
|State||Published - Oct 1998|
- Heterocyclic quinoxaline derivatives
- Human gastric adenocarcinoma cell line