Abstract
A new class of pyridobenzophenoxazine compounds has been developed as topoisomerase II inhibitors for anticancer chemotherapy. These compounds were designed based on a proposed model of a quinobenzoxazine self-assembly complex on DNA. They showed excellent inhibitory effects on several tumor cell lines with nanomolar IC50 values. Their cytotoxic potency correlates with theft ability to unwind DNA and inhibit topoisomerase II.
Original language | English (US) |
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Pages (from-to) | 4273-4278 |
Number of pages | 6 |
Journal | Journal of Medicinal Chemistry |
Volume | 41 |
Issue number | 22 |
DOIs | |
State | Published - Oct 23 1998 |
Externally published | Yes |
ASJC Scopus subject areas
- Molecular Medicine
- Drug Discovery