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Optimized 7-Azaindenoisoquinoline Topoisomerase I Inhibitors Anticancer Agent


Summary

Purdue University researchers have developed a novel process for synthesizing four TOP1 inhibitors and have optimized their structures for the greatest inhibitory activity and cytoxicity towards dividing cells. The compounds consist of 7-, 8-, 9-, and 10-azaindenoisoquinoline structures.


Technology Benefits

TOP1 is a proven target for cancer therapyAzaindenoisoquinolines have enhanced chemical stability and effectiveness over other TOP1 inhibitors


Technology Application

New cancer therapy drugsPharmaceutical industry


Detailed Technology Description

Mark CushmanPurdue Medicinal Chemistry and Molecular Pharmacology


Countries

United States


Application No.

8686146


Country/Region

USA

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