Department of Pharmaceutical Microbiology

Division Integrated Medical and Pharmaceutical Sciences
Great Department Medicinal Chemistry
Website http://www.pharm.kumamoto-u.ac.jp/Labs/bisei/bisei.html
Staff
Professor Tohru Mizushima
mizu@gpo.kumamoto-u.ac.jp
Associate professor Keitaro Suzuki
keitarou@gpo.kumamoto-u.ac.jp
Instructress Kazumi Yokomizo
yokomizo@gpo.kumamoto-u.ac.jp
Research theme


[Full size image]

Structure of fattiviracins FV-8
We are searching for new potent drugs such as antiviral antibiotics, antitumor drugs and other biologically-active substances produced by microorganisms, especially actinomycetes, and studying on their purifications, structure elucidations, biosynthesis pathways and action mechanisms. Among them, fattiviracins found as antiviral agents are novel compounds effective for herpes simplex virus type 1, varicella-zoster virus, human immunodeficiency virus and influenza virus. Fattiviracins will be in clinical use for the treatment of viral diseases.
Topoisomerases are known to be the target enzymes of antitumor drugs, since topoisomerases are critical nuclear enzymes which regulate the three dimensional structures of DNA. We have found 5 kinds of topo inhibitors (antitumor drugs) having novel structures from the cultures of microorganisms. Among them, topostatin and isoaurostatin are the antitumor drugs of new type which do not give DNA damage unlike the conventional antitumor drugs. Now, we have tried to find more effective antitumor drugs by carrying out syntheses of the structure analogues of isoaurostatin.