摘要:
The present invention relates to novel compounds and methods that are useful in treating members of the Flaviviridae family of virtases. Compounds of the present invention will have a structure according to Formulas (I) - (VI) as recited throughout the application.
摘要:
The present invention relates to novel compounds and methods that are useful in treating members of the Flaviviridae family of virtases. Compounds of the present invention will have a structure according to Formulas (I) - (VI) as recited throughout the application.
摘要:
Dicationic compounds that are highly selective for binding G-quadruplex DNA are described. Several compounds exhibit groove binding toward G-quadruplex DNA and in vitro and in vivo activity versus Trypanosoma brucei rhodesiense. The compounds represent novel drugs for the treatment of cancer, malaria, leishmania, and trypanosomiasis.
摘要:
Dicationic compounds that are highly selective for binding G-quadruplex DNA are described. Several compounds exhibit groove binding toward G-quadruplex DNA and in vitro and in vivo activity versus Trypanosoma brucei rhodesiense. The compounds represent novel drugs for the treatment of cancer, malaria, leishmania, and trypanosomiasis.