Dihydroorotate dehydrogenase inhibitors for the treatment of...

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

Reexamination Certificate

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C546S165000, C546S170000, C546S178000

Reexamination Certificate

active

06841561

ABSTRACT:
Flavivirus, rhabdovirus and paramyxovirus infections may be treated by administering an inhibitor of the enzyme dihydroorotate dehydrogenase such as 6-fluoro-2-(2′-fluoro-1,1′-biphenyl-4-yl)-3-methyl-4-quinolinearcarboxylic acid sodium salt (Brequinar). A synergistic effect can be obtained if an interferon such as interferon α2, interferon α8 or interferon β, or an inhibitor of a second enzyme selected from inosine monophosphate dehydrogenase, guanosine monophosphate synthetase, cytidine triphosphate synthetase and S-adenosylhomocysteine hydrolase, is also administered.

REFERENCES:
patent: 4680299 (1987-07-01), Hesson
patent: 0 601 191 (1994-06-01), None
patent: 0 721 942 (1996-07-01), None
patent: WO 2000054003 (2000-08-01), None
patent: WO 2002053138 (2002-07-01), None
Nakazato Yoshisuke, “Tetracyclic Quinoline Derivative”, Patent Abstracts of Japan, vol. 1998, No. 14, Dec. 31, 1998.

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