Rifamycin imino derivatives effective against drug-resistant...

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Heterocyclic carbon compounds containing a hetero ring...

Reexamination Certificate

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Details

C514S253080, C514S312000, C540S456000

Reexamination Certificate

active

11034279

ABSTRACT:
The present invention relates to rifamycin 3-iminomethylenyl (—CH═N—) derivatives having antimicrobial activities, including activities against drug-resistant microorganisms. The claimed rifamycin derivative has a rifamycin moiety covalently linked to a linker through an iminomethylenyl (—CH═N—) group at the C-3 carbon of the rifamycin moiety and the linker is, in turn, covalently linked to a quinolone structure or its pharmacophore within the DNA gyrase and topoisomerase IV inhibitor family. The inventive rifamycins are novel and exhibit activity against both rifampin and ciprofloxacin-resistant microorganisms.

REFERENCES:
patent: 4681938 (1987-07-01), Traxler
patent: 5786350 (1998-07-01), Occelli et al.
patent: 562831 (1975-06-01), None
patent: WO 02/09758 (2002-02-01), None
patent: WO 03/045319 (2003-06-01), None
Brufani, M., et al; “Rifamycins: an Insight into Biological Activity Based on Structural Investigations”; J. Mol. Biol., 1974, vol. 87, pp. 409-435.
Mandell, Gerald L., et al.; “Rifamycins”; Principles and Practice of Infectious Diseases; pp. 348-361; Churchill Livingstone (2001).

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