The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Sep. 20, 2011

Filed:

Dec. 08, 2006
Applicants:

Vickie Brown-driver, San Diego, CA (US);

Kedar Gc, San Diego, CA (US);

John M. Finn, Encinitas, CA (US);

Robert Haselbeck, San Diego, CA (US);

Mark Hilgers, San Diego, CA (US);

Karen Shaw, Poway, CA (US);

Mark Stidham, San Diego, CA (US);

Inventors:

Vickie Brown-Driver, San Diego, CA (US);

Kedar GC, San Diego, CA (US);

John M. Finn, Encinitas, CA (US);

Robert Haselbeck, San Diego, CA (US);

Mark Hilgers, San Diego, CA (US);

Karen Shaw, Poway, CA (US);

Mark Stidham, San Diego, CA (US);

Assignee:

Trius Therapeutics, Inc., San Diego, CA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61K 31/00 (2006.01); A61K 31/43 (2006.01); A61K 39/00 (2006.01);
U.S. Cl.
CPC ...
Abstract

The present invention provides a pharmaceutical composition useful for treating bacterial infections in humans and animals which comprises administering to a human or animal in need thereof, an antibacterially effective combination of a β-lactam antibiotic and an inhibitor of any bacterial peptidoglycan biosynthesis enzyme, especially GlmU, GlmU, MurA, MurB, MurC, MurD, MurE, MurF, MurG, MraY, and UppS. Further provided is a method of discovering synergists for antibiotics including: a) expressing in a cell an antisense nucleic acid against a nucleic acid encoding a gene product so as to reduce the activity or amount of the gene product in the cell, thereby producing a cell sensitized to an antibiotic; b) characterizing the sensitization of the cell to the antibiotic and selecting pairs of antibiotics and genes that result in antibiotic efficacy at one-fifth or less the concentration required in the absence of the antisense gene; c) screening for chemical compounds that inhibit the gene product corresponding to the selected synergistic gene; and d) selecting or creating chemical analogs that inhibit the gene product corresponding to the selected synergistic gene such that the inhibition occurs in the bacteria.


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