Home | Links | Contact Us | More About Intellectual Property | Bookmark
Search patents:
Home Vasodialators Bactericidal-formulations-for-use-in-veterinary-medicine

 Process for the production of sulfenamides
The embodiments of the invention in which an exclusive property or privilege is claimed are defined ...


 Intermediates for triazolobenzazepines
What is claimed: 1. A compound of the formula ##STR6## wherein X and Y are hydrogen or halogen. ...


 Therapeutic uses of the hypervariable region of monoclonal antibody M195 and constructs thereof
OF THE INVENTION The invention provides a polypeptide which consists essentially of an amino acid ...


 Xanthene and thioxanthene derivatives, compositions thereof and treatment therewith
We claim: 1. A compound selected from the group consisting of (1) a xanthene- and thioxanthene ...


 Sulfur and silicon-containing fatty acid amides
What is claimed is: 1. A compound of the formula: ##STR17## wherein each of R.sup.1, R.sup.2 and R....


 Process of making a synthetic resin product containing a molecular inclusion compound in cyclodextrin
Under these circumstances, the present invention provides a synthetic resin product containing a ...


 Aminoalkylethers; composition and method of use
I claim: 1. Pharmaceutical compositions for treatment of Parkinsonism which comprise as active ...


 Method of protecting useful plants and formulations for use in said method
What we claim is: 1. The method of combatting fungi infections of useful plants, or of preventing ...


 Pharmaceutical preparation for treating hemorrhoids and anal fissures
What I claim is: 1. A pharmaceutical preparation of treating hemorrhoids and anal fissures, ...


 Alkylated amine polymers
OF THE INVENTION Compositions Preferred reaction products include the products of one or more ...


 Bactericidal formulations for use in veterinary medicine

Details
Inventors: Metzger, Karl G.; Zeiler, Hans-Joachim; Scheer, Martin; Voege, Herbert; Grohe, Klaus;
Assignee: Bayer Aktiengesellschaft (Leverkusen, DE)
Primary Examiner: Waddell; Frederick E.
Assistant Examiner: Jordan; Kimberly R.
Attorney, Agent or Firm: Sprung, Horn Kramer & Woods

A method of treating livestock infected with, or protecting livestock against infection from, bacteria which comprises administering to such livestock an antibacterially effective amount of a quinolonecarboxylic acid or derivative of the formula ##STR1## in which A represents nitrogen or .dbd.C--R.sup.4, R.sup.4 represents hydrogen, fluorine, chlorine, nitro or methyl, B represents ##STR2## and B also represents ##STR3## when R.sup.1 does not denote cyclopropyl, and R.sup.5 represents hydrogen, a branched or unbranched alkyl group which has 1 to 4 carbon atoms and which can optionally be substituted by a hydroxyl or methoxy group, R.sup.6 represents hydrogen, methyl or phenyl, R.sup.7 represents hydrogen or methyl, R.sup.8 represents amino, alkyl- or dialkylamino having 1 or 2 carbon atoms in the alkyl group, aminomethyl, alkyl- or dialkylaminomethyl having 1 or 2 carbon atoms in the alkyl group, R.sup.1 represents an alkyl radical having 1 to 3 carbon atoms, cyclopropyl, 2-fluoroethyl vinyl, methoxy, 4-fluorophenyl or methylamino, R.sup.2 represents hydrogen, alkyl having 1 to 6 carbon atoms, and cyclohexyl, benzyl, 2-oxopropyl, phenacyl and ethoxycarbonylmethyl, R.sup.3 represents hydrogen, methyl or ethyl, Z represents oxygen, nitrogen which is substituted by methyl or phenyl, and .dbd.CH.sub.2 --, or a pharmaceutically utilizable salt thereof.

DETAILED DESCRIPTION We claim: 1.
A method of treating mycoplasmotic and bacterial infections in fowl which comprises administering drinking water to said fowl, said drinking water containing an antimycoplasmotically or antibacterially effective amount of a quinolonecarboxylic acid and/or derivative of a compound of the formula ##STR11## in which R.
sup.
2 represents hydrogen or C.
sub.
1-4 -alkyl and R.
sup.
5 represents hydrogen, methyl or ethyl.
2.
A method according to claim 1, wherein 10 to 500 mg/l of the compound is added to said drinking water for 1 to 20 days.
3.
A method according to claim 2, wherein 2.
5 to 100 mg/l of the compound is added to said drinking water.
4.
A method according to claim 2, wherein said compound is added to said drinking water for 3 to 10 days.
5.
A method according to claim 1, wherein said fowl are hens.
6.
A method according to claim 1, wherein said compound is 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7 (4-ethyl-1-piperazinyl) quinoline-3-carboxylic acid.




Description:
The present invention relates to bactericidal formulations which contain quinolonecarboxylic acids and their derivatives, for use in the area of veterinary medicine.
It has already been disclosed that quinolonecarboxylic acids and their derivatives have bactericidal properties (U.
S.
Ser.
No.
614,923, filed May 29, 1984, now pending, corresponding to DE OS 3,033,157).
However, nothing has been disclosed about their wide and universal applicability for livestock or about formulations which are especially suitable for applicability for livestock.
In animal medicine the treatment of infections caused by Escherichia coli, salmonellae or mycoplasmas present particular problems, especially when these causative organisms have meanwhile become resistant to known agents.
Bactericidal formulations for use in the area of veterinary medicine have been found, which formulations contain quinolonecarboxylic acids and their derivatives of the formulae I and Ia ##STR4## in which A represents nitrogen or



Related patents
  1-(5-Amino-4H-1,2,4-triazol-3-yl)-4-substituted-piperazines
OF THE INVENTION The novel compounds of the present invention are obtainable as crystalline materials having characteristic melting points and absorption spectra. They ...
  6-C.sub.1-4 Alkyl-7-phenyl or substituted phenyl-1,6-naphthyridine-5(6H)-ones
What is claimed is: 1. A compound of the formula ##STR19## or a pharmaceutically acceptable acid addition salt thereof, wherein R.sub.1 is C.sub.1-4 alkyl, R.sub.2 is ...
  Novel prostaglandins
OF THE INVENTION Also embraced within the scope of the present invention are the non-toxic, pharmaceutically acceptable salts of the novel compounds of the present ...
  Diolefin pheromone mimics as disruptants of sexual communication in insects
We claim: 1. Diolefin insect pheromone mimic (Z)-1,12-heptadecadiene: ##STR1## 2. Diolefin insect pheromone mimic (E)-15-methyl-1,9-heptadecadiene: ##STR2## 3. Diolefin ...
  Substituted phenylguanidines and method
What is claimed is: 1. A compound of the structure ##STR34## wherein R.sup.1 is lower alkyl, cycloalkylalkyl, or phenylalkyl; R.sup.2 is lower alkyl, phenyl or benzyl; ...
  Cephalosporin derivatives
We claim: 1. A cephalosporin derivative of the formula ##STR153## in which n is 0 or 1, (a) the symbol R.sub.1 represents a radical of the formula ##STR154## in the syn ...
  External preparations free of discoloration
What is claimed is: 1. A topical composition free of discoloration with the passage of time comprising at least 0.1 weight percent of kojic acid or a derivative thereof; ...
  Cell-permeable protein inhibitors of calpain
The invention features methods of inhibiting a calpain (e.g., .mu.-calpain and/or m-calpain) in a cell (e.g., a eukaryotic cell). The method can be carried out, for ...
  High molecular weight piperidine derivatives as UV stabilizers
I claim: 1. A compound of the formula ##STR3## wherein X is ##STR4## R being selected from alkyl of 1-6 carbon atoms; with R.sub.1 and R.sub.2 being independently ...
  N.sup.2 -naphthalenesulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof, and antithrombotic compositions and methods employing them
OF THE PREFERRED EMBODIMENTS This invention relates to a group of N.sup.2 -naphthalenesulfonyl-L-argininamides of the formula (I): ##STR2## wherein R.sub.1 is naphthyl, ...

0.004

Archive: All patents - Links

Copyright (c)2006 Eipa-patents.org - All rights reserved