Method for administering ethanolamine derivatives to livestock

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Radical -xh acid – or anhydride – acid halide or salt thereof...

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514533, 514539, 514562, 514563, 514564, 514565, 514597, 514608, 514629, 514630, 514651, 514620, 514653, A61K 31195, A61K 31235, A61K 31195, A61K 3116

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active

048808342

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BRIEF SUMMARY
The present invention relates to the use of certain ethanolamine derivatives in a method for increasing weight gain and/or improving the feed utilisation efficiency and/or increasing the lean body mass and/or decreasing birth mortality rate and increasing post-natal survival rate; of livestock and the veterinary formulations comprising such compounds.
European Published Patent Application No. 0,006,735 discloses compounds of general formula (I): ##STR1## or a pharmaceutically acceptable salt thereof wherein R.sup.1 is a hydrogen, fluorine or chlorine atom or a hydroxyl, hydroxymethyl, methyl, methoxyl, amino, formamido, acetamido, methylsulphonylamido, nitro, benzyloxy, methylsulphonylmethyl, ureido, trifluoromethyl or p-methoxybenzylamino group; R.sup.2 is a hydrogen, fluorine or chlorine atom or a hydroxyl group; R.sup.3 is a hydrogen or chlorine atom or a hydroxyl group; R.sup.4 is a carboxylic acid group or a salt, ester or amide thereof; R.sup.5 is a hydrogen, chlorine or fluorine atom or a methyl, methoxyl or hydroxyl group or a carboxylic acid group or a salt, ester or amide thereof; R.sup.6 is a hydrogen atom or a methyl, ethyl or propyl group; R.sup.7 is a hydrogen atom or a methyl, ethyl or propyl group; X is an oxygen atom or a bond; and Y is an alkylene group of up to 6 carbon atoms or a bond; which compounds show anti-obesity and/or anti-hyperglycaemic activity.
European Patent Specification No. 0,023,385 discloses compounds of a general formula (II): ##STR2## or a pharmaceutically acceptable salt, ester or amide thereof wherein R.sup.1A is a hydrogen, fluorine or chlorine atom or a hydroxyl, hydroxymethyl, methyl, methoxyl, amino, formamido, acetamido, methylsulphonylamido, nitro, benzyloxy, methylsulphonylmethyl, ureido, trifluoromethyl or p-methoxybenzylamino group; R.sup.2A is a hydrogen, fluorine or chlorine atom or a hydroxyl group; R.sup.3A is a hydrogen or chlorine atom or a hydroxyl group; or R.sup.1A, R.sup.2A, and R.sup.3A each represents a bromine atom; R.sup.4A is a hydrogen atom or a methyl group; R.sup.5A is a hydrogen atom or a methyl group; R.sup.6A is a hydrogen, fluorine or chlorine atom or a methyl, methoxyl or hydroxy group; X.sup.1 is an oxygen atom or a bond; Y.sup.1 is an alkylene group of up to 6 carbon atoms or a bond; and Z is an alkylene, alkenylene or alkynylene group of up to 10 carbon atoms; which compounds show anti-obesity and/or anti-hyperglycaemic activity.
European patent specification No. 0,028,105 discloses a particular group of compounds, falling within formula (I), of formula (III): ##STR3## and esters, amides and pharmaceutically acceptable salts thereof wherein A.sup.1 is a hydrogen atom or a methyl group and A.sup.2 is a hydrogen atom or a methyl group and a is 1,2 or 3.
The compounds of formula (III) are described as having good anti-obesity and anti-glycaemic properties coupled with low side effects.
European patent specification No. 0,040,915 also discloses a particular group of compounds, falling within formula (I), of formula (IV) ##STR4## or a pharmaceutically acceptable salt, lower alkyl or aralkyl ester or amide thereof, wherein R.sup.1B and R.sup.2B which may be the same of different, are each a hydrogen atom or a methyl group, b is 1,2 or 3, and Z.sup.1 is a C.sub.1-6 alkyl or C.sub.1-6 alkoxy group, or a halogen or hydrogen atom.
The compounds of formula (IV) are described as having anti-obesity and/or hypoglycaemic activity coupled with low cardiac stimulant activity. Particular compounds of formula (IV) also have anti-inflammatory activity.
European patent specification No. 0,040,000 discloses compounds of formula (V): ##STR5## or a pharmaceutically acceptable salt thereof, in which X.sup.2 is an oxygen atom or a bond, R.sup.1C is a hydrogen, fluorine, chlorine or bromine atom or a trifluoromethyl or C.sub.1-4 alkyl group, each of R.sup.2C and R.sup.3C is a hydrogen atom or a C.sub.1-4 alkyl group, R.sup.4C is a C.sub.1-4 alkyl group, R.sup.5C is a hydrogen atom or a C.sub.1-4 alkyl group and c is an integer of from 1 to 3.
The compounds

REFERENCES:
patent: 4146638 (1979-03-01), Renth et al.
patent: 4404222 (1983-09-01), Baker
patent: 4654371 (1987-03-01), Ainsworth et al.
Blodinger-Formulation of Veterinary Dosage Forms, 1983, Marcel Deckker, Inc, New York and Basel, pp. 176-189.
The Merck Veterinary Manual, Fifth Edition, Merck & Co. Inc., Rahway, N.J., U.S.A., 1979, pp. 201, 202, 524 & 525.
Chemical Abstracts, vol. 94, 1981, 15371m.

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