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Nicotine addiction treatment
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FIELD OF THE INVENTION
The present invention relates to pharmaceutical compositions and methods of using these compositions to treat patients for tobacco addiction and nicotine addiction, to palliate the effects of nicotine withdrawal and to enhance the outcomes of other smoking cessation therapies.
Plantago majorand piper methysticum compound for use in treating a tobacco or nicotine habit
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BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates generally to an aid for use in treating a tobacco or nicotine habit. More particularly, the present invention relates to a composition containing as an active ingredient the herbs Plantago major and Piper methysticum
Plantago major and Piper methysticum compound for use in treating a tobacco or nicotine habit
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BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates generally to an aid for use in treating a tobacco or nicotine habit. More particularly, the present invention relates to a composition containing as an active ingredient the herbs Plantago major and Piper methysticum
Use of Echinacea or preparations thereof in compositions for the treatment of anxiety
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This is the National Stage of International Application PCT/HU2007/000052, filed Jun. 13, 2007.
The present invention relates to the use of Echinacea and preparations made thereof for the treatment of anxiety and to the use of them for the manufacture of the corresponding pharmaceutical
Indole derivatives for the treatment of depression and anxiety
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Pharmaceutical researchers have discovered that the neurons of the brain which contain monoamines are of extreme importance in a great many physiological processes which very strongly affect many psychological and personality-affecting processes as well. In particular, serotonin
Point mutant mice with hypersensitive alpha 4 nicotinic receptors: dopaminergic pathology and increased anxiety
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FIELD OF INVENTION
The invention relates generally to animal model systems useful for examining and manipulating neurobehaviors mediated by nicotine. More specifically, the invention relates to knock-in mice having a leucine-to-serine mutation of the .alpha.4 nicotinic receptor subunit gene
Nicotine derivatives that enhance cognitive function
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TECHNICAL FIELD
This invention relates to nicotine derivatives and pharmaceutical compositions thereof which are cholinergic agonists selective for neuronal nicotinic receptors, to methods for preparing these compounds, to synthetic intermediates employed in these processes and to a method of
Anxiolytic-n-(1-azabicyclo(2.2.2)oct-3-yl) benzamides and thiobenzamides
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The present invention relates to the use of certain N-(3-quinuclidinyl)benzamides and thiobenzamides, namely N-(3-quinuclidinyl)-benzamides and thiobenzamides, otherwise known as N-(1-azabicyclo[2.2.2]oct-3-yl)benzamides and thiobenzamides, which have been observed to exhibit anxiolytic
4-hydroxy-4-methyl-piperidine-1-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-amide
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FIELD OF THE INVENTION
The present invention relates to 4-hydroxy-4-methyl-piperidine-1-carboxylic acid(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-amide, which is a compound of formula
##STR00002## and to pharmaceutically acceptable acid addition salts thereof. This compound is generically
Sulfonamide derivatives as D3-receptor ligands
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FIELD OF THE INVENTION
The present invention relates to new D.sub.3 dopamine receptor subtype selective ligands of formula (I) and/or geometric isomers and/or stereoisomers and/or diastereomers and/or salts and/or hydrates and/or solvates thereof which are useful in the therapy and/or prevention of
Pyridone substituted benzothiazole derivatives
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BACKGROUND OF THE INVENTION
The present invention generally relates to pyridone substituted benzothiazole compounds that are adenosine receptor ligands. Specifically, the compounds of the present invention have a good affinity to the A.sub.2A -receptor and a high selectivity to the A.sub.1 - and
Benzathiazol-acetamides
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BACKGROUND OF THE INVENTION
Adenosine modulates a wide range of physiological functions by interacting with specific cell surface receptors. The potential of adenosine receptors as drug targets was first reviewed in 1982. Adenosine is related both structurally and metabolically to the bioactive
Aminoadamantane derivatives as therapeutic agents
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BACKGROUND OF THE INVENTION
Certain adamantane derivatives have been used to treat illnesses. Rimantadine (1-(1-aminoethyl)adamantane) is used for the prophylaxis and treatment of influenza in humans. Amantadine has been used for the treatment of both influenza and Parkinson's disease (Schwab et
Aminoadamantane derivatives as therapeutic agents
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BACKGROUND OF THE INVENTION
Certain adamantane derivatives have been used to treat illnesses. Rimantadine (1-(1-aminoethyl)adamantane) is used for the prophylaxis and treatment of influenza in humans. Amantadine has been used for the treatment of both influenza and Parkinson's disease (Schwab et
Aminoadamantane derivatives as therapeutic agents
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BACKGROUND OF THE INVENTION
Certain adamantane derivatives have been used to treat illnesses. Rimantadine (1-(1-aminoethyl)adamantane) is used for the prophylaxis and treatment of influenza in humans. Amantadine has been used for the treatment of both influenza and Parkinson's disease (Schwab et
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