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anxiolytic/възпаление
Линкът е запазен в клипборда
15 резултата
Compositions comprising a cannabinoid and spilanthol
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FIELD OF THE INVENTION
The present invention, in some embodiments thereof, relates to fixed dose combination (FDC) compositions, more particularly, but not exclusively, to compositions comprising at least one cannabinoid as a plant isolate or synthetic, in essentially pure form or as a component of
Compositions comprising a cannabinoid and spilanthol
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FIELD OF THE INVENTION
The present invention, in some embodiments thereof, relates to fixed dose combination (FDC) compositions, more particularly, but not exclusively, to compositions comprising at least one cannabinoid as a plant isolate or synthetic, in essentially pure form or as a component of
Method of inducing a histamine agonist action on H.sub.2 receptors
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This invention relates to the therapeutic use of histamine derivatives, a new histamine derivative and the use of these derivatives for the preparation of drugs.
S-[2-(4(5)-imidazolyl)-ethyl] isothiourea (Compound I) has already been described in British Patent GB-A-1,296,544, in which it is
Diphenethylamine derivatives which are inter alia useful as analgesics and method for their production
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FIELD OF THE INVENTION
The present invention relates to diphenethylamine derivatives which can be used as highly active analgesics, diuretics, anxiolytics, for the treatment of neurodegenerative, psychiatric and neuropsychiatric disorders, and also as anti-itch, anti-addiction, anti-inflammatory,
Mixed inhibitors of aminopeptidase N and neprilysin
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CROSS-REFERENCE TO RELATED APPLICATIONS
This application is a National Phase Entry of International Application No. PCT/EP2013/072203, filed on Oct. 23, 2013, which claims priority to French Patent Application Serial No. 1260097, filed on Oct. 23, 2012, both of which are incorporated by reference
Antiinflammatory compositions and methods
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BACKGROUND OF THE INVENTION
The present invention is concerned with an improved antiinflammatory composition and method of treating inflammation which employs antiinflammatory piroxicam, or a pharmaceutically acceptable salt thereof (particularly the ethanolamine salt) in combination with analgesic
Antiinflammatory compositions and methods
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BACKGROUND OF THE INVENTION
The present invention is concerned with an improved antiinflammatory composition and method of treating inflammation which employs antiinflammatory piroxicam, or a pharmaceutically acceptable salt thereof (particularly the ethanolamine salt) in combination with analgesic
Antinflammatory compositions and methods
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BACKGROUND OF THE INVENTION
The present invention is concerned with an improved antiinflammatory composition and method of treating inflammation which employs antiinflammatory piroxicam, or a pharmaceutically acceptable salt thereof (particularly the ethanolamine salt) in combination with analgesic
Substituted alkyltetraamine derivatives
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FIELD OF THE INVENTION
The present invention relates to substituted alkyltetraamine derivatives which are useful as a tachykinin antagonist.
BACKGROUND OF THE INVENTION
Tachykinin is a general term for a group of peptides having similar structures. Substance P (SP), neurokinin A (NKA) and neurokinin
Therapeutically useful sulphur-containing benzylidene derivatives
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The present invention relates to new therapeutically useful sulphur-containing benzylidene derivatives, to a process for their preparation and their application in therapy such as pharmaceutical compositions containing them.
The sulphur-containing benzylidene derivatives of the present invention are
Antibodies that bind stresscopin peptides
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INTRODUCTION
Mammals respond to stress through interlinked endocrine, neuroendocrine, autonomic and behavioral pathways. Activation of the autonomic nervous system elicits the release of catecholamines, whereas hypothalamic secretion of corticotropin releasing hormone (CRH) leads to pituitary
Stresscopins and their uses
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INTRODUCTION
Mammals respond to stress through interlinked endocrine, neuroendocrine, autonomic and behavioral pathways. Activation of the autonomic nervous system elicits the release of catecholamines, whereas hypothalamic secretion of corticotropin releasing hormone (CRH) leads to pituitary
Stresscopins and their uses
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Mammals respond to stress through interlinked endocrine, neuroendocrine, autonomic and behavioral pathways. Activation of the autonomic nervous system elicits the release of catecholamines, whereas hypothalamic secretion of corticotropin releasing hormone (CRH) leads to pituitary secretion of
Halide-free glucosamine-acidic drug complexes
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FIELD OF THE INVENTION
The invention relates to halide-free glucosamine complexes of acidic drugs and to methods for preparing such complexes.
BACKGROUND OF THE INVENTION
Glucosamine is a well-known amino monosaccharide found in chitin. glycoproteins and glycosaminoglycans. Glucosamine is widely
Method for treating warm-blooded vertebrates with halide-free glucosamine-acidic drug complexes
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FIELD OF THE INVENTION
The invention relates to a method for treating warm-blooded vertebrates, i.e., human beings and lower animals, with complexes of halide-free glucosamine and acidic drugs.
BACKGROUND OF THE INVENTION
Glucosamine is a well-known amino monosaccharide found in chitin,
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