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hypersensitivity/turse

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Leht 1 alates 18 tulemused

Method for preventing or treating an allergic disease using extract from illicium verum

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BACKGROUND OF THE INVENTION Field of the Invention The present invention relates to a method for preventing or treating an allergic disease using an extract from Illicium verum. Description of the Related Art Allergies are known as sensitive reaction which is caused by immune dysfunction innately or

Triazine derivatives to treat pain, fever, inflammation, allergies and thrombosis

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N-nicotinoylhalogenobenzoguanamines are known in the art to exhibit strong anti-inflammatory action (see Japanese patent application No. 56-87124). It has now been discovered that triazine derivatives of the formula (I): ##STR2## and pharmaceutically acceptable salts thereof wherein R.sup.1 and

1,3-diaryl cyclopentanes and derivatives thereof as PAF antagonists

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BACKGROUND OF THE INVENTION Platelet-activating factor (PAF) has recently been identified as an acetyl glyceryl ether phosphorylcholine (AGEPC), i.e., 1-O-hexadecyl/octadecyl-2-acetyl-sn-glyceryl-3-phosphorylcholine (Hanahan D. J. et al., J. Biol. Chem. 255:5514, 1980). Even before its chemical

1,3-diaryl cyclopentanes and derivatives thereof as PAF antagonists

Ainult registreeritud kasutajad saavad artikleid tõlkida
Logi sisse
BACKGROUND OF THE INVENTION Platelet-activating factor (PAF) has recently been identified as an acetyl glyceryl ether phosphorylcholine (AGEPC), i.e., 1-0-hexadecyl/octadecyl-2-acetyl-sn-glyceryl-3-phosphorycholine (Hanahan D. J., et al., J. Biol. Chem. 255:5514, 1980). Even before its chemical

Indolylmaleimide derivatives

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The present invention relates to indolylmaleimide derivatives, process for their production and pharmaceutical compositions containing them. More particularly the present invention provides a compound of formula I ##STR00002## wherein R.sub.a is H; CH.sub.3; CH.sub.2--CH.sub.3; or isopropyl, R.sub.b

Indolylmaleimide derivatives

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The present invention relates to indolylmaleimide derivatives, process for their production and pharmaceutical compositions containing them. More particularly the present invention provides a compound of formula I ##STR00002## wherein R.sub.a is H; CH.sub.3; CH.sub.2--CH.sub.3; or isopropyl, R.sub.b

Indolylmaleimide derivatives

Ainult registreeritud kasutajad saavad artikleid tõlkida
Logi sisse
The present invention relates to indolylmaleimide derivatives, process for their production and pharmaceutical compositions containing them. More particularly the present invention provides a compound of formula I ##STR00002## wherein R.sub.a is H; CH.sub.3; CH.sub.2--CH.sub.3; or isopropyl, R.sub.b

Therapeutic treatment for skin disorders

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BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention is broadly directed to a method of inhibiting or decreasing vascular permeability associated with dermal edema, e.g., induration, and especially the increased vascular permeability induced by vascular permeability factor
FIELD OF THE INVENTION The invention relates to the use of biologically active glutarimide derivatives or pharmaceutically acceptable salts thereof as agents for the treatment of eosinophilic diseases. BACKGROUND Eosinophils are cells of the innate immunity. They are produced in the bone marrow and

Phospholipid analogs useful as PAF synthesis inhibitors

Ainult registreeritud kasutajad saavad artikleid tõlkida
Logi sisse
BACKGROUND OF THE INVENTION Platelet-activating factor (PAF) has been identified as an acetyl glyceryl ether phosphorylcholine (AGEPC), i.e., 1-O-hexadecyl/octadecyl-2-O-acetyl-sn-glycerol-3-phosphorylcholine [Hanahan, D. S. et al., J. Biol. Chem., 255:5514, (1980)]. Even before its chemical

Ionic aqueous polysaccharide compositions

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BACKGROUND OF THE INVENTION Sinonasal complaints affect at least 15% of the population in the United States of America with predictable patient morbidity and financial impact. Importantly, any modality that can alleviate sinonasal complaints warrants serious attention. Among various treatments

Nitrosated and nitrosylated phosphodiesterase inhibitors, compositions and methods of use

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This application is related to, not a continuing case to U.S. Pat. Nos. 6,172,060, 6,197,778, 6,177,428, 6,172,068, 6,221,881, 6,232,321, 6,197,782, 6,133,272, and 6,211,179. FIELD OF THE INVENTION The present invention describes novel nitrosated and/or nitrosylated phosphodiesterase inhibitors, and

Nitrosated and nitrosylated phosphodiesterase inhibitors, compositions and methods of use

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FIELD OF THE INVENTION The present invention describes novel nitrosated and/or nitrosylated phosphodiesterase inhibitors, and novel compositions comprising at least one nitrosated and/or nitrosylated phosphodiesterase inhibitor, and, optionally, at least one compound that donates, transfers or

Nitrosated and nitrosylated phosphodiesterase inhibitors, compositions and methods of use

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FIELD OF THE INVENTION The present invention describes novel nitrosated and/or nitrosylated phosphodiesterase inhibitors, and novel compositions comprising at least one nitrosated and/or nitrosylated phosphodiesterase inhibitor, and, optionally, at least one compound that donates, transfers or

Substituted 2,3,3a,6-tetrahydro-6-oxobenzofuran derivative useful as PAF antagonist

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Logi sisse
BACKGROUND OF THE INVENTION Platelet-activating factor (PAF) has recently been identified as an acetyl glyceryl ether phosphorylcholine (AGEPC), i.e., 1-O-hexadecyl/octadecyl-2-O-acetyl-sn-glycero-3-phosphorylcholine (Hanahan, D. S. et al., J. Biol. Chem., 255: 5514, 1980). It is a potent lipid
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