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allyl/gyulladás

A hivatkozás a vágólapra kerül
Oldal 1 tól től 24 eredmények
BACKGROUND OF THE INVENTION Platelet-activating factor (PAF) has recently been identified as an acetyl glyceryl ether phosphorylcholine (AGEPC), i.e., 1O-hexadecyl/octadecyl-2-O-acetyl-sn-glyceryl-3-phosphorylcholine (Hanahan, D. S. et al., J. Biol. Chem., 255:5514, 1980). Even before its chemical
BACKGROUND OF THE INVENTION This invention relates to a new drug and a new technique for obtaining new curative effects from the drug. Almost every internal disease of man is due to internal inflammations or injuries. They result from physical, chemical or biological agents. The latter ones are by
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to 2-(N-substituted-aminoalkyl)-5-(E)-alkylidene cyclopentanones, 2-(N-substituted-aminoalkyl)-5-(E)-arylalkylidene cyclopentanones, and derivatives thereof and their use as anti-inflammatory, analgesic and

Naphthalenepropionic acid derivatives as anti-inflammatory/anti-allergic agents

Csak regisztrált felhasználók fordíthatnak cikkeket
Belépés Regisztrálás
This invention relates to novel naphthalenepropionic acid derivatives possessing lipoxygenase inhibitory and leukotriene antagonist activity, which are useful as anti-inflammatory, antiallergic and cytoprotective agents. It is known that arachidonic acid (AA) is metabolized in mammals by two

Quinoline substituted naphthalenepropionic acid derivatives as anti-inflammatory/antiallergic agents

Csak regisztrált felhasználók fordíthatnak cikkeket
Belépés Regisztrálás
This invention relates to novel naphthalenepropionic acid derivatives possessing lipoxygenase inhibitory and leukotriene antagonist activity, which are useful as anti-inflammatory, antiallergic and cytoprotective agents. It is known that arachidonic acid (AA) is metabolized in mammals by two

Naphthalenepropionic acid derivatives as anti-inflammatory/antiallergic agents

Csak regisztrált felhasználók fordíthatnak cikkeket
Belépés Regisztrálás
This invention relates to novel naphthalenepropionic acid derivatives possessing lipoxygenase inhibitory and leukotriene antagonist activity, which are useful as anti-inflammatory, antiallergic and cytoprotective agents. It is known that arachidonic acid (AA) is metabolized in mammals by two

Anti-inflammatory and anti-arthritic pyrazolo-[1,5-a]-1,3,5-triazine derivatives, compositions, and method of use therefor

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Belépés Regisztrálás
BACKGROUND OF THE INVENTION This invention relates to non-steroidal anti-inflammatory agents, such as are useful for the treatment of arthritis. SUMMARY OF THE INVENTION In general, the invention features in one aspect compounds having the general formula ##STR4## wherein X is an alkyl group (e.g.,

Medical use of esters of acetylsalicylic acid to treat acne

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Belépés Regisztrálás
BACKGROUND OF THE INVENTION 1. Field of the Invention The invention relates generally to a method for topically treating inflammation in humans or animals. More particularly, the invention relates to a method of treating inflammation in humans and animals with acetylsalicylic acid esters. 2.

Quinoline derivatives

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Belépés Regisztrálás
FIELD OF THE INVENTION The present invention relates to novel quinoline derivatives, to methods for their preparation, to compositions containing them, and to methods and use for clinical treatment of diseases resulting from autoimmunity such as multiple sclerosis, insulin-dependent diabetes

Quinoline derivatives

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Belépés Regisztrálás
FIELD OF THE INVENTION The present invention relates to novel substituted quinoline-3-carboxamide derivatives, to methods for their preparation, to compositions containing them, and to methods and use for clinical treatment of diseases resulting from autoimmunity, such as multiple sclerosis,

Quinoline derivatives

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Belépés Regisztrálás
FIELD OF THE INVENTION The present invention relates to novel quinoline derivatives with a thio-substitutent incorporated into the 5-position, to methods for their preparation, to compositions containing them, and to methods and use for clinical treatment of diseases resulting from autoimmunity,

Quinoline derivatives

Csak regisztrált felhasználók fordíthatnak cikkeket
Belépés Regisztrálás
FIELD OF THE INVENTION The present invention relates to novel substituted quinoline-3-carboxamide derivatives, to methods for their preparation, to compositions containing them, and to methods and use for clinical treatment of diseases resulting from autoimmunity, such as multiple sclerosis,

N-(5-aminomethyl-2-oxazolin-2-yl)-N'-phenylureas, compositions and use

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Belépés Regisztrálás
BACKGROUND OF THE INVENTION 1. Field of the Invention This invention relates to new N-(5-aminomethyl-2-oxazolin-2-yl)-N'-phenylureas, the method for producing them and their therapeutic application. 2. Description of the Prior Art 2-Amino-2-oxazolines are already known. Thus,

Compounds

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Belépés Regisztrálás
FIELD OF THE INVENTION The present invention relates to substituted thieno[2,3-b]pyridine-5-carboxamide and 2-thia-4-aza-indene-6-carboxamide derivatives, to methods for their preparation, to compositions containing them, and to methods and use for clinical treatment of diseases resulting from

Substituted dihydrobenzopyran-2-carboxylates

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Belépés Regisztrálás
BACKGROUND OF THE INVENTION (a) Field of the Invention This invention in its broadest aspect, relates to inhibitors of metabolic pathways. In particular the invention relates to novel compounds of Formula I which are inhibitors of leukotriene D.sub.4 (LTD.sub.4) and therefore useful to prevent or
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