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anti inflammatory/edema

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2,3-di-substituted-5,6-dihydroimidazo [2,1-b] thiazole, its salts, production thereof and anti-inflammatory agent containing the same

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This invention relates to novel imidazothiazole derivatives, their salts, a method for the production thereof, and anti-inflammatory compositions containing the same. More particularly, this invention relates to 2,3-di-substituted-5,6-dihydroimidazo [2,1-b] thiazole, its salts, a method for the

2,-3-Di-substituted-5,6-dihydroimidazo [2,1-b] thiazole, its salts, production thereof and anti-inflammatory agent containing the same

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This invention relates to novel imidazothiazole derivatives, their salts, a method for the production thereof, and anti-inflammatory compositions containing the same. More particularly, this invention relates to 2,3-di-substituted-5,6-dihydroimidazo [2,1-b] thiazole, its salts, a method for the

Azaazulene compounds which are useful as antiallergic and antiinflammatory agents

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BACKGROUND OF THE INVENTION The present invention relates to a novel and useful azaazulene derivatives and salts thereof having antiallergic activity and antiinflammatory activity which are based on inhibitory activity against chemical mediator release, 5-lipoxygenase inhibiting activity or relaxing

Plasminogen activator as an anti-inflammatory agent

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BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to the use of plasminogen activator as an anti-inflammatory agent. 2. Description of the Related Art Plasminogen activators play an important physiological role in the regulation of thrombolysis. This action is

Antiinflammatory 2-aminomethyl-6-trihalomethylphenols

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SUMMARY OF THE INVENTION This invention relates to 2-aminomethylphenols useful in the treatment of edema and inflammation, processes for preparing same, compositions and methods of treating inflammation. Particularly, it relates to 2-aminomethyl-4-lower alkyl-6-trihalomethylphenol or its non-toxic,

3,4-Dihydrospiro-2H-1,3-benzoxazines and their use in treating edema, abnormal electrolyte retention, and inflammation

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This invention is concerned with novel 3,4-dihydrospiro-2H-1,3-benzoxazines having therapeutic utility, processes for their preparation, methods of treating inflammation, edema and autoimmune diseases, and novel pharmaceutical formulations comprising at least one of the novel compounds as active

Furo[2, 3d]pyrimidine derivatives and anti-ulcer containing the same

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The present invention relates to furo[2, 3d]pyrimidine derivatives having the general formula (I) ##STR2## wherein R.sub.1 represents a lower alkyl, a lower alkenyl or an aralkyl group, and R.sub.2 represents a lower alkyl, unsubstituted phenyl, carboxyl, methylsulphonyl, methoxycarbonyl or a

Preservative system for ophthalmic formulations

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FIELD OF THE INVENTION The present invention relates to improved ophthalmic formulations, particularly to ophthalmic formulations which use an improved preservative system comprising a quaternary ammonium preservative and a stabilizing amount of a nonionic polyoxyethylated octylphenol surfactant for

Pharmaceutical composition for preventing or treating inflammatory diseases comprising trachelospermi caulis extract and paeonia suffruticosa andrews extract, and method for preparing the same

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CROSS-REFERENCES TO RELATED APPLICATIONS This application is a U.S. national phase application of International PCT Patent Application No. PCT/KR2011/006094, which was filed on Aug. 18, 2011, which claims priority to Korean Patent Application Nos. 10-2010-0123086, filed Dec. 3, 2010;

Protein S protects the nervous system from injury

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BACKGROUND OF THE INVENTION This invention relates to the use of protein S and/or variants thereof as neuroprotective agents for treating brain disorders and other pathological conditions. The ability of protein S and variants thereof to act as cell survival factors on cells of the nervous systems

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

Superoxide dismutase derivatives, method of producing same and medicinal use of same

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BACKGROUND OF THE INVENTION 1. FIELD OF THE INVENTION This invention relates to superoxide dismutase derivatives, a method of producing the same and medicinal use of the same. 2. DESCRIPTION OF THE PRIOR ARTS Superoxide dismutase (hereinafter abbreviated as SOD) has been known so far as an enzyme

Methods of treating and preventing diseases and disorders of the central nervous system

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BACKGROUND OF THE INVENTION The central nervous system (CNS) of an animal, for example, human, contains several important receptor systems such as the glutamate, acetylcholine, GABA.sub.A, and NMDA receptor systems, and injury to the CNS as well as other diseases and disorders of the CNS could be

Methods of treating and preventing diseases and disorders of the central nervous system

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BACKGROUND OF THE INVENTION The central nervous system (CNS) of an animal, for example, human, contains several important receptor systems such as the glutamate, acetylcholine, GABA.sub.A, and NMDA receptor systems, and injury to the CNS as well as other diseases and disorders of the CNS could be

Method of noninvasive treatment of diabetic retinopathy

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FIELD OF THE INVENTION The present invention relates generally to a method for noninvasive treatment of diabetic retinopathy. More so, the present invention relates to a method that prevents and reverses diabetic retinopathy and other vascular retinopathies using a series of non-invasive light and
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