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bromine/inflamación
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Página 1 desde 25 resultados
Anti-inflammatory picolyselenobenzamides and salts thereof
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FIELD OF THE INVENTION
The invention relates to novel picolylselenobenzamides and their salts, method and intermediates for their preparation and pharmaceutical products containing these compounds.
DESCRIPTION OF THE INVENTION
The compounds to which this invention relates correspond to the Formula I
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
6.alpha., 16.beta.-dimethyl corticoids and their anti-inflammatory use
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BACKGROUND OF THE INVENTION
This invention relates to 6,16-dimethyl corticoids, pharmaceutical preparations containing them, processes for their production and to steroids useful as intermediates for the synthesis of these 6,16-dimethyl corticoids.
SUMMARY OF THE INVENTION
It is an object of this
Process for the preparation of N-4-[(substituted phenyl)alkylheterocyclic]- N
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TECHNICAL FIELD
The present invention relates to chemical synthetic processes. More particularly, the present invention concerns a process for the preparation of a class of N-4-[(substituted phenyl)alkylthienyl]-, and N-4-[(substituted phenyl)alkylfuryl]but-3-yn-2-yl]-N-hydroxyurea
Indole derivatives
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This invention relates to novel indole derivatives having pharmacological activity, to pharmaceutical and veterinary compositions containing them and to a method of preparing the said derivatives.
The indole derivatives with which the invention is concerned are represented by the general formula :
Indole derivatives
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This invention relates to novel indole derivatives having pharmacological activity, to pharmaceutical and veterinary compositions containing them and to a method of preparing the said derivatives.
The indole derivatives with which the invention is concerned are represented by the general formula:
Novel 6, 16-dimethylcorticoids, their preparation and use
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BACKGROUND OF THE INVENTION
The present invention relates to new 6,16-dimethylcorticoids, to pharmaceutical preparations containing them, to a process for the preparation of these compounds; and to intermediate steroidal products used in the synthesis of these compounds.
SUMMARY OF THE INVENTION
It
Novel 6,16-dimethylcorticoids their preparation and use
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BACKGROUND OF THE INVENTION
The present invention relates to new 6,16-dimethylcorticoids, to pharmaceutical preparations containing them, to a process for the preparation of these compounds; and to intermediate steroidal products used in the synthesis of these compounds.
SUMMARY OF THE INVENTION
It
4'-Chloro-4-ethynylbiphenyl and method of preparing same
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This invention relates to novel 4-ethynylbiphenyl derivatives, to processes for the production thereof and to pharmaceutical compositions containing the same.
The present invention provides ethynylbiphenyl derivatives of the general formula (I): ##SPC2##
in which R represents a chlorine or bromine
Onychomycosis treatment system and method
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FIELD OF THE DISCLOSURE
The invention in one aspect relates generally to a system and method for the treatment of tissue infected with onychomycosis.
BACKGROUND
Onychomycosis (also known as "dermatophytic onychomycosis," or"tinea unguium") is a fungal infection of the nail. It is the most common
Topical treatment and composition
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This invention relates to pharmaceutical compositions and methods for the treatment of inflammation by topical administration of compounds having anti-inflammatory activity.
United Kingdom Patent No. 1,474,377 refers to pharmaceutical compositions which comprise a compound of the formula (I):
Method for inhibiting osteoclast development
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BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention provides a method for inhibiting osteoclast development and a method for preventing bone erosion by delivering an effective amount of a haloanilide to an osteoclast for inhibiting the osteoclast development and preventing
Derivatives of thiophene-2-carboxylic acid and their pharmaceutically acceptable acid or base addition salts and use in treatment of conditions caused by thromboxane A.sub.2
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SUMMARY OF INVENTION
The present invention relates to novel therapeutically useful derivatives of the thiophene-2-carboxylic acid of the general formula ##STR2## in which R in position 3 or 4 is hydrogen, methyl, chlorine or bromine and R.sub.1 is hydrogen or C.sub.1 -C.sub.4 -alkyl, and the
1-azabicyclo[3.2.2]nonan-3-amine derivatives
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BACKGROUND OF THE INVENTION
This invention relates to novel 1-azabicyclo[3.2.2]-nonan-3-amine derivatives.
The compounds of the invention have the ability to antagonize substance P. They are, therefore, useful in treating conditions such as intestinal disorders, central nervous system disorders,
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