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hydrocarbon/bólga
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Administration of oxazolidinone and pyrolidinone compounds for the treatment of inflammation
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The invention relates to the subject matter characterized in the claims.
Numerous compounds of general Formula I according to claim 1 have been known heretofore. Thus, U.S. Pat. No. 4,012,495, for example, describes pyrrolidone derivatives of general Formula I, and U.S. Pat. No. 4,186,129 discloses
Method and compounds for reducing dermal inflammations
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BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention relates to the treatment of indolent dermal irritations. More specifically, it concerns treatment of persistent inflammations such as chemical ulcers, herpes ulcers, radiation burns, psoriasis and sunburn.
2. General Background of
Topical treatment of skin inflammatory disorders
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This invention relates to the discovery that a certain beeswax fraction affords an effective topical treatment for certain inflammatory skin conditions.
Beeswax is the yellow or white (bleached) wax obtained from the honeycomb of the bee and consists largely of myricyl palmitate, cerotic acid and
Glycerides with anti-inflammatory properties
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DETAILED DESCRIPTION OF THE INVENTION
Acetylsalicylic acid has been used with increasing frequency and amounts over the past 75 years for the treatment of pains and inflammations. It is an inexpensive, yet highly effective drug. Unfortunately, it has a side effect that makes its oral use dangerous
Glycerides with anti-inflammatory properties
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Anti-inflammatories are widely used for the treatment of inflammations associated with rheumatism and similar disease which are very often chronic in nature. In these instances, treatment with anti-inflammatory compositions is required to be continued for prolonged periods of time, often on a
Anti-inflammatory composition and method containing 2-fluoro-4-isopropylbiphenyl
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This invention relates to novel hydrocarbons and ethers and in particular to hydrocarbons and ethers having valuable therapeutic properties.
According to the invention there is provided a compound of formula I ##STR1## in which n = 0 or 1; X is an alkyl or alkenyl group of 2 to 6 carbon atoms, and
Anti-inflammatory nitro and thia-fatty acids
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FIELD OF THE INVENTION
The present invention relates to compounds which include a carbon chain of 14 to 26 carbon atoms and a nitro or sulphur group. In a particular embodiment the invention relates to nitro analogues of polyunsaturated fatty acids. The present invention further relates to the use
2-pyrrolin-3-carbonitril-derivatives, pharmaceutical compositions containing them and their anti-inflammatory and ulcer protective activity
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The present invention is concerned with new 5-oxo-2-pyrroline-3-carbonitriles, with the preparation thereof and with pharmaceutical compositions containing them.
The new 5-oxo-2-pyrroline-3-carbonitriles according to the present invention are compounds of the general formula: ##STR3## wherein
2-Pyrrolin-3-carbonitrile derivatives, and pharmaceutical compositions containing them and their anti-inflammatory and ulcer protective activity
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The present invention is concerned with new 5-oxo-2-pyrroline-3-carbonitriles, with the preparation thereof and with pharmaceutical compositions containing them.
The new 5-oxo-2-pyrroline-3-carbonitriles according to the present invention are compounds of the general formula: ##STR3## wherein
Composition for preventing inflammations
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RELATED APPLICATION
This application is a national stage filing under 35 U.S.C. .sctn.371 of international application PCT/JP2011/070436, filed Sep. 8, 2011, the disclosure of which is incorporated by reference herein in its entirety.
TECHNICAL FIELD
The present invention relates to a probiotic(s)
Method of treating inflammation and pain using heteramino benzofurans
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The invention relates to novel furans, especially benzofuranones of the general formula ##STR2## in which R.sub.1 represents hydrogen or an aliphatic radical, R.sub.2 represents an amino group di-substituted by a divalent hydrocarbon radical, and the aromatic ring A may be additionally substituted,
4-Pregnene-derivatives, a process for their preparation, composition and method for the treatment of inflammatory conditions
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DESCRIPTION
Technical Field
The present invention relates to novel, pharmacologically active compounds, a process for their preparation including the separation of the obtained stereoisomeric mixture into its separate components (diastereoisomers). The invention also relates to pharmaceutical
Anti-inflammatory compounds derived from Pseudopterorgorgia elisabethae
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BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention generally relates to compounds having anti-inflammatory, anti-proliferative and analgesic activity and methods for using these compounds to reduce inflammation, cell proliferation and pain in mammals. Specifically, the
Anti-inflammatory compounds derived from Pseudopterogorgia elisabethae
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BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention generally relates to compounds having anti-inflammatory, anti-proliferative and analgesic activity and methods for using these compounds to reduce inflammation, cell proliferation and pain in mammals.
Specifically, the
Novel 5,6,7,8-tetrahydro-5-quinolines and their use as anti-inflammatory agents
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BACKGROUND OF THE INVENTION
This invention relates to novel, pharmacologically effective pyridine derivatives, a process for the preparation thereof, pharmaceutical preparations containing these compounds and a method of treating inflammation therewith.
SUMMARY OF THE INVENTION
The compounds of this
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Sláðu inn einkenni eða sjúkdóm og lestu um jurtir sem gætu hjálpað, sláðu jurt og sjáðu sjúkdóma og einkenni sem hún er notuð við.
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