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Anti-inflammatory compositions containing monogalactosyl dieicosapentaenoyl glycerol and methods relating thereto
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FIELD OF THE INVENTION
The invention relates generally to anti-inflammatory compositions and, more specifically, to anti-inflammatory compositions derived from marine algae having a high content of monogalactosyl dieicosapentaenoyl glycerol (MGDG-EPA.)
BACKGROUND OF THE
Anti-inflammatory compositions containing monogalactosyl dieicosapentaenoyl glycerol and methods of relating thereto
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FIELD OF THE INVENTION
The invention relates generally to anti-inflammatory compositions and, more specifically, to anti-inflammatory compositions derived from marine algae having a high content of monogalactosyl dieicosapentaenoyl glycerol (MGDG-EPA).
BACKGROUND OF THE
Anti-tumor and anti-inflammatory dicinnamoyl-glycerol esters and their analogues
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BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to anti-cancer drug and, more particularly, to synthetic dicinnamate compounds and their analogues that exhibit anti-tumor activity and/or an anti-inflammatory activity, that has beneficial activity principally in
Zwitteronic-fatty acid compounds having anti-inflammatory properties
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FIELD OF THE INVENTION
This inventions relates to pharmacologically-active, anti-inflammatory compounds, and more specifically to long aliphatic chain esters of selected zwitterionic organic compounds derived from naturally occurring taurine. This invention pertains to novel zwitterionic compounds
Isothiazolyl substituted glycerol derivatives containing phosphate groups
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BACKGROUND TO THE INVENTION
The present invention relates to a series of novel glycerol derivatives containing a heterocyclic system and provides processes for producing these compounds and compositions containing them for therapeutic use, especially for use as antagonists to platelet activating
Composition preventing bacterial inflammation in monogastric animals
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CROSS-REFERENCE TO RELATED APPLICATIONS
This application is a national stage application (under 35 U.S.C. .sctn. 371) of PCT/SE2016/000066, filed Nov. 10, 2016, which claims benefit of European Application No. 1500460.9, filed Nov. 13, 2015, which are incorporated herein by reference in their
Phosphonates as anti-inflammation agents
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FIELD OF THE INVENTION
This invention pertains to the synthesis and use as therapeutic agents of a group of substances with a glycerol backbone or aliphatic chain structure linked to phosphonocholine, phosphinocholine, phosphonoinositol, phosphinoinositol, or other phosphorus-containing head groups.
2,2 disubstituted glycerol and glycerol-like compounds, compositions and methods of use
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The present invention relates to 2,2-disubstituted glycerol and glycerol-like compounds, compositions containing such compounds, and methods of using such compounds.
Various publications have disclosed related compounds. For example, the SCRIP PAF REPORT, PJB Publications, 1986 and Ann. Rep. Med.
2,2-disubstituted glycerol and glycerol-like compounds, compositions and methods of use
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The present invention relates to 2,2-disubstituted glycerol and glycerol-like compounds, compositions containing such compounds, and methods of using such compounds.
Various publications have disclosed related compounds. For example, the SCRIP PAF REPORT, PJB Publications, 1986 and Ann. Rep. Med.
Herbal preparation for accelerating wounds and skin inflammations healing and its application
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BACKGROUND OF THE INVENTION
(1) Field of the Invention
A subject matter of the present invention is a herbal preparation with anti-inflammatory and astringent effects used in a herbal medicine to treat conditions-related to interruption of anatomical continuity of outer layers of skin or deeper
Retinoid glycerol phospholipid conjugates
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Priority is claimed to provisional patent application Ser. No. 60/009,546, filed Jan. 2, 1996.
TECHNICAL FIELD
The present invention relates to certain alkyl and alkenyl glycerophosphoethanolamines substituted with a retinoid ester moiety on the glyceryl backbone, and to pharmaceutical compositions
Reduction of skin irritation during electrotransport delivery
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TECHNICAL FIELD
This invention relates to electrotransport agent delivery devices, compositions, and methods. More particularly, this invention relates to methods of reducing skin irritation during transdermal electrotransport agent delivery.
BACKGROUND ART
The term "electrotransport" as used herein
Reduction of skin irritation during electrotransport delivery
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TECHNICAL FIELD
This invention relates to electrotransport agent delivery devices, compositions, and methods. More particularly, this invention relates to methods of reducing skin irritation during transdermal electrotransport agent delivery.
BACKGROUND ART
The term "electrotransport" as used herein
Enhancement of the action of anti-infective agents and of central and peripheral nervous system agents and transportation of nucleic acid substances
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FIELD OF THE INVENTION
This invention relates to pharmaceutical preparations (which expression is herein intended to include veterinary preparations) for use in combating infective organisms afflicting the animal body (which expression is herein intended to include the human body).
This invention
Enhancement of the action of anti-infective agents and of central and peripheral nervous system agents and transportation of nucleic acid substances
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CROSS-REFERENCE TO RELATED APPLICATIONS
This application is a continuation-in-part of PCT International Applications PCT/ZA01/00098, PCT/ZA01/00099, and PCT/ZA01/00100, all filed Jul. 19, 2001, and all designating the U.S.
FIELD OF THE INVENTION
This invention relates to pharmaceutical preparations
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