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FIELD
The present invention generally relates to NO-releasing coxib compounds, pharmaceutical compositions comprising the compounds, methods useful for treating a subject by administering a therapeutically effective amount of the compounds, and methods for making the compounds. More specifically,
TECHNICAL FIELD
The present invention relates to guanidine compounds for inhibiting mitochondrial oxidative phosphorylation (OXPHOS) and use thereof more specifically, the present invention relates to a pharmaceutical composition for preventing or treating a disease associated with OXPHOS,
BACKGROUND
Some drug compounds act by stimulating certain key aspects of the immune system, as well as by suppressing certain other aspects (e.g., U.S. Pat. Nos. 6,039,969 and 6,200,592). These compounds are sometimes referred to as immune response modifiers (IRMs). Some IRM compounds are useful for
BACKGROUND
Some drug compounds act by stimulating certain key aspects of the immune system, as well as by suppressing certain other aspects (e.g., U.S. Pat. Nos. 6,039,969 and 6,200,592). These compounds are sometimes referred to as immune response modifiers (IRMs). Some IRM compounds are useful for
BACKGROUND
Some drug compounds act by stimulating certain key aspects of the immune system, as well as by suppressing certain other aspects (e.g., U.S. Pat. Nos. 6,039,969 and 6,200,592). These compounds are sometimes referred to as immune response modifiers (IRMs). Some IRM compounds are useful for
CROSS-REFERENCE TO RELATED APPLICATIONS
This application is the U.S. National Stage entry of PCT/CN2011/081238, filed Oct. 25, 2011, which claims benefit of China Patent Application No. 201010519331.8, filed Oct. 26, 2010, the disclosures of each are herein incorporated by reference.
FIELD OF THE
TECHNICAL FIELD OF INVENTION
The present invention is related to a modified hydroxypolymer conjugate, particularly a guanidine-dextran conjugate having a tumor killing effect, and a method for preparation of said conjugates as well as its use.
BACKGROUND OF INVENTION
Guanidine compounds have many
FIELD OF THE INVENTION
The invention relates to new salts of guanidine derivatives and pharmaceutical preparations containing these as the active ingredient, as well as their preparation.
BACKGROUND OF THE INVENTION
WO 97/45401, incorporated by reference herein, discloses guanidine derivatives of
The present invention relates to new series of phenyl-guanidine derivatives for the inhibition of Rac1 which blocks its interaction with guanosine exchange factors (GEFs) belonging to the DBL family as agents for the treatment of aggressive and/or resistant tumours, as well as to processes for their
FIELD OF THE INVENTION
The invention provides inhibitors of F.sub.1F.sub.0-ATPases (e.g., mitochondrial F.sub.1F.sub.0-ATPases) and their therapeutic use. In particular, the invention provides saturated acyl guanidine compounds that inhibit F.sub.1F.sub.0-ATPase, and methods of using saturated acyl
FIELD OF THE INVENTION
The invention provides inhibitors of F.sub.1F.sub.0-ATPases (e.g., mitochondrial F.sub.1F.sub.0-ATPases) and their therapeutic use. In particular, the invention provides pyrazolyl guanidine compounds that inhibit F.sub.1F.sub.0-ATPase, and methods of using pyrazolyl guanidine
FIELD OF THE INVENTION
The invention provides inhibitors of F.sub.1F.sub.0-ATPases (e.g., mitochondrial F.sub.1F.sub.0-ATPases) and their therapeutic use. In particular, the invention provides pyrazolyl guanidine compounds that inhibit F.sub.1F.sub.0-ATPase, and methods of using pyrazolyl guanidine
FIELD OF THE INVENTION
The invention provides inhibitors of F.sub.1F.sub.0-ATPases (e.g., mitochondrial F.sub.1F.sub.0-ATPases) and their therapeutic use. In particular, the invention provides pyrazolyl guanidine compounds that inhibit F.sub.1F.sub.0-ATPase, and methods of using pyrazolyl guanidine
FIELD OF THE INVENTION
The invention provides inhibitors of F.sub.1F.sub.0-ATPases (e.g., mitochondrial F.sub.1F.sub.0-ATPases) and their therapeutic use. In particular, the invention provides pyrazolyl guanidine compounds that inhibit F.sub.1F.sub.0-ATPase, and methods of using pyrazolyl guanidine
FIELD OF THE INVENTION
The invention provides inhibitors of F.sub.1F.sub.0-ATPases (e.g., mitochondrial F.sub.1F.sub.0-ATPases) and their therapeutic use. In particular, the invention provides cycloalkyl guanidine compounds that inhibit F.sub.1F.sub.0-ATPase, and methods of using cyclalkyl guanidine