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uric acid/enflamasyon

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Tetrazole compounds for reducing uric acid

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BACKGROUND OF THE INVENTION Diseases caused by elevated levels of uric acid fall into two major categories: disorders caused by precipitation of uric acid crystals and diseases related to pathological effects of soluble uric acid. Gouty arthritis is the classic example of the former. Deposition of

Tetrazole compounds for reducing uric acid

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BACKGROUND OF THE INVENTION Diseases caused by elevated levels of uric acid fall into two major categories: disorders caused by precipitation of uric acid crystals and diseases related to pathological effects of soluble uric acid. Gouty arthritis is the classic example of the former. Deposition of

Benzoic acid compounds for reducing uric acid

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BACKGROUND OF THE INVENTION Diseases caused by elevated levels of uric acid fall into two major categories: disorders caused by precipitation of uric acid crystals and diseases related to pathological effects of soluble uric acid. Gouty arthritis is the classic example of the former. Deposition of

Method for the preventing and/or treating IL-1 beta lung pathology in mammals by administering a uric acid reducing compound

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This application is a U.S. National Stage application of PCT/EP2009/062159, filed Sept. 18, 2009, which claims priority to European Patent Application No. 083055657, filed Sept. 18, 2008, each and all of which are incorporated herein by reference in their entirety. The present invention is directed

Method for lowering serum uric acid

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This invention relates to a novel method for the preparation of 7-chloro-2-methyl-3,3a-dihydro-2H,9H-isoxazolo (3,2-b) (1,3) benzoxazin-9-one. Prior to the present invention, 6-chloro-2-methyl-3,3a-dihydro-2H,9H-isoxazolo (3,2-b) (1,3) benzoxazin-9-one has been prepared by the reaction of

Prevention or treatment of uratic or gouty diseases

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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/CN2016/000061, filed Jan. 28, 2016, which claims priority to Chinese Application Nos.: 201510048096.3, filed Jan. 30, 2015; 201510079809.2, filed Feb. 13, 2015; 201510080714.2,

2-phenylpyridine derivative

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This is a national stage application under 35 U.S.C. .sctn.371 of PCT/JP2005/015549 filed on Aug. 26, 2005, which claims priority from Japanese patent application P.2004-249275 filed on Aug. 27, 2004 and from Japanese patent application P.2005-078222 filed on Mar. 17, 2005, all of which are

2-phenylthiophene derivative

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TECHNICAL FIELD The present invention relates to a 2-phenylthiophene derivative useful as a medicament, particularly a therapeutic or preventive agent for diseases in which xantine oxidase participates, such as hyperuricemia, gout, inflammatory bowel diseases, diabetic kidney diseases, and diabetic

5-Methyl-1-phenyl-2-(1H)-pyridone compositions and methods of use

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BACKGROUND OF THE INVENTION The present invention relates to novel pharmaceutical compositions containing as the active ingredient the compound 5-methyl-1-phenyl-2-(1H)-pyridone (AMR-69) having the formula Certain substituted pyridones and particularly those wherein the N-substituents are
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