Heart failure / napad padaczkowy

Spider toxins and methods for their use as blockers of calcium channels and amino acid receptor function

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BACKGROUND 1. The Field of the Invention The present invention generally relates to the isolation of certain toxins from spider venoms and the use of those toxins as inhibitors of the functions of ion channels and neurotransmitter receptors. In particular, the present invention relates to spider

Spider toxins and methods for their use as blockers of calcium channels and amino acid receptor function

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BACKGROUND 1. The Field of the Invention The present invention generally relates to the isolation of certain toxins from spider venoms and the use of those toxins as inhibitors of the functions of ion channels and neurotransmitter receptors. In particular, the present invention relates to spider

Compositions and methods for the suppression of carbonic anhydrase activity

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PRIORITY This application is a national phase filing of the Patent Cooperation Treaty (PCT) application # PCT/IB2013/050899 titled "COMPOSITIONS AND METHODS FOR THE SUPPRESSION OF CARBONIC ANHYDRASE ACTIVITY" filed on Feb. 3, 2013 Published with WIPO Publication # WO/2013/167994, which further

Aryl sulfonamides and sulfamide derivatives and uses thereof

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Throughout this application, various references are referred to within parentheses. Disclosures of these publications in their entireties are hereby incorporated by reference into this application to more fully describe the state of the art to which this invention pertains. Full bibliographic

Aryl sulfonamides and sulfamide derivatives and uses thereof

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Throughout this application, various references are referred to within parentheses. Disclosures of these publications in their entireties are hereby incorporated by reference into this application to more fully describe the state of the art to which this invention pertains. Full bibliographic

Aryl sulfonamides and sulfamide derivatives and uses thereof

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Throughout this application, various references are referred to within parentheses. Disclosures of these publications in their entireties are hereby incorporated by reference into this application to more fully describe the state of the art to which this invention pertains. Full bibliographic

Pyridone derivatives

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This application is a U.S. national stage of International Application No. PCT/JP03/03115 filed Mar. 14, 2003. TECHNICAL FIELD The present invention is useful in medical fields. In more detail, novel pyridone derivatives of the present invention have an effect as neuropeptide Y receptor antagonists

Spider toxins and methods for their use as blockers of amino acid receptor function

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BACKGROUND 1. The Field of the Invention The present invention generally relates to the isolation of certain toxins from spider venoms and the use of those toxins as inhibitors of the functions of ion channels and neurotransmitter receptors. In particular, the present invention relates to spider

Substituted saturated aza heterocycles as inhibitors of nitric oxide synthase

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CROSS REFERENCE TO RELATED APPLICATION The present invention is based on, and claims priority from 60/008,390, filed Dec. 8, 1995. BACKGROUND OF THE INVENTION This application is directed to inhibitors of nitric oxide synthase, and in particular substituted azacycle derivatives. Nitric Oxide in

Cyclic amidine analogs as inhibitors of nitric oxide synthase

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BACKGROUND OF THE INVENTION This application is directed to inhibitors of Nitric oxide synthase, and in particular cyclic amidines. Nitric Oxide in Biology. The emergence of nitric oxide (NO), a reactive, inorganic radical gas as a molecule contributing to important physiological and pathological

Pyridone substituted benzothiazole derivatives

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BACKGROUND OF THE INVENTION The present invention generally relates to pyridone substituted benzothiazole compounds that are adenosine receptor ligands. Specifically, the compounds of the present invention have a good affinity to the A.sub.2A -receptor and a high selectivity to the A.sub.1 - and

Benzathiazol-acetamides

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BACKGROUND OF THE INVENTION Adenosine modulates a wide range of physiological functions by interacting with specific cell surface receptors. The potential of adenosine receptors as drug targets was first reviewed in 1982. Adenosine is related both structurally and metabolically to the bioactive

Benzothiazole derivatives

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BACKGROUND OF THE INVENTION Adenosine modulates a wide range of physiological functions by interacting with specific cell surface receptors. The potential of adenosine receptors as drug targets was first reviewed in 1982. Adenosine is related both structurally and metabolically to the bioactive

heart failure/napad padaczkowy

Spider toxins and methods for their use as blockers of calcium channels and amino acid receptor function

Spider toxins and methods for their use as blockers of calcium channels and amino acid receptor function

Compositions and methods for the suppression of carbonic anhydrase activity

Aryl sulfonamides and sulfamide derivatives and uses thereof

Aryl sulfonamides and sulfamide derivatives and uses thereof

Aryl sulfonamides and sulfamide derivatives and uses thereof

Pyridone derivatives

Spider toxins and methods for their use as blockers of amino acid receptor function

Substituted saturated aza heterocycles as inhibitors of nitric oxide synthase

Cyclic amidine analogs as inhibitors of nitric oxide synthase

Pyridone substituted benzothiazole derivatives

Benzathiazol-acetamides

Benzothiazole derivatives

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