Antidepressants / zápal

Muscle-strengthening drugs and anti-inflammatory drugs

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TECHNICAL FIELD The present invention relates to a novel agent or composition for use as a muscle-strengthening drug, an anti-inflammatory drug, an antiasthmatic, an antidiarrheal, an antidepressant, or a drug for the treatment of secondary diseases following cerebral infarction (human stroke

Combinations for the treatment of inflammatory disorders

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BACKGROUND OF THE INVENTION The invention relates to the treatment of inflammatory disorders. Inflammation occurs when tissues are injured by viruses, bacteria, trauma, chemicals, heat, cold or any other harmful stimulus. Chemicals including bradykinin, histamine, serotonin and others are released,

Therapeutic neuropathic pain lotion

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BACKGROUND Damage or disease may affect the somatosensory nervous system and may cause neuropathic pain. Abnormal sensations or pain from normally non-painful stimuli may be associated with neuropathic pain and may occur episodically or continuously. Neuropathic pain sensations may include feelings

Compositions and methods for treating neuropsychiatric disorders using an endothelin-B receptor agonist

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INCORPORATION BY REFERENCE OF MATERIAL SUBMITTED ELECTRONICALLY This application contains, as a separate part of disclosure, a Sequence Listing in computer-readable form (filename: 48812_SeqListing.txt; created Jul. 8, 2014, 659 bytes--ASCII text file) which is incorporated by reference in its

.beta.3 adrenergic agonists

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FIELD OF THE INVENTION The present invention is in the field of medicine, particularly in the treatment of Type II diabetes and obesity. More specifically, the present invention relates to .beta..sub.3 adrenergic receptor agonists useful in the treatment of Type II diabetes and obesity. BACKGROUND

Amide derivatives as .beta. 3 agonists

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SUMMARY OF THE INVENTION The instant invention is concerned with amide derivatives which are useful as antiobesity and antidiabetic compounds. Thus, it is an object of this invention to describe such compounds. It is a further object to describe the specific preferred stereoisomers of the present

Fused piperidine substituted arylsulfonamides as .beta.3-agonists

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SUMMARY OF THE INVENTION The instant invention is concerned with fused piperidine substituted arylsulfonamides which are useful as antiobesity and antidiabetic compounds. Thus, it is an object of this invention to describe such compounds. It is a further object to describe the specific preferred

Oxadiazole benzenesulfonamides as selective .beta..sub.3 Agonist for the treatment of Diabetes and Obesity

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BACKGROUND OF THE INVENTION .beta.-Adrenoceptors have been subclassified as .beta..sub.1 and .beta..sub.2 since 1967. Increased heart rate is the primary consequence of .beta..sub.1 -receptor stimulation, while bronchodilation and smooth muscle relaxation typically result from .beta..sub.2

Substituted sulfonamides as selective .beta..sub.3 agonists for the treatment of diabetes and obesity

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BACKGROUND OF THE INVENTION .beta.-Adrenoceptors have been subclassified as .beta..sub.1 and .beta..sub.2 since 1967. Increased heart rate is the primary consequence of .beta..sub.1 -receptor stimulation, while bronchodilation and smooth muscle relaxation typically result from .beta..sub.2

Substituted sulfonamides as selective .beta..sub.3 agonists for the treatment of diabetes and obesity

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BACKGROUND OF THE INVENTION .beta.-Adrenoceptors have been subclassified as .beta..sub.1 and .beta..sub.2 since 1967. Increased heart rate is the primary consequence of .beta..sub.1 -receptor stimulation, while bronchodilation and smooth muscle relaxation typically result from .beta..sub.2

Substituted phenyl sulfonamides as selective .beta. 3 agonists for the treatment of diabetes and obesity

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BACKGROUND OF THE INVENTION .beta.-Adrenoceptors have been subclassified as .beta..sub.1 and .beta..sub.2 since 1967. Increased heart rate is the primary consequence of .beta..sub.1 -receptor stimulation, while bronchodilation and smooth muscle relaxation typically result from .beta..sub.2

Substituted sulfonamides as selective .beta.-3 agonists for the treatment of diabetes and obesity

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BACKGROUND OF THE INVENTION .beta.-Adrenoceptors have been subclassified as .beta..sub.1 and .beta..sub.2 since 1967. Increased heart rate is the primary consequence of .beta..sub.1 -receptor stimulation, while bronchodilation and smooth muscle relaxation typically result from .beta..sub.2

Thiazole benzenesulfonamides as .beta.3 agonists for treatment of diabetes and obesity

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BACKGROUND OF THE INVENTION .beta.-Adrenoceptors have been subclassified as .beta..sub.1 and .beta..sub.2 since 1967. Increased heart rate is the primary consequence of .beta..sub.1 -receptor stimulation, while bronchodilation and smooth muscle relaxation typically result from .beta..sub.2

Selective .beta..sub.3 agonists for the treatment of diabetes and obesity

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RELATED APPLICATIONS This application claims priority to U.S. provisional application Ser. No. 60/006,070, filed Oct. 24, 1995, and to U.S. provisional application Ser. No. 60/004,332, filed Sep. 26, 1995. BACKGROUND OF THE INVENTION .beta.-Adrenoceptors have been subclassified as .beta..sub.1 and

Method of modifying angiotensin receptor activity for mediation of pain

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FIELD OF THE INVENTION The present invention relates to a method of modifying Angiotensin II subtype 1 (AT.sub.1) receptor activity for the treatment of premenstrual syndrome (PMS) and for the mediation and alleviation of pain. More specifically, the present invention relates to the use of AT.sub.1

antidepressants/zápal

Muscle-strengthening drugs and anti-inflammatory drugs

Combinations for the treatment of inflammatory disorders

Therapeutic neuropathic pain lotion

Compositions and methods for treating neuropsychiatric disorders using an endothelin-B receptor agonist

.beta.3 adrenergic agonists

Amide derivatives as .beta. 3 agonists

Fused piperidine substituted arylsulfonamides as .beta.3-agonists

Oxadiazole benzenesulfonamides as selective .beta..sub.3 Agonist for the treatment of Diabetes and Obesity

Substituted sulfonamides as selective .beta..sub.3 agonists for the treatment of diabetes and obesity

Substituted sulfonamides as selective .beta..sub.3 agonists for the treatment of diabetes and obesity

Substituted phenyl sulfonamides as selective .beta. 3 agonists for the treatment of diabetes and obesity

Substituted sulfonamides as selective .beta.-3 agonists for the treatment of diabetes and obesity

Thiazole benzenesulfonamides as .beta.3 agonists for treatment of diabetes and obesity

Selective .beta..sub.3 agonists for the treatment of diabetes and obesity

Method of modifying angiotensin receptor activity for mediation of pain

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