Abstract:
PROBLEM TO BE SOLVED: To provide adamantyl derivatives as an 11-β-hydroxysteroid dehydrogenase (HSD) 1, whose inhibition prevents or decreases the tissue specific amplification of glucocorticoid action thus imparting beneficial effects on blood pressure and glucose- and lipid-metabolism.SOLUTION: Compounds are used which are inhibitors of the 11-β-hydroxysteroid dehydrogenase Type 1 enzyme. The present invention further relates to the use of inhibitors of 11-β-hydroxysteroid dehydrogenase Type 1 enzyme, e.g. acylamino-substituted adamantane carboxylic amides, for the treatment of non-insulin dependent type 2 diabetes, insulin resistance, obesity, lipid disorders, metabolic syndrome and other diseases and conditions that are mediated by excessive glucocorticoid action.
Abstract:
PROBLEM TO BE SOLVED: To provide a therapeutic agent for a patient suffering from disorders and deficits of the central nervous system associated with diabetes, associated with aging and neurodegeneration, comprising attention deficit disorder in general, attention deficit hyperactivity disorder (ADHD), Alzheimer's disease (AD), mild cognitive impairment, senile dementia, AIDS dementia, neurodegeneration, and schizophrenia.SOLUTION: A pharmaceutical composition includes an effective amount of a selective inhibitor of the 11-β-hydroxysteroid dehydrogenase type 1 enzyme activity represented by formula.
Abstract:
PROBLEM TO BE SOLVED: To provide a pharmaceutical composition for treating patients with diabetes-, aging- and neurodegeneration-related central-nervous-system disorders and deletions including ordinary attention-deficit disorders, attention-deficit hyperactivity disorders (ADHD), Alzheimer's disease (AD), mild cognitive damage, senile dementia, AIDS dementia, neurodegeneration and schizophrenia. SOLUTION: The pharmaceutical composition for treating glucocorticoid-related central-nervous-system disorders contains a selective inhibitor for 11-β-hydroxysteroid dehydrogenase 1-type enzyme activity. COPYRIGHT: (C)2009,JPO&INPIT
Abstract:
A GENERAL PREPARATION OF IODOMETHYLSULFONES IN WHICH IODINE MONOCHLORIDE IS REACTED WITH A SUBSTITUTED SULFONYL ACETIC ACID IN A REACTION MIXTURE MAINTAINED AT A NEARLY NEUTRAL PH TO PRODUCE A SUPERIOR CONVERSION.
Abstract:
Alkylphenyl benzopyrans represented by the formula
WHEREIN N IS 1 OR 2; EACH R and R1 are the same or different members of the group consisting of hydrogen or loweralkyl; R2 is loweralkyl; R3 is hydrogen; Y is a straight or branched chain alkylene group having from one to ten carbon atoms; and each R4 and R5 and R6 are the same or different members of the group consisting of hydrogen, halo, trifluoromethyl or loweralkyl and Z is C or N and the pharmaceutically acceptable salts thereof.
Abstract:
Covers pyrazolo naphthyridines having the formula:
WHEREIN R1 is hydrogen or lower alkyl, R2 is hydrogen, lower alkyl, phenyl or cyclohexyl and R3 is phenyl, benzyl or halo benzyl. Compounds exhibit anti-inflammatory and other properties.
Abstract:
The present invention relates to compounds which are inhibitors of the 11-beta-hydroxysteroid dehydrogenase Type 1 enzyme. The present invention further relates to the use of inhibitors of 11-beta-hydroxysteroid dehydrogenase Type 1 enzyme for the treatment of non-insulin dependent type 2 diabetes, insulin resistance, obesity, lipid disorders, metabolic syndrome and other diseases and conditions that are mediated by excessive glucocorticoid action.
Abstract:
A method for treating a patient suffering from disorders and deficits of the central nervous system associated with diabetes, associated with aging and neurodegeneration, comprising attention deficit disorder in general, attention deficit hyperactivity disorder (ADHD), Alzheimer's disease (AD), mild cognitive impairment, senile dementia, AIDS dementia, neurodegeneration, depression, and schizophrenia, comprising administering to a patient in need of such treatment an effective amount of a selective inhibitor of the 11-ß-hydroxysteroid dehydrogenase Type 1 enzyme activity.
Abstract:
A compound of formula (I), or a pharmaceutically acceptable salt thereof, is disclosed, as well as processes for and intermediates in the preparation thereof, and a method of antagonizing endothelin.