US2008183003A1PendingUtilityA1

Aminoadamantane derivatives as therapeutic agents

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Assignee: ADAMAS PHARMACEUTICALS INCPriority: Feb 22, 2000Filed: Feb 4, 2008Published: Jul 31, 2008
Est. expiryFeb 22, 2020(expired)· nominal 20-yr term from priority
A61P 9/04A61P 9/02A61P 9/10A61P 25/28A61P 27/02A61P 25/36A61P 25/34A61P 25/22A61P 25/04A61P 25/06A61P 25/14A61P 25/08A61P 25/00A61P 25/16A61P 21/00A61P 17/02C07C 233/23C07C 219/24C07C 2603/74A61P 1/08A61P 13/10
63
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Claims

Abstract

The present invention provides novel aminoadamantane derivatives, methods of making the derivatives, compositions including the novel aminoadamantane derivatives, and methods for the treatment and prevention of neurological diseases using the derivatives and compositions. There are a variety of neurological disorders that can be treated using the present invention, including, for example, the following: neurological disorders arising from trauma, ischemic or hypoxic conditions that can be treated include stroke, hypoglycemia, cerebral ischemia, cardiac arrest, spinal cord trauma, head trauma, perinatal hypoxia, cardiac arrest and hypoglycemic neuronal damage; neurodegenerative disorders such as epilepsy, Alzheimer's disease, Huntington's disease Parkinsonism, and amyotrophic lateral sclerosis; other diseases or disorders such as convulsion, pain, depression, anxiety, schizophrenia, muscle spasms, migraine headaches, urinary incontinence, nicotine withdrawal, opiate tolerance and withdrawal, emesis, brain edema, tardive dyskinesia, AIDS-induced dementia, ocular damage, retinopathy, cognitive disorders, and neuronal injury associated with HIV-infection such as dysfunction in cognition, movement and sensation.

Claims

exact text as granted — not AI-modified
1 . A compound having the formula: 
       
         
           
           
               
               
           
         
         or a pharmaceutically acceptable salt thereof, wherein: 
         R 1  is H, alkyl, heteroalkyl, aryl, heteroaryl, C(O)OR 6  or C(O)R 6 ; 
         R 2  is H, alkyl, heteroalkyl, aryl, heteroaryl, C(O)OR 6  or C(O)R 6 ; 
         R 3  is H, alkyl, heteroalkyl, aryl, or heteroaryl; 
         R 4  is H, alkyl, heteroalkyl, aryl, or heteroaryl; 
         R 5  is OR 7 , alkyl-OR 7 , or heteroalkyl-OR 7 ; 
         R 6  is alkyl, heteroalkyl, aryl, or heteroaryl; 
         R 7  is NO 2 , C(O)R 6 , C(O)alkyl-ONO 2  or C(O)heteroalkyl-ONO 2 ; 
         provided that when R 5  is OR 7 , R 7  is not NO 2  or C(O)R 6 ; 
         further provided that at least one of R 3  is and R 4  is not H or alkyl. 
       
     
     
         2 . A compound having the formula: 
       
         
           
           
               
               
           
         
         or a pharmaceutically acceptable salt thereof, wherein: 
         R 1  is H, alkyl, heteroalkyl, aryl, heteroaryl, C(O)OR 6  or C(O)R 6 ; 
         R 2  is H, alkyl, heteroalkyl, aryl, heteroaryl, C(O)OR 6  or C(O)R 6 ; 
         R 3  is H, alkyl, heteroalkyl, aryl, or heteroaryl; 
         R 4  is H, alkyl, heteroalkyl, aryl, or heteroaryl; 
         R 5  is OR 7 , alkyl-OR 7 , or heteroalkyl-OR 7 ; 
         R 6  is alkyl, heteroalkyl, aryl, or heteroaryl; 
         R 7  is NO 2 , C(O)R 6 , C(O)alkyl-ONO 2  or C(O)heteroalkyl-ONO 2 ; 
         provided that when R 5  is OR 7 , R 7  is not NO 2  or C(O)R 6 ; 
         further provided that at least one of R 3  is and R 4  is not H, alkyl, or heteroalkyl.

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