US2012157549A1PendingUtilityA1

Methods of preventing, treating and diagnosing disorders of protein aggregation

Assignee: MCLAURIN JOANNEPriority: Feb 27, 2003Filed: Feb 29, 2012Published: Jun 21, 2012
Est. expiryFeb 27, 2023(expired)· nominal 20-yr term from priority
Inventors:Joanne Mclaurin
A61P 9/00A61P 25/08A61P 25/02A61P 25/28A61P 35/00A61P 29/00A61P 3/10A61P 25/00A61P 31/00A61P 25/16A61P 25/14A61K 31/70A61K 51/04A61K 51/0491G01N 33/60G01N 33/6896A61K 31/047A61P 11/02A61P 21/00A61K 45/06
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Claims

Abstract

Disclosed are methods of preventing, treating, or diagnosing in a subject a disorder in protein folding or aggregation, or amyloid formation, deposition, accumulation, or persistence consisting of administering to said subject a pharmaceutically effective amount of inositol stereoisomers, enantiomers or derivatives thereof.

Claims

exact text as granted — not AI-modified
1 . A method of treating or preventing in a subject a condition of the central or peripheral nervous system or systemic organ associated with a disorder in protein folding or aggregation, or amyloid formation, deposition, accumulation, or persistence comprising administering to said subject a pharmaceutically effective amount of a compound having the following structure: 
       
         
           
           
               
               
           
         
         wherein each of R 1 , R 1′ , R 2 , R 2′ , R 3 , R 3′ , R 4 , R 4′ , R 5 , R 5′ , R 6 , and R 6′  is independently selected from the group of: 
         (a) hydrogen atom; 
         (b) NHR 7 , wherein said R 7  is selected from the group of hydrogen; C 2 -C 10  acyl and C 1 -C 10  alkyl; 
         (c) NR 8 R 9 , wherein said R 8  is C 2 -C 10  acyl or C 1 -C 10  alkyl and said R 9  is C 2 -C 10  acyl or C 1 -C 10  alkyl; 
         (d) OR 10 , wherein said R 10  is selected from the group of no group, hydrogen, C 2 -C 10  acyl, C 1 -C 10  alkyl and SO 3 H; 
         (e) C 5 -C 7  glycosyl; 
         (f) C 3 -C 8  cycloalkyl optionally substituted with a substituent selected from the group of hydrogen, OH, NH 2 , SH, OSO 3 H and OPO 3 H 2 ; 
         (g) SR 11 , wherein R 11  is selected from the group of hydrogen, C 1 -C 10  alkyl and O 3 H; 
         (h) C 1 -C 10  alkyl optionally substituted with a substituent selected from the group of hydrogen, OR 10 , NH R7 , NR 8 R 9  and SR 11 ; and 
         (i) C 3 -C 8  cycloalkyl optionally substituted with a substituent selected from the group of hydrogen, OR 10 , NHR 7 , NR 8 , R 9  and SR 11 , 
       
       providing that the compound is not myo-inositol. 
     
     
         2 .- 201 . (canceled)

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