US2022001033A1PendingUtilityA1

Phosphate compounds for detecting neurological disorders

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Assignee: AMYDIS INCPriority: Nov 2, 2018Filed: Nov 1, 2019Published: Jan 6, 2022
Est. expiryNov 2, 2038(~12.3 yrs left)· nominal 20-yr term from priority
C07F 9/59C07D 295/155A61K 49/0021A61K 9/0048A61P 25/28A61P 25/16
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Claims

Abstract

Provided herein are compounds, methods and compositions for determining whether a patient has a neurological disease or disorder is provided, comprising detecting the presence of a detectable target protein, or an accumulated mass thereof, for example, amyloid beta protein or phosphorylated tau protein, or an accumulated mass thereof, in a tissue or a sample of the patient. The detecting may comprise contacting the target protein with a compound described herein.

Claims

exact text as granted — not AI-modified
1 .- 24 . (canceled) 
     
     
         25 . A compound of formula I, or a pharmaceutically acceptable salt thereof: 
       
         
           
           
               
               
           
         
       
       wherein R 1  is selected from 
       
         
           
           
               
               
           
         
         each X is independently O or S; 
         each R 11  is independently selected from hydrogen, C 1-10  alkyl, C 2-6  alkenyl, C 2-6  alkynyl, C 3-10  cycloalkyl, C 6-10  aryl, 5- to 10-membered heteroaryl and 4- to 10-membered heterocyclyl; 
         wherein alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl and heterocyclyl are optionally substituted with one to four R 21 ; or each XR 11  may independently be —XP(X)(R 12 ) 2 ; 
         each R 12  is independently selected from hydroxy, thiol, —XP(X)(R 13 ) 2 , C 1-10  alkyl, —O—C 1-10  alkyl, and —S—C 1-10  alkyl; 
         each R 13  is independently selected from hydroxy, thiol, C 1-10  alkyl, —O—C 1-10  alkyl, and —S—C 1-10  alkyl; 
         each R 21  is independently selected from halo, hydroxy, thiol, —NO 2 , —N 3 , cyano, C 1-10  alkyl, C 2-6  alkenyl, C 2-6  alkynyl, C 3-10  cycloalkyl, C 1-8  haloalkyl, C 6-10  aryl, 5- to 10-membered heteroaryl, 4- to 10-membered heterocyclyl, —O—C 1-10  alkyl, —O—C 2-6  alkenyl, —O—C 2-6  alkynyl, —O—C 3-10  cycloalkyl, —O—C 1-8  haloalkyl, —O-aryl, —O-heteroaryl, —O-heterocyclyl, —NH 2 , —NH(R 31 ), —N(R 31 ) 2 , —C(O)(R 31 ), —C(O)O(R 31 ), —C(O)OH, —C(O)NH 2 , —C(O)NH(R 31 ), —C(O)N(R 31 ) 2 , —NHC(O)(R 31 ), —NHC(O)O(R 31 ), —NHC(O)NH(R 31 ), —S(R 31 ), —NHS(O) y (R 31 ), —N(C 1-10  alkyl)S(O) y (R 31 ), —S(O) y N(R 31 ) 2 , —S(O)NH(R 31 ), and —S(O) y (R 31 ); 
         each R 31  is independently selected from C 1-10  alkyl, C 2-6  alkenyl, C 2-6  alkynyl, C 3-10  cycloalkyl, C 1-8  haloalkyl, aryl, heteroaryl, and heterocyclyl; and 
         each y is independently 1 or 2. 
       
     
     
         26 . The compound of  claim 25 , wherein R 1  is 
       
         
           
           
               
               
           
         
       
     
     
         27 . The compound of  claim 25 , wherein each X is independently O. 
     
     
         28 . The compound of  claim 25 , wherein R 1  is 
       
         
           
           
               
               
           
         
       
     
     
         29 . The compound of  claim 25 , wherein R 1  is 
       
         
           
           
               
               
           
         
       
     
     
         30 . The compound of  claim 25 , having the formula 
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt thereof. 
     
     
         31 . The compound of  claim 25 , having the formula 
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt thereof. 
     
     
         32 . A compound 
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt thereof. 
     
     
         33 . The compound of  claim 30  as a sodium salt, potassium salt, lithium salt, calcium salt, magnesium salt, zinc salt, diisopropylamine salt, triethylamine salt, diethylamine salt, ammonium salt, diammonium salt, tri(iso-propyl)amine salt, tri(n-propyl)amine salt, ethanolamine salt, 2-dimethylaminoethanol salt, piperazine salt, piperidine salt, morpholine salt, N-ethylpiperidine salt, or a mixed alkyl and aryl amine salt. 
     
     
         34 . The compound of  claim 31 , as a sodium salt, potassium salt, lithium salt, calcium salt, magnesium salt, zinc salt, diisopropylamine salt, triethylamine salt, diethylamine salt, ammonium salt, diammonium salt, tri(iso-propyl)amine salt, tri(n-propyl)amine salt, ethanolamine salt, 2-dimethylaminoethanol salt, piperazine salt, piperidine salt, morpholine salt, N-ethylpiperidine salt, or a mixed alkyl and aryl amine salt. 
     
     
         35 . The compound of  claim 32 , a sodium salt, potassium salt, lithium salt, calcium salt, magnesium salt, zinc salt, diisopropylamine salt, triethylamine salt, diethylamine salt, ammonium salt, diammonium salt, tri(iso-propyl)amine salt, tri(n-propyl)amine salt, ethanolamine salt, 2-dimethylaminoethanol salt, piperazine salt, piperidine salt, morpholine salt, N-ethylpiperidine salt, or a mixed alkyl and aryl amine salt. 
     
     
         36 . A pharmaceutical composition comprising the compound of  claim 25  and a pharmaceutically acceptable carrier. 
     
     
         37 . A method for determining whether a patient has a neurological disease or disorder, comprising administering to the patient a compound according to  claim 25 . 
     
     
         38 . The method of  claim 37 , wherein the compound is administered to the eye of the patient. 
     
     
         39 . The method of  claim 37 , further comprising detecting the presence or absence of binding of the compound or its parent compound with a detectable target protein. 
     
     
         40 . The method of  claim 39 , wherein the detection comprises activation of a tissue of the patient to be examined by a light thereby producing emission of a detectable signal, and detecting the detectable signal. 
     
     
         41 . The method of  claim 37 , wherein the neurological disease or disorder is Alzheimer's disease or traumatic brain injury (TBI). 
     
     
         42 . The method of  claim 37 , wherein the neurological disease or disorder is selected from an age-related disease or disorder, a genetic disease or disorder, an injury-related disease or disorder, and a psychiatric disease or disorder. 
     
     
         43 . The method of  claim 42 , wherein the age-related disease or disorder is selected from Parkinson's disease, vascular dementia, and Amyotrophic lateral sclerosis, wherein the genetic disease or disorder is Down syndrome, wherein the injury-related disease or disorder is selected from traumatic brain injury and chronic traumatic encephalopathy, and wherein the psychiatric disease or disorder is selected from schizophrenia and depression.

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