Nlrx1 ligands

Abstract

Provided are compounds that target the nucleotide-binding oligomerization domain, leucine rich repeat containing X1 (NLRX1) pathway. The compounds can be used to treat conditions such as autoimmune diseases, allergic diseases, chronic and/or inflammatory central nervous system diseases, chronic and/or inflammatory respiratory diseases, cancer, and infectious diseases. Exemplary conditions include multiple sclerosis, asthma, Alzheimer's disease, Parkinson's disease, neuroinflammation resulting from, for example, stroke, traumatic brain injury, or spinal cord injury, chronic obstructive pulmonary disease, idiopathic pulmonary fibrosis, and inflammatory bowel disease.

1 - 28 . (canceled) 
     
     
         29 . A method of treating a condition in which NLRX1 is implicated in an animal with a compound, the method comprising administering an effective amount of the compound to the animal, wherein:
 the condition is selected from the group consisting of an autoimmune disease, an allergic disease, a chronic and/or inflammatory central nervous system disease, a chronic and/or inflammatory respiratory disease, cancer, and an infectious disease; and   the compound is a compound of Formula (I) having an A ring, a B ring, a C ring, a D ring, and an E ring:   
       
         
           
           
               
               
           
         
       
       or a salt or ester thereof, wherein:
 A′ and A 5  are each independently O, N(R A ), N(R ALK K), C(R A ) 2 , C(R A ), or N; 
 A 2 , A 3 , and A 4  are each independently O, N(R A ), N(R ALK ), C(R A ) 2 , C(R A ), N, C(R A )(R O ), C(R O ), or C(═O), with the proviso that A 4  is optionally absent; 
 A 6  and A 7  are each independently C(R A ) or N; 
 A 8 , A 9 , and A 0  are each independently O, N(R A ), N(R ALK ), C(R A ) 2 , C(R A ), or N; 
 A 11 , A 12 , A 13 , A 14 , and A 15  are each independently O, N(R A ), N(R ALK ), C(R A ) 2 , C(R A ), N, C(R A )(R O ), C(R O ), or C(═O), with the proviso that A 4  is optionally absent; 
 each --- between adjacent atoms represents a bond that is present or absent; 
 L is O, N(R L ), or C(R L ) 2 ; 
 R O  in each instance is independently hydroxyl or optionally substituted alkyloxy; 
 R ALK  in each instance is independently C1-C6 alkyl; and 
 R A , R B , and R L  in each instance is independently, hydrogen, halogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted cycloalkyl, optionally substituted cycloalkenyl, hydroxyl, carboxyl, optionally substituted alkyloxy, optionally substituted alkenyloxy, optionally substituted alkynyloxy, optionally substituted cycloalkyloxy, optionally substituted cycloalkenyloxy, mercapto, optionally substituted alkylthio, optionally substituted alkenylthio, optionally substituted alkynylthio, optionally substituted alkylsulfinyl, optionally substituted alkylsulfonyl, optionally substituted alkylsulfonyloxy, optionally substituted cycloalkylthio, optionally substituted cycloalkylsulfinyl, optionally substituted cycloalkylsulfonyl, optionally substituted cycloalkylsulfonyloxy, optionally substituted cycloalkenylthio, optionally substituted cycloalkenylsulfinyl, optionally substituted cycloalkenylsulfonyl, optionally substituted cycloalkenylsulfonyloxy, optionally substituted amino, acyl, optionally substituted alkyloxycarbonyl, optionally substituted alkenyloxycarbonyl, optionally substituted alkynyloxycarbonyl, optionally substituted aryloxycarbonyl, optionally substituted carbamoyl, optionally substituted sulfamoyl, cyano, nitro, optionally substituted aryl, optionally substituted aryloxy, optionally substituted arylthio, optionally substituted arylsulfinyl, optionally substituted arylsulfonyl, optionally substituted arylsulfonyloxy, optionally substituted heteroaryl, optionally substituted heteroaryloxy, optionally substituted heteroarylthio, optionally substituted heteroarylsulfinyl, optionally substituted heteroarylsulfonyl, optionally substituted heteroarylsulfonyloxy, or an optionally substituted non-aromatic heterocyclic group. 
 
     
     
         30 . The method of  claim 29 , wherein the condition is selected from the group consisting of multiple sclerosis, Alzheimer's disease, Parkinson's disease, and neuroinflammation. 
     
     
         31 . The method of  claim 29 , wherein the condition is selected from the group consisting of asthma, chronic obstructive pulmonary disease, and idiopathic pulmonary fibrosis. 
     
     
         32 . The method of  claim 29 , wherein the condition is inflammatory bowel disease. 
     
     
         33 . The method of  claim 29 , wherein A 2  is N. 
     
     
         34 . The method of  claim 29 , wherein A 3  is O, N(R A ), N(R ALK ), N, C(R O ), or C(═O). 
     
     
         35 . The method of  claim 29 , wherein:
 A 4  is present; A 1  and A 5  are each independently C(R A ) or N; and A 2 , A 3 , and A 4  are each independently C(R A ), N, or C(R O ); or   A 4  is absent and A 1 , A 2 , A 3 , and A 5  are each independently O, N(R A ), N(R ALK ), C(R A ), or N, with the proviso that exactly one of A 1 , A 2 , A 3 , and A 5  is O, N(R A ), or N(R ALK ).   
     
     
         36 . The method of  claim 35 , wherein A 2  is N. 
     
     
         37 . The method of  claim 35 , wherein A 3  is C(R O ), O, N(R A ), or N(R ALK ). 
     
     
         38 . The method of  claim 29 , wherein A 4  is present; A 1  and A 5  are each independently C(R A ) or N; and A 2 , A 3 , and A 4  are each independently C(R A ), N, or C(R O ). 
     
     
         39 . The method of  claim 38 , wherein A 2  is N. 
     
     
         40 . The method of  claim 39 , wherein A 3  is C(R O ). 
     
     
         41 . The method of  claim 40 , wherein the R O  of A 3  is hydroxyl. 
     
     
         42 . The method of  claim 29 , wherein A 10  is O, N, or NH. 
     
     
         43 . The method of  claim 29 , wherein A 11  is O, N(R A ), N(R ALK ), or N. 
     
     
         44 . The method of  claim 43 , wherein A 12  is C(═O). 
     
     
         45 . The method of  claim 43 , wherein A 14  is present. 
     
     
         46 . The method of  claim 29 , wherein R A , R B , and R L  in each instance are independently hydrogen, halogen, unsubstituted C1-C6 alkyl, hydroxyl, carboxyl, unsubstituted cycloalkyl, unsubstituted C1-C6 alkyloxy, unsubstituted amino, acyl, unsubstituted alkyloxycarbonyl, unsubstituted aryl, unsubstituted heteroaryl, or unsubstituted non-aromatic heterocyclic group. 
     
     
         47 . The method of  claim 29 , wherein R A , R B , and R L  in each instance are hydrogen. 
     
     
         48 . The method of  claim 29 , wherein the compound is any one of: 
       
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
       
       or a salt or ester thereof.