Water soluble tetrapyrollic photosensitizers for photodynamic therapy

Abstract

A tetrapyrollic photosensitizer compound having at least one pendant —CH 2 CH 2 CON(CH 2 CON(CH 2 COOH) 2 ) 2 or —N(CH 2 COOH) 2 group or esters thereof said tetrapyrollic compound being a chlorin, bacteriochlorin, porphyrin, pyropheophorbide, purpurinimide, or bacteriopurpurinimide. Desirably the compound has the formula: or a pharmaceutically acceptable derivative thereof, wherein R 1 —R 8 and R 10 are various substituents and R 9 is substituted or unsubstituted —CH 2 CH 2 CON(CH 2 CON(CH 2 COOH) 2 ) 2 ; or —N(CH 2 COOH) 2 . The invention also includes a method of treatment by photodynamic therapy by treatment with light after injecting the compound and a method of imaging by fluorescence after injection of the compound.

1 - 24 . (canceled) 
     
     
         25 . A method for detecting the presence of a hyperproliferative tissue in a subject comprising:
 (i) administering to the subject a sufficient quantity of a compound or a pharmaceutically acceptable derivative thereof, said compound or pharmaceutically acceptable derivative thereof being fluorescent or magnetically resonant and that preferentially associates with the hyperproliferative tissue; and   (ii) visualizing the compound within the patient by fluorescent spectroscopy when the compound is fluorescent or MRI when the compound is magnetically resonant;
 where the compound is a tetrapyrollic photosensitizer compound having at least one pendant —CH 2 CH 2 CON(CH 2 CON(CH 2 COOH) 2 ) 2  or —N(CH 2 COOH) 2  group or esters thereof said tetrapyrollic compound being a chlorin, bacteriochlorin, porphyrin, pyropheophorbide, purpurinimide, or bacteriopurpurinimide. 
   
     
     
         26 . The method of  claim 25  where the compound has the formula: 
       
         
           
           
               
               
           
         
         or a pharmaceutically acceptable derivative thereof, wherein:
 R 1  and R 2  are each independently substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, —C(O)R a  or —COOR a  or —CH(CH 3 )(OR) or —CH(CH 3 )(O(CH 2 ) n XR) where R a  is hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, or substituted or unsubstituted cycloalkyl where R 2  may be CH═CH 2 , CH(OR 20 )CH 3 , C(O)Me, C(═NR 21 )CH 3  or CH(NHR 21 )CH 3 ; 
 where X is an aryl or heteroaryl group; 
 n is an integer of 0 to 6; 
 R and R′ are independently H or lower alkyl of 1 through 8 carbon atoms; 
 where R 20  is methyl, butyl, heptyl, docecyl or 3,5-bis(trifluoromethyl)-benzyl; and R 21  is 3,5-bis(trifluoromethyl)benzyl; 
 R 1a  and R 2a  are each independently hydrogen or substituted or unsubstituted alkyl, or together form a covalent bond; 
 R 3  and R 4  are each independently hydrogen or substituted or unsubstituted alkyl; 
 R 3a  and R 4a  are each independently hydrogen or substituted or unsubstituted alkyl, or together form a covalent bond; 
 R 5  is hydrogen or substituted or unsubstituted alkyl; 
 R 6  and R 6a  are each independently hydrogen or substituted or unsubstituted alkyl, or together form ═O; 
 R 7  is a covalent bond, alkylene, azaalkyl, or azaaraalkyl or ═NR 20  where R 20  is hydrogen or lower alkyl of 1 through 8 carbon atoms or —CH 2 -3,5-bis(tri-fluoromethyl)benzyl or —CH 2 X—R 1  or —YR 1  where Y is an aryl or heteroaryl group; 
 R 8  and R 8a  are each independently hydrogen or substituted or unsubstituted alkyl or together form ═O; 
 R 9  is —CH 2 CH 2 CON(CH 2 CON(CH 2 COOH) 2 ) 2 ; or —N(CH 2 COOH) 2    
 R 10  is hydrogen, or substituted or unsubstituted alkyl and; 
 each of R 1 -R 10 , when substituted, is substituted with one or more substituents each independently selected from Q, where Q is alkyl, haloalkyl, halo, pseudohalo, or —COOR b  where R b  is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl, araalkyl, or OR c  where R c  is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, or aryl or CONR d R e  where R d  and R e  are each independently hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, or aryl, or NR f R g  where R f  and R g  are each independently hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, or aryl, or ═NR h  where R h  is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, or aryl, or is an amino acid residue; 
 each Q is independently unsubstituted or is substituted with one or more substituents each independently selected from Q 1 , where Q 1  is alkyl, haloalkyl, halo, pseudohalo, or —COOR b  where R b  is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl, araalkyl, or OR c  where R c  is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, or aryl or CONR d R e  where R d  and R e  are each independently hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, or aryl, or NR f R g  where R f  and R g  are each independently hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, or aryl, or ═NR h  where R h  is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, or aryl, or is an amino acid residue.