Compositions and Methods For Increasing Telomerase Activity

Abstract

The present invention relates to methods and compositions for increasing telomerase activity in cells. Such compositions include pharmaceutical formulations. The methods and compositions are useful for treating diseases subject to treatment by an increase in telomerase activity in cells or tissue of a patient. They are also useful for enhancing replicative capacity of cells in culture, as in ex vivo cell therapy and for enhancing proliferation of stem and progenitor cells.

It is claimed: 
     
         1 . A compound of formula I: 
       
         
           
           
               
               
           
         
         wherein X 1 , is selected from keto, hydroxy, and 
       
       
         
           
           
               
               
           
         
         wherein X 2  is selected from keto, hydroxy, and 
       
       
         
           
           
               
               
           
         
         wherein X 3  is selected from keto, hydroxy, and 
       
       
         
           
           
               
               
           
         
         wherein at least one of X 1 , X 2 , and X 3  are 
       
       
         
           
           
               
               
           
         
         respectively; 
         wherein R 1  or R 2  are independently selected from —CH(CH 3 ) 2 , and —CH(CH 3 )CH 2 CH 3  and pharmaceutically acceptable salts thereof. 
       
     
     
         2 . The compound of  claim 1 , wherein X 1  is 
       
         
           
           
               
               
           
         
       
       wherein R 1  is selected from the group consisting of —CH(CH 3 ) 2  or —CH(CH 3 )CH 2 CH 3 . 
     
     
         3 . The compound of  claim 1 , wherein X 2  is 
       
         
           
           
               
               
           
         
       
       wherein R 2  is selected from the group consisting of —CH(CH 3 ) 2  or —CH(CH 3 )CH 2 CH 3 . 
     
     
         4 . The compound of  claim 1 , wherein X 3  is 
       
         
           
           
               
               
           
         
       
     
     
         5 . The compound of  claim 1 , wherein at least one of X 1 , X 2  or X 3  is 
       
         
           
           
               
               
           
         
       
     
     
         6 . The compound of  claim 1 , wherein both X 1  and X 2  are 
       
         
           
           
               
               
           
         
       
     
     
         7 . The compound of  claim 1 , wherein at least one of X 1  or X 2  is —OC(O)CH(NH 2 )CH(CH 3 )CH 2 CH 3 . 
     
     
         8 . The compound of  claim 1 , wherein both X 1  and X 2  are —OC(O)CH(NH 2 )CH(CH 3 )CH 2 CH 3 . 
     
     
         10 . The compound of  claim 1 , wherein X 1  is a —OC(O)CH(NH 2 )CH(CH 3 ) 2  and X 2  and X 3  are OH. 
     
     
         11 . The compound of  claim 1 , wherein X 1  is a —OC(O)CH(NH 2 )CH(CH 3 )CH 2 CH 3  and X 2  and X 3  are —OH. 
     
     
         12 . The compound of  claim 1 , wherein X 2  is a —OC(O)CH(NH 2 )CH(CH 3 ) 2  and X 1  and X 3  are OH. 
     
     
         13 . The compound of  claim 1 , wherein X 2  is a —OC(O)CH(NH 2 )CH(CH 3 )CH 2 CH 3  and X 1  and X 3  are OH. 
     
     
         14 . A compound selected from the group consisting of: 
       
         
           
           
               
               
           
         
         and pharmaceutically acceptable salts thereof. 
       
     
     
         15 . The compound of  claim 14  wherein the pharmaceutically acceptable salt is hydrochloride salt. 
     
     
         16 . A compound selected from the group consisting of:
 2-(L)-amino-3-methyl-butyric acid 6α, 16β-dihydroxy-17-[5-(1-hydroxy-1-methyl-ethyl)-2-methyl-tetrahydro-furan-2-yl]-4,4,13,14-tetramethyl-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-30-yl ester;   2-(L)-amino-3-methyl-butyric acid 6α-(2-amino-3-methyl-butyryloxy)-16β-hydroxy-17-[5-(1-hydroxy-1-methyl-ethyl)-2-methyl-tetrahydro-furan-2-yl]-4,4,13,14-tetramethyl-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-3β-yl ester;   2-(L)-tert-butoxycarbonylamino-3-methyl-butyric acid 3b-acetoxy-16b-hydroxy-17-[5-(1-hydroxy-1-methyl-ethyl)-2-methyl-tetrahydro-furan-2-yl]-4,4,13,14-tetramethyl-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-6a-yl ester;   2-(L),3-dimethyl-pentanoic acid 6α,16β-di hydroxy-17-[5-(1-hydroxy-1-methyl-ethyl)-2-methyl-tetrahydro-furan-2-yl]-4,4,13,14-tetramethyl-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-3β-yl ester,   2-(L)-Amino-3-methyl-butyric acid, 16β-hydroxy-17-[5-(1-hydroxy-1-methyl-ethyl)-2-methyl-tetrahydro-furan-2-yl]-4,4,13,14-tetramethyl-3-oxo-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-6α-yl ester;   2-(L)-Amino-3-methyl-pentanoic acid 6α-(2-amino-3-methyl-pentanoyloxy)-16β-hydroxy-17-[5-(1-hydroxy-1-methyl-ethyl)-2-methyl-tetrahydro-furan-2-yl]-4,4,13,14-tetramethyl-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-3β-yl ester;   2-(L)-Amino-3-methyl-butyric acid, 3β,6α-dihydroxy-16-hydroxy-17-[5-(1-hydroxy-1-methyl-ethyl)-2-methyl-tetrahydro-furan-2-yl]-4,4,13,14-tetramethyl-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-16β-yl ester;   and pharmaceutically acceptable salts thereof.   
     
     
         17 . The compound of  claim 16  wherein the pharmaceutically acceptable salt is hydrochloride salt. 
     
     
         18 . The compound of  claim 17  wherein the compound is selected from the group consisting of:
 2-(L)-amino-3-methyl-butyric acid 6α,16β-dihydroxy-17-[5-(1-hydroxy-1-methyl-ethyl)-2-methyl-tetrahydro-furan-2-yl]-4,4,13,14-tetramethyl-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-3β-yl ester hydrochloride salt; 
 2-(L)-amino-3-methyl-butyric acid 6α-(2-amino-3-methyl-butyryloxy)-16-hydroxy-17-[5-(1-hydroxy-1-methyl-ethyl)-2-methyl-tetrahydro-furan-2-yl]-4,4,13,14-tetramethyl-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-3β-yl ester hydrochloride salt; 
 2-(L)-tert-butoxycarbonylamino-3-methyl-butyric acid 3b-acetoxy-16b-hydroxy-17-[5-(1-hydroxy-1-methyl-ethyl)-2-methyl-tetrahydro-furan-2-yl]-4,4,13,14-tetramethyl-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-6α-yl ester hydrochloride salt; and 
 2-(L),3-dimethyl-pentanoic acid 6α,16β-di hydroxy-17-[5-(1-hydroxy-1-methyl-ethyl)-2-methyl-tetrahydro-furan-2-yl]-4,4,13,14-tetramethyl-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-3β-yl ester hydrochloride salt. 
 
     
     
         19 . A method of increasing telomerase activity in a cell or tissue comprising contacting said cell or tissue with an isolated compound of  claim 1 . 
     
     
         20 . The method of  claim 19  wherein the cell or tissue is identified as requiring increased telomerase activity. 
     
     
         21 . A pharmaceutical composition comprising the compound of  claim 1  in a pharmaceutically acceptable vehicle 
     
     
         22 . The composition of  claim 21 , wherein said compound is present in said composition at a concentration of at least 0.1% (w/v). 
     
     
         23 . The pharmaceutical composition comprising a topical formulation of the compound of  claim 1 . 
     
     
         24 . The composition of  claim 23 , wherein said topical formulation comprises one or more components selected from the group consisting of an emulsifier, a thickener, a carrier, and a skin emollient. 
     
     
         25 . A method of enhancing replicative capacity of cells in vitro or ex vivo, comprising contacting said cells with the compound of  claim 1 , in an amount effect to increase telomerase activity in said cells. 
     
     
         26 . The method of  claim 25 , wherein said cells are explant cells obtained from a patient.