US2015216830A1PendingUtilityA1

5-aminolevulinic acid derivatives, methods for their preparation and uses thereof

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Assignee: UNIV BAR ILANPriority: Mar 24, 2011Filed: Mar 20, 2015Published: Aug 6, 2015
Est. expiryMar 24, 2031(~4.7 yrs left)· nominal 20-yr term from priority
A61K 45/06A61K 31/221A61K 41/0061A61K 31/197A61K 47/54A61K 47/55C07C 229/22A61K 31/225A61N 5/062A61K 2300/00
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Claims

Abstract

There are provided conjugates comprising 5-aminolevulinic acid (5-ALA), an aldehyde and a carboxylic acid (e.g., a histone deacetylase inhibitor), compositions comprising same, methods for their preparation and uses thereof for treatment of cancer and anemia, and for inducing erythropoiesis.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method for the treatment or prevention of anemia, or for the induction of erythropoiesis comprising the step of administering to a subject in need thereof a composition comprising Histone deacetylase (HDAC)-inhibitor and 5-aminolevulinic acid (5-ALA) or an ester thereof. 
     
     
         2 . The method of  claim 1 , wherein the ester is a methyl or a hexyl ester. 
     
     
         3 . The method of  claim 1 , wherein the HDAC inhibitor is a carboxylic acid. 
     
     
         4 . The method of  claim 3 , wherein the carboxylic acid is selected from the group consisting of pivalic, butyric, valeric, hexanoic, heptanoic, octanoic, decanoic, 4-phenylbutyric, 4-phenylacetic and retinoic acid. 
     
     
         5 . The method of  claim 3 , wherein the carboxylic acid is butyric, octanoic, decanoic or valeric acid. 
     
     
         6 . The method of  claim 3 , wherein the carboxylic acid is butyric acid or octanoic acid. 
     
     
         7 . The method of  claim 1 , wherein the composition is in a form suitable for oral administration, parenteral administration, topical administration, dermatological administration, administration by inhalation, or administration via a suppository. 
     
     
         8 . The method of  claim 1 , wherein the composition is in a form suitable for oral administration, intravenous administration by injection, or administration by inhalation. 
     
     
         9 . The method of  claim 1 , wherein the HDAC inhibitor is an inhibitor of a Class I HDAC and/or a Class II HDAC. 
     
     
         10 . The method of  claim 1 , wherein the HDAC inhibitor is a lysine deacetylase inhibitor.

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