US2021130271A1PendingUtilityA1

Pharmaceutical compositions comprising monoterpenes

79
Assignee: NEONC TECH INCPriority: Mar 3, 2010Filed: Dec 16, 2020Published: May 6, 2021
Est. expiryMar 3, 2030(~3.6 yrs left)· nominal 20-yr term from priority
C07C 29/78C07C 67/14A61K 31/045A61K 31/4188C07C 29/86A61N 5/10C07C 29/92C07C 201/16C07B 2200/07C07C 29/88C07C 201/12C07C 2601/16A61P 35/00A61K 45/06
79
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Claims

Abstract

The present invention provides a process for purifying a monoterpene or sesquiterpene having a purity greater than about 98.5% (w/w). The process comprises the steps of derivatizing the monoterpene (or sesquiterpene) to produce a monoterpene (or sesquiterpene) derivative, separating the monoterpene (or sesquiterpene) derivative, and releasing the monoterpene (or sesquiterpene) from the derivative. Also encompassed by the scope of the present invention is a pharmaceutical composition comprising a monoterpene (or sesquiterpene) having a purity greater than about 98.5% (w/w). The purified monoterpene can be used to treat a disease such as cancer. The present monoterpene (or sesquiterpene) may be administered alone, or may be co-administered with radiation or other therapeutic agents, such as chemotherapeutic agents.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A process for purifying (S)-perillyl alcohol comprising the steps of:
 (a) derivatizing a mixture comprising (S)-perillyl alcohol to form a perillyl alcohol derivative;   (b) crystallizing the perillyl alcohol derivative;   (c) separating the perillyl alcohol derivative crystals from the mixture;   (d) releasing the (S)-perillyl alcohol from the separated perillyl alcohol derivative from step (c); and,   (e) isolating the (S)-perillyl alcohol from step (d),   
       wherein the isolated (S)-perillyl alcohol has a purity of greater than about 98.5% (w/w). 
     
     
         2 . The process of  claim 1 , wherein the perillyl alcohol derivative is a perillyl alcohol ester. 
     
     
         3 . The process of  claim 2 , wherein the ester is a benzoate ester. 
     
     
         4 . The process of  claim 3 , wherein the benzoate ester is 3,5-dinitrobenzoate ester. 
     
     
         5 . The process of  claim 1 , wherein the isolated (S)-perillyl alcohol has a purity of greater than about 99.0% (w/w). 
     
     
         6 . The process of  claim 5 , wherein the isolated (S)-perillyl alcohol has a purity of greater than about 99.5% (w/w). 
     
     
         7 . The process of  claim 1 , wherein the mixture further comprises natural-product-derived or other impurities.

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