IP Library Granted Patent US 10,457,618
Granted Patent B2
US 10,457,618 · App. 15/220,135 · Granted Oct 29, 2019

Pharmaceutical compositions comprising monoterpenes

Inventors: Thomas Chen (La Canada, CA); Daniel Levin (La Canada, CA); Satish Puppali (Rancho Cucamonga, CA)
Assignee: NeOnc Technologies, Inc.
C07C29/92A61K31/045A61K31/4188A61K45/06A61N5/10C07C29/78C07C29/86C07C29/88C07C67/14C07C201/12C07C201/16C07B2200/07C07C2601/16
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Quick Facts
Patent No.
US 10,457,618
App. No.
15/220,135
Granted
Oct 29, 2019
Kind
B2
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 (21)

1. A process for purifying (S)-perillyl alcohol consisting essentially of the steps of:

(a) derivatizing a mixture comprising (S)-perillyl alcohol to form a perillyl alcohol derivative, wherein the perillyl alcohol derivative is a 3,5-dinitrobenzoate ester derivative of perillyl alcohol;

(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).

2. The process of claim 1 , wherein the isolated (S)-perillyl alcohol has a purity of greater than about 98.5% (w/w).

3. The process of claim 2 , wherein the isolated (S)-perillyl alcohol has a purity of greater than about 99.0% (w/w).

4. The process of claim 1 , wherein the mixture further comprises natural-product-derived or other impurities.

5. The process of claim 3 , wherein the isolated (S)-perillyl alcohol has a purity of greater than about 99.5% (w/w).

6. A process for purifying perillyl alcohol comprising the steps of:

(a) derivatizing a mixture comprising perillyl alcohol to form a perillyl alcohol derivative, wherein the perillyl alcohol derivative is a 3,5-dinitrobenzoate ester derivative of perillyl alcohol;

(b) crystallizing the perillyl alcohol derivative;

(c) separating the perillyl alcohol derivative crystals from the mixture;

(d) releasing the perillyl alcohol from the separated perillyl alcohol derivative from step (c); and,

(e) isolating the perillyl alcohol from step (d).

7. The process of claim 6 , wherein the isolated perillyl alcohol has a purity of greater than about 98.5% (w/w).

8. The process of claim 7 , wherein the isolated perillyl alcohol has a purity of greater than about 99.0% (w/w).

9. The process of claim 8 , wherein the isolated perillyl alcohol has a purity of greater than about 99.5% (w/w).

10. The process of claim 6 , wherein the mixture further comprises natural-product-derived or other impurities.

11. The process of claim 6 , wherein the perillyl alcohol is (S)-perillyl alcohol.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 23, 2023
From: NEONC TECHNOLOGIES INC.
To: UNIVERSITY OF SOUTHERN CALIFORNIA
Reel/Frame 063726/0859 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 23, 2018
From: CHEN, THOMAS; LEVIN, DANIEL; PUPPALI, SATISH
To: NEONC TECHNOLOGIES INC.
Reel/Frame 045885/0396 →
Continuity (5)
Continuation 14843097 · Sep 2, 2015
Continuation 13939834 · Jul 11, 2013
Continuation 13040059 · Mar 3, 2011
Provisional Application 61310231 · Mar 3, 2010
Related Publication 20160332942A1 · Nov 17, 2016
Cited By (1)
US 12,245,355