IP Library Granted Patent US 9,133,097
Granted Patent B2
US 9,133,097 · App. 14/261,175 · Granted Sep 15, 2015

Use of unsaturated sphingosine compounds as chemotherapeutic agents for the treatment of cancer

Inventors: Julie D. Saba (Oakland, CA); Henrik Fyrst (Oakland, CA); Robert Bittman (Roslyn Heights, NY)
Assignees: Children's Hospital & Research Center at Oakland; Research Foundation of the City University of New York
C07C215/24A61K8/68A61K31/133A61K31/352A61K31/436A61K31/5377
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,133,097
App. No.
14/261,175
Granted
Sep 15, 2015
Kind
B2
Abstract

The present invention is directed to unsaturated sphingosine compounds which are useful as therapeutic agents for the treatment of cancer and for the treatment of other diseases including diabetes and infection with intracellular bacteria. The invention is also directed to methods of using the compounds and pharmaceutical compositions comprising the compounds in treating these diseases.

Claims (35)

1. A method of treating a cancer in a mammal, wherein the method comprises administering to the mammal a therapeutically effective amount of a compound selected from the group consisting of:

as an isolated stereoisomer or mixture thereof, or a pharmaceutically acceptable salt thereof, wherein at least one of:

a) the cancer is associated with activation of AKT,

b) the cancer is associated with activation of PI3 kinase,

c) the cancer is associated with a deficiency of PTEN activity,

d) the cancer is associated with activation of the Wnt signaling pathway,

e) the cancer comprises a gastrointestinal cancer,

f) the cancer is colon cancer,

g) the cancer is breast cancer,

h) the cancer is neuroblastoma,

i) the cancer is leukemia, or

j) the cancer comprises a brain tumor.

2. The method of claim 1 wherein at least one of:

(a) the compound is administered orally,

(b) the compound alters activity of a component of the AKT/PI 3 kinase signaling pathway,

(c) the compound inhibits activity of AKT,

(d) the compound inhibits cytosolic to membrane translocation of AKT, or

(e) the compound activates PTEN phosphatase.

3. A method for altering the activity of an AKT/PI 3 kinase signaling pathway component in a mammal, or for inhibiting a Wnt signaling pathway in a mammal in need thereof, comprising administering to the mammal a therapeutically effective amount of a compound selected from the group consisting of:

as an isolated stereoisomer or mixture thereof, or a pharmaceutically acceptable salt thereof.

4. The method of claim 3 wherein at least one of:

(a) the compound inhibits activity of AKT,

(b) the compound inhibits cytosolic to membrane translocation of AKT,

(c) the compound activates PTEN phosphatase, or

(d) inhibiting the Wnt signaling pathway comprises inducing translocation of β-catenin from a nucleus of a cell to cytoplasm of the cell.

5. A method for inducing apoptosis in a cell or for inducing autophagy in a cell in a patient in need thereof, comprising contacting the cell within the patient with a therapeutically effective amount of a compound selected from the group consisting of:

as an isolated stereoisomer or mixture thereof, or a pharmaceutically acceptable salt thereof.

6. A composition comprising a therapeutically effective amount of an mTOR inhibitor, rapamycin, or a PI 3 K inhibitor in combination with a compound selected from the group consisting of:

as an isolated stereoisomer or mixture thereof, or a pharmaceutically acceptable salt thereof.

7. A method of treating a cancer in a mammal, wherein the method comprises administering to the mammal a therapeutically effective amount of the composition of claim 6 .

8. A method for inducing apoptosis in a cell wherein the method comprises contacting the cell with the composition of claim 6 .

9. The method of claim 1 further comprising administering to the mammal a therapeutically effective amount of an mTOR inhibitor, rapamycin or a PI 3 K inhibitor.

10. The method of claim 9 wherein the PI 3 K inhibitor is selected from the group consisting of wortmannin and LY294002.

11. The method of claim 5 further comprising administering to the mammal a therapeutically effective amount of an mTOR inhibitor, rapamycin or a PI 3 K inhibitor.

12. The method of claim 11 wherein the PI 3 K inhibitor is selected from wortmannin and LY294002.

Assignments (1)
CONFIRMATORY LICENSE Recorded Jul 27, 2017
From: CHILDREN'S HOSPITAL & RES CTR AT OAKLAND
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 043115/0981 →
Continuity (3)
Division 12747253
Provisional Application 61013230 · Dec 12, 2007
Related Publication 20150051207A1 · Feb 19, 2015