IP Library Granted Patent US 9,044,518
Granted Patent B2
US 9,044,518 · App. 14/007,743 · Granted Jun 2, 2015

Auristatin tyramine phosphate salts and auristatin aminoquinoline derivatives and prodrugs thereof

Inventors: George R. Pettit (Paradise Valley, AZ); Fiona Hogan (Gilbert, AZ); Steven Toms (Wellington, NZ)
Assignee: ARIZONA BOARD OF REGENTS, A BODY CORPORATE OF THE STATE OF ARIZONA ACTING FOR AND ON BEHALF OF ARIZONA STATE UNIVERSITY
A61K47/48415C07D401/12C07D207/12C07K7/02G01N33/5014A61K38/00C07K5/0205A61K45/06A61K38/08A61K31/4709A61K31/472
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Quick Facts
Patent No.
US 9,044,518
App. No.
14/007,743
Granted
Jun 2, 2015
Kind
B2
Abstract

The present invention relates to new auristatin compounds and prodrugs thereof, compositions comprising them and uses thereof.

Claims (26)

1. A compound of formula (I):

wherein R is selected from the group consisting of:

R 1 and R 2 are independently selected from the group consisting of H, alkyl, alkenyl, alkynyl and a Linker Unit;

R 3 and R 4 are independently selected from the group consisting of lithium (Li + ), sodium (Na + ), potassium (K + ), hydrogen (H), morpholine, quinine, tris(hydroxymethyl)aminomethane (TRIS), serine, nitroarginine and a Linker Unit; and

each R 5 is selected from the group consisting of H, alkyl, alkenyl, alkynyl and a Linker Unit.

2. The compound of claim 1 , wherein R is:

3. The compound of claim 2 , wherein R 3 and R 4 are sodium.

4. The compound of claim 3 , wherein R 5 is H.

5. The compound of claim 1 , wherein R is

6. The compound of claim 1 , wherein R is

7. The compound of claim 1 , wherein R 1 is methyl and R 2 is methyl.

8. The compound of claim 1 , wherein one of R 1 or R 2 is a Linker Unit.

9. The compound of claim 8 , wherein the Linker Unit comprises an antibody.

10. A pharmaceutical composition comprising a compound of claim 1 or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier.

11. A pharmaceutical composition comprising a combination of compounds of claim 1 or pharmaceutically acceptable salts thereof and a pharmaceutically acceptable carrier.

12. The pharmaceutical composition of claim 10 or claim 11 , further comprising a therapeutically effective amount of chemotherapeutic agent selected from the group consisting of a tubulin-forming inhibitor, a topoisomerase inhibitor, and a DNA binder.

13. A method for killing or inhibiting the proliferation of tumor cells or cancer cells comprising treating tumor cells or cancer cells with a compound of claim 1 , or a pharmaceutically acceptable salt or solvate thereof, in an amount effective to kill or inhibit the proliferation of the tumor cells or cancer cells.

14. A method for treating cancer in a patient comprising administering to the patient a compound of claim 1 , or a pharmaceutically acceptable salt or solvate thereof, wherein the compound is administered in an amount effective to treat cancer.

15. The method of claim 12 , further comprising administering an effective amount of a chemotherapeutic agent.

16. The method of claim 13 or 14 , wherein the compound is in a formulation comprising a pharmaceutically acceptable carrier.

17. A method of inhibiting the growth of tumor cells that overexpress a tumor-associated antigen comprising administering to a patient the compound of claim 1 conjugated to an antibody that is specific for said tumor-associated antigen, and optionally a chemotherapeutic agent wherein the compound and said chemotherapeutic agent are each administered in amounts effective to inhibit growth of tumor cells in the patient.

18. The method of claim 17 , wherein the compound sensitizes the tumor cells to said chemotherapeutic agent.

19. The method of claim 17 , wherein the compound induces cell death.

20. The method of claim 17 , wherein the compound induces apoptosis.

21. The method of claim 17 , wherein the cancer is selected from the group consisting of breast, ovarian, stomach, endometrial, salivary gland, lung, kidney, colon, colorectal, thyroid, pancreatic, prostate and bladder cancer.

22. An article of manufacture comprising the compound of claim 1 , a container, and a package insert or label indicating that the compound can be used to treat cancer characterized by the overexpression of at least one tumor-associated antigen.

Assignments (3)
CONFIRMATORY LICENSE Recorded Aug 12, 2016
From: ARIZONA STATE UNIVERSITY-TEMPE CAMPUS
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 039670/0663 →
CONFIRMATORY LICENSE Recorded Aug 17, 2015
From: ARIZONA STATE UNIVERSITY-TEMPE CAMPUS
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 036374/0755 →
CONFIRMATORY LICENSE Recorded Dec 9, 2014
From: ARIZONA BOARD OF REGENTS, A BODY CORPORATE OF THE STATE OF ARIZONA ACTING FOR AND ON BEHALF OF ARIZONA STATE UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 034560/0817 →
Continuity (2)
Provisional Application 61469428 · Mar 30, 2011
Related Publication 20140023666A1 · Jan 23, 2014