IP Library Granted Patent US 9,611,266
Granted Patent B2
US 9,611,266 · App. 14/993,029 · Granted Apr 4, 2017

Compounds and anti-tumor NQO1 substrates

Inventors: Paul J. Hergenrother (Champaign, IL); David A. Boothman (Dallas, TX); Joseph S. Bair (Albany, CA); Rahul Palchaudhuri (Cambridge, MA); Elizabeth I. Parkinson (Champaign, IL)
Assignees: The Board of Trustees of the University of Illinois; The Board of Regents of the University of Texas System
C07D471/04A61K31/47C07F9/6561C07H15/26
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 9,611,266
App. No.
14/993,029
Granted
Apr 4, 2017
Kind
B2
Abstract

Compounds of Formula (I) can be selectively lethal toward a variety of different cancer cell types. The compounds are useful for the management, treatment, control, or adjunct treatment of diseases, where the selective lethality is beneficial in chemotherapeutic therapy.

Claims (44)

1. A compound of the Formula (I):

wherein

R 1 is alkyl;

R 3 is H;

R 2 and R 4 are each independently —X—R;

each X is independently a direct bond, —C(═O)—, or (C 1 -C 20 )alkyl;

each R is independently alkyl, alkenyl, alkynyl, heteroalkyl, cycloalkyl, (cycloalkyl)heteroalkyl, aryl, heteroaryl, alkoxy, (alkoxy)alkyl, or saccharide;

wherein any alkyl or aryl can be optionally substituted with one or more hydroxy, amino, cyano, nitro, or halo groups;

provided that R 1 , R 2 , and R 4 are not each methyl;

or a salt or solvate thereof

provided that when R 1 , R 2 , and R 3 are methyl, R 4 is not H or methyl; and provided that when R 1 , R 3 , and R 4 are methyl, the group —X—R of R 2 is not acyloxy.

2. The compound of claim 1 wherein R 1 is a straight chain or branched (C 1-20 )alkyl group.

3. The compound of claim 1 wherein R 2 or R 4 is a straight chain or branched (C 1-20 )alkyl group.

4. The compound of claim 1 wherein R 1 is methyl, R 2 is methyl, or R 1 and R 2 are both methyl.

5. The compound of claim 1 wherein R 4 is methyl.

6. The compound of claim 1 wherein:

R 1 and R 2 are methyl; R 3 is hydrogen; and R 4 is ethyl; propyl; isopropyl; n-butyl; tert-butyl; isobutyl; n-pentyl; n-hexyl; 3-methybutyl; 3,3-dimethylbutyl; C 8-12 alkyl; cyclooctyl; cyclopropyl; methylcyclopropyl; ethylcyclopropyl; —CH 2 OPO 3 Na 2 ; —CH 2 CH 2 OPO 3 Na 2 ; —CH 2 OH; —CH 2 CH 2 OH; or hydroxypropyl;

R 1 and R 2 are ethyl; R 3 is hydrogen; and R 4 is alkyl;

R 1 and R 2 are propyl; R 3 is hydrogen; and R 4 is alkyl;

R 1 is methyl; R 2 is propyl; R 3 is hydrogen; and R 4 is alkyl;

R 1 is propyl; R 2 is methyl; R 3 is hydrogen; and R 4 is alkyl;

R 1 and R 4 are methyl; R 3 is hydrogen; and R 2 is ethyl, propyl; C 8-12 alkyl; —CH 2 OPO 3 Na 2 ; or —CH 2 OH; or

R 2 and R 4 are methyl, R 3 is hydrogen; and R 1 is ethyl, propyl, C 8-12 alkyl; —CH 2 OPO 3 Na 2 ; or —CH 2 OH.

7. The compound of claim 1 wherein the compound is a compound of Formula IA:

wherein

R 4 is —X—R;

X is a direct bond, —C(═O)—, or (C 1 -C 20 )alkyl;

each R is independently alkyl, alkenyl, alkynyl, heteroalkyl, cycloalkyl, (cycloalkyl)heteroalkyl, aryl, heteroaryl, alkoxy, or saccharide;

wherein any alkyl or aryl can be optionally substituted with one or more hydroxy, amino, cyano, nitro, or halo groups;

or a salt or solvate thereof.

8. The compound of claim 1 wherein the compound is:

or a salt or solvate thereof.

9. A pharmaceutical composition comprising a compound of claim 1 and a pharmaceutically acceptable carrier.

10. The pharmaceutical composition of claim 9 wherein the composition comprises a cyclodextrin.

11. The pharmaceutical composition of claim 9 wherein the composition is a liquid for injection or infusion.

12. The pharmaceutical composition of claim 9 wherein the composition is a solid for oral administration.

13. The compound of claim 1 wherein R 1 is a straight chain or branched (C 1-20 )alkyl group and wherein R 2 or R 4 is a straight chain or branched (C 1-20 )alkyl group.

14. The compound of claim 1 wherein R 1 is a straight chain or branched (C 1-12 )alkyl group and wherein R 2 or R 4 is a straight chain or branched (C 1-12 )alkyl group.

15. The compound of claim 7 wherein X is a direct bond and R is (C 1 -C 20 )alkyl.

16. The compound of claim 7 wherein X is a direct bond and R is a substituted (C 1 -C 12 )alkyl.

17. The compound of claim 7 wherein X is a direct bond and R is an unsubstituted (C 1 -C 12 )alkyl.

18. The compound of claim 7 wherein the compound is:

19. A pharmaceutical composition comprising a compound of claim 18 and a pharmaceutically acceptable carrier.

20. The pharmaceutical composition of claim 19 wherein the composition comprises a cyclodextrin.

Assignments (3)
CONFIRMATORY LICENSE Recorded May 24, 2017
From: UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 042550/0948 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 27, 2016
From: BOOTHMAN, DAVID A.
To: THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM
Reel/Frame 038396/0391 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 27, 2016
From: HERGENROTHER, PAUL J.; BAIR, JOSEPH S.; PALCHAUDHURI, RAHUL; PARKINSON, ELIZABETH I.
To: THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS
Reel/Frame 038396/0394 →
Continuity (4)
Continuation 14351861
Provisional Application 61662163 · Jun 20, 2012
Provisional Application 61547166 · Oct 14, 2011
Related Publication 20160122348A1 · May 5, 2016