IP Library Granted Patent US 10,363,261
Granted Patent B2
US 10,363,261 · App. 15/557,288 · Granted Jul 30, 2019

Enolase inhibitors and methods of treatment therewith

Inventors: Florian Muller (Houston, TX); David S. Maxwell (Pearland, TX); William G. Bornmann (Missouri City, TX); Yu-Hsi Lin (Houston, TX); Basvoju A. Bhanu Prasad (Katy, TX); Zhenghong Peng (Missouri City, TX); Duoli Sun (Houston, TX); Nikunj Satani (Houston, TX); M. Emilia Di Francesco (Houston, TX); Ronald A. Depinho (Houston, TX); Barbara Czako (Houston, TX); Federica Pisaneschi (Houston, TX)
Assignee: Board of Regents, The University of Texas System
A61K31/675A61K45/06A61P35/00C07F9/5532C07F9/572C07F9/59A61K2300/00Y02A50/414Y02A50/415
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 10,363,261
App. No.
15/557,288
Granted
Jul 30, 2019
Kind
B2
Abstract

Provided herein are compounds of the formula (I) wherein the variables R 1 , R 2 , R 3 , R 4 , X 1 , X 2 , Y 1 , and A 1 are as defined herein. Such compounds may be used, for example, for the inhibition of enolase enzymes, including preferential inhibition of one isoenzyme of over one or more of the other isoenzymes. Methods of treatment using these compounds, as well as pharmaceutical compositions thereof, are also provided.

Claims (59)

1. A compound of the formula:

or a pharmaceutically acceptable salt, wherein:

R 1 is hydrogen, acyl (C≤12) or substituted acyl (C≤12) ;

R 2 is hydrogen, acyloxy (C≤12) , or substituted acyloxy (C≤12) ;

X 1 and X 2 are each independently O, S, or NR a , wherein:

R a is hydrogen, alkyl (C≤6) , or substituted alkyl (C≤6) ;

R 3 and R 4 are each independently hydrogen or alkyl (C≤12) , aryl (C≤12) , aralkyl (C≤12) , heteroaryl (C≤12) , heteroaralkyl (C≤12) , or a substituted version of these groups; or a phosphate protecting group; or R 3 and R 4 are taken together and are alkanediyl (C≤8) or substituted alkanediyl (C≤8) ; or —X 3 —R 5 ; wherein:

X 3 is a covalent bond, alkanediyl (C≤8) , or substituted alkanediyl (C≤8) ; and

R 5 is acyl (C≤18) , alkoxy (C≤18) , —C(O)-alkoxy (C≤18) , acyloxy (C≤18) , or a substituted version of any of these groups;

A 1 is alkanediyl (C1-3) ; and

Y 1 is hydrogen, amino, halo, hydroxy, phosphate, alkyl (C≤12) , or substituted alkyl (C≤12) .

2. The compound of claim 1 further defined as:

wherein:

R 2 is hydrogen, acyloxy (C≤12) , or substituted acyloxy (C≤12) ;

R 3 and R 4 are each independently hydrogen, alkyl (C≤12) , substituted alkyl (C≤12) , or a phosphate protecting group; and

A 1 is alkanediyl (C1-3) ; or

wherein:

R 1 is acyl (C≤12) or substituted acyl (C≤12) ;

R 2 is acyloxy (C≤12) , or substituted acyloxy (C≤12) ;

R 3 is alkyl (C≤12) , substituted alkyl (C≤12) , or a phosphate protecting group;

R 4 is hydrogen, alkyl (C≤12) , substituted alkyl (C≤12) , or a phosphate protecting group; and

A 1 is alkanediyl (C1-3) ;

or a pharmaceutically acceptable salt of either formula.

3. The compound of claim 2 further defined as:

wherein:

R 2 is hydrogen;

R 3 and R 4 are each independently hydrogen, alkyl (C≤12) , substituted alkyl (C≤12) , or a phosphate protecting group; and

A 1 is alkanediyl (C1-3) ;

or a pharmaceutically acceptable salt thereof.

4. The compound of claim 1 , wherein R 1 is hydrogen.

5. The compound of claim 1 , wherein R 2 is acyloxy (C≤8) or substituted acyloxy (C≤8) .

6. The compound of claim 1 , wherein R 2 is hydrogen.

7. The compound of claim 1 , wherein R 3 is a phosphate protecting group.

8. The compound of claim 7 , wherein R 3 is a phosphate protecting group of the formula: -alkanediyl (C≤6) -acyloxy (C≤12) or substituted -alkanediyl (C≤6) -acyloxy (C≤12) .

9. The compound of claim 8 , wherein R 3 is pivaloyloxymethyl.

10. The compound of claim 1 , wherein X 1 and X 2 are each O.

11. The compound of claim 1 , wherein R 4 is a phosphate protecting group.

12. The compound of claim 11 , wherein R 4 is a phosphate protecting group of the formula: -alkanediyl (C≤6) -acyloxy (C≤12) or substituted -alkanediyl (C≤6) -acyloxy (C≤12) .

13. The compound of claim 11 , wherein R 4 is pivaloyloxymethyl.

14. The compound of claim 1 , wherein A 1 is —CH 2 —, —CH 2 CH 2 —, or —CH 2 CH 2 CH 2 —.

15. The compound of claim 1 , wherein Y 1 is hydrogen.

16. The compound of claim 1 , wherein the compound is further defined as:

or a pharmaceutically acceptable salt of any of these formulas.

17. The compound of claim 16 , wherein the compound is further defined as:

or a pharmaceutically acceptable salt of any of these formulas.

18. A method of treating a glioma, a melanoma, lung cancer and/or a kidney cancer comprising administering to a patient in need thereof a therapeutically effective amount of a compound of the formula:

wherein:

R 1 is hydrogen, acyl (C≤12) or substituted acyl (C≤12) ;

R 2 is hydrogen, hydroxy, alkoxy (C≤12) , substituted alkoxy (C≤12) , acyloxy (C≤12) , or substituted acyloxy (C≤12) ;

X 1 and X 2 are each independently O, S, or NR a , wherein:

R a is hydrogen, alkyl (C≤6) , or substituted alkyl (C≤6) ;

R 3 and R 4 are each independently hydrogen or alkyl (C≤12) , aryl (C≤12) , aralkyl (C≤12) , heteroaryl (C≤12) , heteroaralkyl (C≤12) , or a substituted version of these groups; or a phosphate protecting group; or R 3 and R 4 are taken together and are alkanediyl (C≤8) or substituted alkanediyl (C≤8) ; or —X 3 —R 5 ; wherein:

X 3 is a covalent bond, alkanediyl (C≤8) , or substituted alkanediyl (C≤8) ; and

R 5 is acyl (C≤18) , alkoxy (C≤18) , —C(O)-alkoxy (C≤18) , acyloxy (C≤18) , or a substituted version of any of these groups;

A 1 is alkanediyl (C1-3) ; and

Y 1 is hydrogen, amino, halo, hydroxy, phosphate, alkyl (C≤12) , or substituted alkyl (C≤12) ;

or a pharmaceutically acceptable salt thereof.

19. A compound of the formula:

or a pharmaceutically acceptable salt of any of these formulas.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2019
From: MULLER, FLORIAN; MAXWELL, DAVID S.; BORNMANN, WILLIAM G.; LIN, YU-HSI; SATANI, NIKUNJ; DIFRANCESCO, M. EMILIA; DEPINHO, RONALD A.; CZAKO, BARBARA; PISANESCHI, FEDERICA
To: BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM
Reel/Frame 047946/0826 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2019
From: BHANU PRASAD, BASVOJU A.; PENG, ZHENGHONG; SUN, DUOLI
To: BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM
Reel/Frame 047946/0871 →
CONFIRMATORY LICENSE Recorded Apr 11, 2018
From: UNIVERSITY OF TX MD ANDERSON CAN CTR
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 045889/0710 →
Continuity (2)
Provisional Application 62130431 · Mar 9, 2015
Related Publication 20180147219A1 · May 31, 2018
Cited By (1)
US 12,679,855