IP Library Granted Patent US 10,363,237
Granted Patent B2
US 10,363,237 · App. 15/072,194 · Granted Jul 30, 2019

Compositions and methods of inhibiting N-acylethanolamine-hydrolyzing acid amidase

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Quick Facts
Patent No.
US 10,363,237
App. No.
15/072,194
Granted
Jul 30, 2019
Kind
B2
Abstract

Compounds and pharmaceutical compositions are contemplated that inhibit N-acyl-ethanolamine-hydrolyzing acid amidase (NAAA) to so increase the concentration of the substrate of NAAA, palmitoylethanolamide (PEA). NAAA inhibition is contemplated to be effective to alleviate conditions associated with a reduced concentration of PEA. Among other uses, various NAAA inhibitors are especially contemplated as therapeutic agents in the treatment of inflammatory diseases.

Claims (28)

1. A method of treating a patient in need of increased levels of palmitoylethanolamide, comprising administering a pharmaceutical composition comprising a pharmaceutically acceptable carrier and a compound according to Formula I

wherein

A is O; B is O, or NR a ; R 1 and R 2 are independently H, halogen, or optionally substituted lower alkyl; n is 1; X is NR b or CHR b ; Y is C(O), C(S), or CHR c ; Z is O, S, NR d , or CHR d ; V is optionally substituted lower alkyl or optionally substituted lower alkenyl; wherein W is optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted cycloheteroalkyl, or C(R 3 R 4 R 5 ); and wherein Y and V may optionally form a 5- or 6 membered ring;

wherein R a , R b , R c , and R d are independently selected from the group consisting of H, optionally substituted lower alkyl, or optionally substituted lower thioalkyl; and

wherein R 3 , R 4 , and R 5 are independently H, optionally substituted lower alkyl, optionally substituted lower aryl, optionally substituted lower cycloheteroalkyl, or optionally substituted lower heteroaryl.

2. The method of claim 1 wherein X is NR b and Y is C(O) or C(S).

3. The method of claim 2 wherein Z is O or CHR d , V is lower alkyl, and wherein W is aryl or lower alkyl.

4. The method of claim 2 wherein W is aryl or lower alkyl.

5. The method of claim 1 wherein the patient has a condition associated with reduced levels of palmitoylethanolamide.

6. The method of claim 5 wherein the condition associated with reduced levels of palmitoylethanolamide includes an inflammatory component, and wherein administration of the composition reduces inflammation in the patient.

7. The method of claim 5 wherein the condition is rheumatoid arthritis, osteoarthritis, asthma, allergic dermatitis, psoriasis, an inflammatory bowel disease, or a spinal cord injury.

8. The method of claim 1 wherein the compound has the formula:

wherein

A is O; B is O, or NR a ; R 1 and R 2 are independently H, halogen, or optionally substituted lower alkyl; X is NR b or CHR b ; Y is C(O), C(S), or CHR c ; Z is O, S, NR d , or CHR d ; V is optionally substituted lower alkyl or optionally substituted lower alkenyl; wherein W is optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted cycloheteroalkyl, or C(R 3 R 4 R 5 );

wherein R a , R b , R c , and R d are independently selected from the group consisting of H, optionally substituted lower alkyl, or optionally substituted lower thioalkyl; and

wherein R 3 , R 4 , and R 5 are independently H, optionally substituted lower alkyl, optionally substituted lower aryl, optionally substituted lower cycloheteroalkyl, or optionally substituted lower heteroaryl.

9. The method of claim 8 wherein R 3 , R 4 , and R 5 are independently H or lower alkyl.

10. The method of claim 8 wherein R 3 , R 4 , and R 5 are independently H.

11. The method of claim 8 wherein B is O.

12. The method of claim 8 wherein X is NR b and Y is C(O) or C(S).

13. The method of claim 8 wherein R 1 is H and R 2 is lower alkyl.

14. The method of claim 12 wherein R 1 is H and R 2 is lower alkyl.

15. The method of claim 8 wherein V is methyl, ethyl, n-propyl, n-butyl, t-butyl, i-butyl, 2-methylpropyl, cyclopropylmethyl, i-amyl, n-amyl, hexyl or optionally substituted lower alkenyl.

16. The method of claim 8 wherein V is n-amyl.

17. The method of claim 8 wherein Z is O or CHR d .

18. The method of claim 8 wherein W is phenyl substituted with hydroxyl, thiol, alkylthiol, halogen, alkoxy, amino, amido, nitro, carboxyl, cycloalkyl, heterocycle, cycloheteroalkyl, acyl, carboxyl, aryl, aryloxy, heteroaryl, arylalkyl, heteroarylalkyl, alkyl, alkenyl, alknyl or cyano.

19. The method of claim 8 wherein W is biphenyl.

20. The method of claim 8 wherein W is phenyl.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 28, 2018
From: PIOMELLI, DANIELE
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 047012/0713 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 28, 2018
From: MOR, MARCO
To: UNIVERSITA DEGLI STUDI DI PARMA
Reel/Frame 047012/0721 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 28, 2018
From: TARZIA, GIORGIO; DURANTI, ANDREA; TONTINI, ANDREA
To: UNIVERSITA DEGLI STUDI DI URBINO "CARLO BO"
Reel/Frame 047012/0750 →