IP Library › Granted Patent US 12,370,185
Granted Patent B2
US 12,370,185 · App. 17/590,061 · Granted Jul 29, 2025

TRPV2 antagonists

Inventors: Gonçalo Bernardes (Lisbon, PT); Tiago Rodrigues (Lisbon, PT); João Conde (Lisbon, PT); Charlotte Baker (Lisbon, PT)
Assignee: FUNDAÃO GIMM—GULBENKIAN INSTITUTE FOR MOLECULAR MEDICINE
A61K31/4412A61K9/06A61K45/06A61K47/40A61P35/00
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Quick Facts
Patent No.
US 12,370,185
App. No.
17/590,061
Granted
Jul 29, 2025
Kind
B2
Abstract

This invention relates to the finding that Piperlongumine compounds, such as Piperlongumine and analogues, derivatives and prodrugs thereof, are reversible, allosteric antagonists of transient receptor potential vanilloid 2 channel (TRPV2). Methods of treatment of conditions that are characterised by TRPV2 expression using Piperlongumine compounds and Piperlongumine compounds for use in such treatments are provided.

Claims (32)

1. A method of treating cancer characterized by transient receptor potential vanilloid 2 channel (TRPV2) expression comprising: providing a sample of cancer cells from a cancer patient, determining TRPV2 expression in the cancer cells, and administering a piperlongumine compound to the patient if TRPV2 is expressed in the cancer cells.

2. The method according to claim 1 wherein the piperlongumine compound is a reversible antagonist of TRPV2.

3. The method according to claim 1 wherein the piperlongumine compound is piperlongumine or an analogue, derivative or prodrug thereof.

4. The method according to claim 3 wherein the piperlongumine compound has the formula 1:

where Q 1 is O or S,

—Ar is an optionally substituted aryl group,

-D- is selected from —C(O)—, —C(S)—, —CH(OH)— and —CH(SH)—, and

—R 1 and —R 2 , together with —N-D- to which they are attached, form an optionally substituted heterocyclic ring, or —R 1 and —R 2 are each independently selected from hydrogen and optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl and aryl, and salts, solvates and protected forms thereof.

5. The method according to claim 4 , wherein Q 1 is O.

6. The method according to claim 3 , wherein -D- is —C(O)— or —C(S)—.

7. The method according to any one of claim 4 , wherein —R 1 and —R 2 , together with —N-D- to which they are attached, form an optionally substituted heterocyclic ring.

8. The method according to claim 7 , wherein the heterocyclic ring is partially unsaturated.

9. The method according to claim 8 , wherein -D- is —C(O)— or —C(S)—, and the unsaturation is conjugated with the —C(O)— or —C(S)—.

10. The method according to claim 9 , wherein the heterocyclic ring is a 4- to 9-membered ring.

11. The method according to any one of claim 10 , wherein —R 1 and —R 2 , together with —N-D- to which they are attached, form a β-unsaturated δ-lactam.

12. The method according to claim 4 , wherein Ar— is an optionally substituted carboaryl group, or an optionally substituted heteroaryl group.

13. The method according to claim 12 , wherein Ar— is optionally substituted phenyl.

14. The method according to any one of claim 13 , wherein Ar— is phenyl substituted with one or more groups selected from halo, cyano, —R S1 , —OH, —OR S1 , —SH, —SR S1 , —NH 2 , —NHR S1 , —NR S1 R S2 , —COON, —CONH 2 , —CONHR S1 , —CONR S1 R S2 , NHCOR S1 , —N(R S1 )COR S1 , where each —R S1 and each —R S2 is independently alkyl, alkenyl, alkynyl, aryl or aralkyl, which are optionally substituted with halo, or —R S1 and —R S2 may together form a heterocyclic ring.

15. The method according to claim 1 wherein cancer is a skin cancer, breast cancer, prostate cancer, brain cancer or blood cancer.

16. The method according to claim 15 wherein the cancer is a metastatic cancer.

17. The method according to claim 1 wherein the piperlongumine compound is encapsulated in a hydrogel.

18. The method of claim 6 , wherein -D- is —C(O).

19. The method of claim 10 , wherein the heterocyclic ring is a 4- to 6-membered ring.

20. The method of claim 19 , wherein the heterocyclic ring is a 6-membered ring.

21. The method of claim 11 , wherein —R1 and —R2, together with —N-D- to which they are attached is 5,6-dihydropyridin-2-one-1-yl.

22. The method of claim 12 , wherein Ar— is phenyl, pyridinyl, pyrimidinyl, furanyl, thiophenyl, or pyrrolyl.

23. The method of claim 1 , wherein the piperlongumine compound is piperlongumine.

24. The method of claim 1 , wherein TRPV2 expression is determined by a technique selected from PCR-based method, ELISA, immunofluorescent assay, chemiluminescent assay, and immunohistochemistry.

25. The method of claim 23 , wherein the technique comprises reverse transcription PCR.

26. The method of claim 1 , wherein the patient is a mammal.

27. The method of claim 25 , wherein the patient is a human.

28. The method of claim 1 , wherein the piperlongumine compound is administered to the patient if TRPV2 is expressed in one or more cancer cells greater than a predetermined threshold value.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 17, 2025
From: BERNARDES, GONÇALO JOSÉ LOPES; RODRIGUES, TIAGO CORREIA DE OLIVEIRA; CONDE, JOÃO; BAKER, CHARLOTTE
To: INSTITUTO DE MEDICINA MOLECULAR
Reel/Frame 071434/0401 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 17, 2025
From: INSTITUTO DE MEDICINA MOLECULAR JOÃO LOBO ANTUNES
To: FUNDAÇÁO GIMM - GULBENKIAN INSTITUTE FOR MOLECULAR MEDICINE
Reel/Frame 071434/0605 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 19, 2025
From: INSTITUTO DE MEDICINA MOLECULAR JOÃO LOBO ANTUNES
To: FUNDAÇÃO GIMM – GULBENKIAN INSTITUTE FOR MOLECULAR MEDICINE
Reel/Frame 070557/0903 →
Continuity (2)
Continuation 16647995
Related Publication 20220152006A1 · May 19, 2022
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