IP Library Granted Patent US 12,303,511
Granted Patent B2
US 12,303,511 · App. 18/740,610 · Granted May 20, 2025

Methods related to opioid therapeutics

Inventors: Kirill Martemyanov (Jupiter, FL); Brock Grill (Lake Worth, FL)
Assignee: University of Florida Research Foundation, Incorporated
A61K31/519A61K31/095A61K31/166A61K31/175A61K31/397A61P25/36
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 12,303,511
App. No.
18/740,610
Granted
May 20, 2025
Kind
B2
Abstract

The present invention provides methods for modulating opioid receptor mediated analgesic effect, e.g., promoting or enhancing analgesia in subjects in need of pain relief. Also provided in the invention are methods for ameliorating or suppressing withdrawal symptoms in subjects with chronic opioid use. These methods of the invention entail administering to the subjects in need of treatment a therapeutically effective amount of a GPR139 antagonist compound. The invention further provides methods for identifying novel compounds that can be useful for modulating opioid receptor mediated analgesic effect.

Claims (12)

1. A method for suppressing or ameliorating withdrawal symptoms in subjects with chronic use of an opioid drug, comprising administering to the subject a pharmaceutical composition comprising an effective amount of a compound that down-regulates expression or cellular activity of GPR139 or an ortholog thereof, wherein the compound is a small organic molecule, thereby suppressing or ameliorating withdrawal symptoms in the subject.

2. The method of claim 1 , wherein the subject is administered the pharmaceutical composition after discontinuing use of the opioid drug.

3. The method of claim 2 , wherein the opioid drug is oxycodone, hydrocodone, morphine, codeine or fentanyl.

4. The method of claim 1 , wherein the subject is at risk of developing withdrawal symptoms or is a risk of relapse.

5. The method of claim 1 , wherein the subject is a human.

6. The method of claim 1 , wherein the compound down-regulates GPCR signaling activity of GPR139 or an ortholog thereof.

7. The method of claim 1 , wherein the compound is a small organic compound selected from the group consisting of:

8. A method for diminishing reinforcing effects of, or preventing or treating addiction to, opioid drugs in a subject, comprising administering to the subject a pharmaceutical composition comprising an effective amount of a compound that up-regulates expression or cellular activity of GPR139 or an ortholog thereof, wherein the compound is a small organic molecule, thereby diminishing reinforcing effects of, or preventing or treating addiction to, opioid drugs in the subject.

9. The method of claim 8 , wherein the GRP139 agonist compound administered to the subject is selected from following table:

or

or a Glycine benzamide.

10. A method for identifying an agent that modulates the μ-opioid receptor (MOR) signaling, comprising (a) screening test compounds to identify one or more modulating compounds that modulate expression or cellular activity of GPR139 or an ortholog thereof, and (b) testing the modulating compounds for ability to modulate an MOR signaling related activity; thereby identifying a MOR modulator.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 12, 2024
From: MARTEMYANOV, KIRILL; GRILL, BROCK
To: THE SCRIPPS RESEARCH INSTITUTE
Reel/Frame 067699/0641 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 12, 2024
From: THE SCRIPPS RESEARCH INSTITUTE
To: UNIVERSITY OF FLORIDA BOARD OF TRUSTEES
Reel/Frame 067700/0868 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 12, 2024
From: UNIVERSITY OF FLORIDA BOARD OF TRUSTEES
To: UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INCORPORATED
Reel/Frame 067701/0090 →
Continuity (3)
Division 17286187
Provisional Application 62746343 · Oct 16, 2018
Related Publication 20240342180A1 · Oct 17, 2024
References Cited (18)
US 12042496B2 · Martemyanov · 2024 [cited by examiner]
US 20160022636A1 · Dvorak et al. · 2016 [cited by applicant]
US 20170095480A1 · Hitchcock et al. · 2017 [cited by applicant]
US 20170348319A1 · Hitchcock · 2017 [cited by applicant]
WO WO2014152917A2 · 2014 [cited by applicant]
WO WO2020081538A1 · 2020 [cited by applicant]
Wang et al., Genetic behavioral screen identifies an orphan anti-opioid system, Science. Aug. 15, 2019;365(6459):1267-1273. [cited by examiner]
Kononoff, et al., “Systemic and Intra-Habenular Activation of the Orphan G Protein-Coupled Receptor GPR139 Decreases Compulsive-Like Alcohol Drinking and Hyperalgesia in Alcohol-Dependent Rats”, [cited by applicant]
Wang, et al., “High-throughput Screening of Antagonists for the Orphan G-protein Coupled Receptor GPR139”, [cited by applicant]
Carney, “Identification of a Novel Molecular Target for Alcohol Dependence”, [cited by applicant]
Hashimoto, et al., “Enhancement of Morphine Analgesic Effect with Induction of μ-Opioid Receptor Endocytosis in Rats”, [cited by applicant]
International Search Report and Written Opinion for Patent Cooperation Treaty Application No. PCT/US2019/056284, dated Jan. 30, 2020, 7 pages. [cited by applicant]
International Preliminary Report on Patentability for Patent Cooperation Treaty Application No. PCT/US2019/056284, dated Apr. 29, 2021, 6 pages. [cited by applicant]
Dvorak, “Identification and SAR of Glycine Benzamides as Potent Agonists for the GPR139 Receptor”, [cited by applicant]
Hu, “Identification of Surrogate Agonists and Antagonists for Orphan G-Protein-Coupled Receptor PR139”, [cited by applicant]
Ju, “GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids L-Tryptophan and L-Phenylalanine”, [cited by applicant]
Nohr, “The Orphan G Protein-Coupled Receptor GPR139 is Activated by the Peptides: Mrenocorticotropic Hormone (ACTH), a-, and b-Melanocyte Stimulating Hormone (a-MSH, and b-MSH), and the nserved core motif HFRW”, [cited by applicant]
Shi, “Discovery and SAR of a Series of Agonists at Orphan G Protein-Coupled Receptor 139”, [cited by applicant]