IP Library Granted Patent US 7,879,866
Granted Patent B2
US 7,879,866 · App. 11/632,818 · Granted Feb 1, 2011

Inhibition of the activity of the capsaicin receptor in the treatment of obesity or obesity-related diseases and disorders

Assignee: Dorte Xenia Gram
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 7,879,866
App. No.
11/632,818
Granted
Feb 1, 2011
Kind
B2
Abstract

The present invention provides a method of treating diseases or disorders benefiting from inactivating or down regulating the activity of the capsaicin receptor in a mammal by inhibiting the activity of the capsaicin receptor. The present invention also provides a method of treating obesity and obesity-related diseases and disorders in a mammal by inhibiting the activity of the capasaicin receptor.

Claims (6)

1. A method for treating obesity in a mammal comprising:

administering to the mammal a therapeutically-effective amount of a compound that is a halogenated analog of resiniferatoxin; N-(3-acyloxy-2-benzylpropyl)-N-[4-(methylsulfonylamino)benzyl-thiourea; [N-(4-tert-butylbenzyl)-N′-[4-(methylsulfonylamino)benzyl]thiourea]; [N-(4-tertbutylbenzyl)-N′-[3-fluoro-4-(methylsulfonylamino)benzyl]thiourea; N-(4-chlorobenzyl)-N′-(4-hydroxy-3-iodo-5-methoxybenzyl)thiourea; 4-(3-Chloro-pyridin-2-yl)-piperazine-1-carboxylic acid (4-tert-butyl-phenyl)-amide, or (N-(3-methoxyphenyl)-4-chlorocinnamide.

2. The method according to claim 1 wherein the mammal is a human.

3. The method according to claim 1 , wherein the compound is 4-(3-Chloro-pyridin-2-yl)-piperazine-1-carboxylic acid (4-tert-butyl-phenyl)-amide.

4. A kit for treating obesity in a mammal in need thereof by inactivating or down regulating the activity of the capsaicin receptor, comprising a compound that is a halogenated analog of resiniferatoxin; N-(3-acyloxy-2-benzylpropyl)-N-[4-(methylsulfonylamino)benzyl-thiourea; [N-(4-tert-butylbenzyl)-N′-[4-(methylsulfonylamino)benzyl]thiourea]; [N-(4-tertbutylbenzyl)-N′-[3-fluoro-4-(methylsulfonylamino)benzyl]thiourea; N-(4-chlorobenzyl)-N′-(4-hydroxy-3-iodo-5-methoxybenzyl)thiourea; N-(4-tertiarybutylphenyl)-4-(3-chloropyridin-2-yl)tetrahydropyrazine-1(2H)-carboxamide, or (N-(3-methoxyphenyl)-4-chlorocinnamide.

5. A kit according to claim 4 , wherein the mammal is a human.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 10, 2014
From: XENIA PHARMA
To: P?LA PHARMA AB
Reel/Frame 032642/0890 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 28, 2014
From: GRAM, DORTE X.
To: XENIA PHARMA
Reel/Frame 032324/0232 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 24, 2009
From: NOVO NORDISK A/S
To: GRAM, DORTE XENIA
Reel/Frame 022326/0075 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 13, 2007
From: GRAM, DORTE XENIA; HANSEN, ANKER JON
To: NOVO NORDISK A/S
Reel/Frame 019821/0139 →
Priority Claims (1)
DK 2004 01126 · Jul 19, 2004 · national
Continuity (2)
Provisional Application 60589242 · Jul 20, 2004
Related Publication 20080214574A1 · Sep 4, 2008