IP Library Granted Patent US 9,340,544
Granted Patent B2
US 9,340,544 · App. 13/720,956 · Granted May 17, 2016

Purinyl derivatives and their use as potassium channel modulators

Inventors: Birgitte L. Eriksen (Farum, DK); Ulrik Svane Sørensen (Søborg, DK); Charlotte Hougaard (Bagsværd, DK); Dan Peters (Malmö, DK); Tina Holm Johansen (Smørum, DK); Palle Christophersen (Ballerup, DK)
Assignee: ATAXION, INC.
C07D473/16C07D473/24
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Quick Facts
Patent No.
US 9,340,544
App. No.
13/720,956
Granted
May 17, 2016
Kind
B2
Abstract

This invention relates to novel purinyl derivatives and their use as potassium channel modulating agents. Moreover the invention is directed to pharmaceutical compositions useful for the treatment or alleviation of diseases or disorders associated with the activity of potassium channels.

Claims (47)

1. A method of treatment or alleviation of a disease, or a disorder, or a condition of a mammal, comprising administering to a patient in need thereof an effective amount of a purinyl derivative of Formula Ia or Ib

a stereoisomer thereof or a mixture of its stereoisomers, an N-oxide thereof, or a pharmaceutically acceptable salt thereof, wherein

n is 0, 1, 2 or 3;

X represents O, S or NR′, wherein R′ represents hydrogen, alkyl, cycloalkyl, phenyl or benzyl;

Y represents alkyl, cycloalkyl, phenyl, benzo[1,3]dioxolyl or pyridyl; which alkyl, cycloalkyl, phenyl, benzo[1,3]dioxolyl and pyridyl are optionally substituted with one substituent selected from the group consisting of alkyl, cycloalkyl, halo, trifluoromethyl, trifluoromethoxy, hydroxy, alkoxy, cyano, nitro and amino;

R 1 represents hydrogen, alkyl or alkoxy-alkyl; and

Het represents a heterocyclic group selected from pyrazolyl, imidazolyl, indazolyl, benzimidazolyl and pyridinyl, which pyrazolyl, imidazolyl, indazolyl, benzimidazolyl and pyridinyl are substituted two or more times with substituents selected from the group consisting of alkyl, hydroxy-alkyl, cycloalkyl, cycloalkyl-alkyl, alkenyl, alkynyl, halo, trifluoromethyl, trifluoromethoxy, hydroxy, alkoxy, alkoxy-carbonyl, carboxy, cyano, nitro, amino, amino-carbonyl, N,N-dialkyl-amino-carbonyl, phenyl, benzyl and furanyl,

wherein the disease, disorder or condition is a epilepsy, overactive bladder, cerebral ischaemia, or ataxia.

2. The method of claim 1 , wherein the mammal is a human.

3. A method of activating small conductance calcium-activated potassium channels (SK channels) in a mammal comprising administering to the mammal a purinyl derivative of Formula Ia or Ib

a stereoisomer thereof or a mixture of its stereoisomers, an N-oxide thereof, or a pharmaceutically acceptable salt thereof, wherein

n is 0, 1, 2 or 3;

X represents O, S or NR′, wherein R′ represents hydrogen, alkyl, cycloalkyl, phenyl or benzyl;

Y represents alkyl, cycloalkyl, phenyl, benzo[1,3]dioxolyl or pyridyl; which alkyl, cycloalkyl, phenyl, benzo[1,3]dioxolyl and pyridyl are optionally substituted with one substituent selected from the group consisting of alkyl, cycloalkyl, halo, trifluoromethyl, trifluoromethoxy, hydroxy, alkoxy, cyano, nitro and amino;

R 1 represents hydrogen, alkyl or alkoxy-alkyl; and

Het represents a heterocyclic group selected from pyrazolyl, imidazolyl, indazolyl, benzimidazolyl and pyridinyl, which pyrazolyl, imidazolyl, indazolyl, benzimidazolyl and pyridinyl are substituted two or more times with substituents selected from the group consisting of alkyl, hydroxy-alkyl, cycloalkyl, cycloalkyl-alkyl, alkenyl, alkynyl, halo, trifluoromethyl, trifluoromethoxy, hydroxy, alkoxy, alkoxy-carbonyl, carboxy, cyano, nitro, amino, amino-carbonyl, N,N-dialkyl-amino-carbonyl, phenyl, benzyl and furanyl.

4. The method of treatment or alleviation of a disease, or a disorder, or a condition of a mammal, comprising:

administering to a patient in need thereof an effective amount of a purinyl derivative of Formula Ia or Ib

a stereoisomer thereof or a mixture of its stereoisomers, an N-oxide thereof, or a pharmaceutically acceptable salt thereof, wherein

n is 0, 1, 2 or 3;

X represents O S or NR′, wherein R′ represents hydrogen, alkyl, phenyl or benzyl;

Y represents alkyl, cycloalkyl, phenyl, benzo[1,3]dioxolyl or pyridyl; which alkyl, cycloalkyl, phenyl, benzo[1,3]dioxolyl and pyridyl are optionally substituted with one substituent selected from the group consisting of alkyl, cycloalkyl, halo, trifluoromethyl, trifluoromethoxy, hydroxy, alkoxy, cyano, nitro and amino;

R 1 represents hydrogen, alkyl or alkoxy-alkyl; and

Het represents a heterocyclic group selected from pyrazolyl, imidazolyl, indazolyl, benzimidazolyl and pyridinyl, which pyrazolyl, imidazolyl, indazolyl, benzimidazolyl and pyridinyl are substituted two or more times with substituents selected from the group consisting of alkyl, hydroxy-alkyl, cycloalkyl, cycloalkyl-alkyl, alkenyl, alkynyl, halo, trifluoromethyl, trifluoromethoxy, hydroxy, alkoxy, alkoxy-carbonyl, carboxy, cyano, nitro, amino, amino-carbonyl, N,N-dialkyl-amino-carbonyl, phenyl, benzyl and furanyl,

wherein the disease, disorder or condition is epilepsy.

5. The method of treatment or alleviation of a disease, or a disorder, or a condition of a mammal, comprising:

administering to a patient in need thereof an effective amount of a purinyl derivative of Formula Ia or Ib

a stereoisomer thereof or a mixture of its stereoisomers, an N-oxide thereof, or a pharmaceutically acceptable salt thereof, wherein

n is 0, 1, 2 or 3;

X represents O, S or NR′, wherein R′ represents hydrogen, alkyl, cycloalkyl, phenyl or benzyl;

Y represents alkyl, cycloalkyl, phenyl, benzo[1,3]dioxolyl or pyridyl; which alkyl, cycloalkyl, phenyl, benzo[1,3]dioxolyl and pyridyl are optionally substituted with one substituent selected from the group consisting of alkyl, cycloalkyl, halo, trifluoromethyl, trifluoromethoxy, hydroxy, alkoxy, cyano, nitro and amino;

R 1 represents hydrogen, alkyl or alkoxy-alkyl; and

Het represents a heterocyclic group selected from pyrazolyl, imidazolyl, indazolyl, benzimidazolyl and pyridinyl, which pyrazolyl, imidazolyl, indazolyl, benzimidazolyl and pyridinyl are substituted two or more times with substituents selected from the group consisting of alkyl, hydroxy-alkyl, cycloalkyl, cycloalkyl-alkyl, alkenyl, alkynyl, halo, trifluoromethyl, trifluoromethoxy, hydroxy, alkoxy, alkoxy-carbonyl, carboxy, cyano, nitro, amino, amino-carbonyl, N,N-dialkyl-amino-carbonyl, phenyl, benzyl and furanyl,

wherein the disease, disorder or condition is ataxia.

6. The method of treatment or alleviation of a disease, or a disorder, or a condition of a mammal, comprising:

administering to a patient in need thereof an effective amount of a purinyl derivative of Formula Ia or Ib

a stereoisomer thereof or a mixture of its stereoisomers, an N-oxide thereof, or a pharmaceutically acceptable salt thereof, wherein

n is 0, 1, 2 or 3;

X represents O, S or NR′, wherein R′ represents hydrogen, alkyl, cycloalkyl, phenyl or benzyl;

Y represents alkyl, cycloalkyl, phenyl, benzo[1,3]dioxolyl or pyridyl; which alkyl, cycloalkyl, phenyl, benzo[1,3]dioxolyl and pyridyl are optionally substituted with one substituent selected from the group consisting of alkyl, cycloalkyl, halo, trifluoromethyl, trifluoromethoxy, hydroxy, alkoxy, cyano, nitro and amino;

R 1 represents hydrogen, alkyl or alkoxy-alkyl; and

Het represents a heterocyclic group selected from pyrazolyl, imidazolyl, indazolyl, benzimidazolyl and pyridinyl, which pyrazolyl, imidazolyl, indazolyl, benzimidazolyl and pyridinyl are substituted two or more times with substituents selected from the group consisting of alkyl, hydroxy-alkyl, cycloalkyl, cycloalkyl-alkyl, alkenyl, alkenyl, halo, trifluoromethyl, trifluoromethoxy, hydroxy, alkoxy, alkoxy-carbonyl, carboxy, cyano, nitro, amino, amino-carbonyl, N,N-dialkyl-amino-carbonyl, phenyl, benzyl and furanyl,

wherein the disease, disorder or condition is Parkinson's disease.

7. The method of claim 3 , wherein the mammal is a human.

8. The method of claim 4 , wherein the mammal is a human.

9. The method of claim 5 , wherein the mammal is a human.

10. The method of claim 6 , wherein the mammal is a human.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 10, 2023
From: CADENT THERAPEUTICS, INC.
To: NOVARTIS AG
Reel/Frame 062321/0679 →
CHANGE OF NAME Recorded Jan 3, 2023
From: LUC THERAPEUTICS, INC.
To: CADENT THERAPEUTICS, INC.
Reel/Frame 062265/0889 →
MERGER Recorded Dec 20, 2022
From: ATAXION, INC.
To: LUC THERAPEUTICS, INC.
Reel/Frame 062155/0043 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 6, 2013
From: ANIONA APS
To: ATAXION, INC.
Reel/Frame 030946/0329 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 20, 2013
From: NEUROSEARCH A/S
To: ANIONA APS
Reel/Frame 030049/0894 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 4, 2013
From: ERIKSEN, BIRGITTE L; SORENSEN, ULRIK; HOUGAARD, CHARLOTTE; PETERS, DAN; JOHANSEN, TINA; CHRISTOPHERSEN, PALLE
To: NEUROSEARCH A/S
Reel/Frame 029917/0830 →
Priority Claims (1)
DK 200700482 · Mar 28, 2007 · national
Continuity (3)
Division 12593194
Provisional Application 60908503 · Mar 28, 2007
Related Publication 20130109704A1 · May 2, 2013