US2013178520A1PendingUtilityA1
Methods of treatment using arylcyclopropylamine compounds
Est. expiryDec 23, 2031(~5.4 yrs left)· nominal 20-yr term from priority
Inventors:Dewey G. MccaffertyJulie PollockDavid GoodenMarc G. CaronRaul R. GainetdinovTatyana D. Sotnikova
A61K 31/343A61K 31/135A61K 31/198C07D 317/58C07C 323/31C07C 217/74C07C 211/40C07C 211/42
53
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Claims
Abstract
Described herein are methods of treating Parkinson's disease using arylcyclopropylamine compounds.
Claims
exact text as granted — not AI-modified1 . A method of treating Parkinson's disease in a subject in need of treatment, comprising administering to the subject an effective amount of a compound of formula (I):
wherein R 1 , R 2 , R 3 , R 4 and R 5 are independently selected from hydrogen, C 1-7 alkyl, C 3-20 heterocyclyl, C 5-20 aryl, C 1-7 alkoxy, C 1-7 haloalkyl, halo, amino, cyano, nitro, ether and thioether, or any two of R 1 , R 2 , R 3 , R 4 and R 5 may be taken together with the carbon atoms to which they are attached to form an optionally substituted ring; and
R 6 is selected from hydrogen and optionally substituted C 5-20 aryl;
or an isomer, prodrug or pharmaceutically acceptable salt thereof.
2 . The method of claim 1 , wherein R 1 , R 2 , R 4 and R 5 are hydrogen.
3 . The method of claim 1 , wherein R 3 is selected from C 1-7 haloalkyl, halo, C 1-7 alkoxy, and C 5-20 aryloxy.
4 . The method of claim 1 , wherein R 2 and R 3 are taken together with the carbon atoms to which they are attached to form a C 3-20 heterocyclyl ring.
5 . The method of claim 4 , wherein R 2 and R 3 are taken together to form a five-membered heterocyclyl ring.
6 . The method of claim 1 , wherein R 6 is hydrogen.
7 . The method of claim 1 , wherein the compound of formula (I) is selected from the group consisting of:
or a pharmaceutically acceptable salt thereof.
8 .- 18 . (canceled)
19 . A method of treating Parkinson's disease in a subject in need of treatment, comprising administering to the subject an effective amount of a compound of formula (IX):
wherein:
A is a C 5 -C 6 aryl, cycloalkenyl or heterocyclyl ring;
or an isomer, prodrug or pharmaceutically acceptable salt thereof.
20 . The method of claim 19 , wherein A is a heterocyclyl ring.
21 . The method of claim 19 , wherein A is a bicyclic heterocyclyl ring.
22 . The method of claim 19 , wherein the compound is of formula (X):
wherein X 1 is selected from CH 2 , O, S, and NH; and
- - - represents the presence or absence of a bond.
23 . The method of claim 19 , wherein the compound is of formula (XI):
wherein X 1 is selected from CH 2 , O, S, and NH; and
- - - represents the presence or absence of a bond.
24 . The method of claim 19 , wherein the compound is of formula (XII):
wherein X 1 is selected from CH 2 , O, S, and NH;
n is 1 or 2; and
- - - represents the presence or absence of a bond.
25 . The method of claim 19 , wherein the compound is of formula (XIII):
wherein X 2 , X 3 , X 4 and X 5 are independently selected from CH and N.
26 . The method of claim 19 , wherein the compound is of formula (XIV):
wherein X 1 and X 2 are independently selected from O and S; and
n is 1 or 2.
27 . The method of claim 26 , wherein X 1 and X 2 are O.
28 . The method of claim 26 , wherein n is 1.
29 .- 39 . (canceled)
40 . A pharmaceutical composition comprising a compound having the following formula:
or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.Join the waitlist — get patent alerts
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