IP Library › Granted Patent US 9,957,214
Granted Patent B2
US 9,957,214 · App. 14/434,725 · Granted May 1, 2018

Multifunctional radical quenchers

Inventors: Manikandadas Mathilakathu Madathil (Tempe, AZ); Omar Khdour (Phoenix, AZ); Sidney Hecht (Phoenix, AZ)
Assignee: ARIZONA BOARD OF REGENTS ON BEHALF OF ARIZONA STATE UNIVERSITY
C07C49/753C07C46/02C07C225/20C07C229/10C07D225/06A61K9/008A61K9/0019A61K9/08A61K9/2018A61K9/2054A61K9/4858
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Quick Facts
Patent No.
US 9,957,214
App. No.
14/434,725
Granted
May 1, 2018
Kind
B2
Abstract

The invention provides a compound of formula (I): [insert formula (I)] wherein X, Y, and R 1 -R 4 have any of the values defined in the specification, and salts thereof, as well as compositions comprising the compounds or salts. The compounds are useful for treating diseases associated with impaired mitochondrial function in an animal.

Claims (34)

1. A compound of formula Ib:

wherein:

R 2 is H, cyano, nitro, halo, aryloxy, —OC 1 -C 20 alkyl, —OC 2 -C 20 alkenyl, —OC 2 -C 20 alkynyl, —NR b R c , —C(═O)NR b R c , or —C(═O)OR d ;

Y and R 3 taken together are H, cyano, nitro, halo, aryloxy, —OC 1 -C 20 alkyl, —NR a (C 1 -C 20 alkyl), —NR a (aryl), —C 1 -C 20 alkyl, —C 2 -C 20 alkenyl, or —C 2 -C 20 alkynyl;

R 4 is a C 1 -C 20 alkyl, C 2 -C 20 alkenyl, or C 2 -C 20 alkynyl;

R a is H, C 1 -C 20 alkyl, C 2 -C 20 alkenyl, C 2 -C 20 alkynyl, or C 1 -C 20 alkanoyl;

R x is C 1 -C 16 alkyl, C 2 -C 16 alkenyl, C 2 -C 16 alkynyl, aryl, —OC 1 -C 16 alkyl, —OC 2 -C 16 alkenyl, —OC 2 -C 16 alkynyl, aryloxy, —N(H)C 1 -C 16 alkyl, —N(H)C 2 -C 16 alkenyl, —N(H)C 2 -C 16 alkynyl, or —N(H)aryl;

or a salt thereof.

2. A compound selected from:

and salts thereof.

3. A compound selected from:

4. A compound of formula I:

wherein:

X is NR a or —C(═O)N(R a )—;

R a is H or methyl;

R 1 is a C 1 -C 20 straight or branched, saturated or unsaturated carbon chain, wherein one or more carbon atoms can optionally be replaced with —O—, —NH—, a divalent phenyl group, or a divalent C 3 -C 6 cycloalkyl group; wherein R 1 can be optionally substituted with one or more groups independently selected from halo, aryl, and oxo (═O);

R 2 is H or methyl;

Y and R 3 taken together are methoxy, 3-(tert-butoxycarbonyl)prop-1-yloxy, N-(3-(butoxycarbonyl)prop-1-yl)amino, N-(3-(hexyloxycarbonyl)prop-1-yl)amino, 3-(butoxycarbonyl)prop-1-yloxy, or 3-(hexyloxycarbonyl)prop-1-yloxy; and

R 4 is tridecyl, hexadecyl, or 10-undecen-1-yl;

or a salt thereof;

provided the compound is not:

5. The compound of claim 4 wherein X is NR a .

6. The compound of claim 4 wherein R a is H.

7. The compound of claim 4 wherein R 1 is a C 1 -C 20 straight or branched, saturated or unsaturated carbon chain, wherein one or more carbon atoms can optionally be replaced with —O—; wherein R 1 can be optionally substituted with one or more groups independently selected from aryl and oxo (═O).

8. A compound of formula I:

wherein:

X is NR a , or —C(═O)N(R a )—;

R 1 is a C 1 -C 20 straight or branched, saturated or unsaturated carbon chain, wherein one or more carbon atoms can optionally be replaced with —O—, —NH—, a divalent phenyl group, or a divalent C 3 -C 6 cycloalkyl group; wherein R 1 can be optionally substituted with one or more groups independently selected from halo, aryl, and oxo (═O);

R 2 is H,

Y is O,

R 3 is aryl, or a C 1 -C 20 straight or branched, saturated or unsaturated carbon chain other than methyl;

R 4 is a C 1 -C 20 straight or branched, saturated or unsaturated carbon chain, wherein one or more carbon atoms can optionally be replaced with a divalent phenyl group, or a divalent C 3 -C 6 cycloalkyl group; wherein R 4 can be further optionally substituted with one or more groups independently selected from halo, oxo (═O), carboxy, C 1 -C 3 alkyl, C 1 -C 3 alkoxy, nitro, —SO 3 H, or tetrazolyl; or R 1 and R 4 taken together form a C 3 -C 18 straight or branched, saturated or unsaturated carbon chain that can be optionally substituted with one or more groups independently selected from halo and oxo (═O); and

R a is H;

or a salt thereof.

Continuity (2)
Provisional Application 61712170 · Oct 10, 2012
Related Publication 20150274628A1 · Oct 1, 2015