Compositions and methods for treating amyloidosis
Therapeutic compounds and methods for modulating amyloid aggregation in a subject, whatever its clinical setting, are described. Amyloid aggregation is modulated by the administration to a subject of an effective amount of a therapeutic compound of the formula or a pharmaceutically acceptable salt or ester, such that modulation of amyloid aggregation occurs. R 1 and R 2 are each independently a hydrogen atom or a substituted or unsubstituted aliphatic or aryl group. Z and Q are each independently a carbonyl (C═O), thiocarbonyl (C═S), sulfonyl (SO 2 ), or sulfoxide (S═O) group. “k” and “m” are 0 or 1, provided when k is 1, R 1 is not a hydrogen atom, and when m is 1, R 2 is not a hydrogen atom. In an embodiment, at least one of k or m must equal 1. “p” and “s” are each independently positive integers selected such that the biodistribution of the therapeutic compound for an intended target site is not prevented while maintaining activity of the therapeutic compound. T is a linking group and Y is a group of the formula -A X wherein A is an anionic group at physiological pH, and X is a cationic group.
1 . A method for treating or preventing an amyloid-related disease or disorder comprising administering an effective amount of a therapeutic compound to a subject in need thereof, where said therapeutic compound has the formula:
wherein
R 1 is an aliphatic group selected from a branched or unbranched, hydroxyl-substituted lower alkyl or an unsubstituted straight-chain C 1 -C 22 alkyl; R 2 is a hydrogen atom;
Z and Q are absent;
k and m are 0;
p and s are one;
T is an alkylene group; Y is SO 3 X, and X is a cationic group;
or a pharmaceutically acceptable salt thereof.
2 . The method of claim 1 , wherein R 1 is an unsubstituted straight-chain C 5 -C 18 alkyl.
3 . The method of claim 2 , wherein R 1 is an unsubstituted straight-chain C 5 -C 9 alkyl.
4 . The method of claim 1 , wherein R 1 is a branched or unbranched C 2 -C 6 alkyl group substituted with a hydroxyl group.
5 . The method of claim 4 , wherein R 1 is a branched C 2 -C 6 alkyl group substituted with a hydroxyl group.
6 . The method of claim 4 , wherein R 1 is an unbranched C 2 -C 6 alkyl group substituted with a hydroxyl group.
7 . The method of claim 1 , wherein said therapeutic compound is selected from the group consisting of 3-amylamino-1-propanesulfonic acid, 3-hexylamino-1-propanesulfonic acid, 3-heptylamino-1-propanesulfonic acid, 3-octylamino-1-propanesulfonic acid, 3-nonylamino-1-propanesulfonic acid, 3-decylamino-1-propanesulfonic acid, 3-undecylamino-1-propanesulfonic acid, 3-dodecylamino-1-propanesulfonic acid, 3-tridecylamino-1-propanesulfonic acid, 3-tetradecylamino-1-propanesulfonic acid, 3-hexadecylamino-1-propanesulfonic acid, and 3-octadecylamino-1-propanesulfonic acid; and pharmaceutically acceptable salts thereof.
8 . The method of claim 1 , wherein said therapeutic compound is selected from the group consisting of 2-deoxy-2-(3-sulfopropyl)amino-D-glucose; 3-(2-hydroxyethyl)amino-1-propanesulfonic acid; 3-(3-hydroxy-1-propyl)amino-1-propanesulfonic acid; (−)-(3)-[(R)-2-hydroxy-1-propyl]amino-1-propanesulfonic acid; (3)-[(d,l)-1-hydroxy-2-propyl]amino-1-propanesulfonic acid; 3-(4-hydroxy-1-butyl)amino-1-propanesulfonic acid; 3-(5-hydroxy-1-pentyl)amino-1-propanesulfonic acid; 3-(6-hydroxy-1-hexyl)amino-1-propanesulfonic acid; (+)-3-[(S)-2-hydroxy-1-propyl]amino-1-propanesulfonic acid; (+)-3-[(S)-1-hydroxy-2-propyl]amino-1-propanesulfonic acid; (−)-3-[(R)-1-hydroxy-2-propyl]amino-1-propanesulfonic acid; (+)-3-[(S)-1-hydroxy-2-butyl]amino-1-propanesulfonic acid; (−)-3-[(R)-1-hydroxy-2-butyl]amino-1-propanesulfonic acid; 3-[(dl)-5-hydroxy-2-pentyl]amino-1-propanesulfonic acid; 3-[(dl)-6-hydroxy-2-hexyl]amino-1-propanesulfonic acid; 3-(1-hydroxymethyl-1-cyclopentyl)amino-1-propanesulfonic acid, and pharmaceutically acceptable salts thereof.
9 . The method of claim 1 , wherein said amyloid-related disease or disorder is a disease associated with Amyloid-β, Amyloid A or IAPP.
10 . The method of claim 9 , wherein the disease or disorder is selected from Alzheimer's disease, Down's syndrome, or hereditary cerebral hemorrhage.
11 . The method of claim 10 , wherein the disease or disorder is Alzheimer's disease.
12 . The method of claim 9 , wherein the disease or disorder is adult onset diabetes.
13 . The method of claim 7 , wherein said amyloid-related disease or disorder is a disease associated with Amyloid-β, Amyloid A or LAPP.
14 . The method of claim 13 , wherein the disease or disorder is selected from Alzheimer's disease, Down's syndrome, or hereditary cerebral hemorrhage.
15 . The method of claim 14 , wherein the disease or disorder is Alzheimer's disease.
16 . The method of claim 13 , wherein the disease or disorder is adult onset diabetes.
17 . The method of claim 8 , wherein said amyloid-related disease or disorder is a disease associated with Amyloid-β, Amyloid A or IAPP.
18 . The method of claim 17 , wherein the disease or disorder is selected from Alzheimer's disease, Down's syndrome, or hereditary cerebral hemorrhage.
19 . The method of claim 18 , wherein the disease or disorder is Alzheimer's disease.
20 . The method of claim 17 , wherein the disease or disorder is adult onset diabetes.