Identification of stabilizers of multimeric proteins
View Patent ↗Disclosed herein are compounds and compositions thereof which find use in increasing stability of TTR tetramers reducing its tendency to misfold and form aggregates. Also provided herein are methods for using these compounds and compositions for increasing stability of TTR and therby decreasing aggegate formation by TTR. Also disclosed herein are methods to screen for candidate compounds that increase stability of TTR. Also disclosed herein are heterobifunctional compounds that include a TTR binding compound connected to a targeting moiety via a linker, for use in disrupting PP is of a target protein.
1. A method of stabilizing Transthyretin (TTR) in a subject, comprising administering a therapeutically effective amount of a compound of formula VIII
or a pharmaceutically acceptable salt thereof, wherein
Z 4 is selected from the group consisting of, a methylene, an aminomethylene, a hydroxymethylene and a linker of 1 to 3 atoms in length; and
R 14 and R 15 are independently one or more groups,
each R 14 and R 15 group is independently selected from hydrogen, an alkyl, an aryl, an alkoxy, an aryloxy, an acetyl, a carboxy, a formyl, an amido, a hydroxyl, a heterocyclic group, a halo, a nitro, and a cyano, where optionally two or more R 14 or R 15 groups may be cyclically linked.
2. The method of claim 1 , wherein Z 4 is selected from the group consisting of, a methylene, an aminomethylene, and a hydroxymethylene.
3. A method of stabilizing Transthyretin (TTR) in a subject, comprising administering a therapeutically effective amount of a compound of formula IX:
wherein,
R 16 is one or more groups selected from the group consisting of a halo, an alkyl, and a hydroxyl,
R 17 is one or more groups selected from the group consisting of an alkyl, an aryl, an alkoxy, an aryloxy, an acetyl, a carboxy, a formyl, an amido, a hydroxyl, a heterocyclic group, a halo, a nitro, and a cyano.
4. The method of claim 3 , wherein each R 17 is selected from a lower alkoxy, a trifluoromethyl, a carboxy, a formyl, a lower alkyl, a hydroxyl, a nitro, and a halo.
5. The method of claim 4 , wherein at least one R 17 is selected from a carboxy, a formyl, and a hydroxyl, and is attached at the 2-position of the phenyl ring.
6. The method of claim 4 , wherein at least one of R 17 is selected from a carboxy, a formyl, and a hydroxyl, and is attached at the 3-position of the phenyl ring.
7. The method of claim 4 , wherein at least one R 17 is selected from a carboxy, a formyl, and a hydroxyl, and is attached at the 4-position of the phenyl ring.
8. The method of claim 3 , wherein each R 17 is selected from a lower alkoxy, a hydroxyl, and a nitro.
9. The method of claim 3 , wherein R 17 is hydroxyl at the 3- and 4-position of the phenyl ring.
10. The method of claim 2 , wherein said compound is selected from the group consisting of
11. The method of claim 3 , wherein said compound is
12. The method of claim 3 , wherein said stabilization of TTR in a subject treats a transthyretin amyloid disease.
13. The method of claim 12 , wherein said transthyretin amyloid disease is selected from the group consisting of familial amyloid polyneuropathy, familial amyloid cardiomyopathy, and senile systemic amyloidosis.
14. The method of claim 13 , wherein said transthyretin amyloid disease is familial amyloid polyneuropathy.
15. The method of claim 13 , wherein said transthyretin amyloid disease is familial amyloid cardiomyopathy.
16. The method of claim 13 , wherein said transthyretin amyloid disease is senile systemic amyloidosis.
17. The method of claim 3 , wherein said subject is a human.
18. The method of claim 3 , wherein said subject is an ungulate.
19. The method of claim 18 , wherein said ungulate is a bovine.