PRMT5 inhibitors and uses thereof
View Patent ↗Described herein are compounds of formula (A), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. Compounds of the present invention are useful for inhibiting PRMT5 activity. Methods of using the compounds for treating PRMT5-mediated disorders are also described.
1. A compound of Formula (A):
or a pharmaceutically acceptable salt thereof;
wherein:
R 12 is hydrogen, and —R 13 is halogen; or
R 12 is hydrogen, and R 13 is —OR 1 ;
R 1 is hydrogen, R z , or —C(O)R z , wherein R z is optionally substituted C 1-6 alkyl;
L z is —C(O)N(R)— or —X A —C(R 2A )(R 3A )C(═O)N(R)—, wherein X A is —CR 4A R 5A —, and each instance of R 2A , R 3A , R 4A , and R 5A is hydrogen;
R is hydrogen or optionally substituted C 1-6 aliphatic;
Ring Z is a monocyclic or bicyclic aromatic ring having 0-4 heteroatoms selected from nitrogen, wherein Ring Z is substituted with 0, 1, 2, 3, 4, or 5 R y groups, as valency permits;
each R y is independently selected from the group consisting of halo, —CN, —NO 2 , optionally substituted aliphatic, optionally substituted carbocyclyl, optionally substituted aryl, optionally substituted heterocyclyl, optionally substituted heteroaryl, —OR A , —N(R B ) 2 , —SR A , —C(═O)R A , —C(O)OR A , —C(O)SR A , —C(O)N(R B ) 2 , —C(O)N(R B )N(R B ) 2 , —OC(O)R A , —OC(O)N(R B ) 2 , —NR B C(O)R A , —NR B C(O)N(R B ) 2 , —NR B C(O)N(R B )N(R B ) 2 , —NR B C(O)OR A , —SC(O)R A , —C(═NR B )R A , —C(═NNR B )R A , —C(═NOR A )R A , —C(═NR B )N(R B ) 2 , —NR B C(═NR B )R B , —C(═S)R A , —C(═S)N(R B ) 2 , —NR B C(═S)R A , —S(O)R A , —OS(O) 2 R A , —SO 2 R A , —NR B SO 2 R A , and —SO 2 N(R B ) 2 ;
each R A is independently selected from the group consisting of hydrogen, optionally substituted aliphatic, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, and optionally substituted heteroaryl;
each R B is independently selected from the group consisting of hydrogen, optionally substituted aliphatic, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, and optionally substituted heteroaryl, or two R B groups are taken together with their intervening atoms to form an optionally substituted heterocyclic ring;
R 21 , R 22 , R 23 , and R 24 are each independently hydrogen, halo, or optionally substituted aliphatic;
each R x is independently selected from the group consisting of halo, —CN, optionally substituted aliphatic, and —OR′;
R′ is hydrogen or optionally substituted aliphatic;
n is 0, 1, 2, 3, 4, 5, 6, 7, or 8; and
x is 1, and y is 1; or
x is 0, and y is 2, 3, or 4; or
x is 1, and y is 3.
2. The compound of claim 1 , wherein the compound is of Formula (A-3-iv):
or a pharmaceutically acceptable salt thereof, wherein R 12 is hydrogen.
3. The compound of claim 1 , wherein Ring Z is of the formula:
X 1 , X 2 , X 3 , and X 4 are independently selected from the group consisting of N, CH, and CR y , provided that at least one of X 2 , X 3 , and X 4 is not N;
L 1 is a bond, —O—, or —N(R)—;
R is hydrogen or optionally substituted C 1-6 aliphatic; and
Cy D is an optionally substituted 5- to 6-membered heteroaryl having 1-3 heteroatoms independently selected from nitrogen, oxygen, and sulfur, or an optionally substituted 3- to 8-membered heterocyclic ring having 1-2 heteroatoms independently selected from nitrogen, oxygen, and sulfur.
4. The compound of claim 3 , wherein:
X 1 , X 2 , X 3 , and X 4 are independently selected from the group consisting of CH and CR y ; or
X 1 is N, and each of X 2 , X 3 , and X 4 are independently selected from the group consisting of CH and CR y ; or
X 2 is N, and each of X 1 , X 3 , and X 4 are independently selected from the group consisting of CH and CR y ; or
X 3 is N, and each of X 1 , X 2 , and X 4 are independently selected from the group consisting of CH and CR y ; or
X 4 is N, and each of X 1 , X 2 , and X 3 are independently selected from the group consisting of CH and CR y ; or
each of X 1 and X 2 is N, and each of X 3 and X 4 is independently CH or CR y ; or
each of X 1 and X 3 is N, and each of X 2 and X 4 is independently CH or CR y ; or
each of X 1 and X 4 is N, and each of X 2 and X 3 is independently CH or CR y ; or
each of X 2 and X 4 is N, and each of X 1 and X 3 is independently CH or CR y ; or
each of X 2 and X 3 is N, and each of X 1 and X 4 is independently CH or CR y ; or
each of X 3 and X 4 is N, and each of X 1 and X 2 is independently CH or CR y .
5. The compound of claim 3 , wherein L 1 is —O—, or —N(R)—; R is hydrogen or optionally substituted C 1-6 aliphatic; and Cy D is an optionally substituted 3- to 8-membered heterocyclic ring having 1-2 heteroatoms independently selected from nitrogen, oxygen, and sulfur.
6. The compound of claim 3 , wherein the compound is of Formula (V D -c):
or a pharmaceutically acceptable salt thereof, wherein L D is —C(O)N(R)—.
7. The compound of claim 1 , wherein L z is —C(O)N(R)—.
8. The compound of claim 1 , wherein L z is —X A —C(R 2A )(R 3A )C(═O)N(R)—.
9. The compound of claim 1 , wherein R 1 is hydrogen.
10. The compound of claim 1 , wherein n is 0.
11. The compound of claim 1 , wherein Ring Z is a monocyclic aromatic ring having 0-4 heteroatoms selected from nitrogen and wherein Ring Z is substituted with 1 or 2 R y groups, as valency permits;
R y is independently selected from the group consisting of optionally substituted carbocyclyl, optionally substituted aryl, optionally substituted heterocyclyl, optionally substituted heteroaryl, —OR A , and —N(R B ) 2 ;
each R A is independently selected from the group consisting of optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, and optionally substituted heteroaryl; and
each R B is independently selected from the group consisting of hydrogen, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, and optionally substituted heteroaryl, or two R B groups are taken together with their intervening atoms to form an optionally substituted heterocyclic ring.
12. The compound of claim 1 , wherein Ring Z is selected from the group consisting of:
13. The compound of claim 1 selected from the group consisting of:
and pharmaceutically acceptable salts thereof.
14. The compound of claim 1 selected from the group consisting of:
and pharmaceutically acceptable salts thereof.
15. The compound of claim 1 selected from the group consisting of:
and pharmaceutically acceptable salts thereof.
16. A pharmaceutical composition comprising a compound of claim 1 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable excipient.
17. A kit or packaged pharmaceutical comprising a compound of claim 1 , or a pharmaceutically acceptable salt thereof, and instructions for use thereof.
18. A pharmaceutical composition comprising a compound of claim 13 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable excipient.
19. A kit or packaged pharmaceutical comprising a compound of claim 13 , or a pharmaceutically acceptable salt thereof, and instructions for use thereof.
20. A pharmaceutical composition comprising a compound of claim 14 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable excipient.
21. A kit or packaged pharmaceutical comprising a compound of claim 14 , or a pharmaceutically acceptable salt thereof, and instructions for use thereof.
22. A pharmaceutical composition comprising a compound of claim 15 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable excipient.
23. A kit or packaged pharmaceutical comprising a compound of claim 15 , or a pharmaceutically acceptable salt thereof, and instructions for use thereof.