SUMO inhibitor compounds and uses thereof

1. A compound of formula:

wherein

is a single bond or double bond;

L 3 is —O—, —S—, or —N(R 7 )—;

L 7 is —O— or —N(R 10 )—;

R 1A is hydrogen, halogen, —CX 1A 3 ,—CHX 1A 2 , —CH 2 X 1A , —OCX 1A 3 , —OCH 2 X 1A , —OCHX 1A 2 , —CN, —SO n1A R 1AA , —SO v1A NR 1AA R 1AB , —NHC(O)NR 1AA R 1AB , —N(O) m1A , —NR 1AA R 1AB , —NHNR 1AA R 1AB , —C(O)R 1AA , —C(O)—OR 1AA , —C(O)NR 1AA R 1AB , —OR 1AA , —NR 1AA SO 2 R 1AB , —NR 1AA C(O)R 1AB , —NR 1AA C(O)OR 1AB , —NR 1AA OR 1AB , —N 3 , substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;

R 2A is hydrogen, halogen, —CX 2A 3 , —CHX 2A 2 , —CH 2 X 2A , —OCX 2A 3 , —OCH 2 X 2A , —OCHX 2A 2 , —CN, —SO n2A R 2AA , —SO v2A NR 2AA R 2AB , —NHC(O)NR 2AA R 2AB , —N(O) m2A , —NR 2AA R 2AB , —NHNR 2AA R 2AB , —C(O)R 2AA , —C(O)—OR 2AA , —C(O)NR 2AA R 2AB , —OR 2AA , —NR 2AA SO 2 R 2AB , —NR 2AA C(O)R 2AB , —NR 2AA C(O)OR 2AB , —NR 2AA OR 2AB , —N 3 , substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;

R 2B is hydrogen, halogen, —CX 2B 3 , —CHX 2B 2 , —CH 2 X 2B , —OCX 2B 3 , —OCH 2 X 2B , —OCHX 2B 2 , —CN, —SO n2B R 2BA , —SO v2B NR 2BA R 2BB , —NHC(O)NR 2BA R 2BB , —N(O) m2B , —NR 2BA R 2BB , —NHNR 2BA R 2BB , —C(O)R 2BA , —C(O)—OR 2BA , —C(O)NR 2BA R 2BB , —OR 2BA , —NR 2BA SO 2 R 2BB , —NR 2BA C(O)R 2BB , —NR 2BA C(O)OR 2BB , —NR 2BA OR 2BB , —N 3 , substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;

R 3 is hydrogen, halogen, —CX 3 3 , —CHX 3 2 , —CH 2 X 3 , —OCX 3 3 , —OCH 2 X 3 , —OCHX 3 2 , —CN, —SO n3 R 3A , —SO v3 NR 3A R 3B , —NHC(O)NR 3A R 3B , —N(O) m3 , —NR 3A R 3B , —NHNR 3A R 3B , —C(O)R 3A , —C(O)—OR 3A , —C(O)NR 3A R 3B , —OR 3A , —NR 3A SO 2 R 3B , —NR 3A C(O)R 3B , —NR 3A C(O)OR 3B , —NR 3A OR 3B , —N 3 , substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;

R 4 is hydrogen, halogen, —CX 4 3 , —CHX 4 2 , —CH 2 X 4 , —OCX 4 3 , —OCH 2 X 4 , —OCHX 4 2 , —CN, —SO n4 R 4A , —SO v4 NR 4A R 4B , —NHC(O)NR 4A R 4B , —N(O) m4 , —NR 4A R 4B , —NHNR 4A R 4B , —C(O)R 4A , —C(O)—OR 4A , —C(O)NR 4A R 4B , —C(O)NHNR 4A R 4B , —OR 4A , —NR 4A SO 2 R 4B , —NR 4A C(O)R 4B , —NR 4A C(O)OR 4B , —NR 4A OR 4B , —N 3 , substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;

R 5 is hydrogen, halogen, —CX 5 3 , —CHX 5 2 , —CH 2 X 5 , —OCX 5 3 , —OCH 2 X 5 , —OCHX 5 2 , —CN, —SO n5 R 5A , —SO v5 NR 5A R 5B , —NHC(O)NR 5A R 5B , —N(O) m5 , —NR 5A R 5B , —NHNR 5A R 5B ,—C(O)R 5A , —C(O)—OR 5A , —C(O)NR 5A R 5B , —C(O)NHNR 5A R 5B , —OR 5A , —NR 5A SO 2 R 5B , —NR 5A C(O)R 5B , —NR 5A C(O)OR 5B , —NR 5A OR 5B , —N 3 , substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;

R 7 is hydrogen, halogen, —CX 7 3 , —CHX 7 2 , —CH 2 X 7 , —OCX 7 3 , —OCH 2 X 7 , —OCHX 7 2 , —CN, —SO n7 R 7A , —SO v7 NR 7A R 7B , —NHC(O)NR 7A R 7B , —N(O) m7 , —NR 7A R 7B , —NHNR 7A R 7B , —C(O)R 7A , —C(O)—OR 7A , —C(O)NR 7A R 7B , —C(O)NHNR 7A R 7B , —OR 7A , —NR 7A SO 2 R 7B , —NR 7A C(O)R 7B , —NR 7A C(O)OR 7B , —NR 7A OR 7B , —N 3 , substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;

R 8 is hydrogen, halogen, —CX 8 3 , —CHX 8 2 , —CH 2 X 8 , —OCX 8 3 , —OCH 2 X 8 , —OCHX 8 2 , —CN, —SO n8 R 8A , —SO v8 NR 8A R 8B , —NHC(O)NR 8A R 8B , —N(O) m8 , —NR 8A R 8B , —NHNR 8A R 8B , —C(O)R 8A , —C(O)—OR 8A , —C(O)NR 8A R 8B , —C(O)NHNR 8A R 8B , —OR 8A , —NR 8A SO 2 R 8B , —NR 8A C(O)R 8B , —NR 8A C(O)OR 8B , —NR 8A OR 8B , —N 3 , substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;

R 9 is halogen, —CX 9 3 , —CHX 9 2 , —CH 2 X 9 , —OCX 9 3 , —OCH 2 X 9 , —OCHX 9 2 , —CN, —SO n9 R 9A , —SO v9 NR 9A R 9B , —NHC(O)NR 9A R 9B , —N(O) m9 , —NR 9A R 9B , —NHNR 9A R 9B , —C(O)R 9A , —C(O)—OR 9A , —C(O)NR 9A R 9B , —C(O)NHNR 9A R 9B , —OR 9A , —NR 9A SO 2 R 9B , —NR 9A C(O)R 9B , —NR 9A C(O)OR 9B , —NR 9A OR 9B , —N 3 , substituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;

R 10 is hydrogen, halogen, —CX 10 3 , —CHX 10 2 , —CH 2 X 10 , —OCX 10 3 , —OCH 2 X 10 , —OCHX 10 2 , —CN, —SO n10 R 10A , —SO v10 NR 10A R 10B , —NHC(O)NR 10A R 10B , —N(O) m10 , —NR 10A R 10B , —NHNR 10A R 10B , —C(O)R 10A , —C(O)—OR 10A , —C(O)NR 10A R 10B , —C(O)NHNR 10A R 10B , —OR 10A , —NR 10A SO 2 R 10B , —NR 10A C(O)R 10B , —NR 10A C(O)OR 10B , —NR 10A OR 10B , —N 3 , substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;

each R 1AA , R 1AB , R 2AA , R 2AB , R 2BA , R 2BB , R 3A , R 3B , R 4A , R 4B , R 5A , R 5B , R 7A , R 7B , R 8A , R 8B , R 9A , R 9B , R 10A , and R 10B is independently hydrogen, —CX 3 , —CHX 2 , —CH 2 X, —C(O)OH, —C(O)NH 2 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC═(O)NHNH 2 , —NHC═(O)NH 2 , —NHSO 2 H, —NHC═(O)H, —NHC(O)OH, —NHOH, —OCX 3 , —OCHX 2 , —OCH 2 X, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; R 1AA and R 1AB substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl; R 2AA and R 2AB substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl; R 2BA and R 2BB substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl; R 3A and R 3B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl; R 4A and R 4B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl; R 5A and R 5B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl; R 7A and R 7B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl; R 8A and R 8B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl; R 9A and R 9B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl; R 10A and R 10B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl;

m1A, m2A, m2B, m3, m4, m5, m7, m8, m9, and m10 are independently 1 or 2;

v1A, v2A, v2B, v3, v4, v5, v7, v8, v9, and v10 are independently 1 or 2;

n1A, n2A, n2B, n3, n4, n5, n7, n8, n9, and n10 are independently an integer from 0 to 4;

X, X 1A , X 2A , X 2B , X 3 , X 4 , X 5 , X 7 , X 8 , X 9 , and X 10 are independently —Cl, —Br, —I, or —F;

L 6 is substituted or unsubstituted alkylene, substituted or unsubstituted heteroalkylene, substituted or unsubstituted cycloalkylene, substituted or unsubstituted heterocycloalkylene, substituted or unsubstituted arylene, or substituted or unsubstituted heteroarylene;

L 8 is a bond, —C(O)—, —C(O)NH—, —C(O)O—, substituted or unsubstituted alkylene, substituted or unsubstituted heteroalkylene, substituted or unsubstituted cycloalkylene, substituted or unsubstituted heterocycloalkylene, substituted or unsubstituted arylene, or substituted or unsubstituted heteroarylene;

L 9 is a bond, —O—, —S—, —NH—, —C(O)—, —C(O)O—, —C(O)NH—, —OC(O)—, —NHC(O)—, —NHC(O)NH—, —OC(O)NH—, —NHC(O)O—, substituted or unsubstituted alkylene, substituted or unsubstituted heteroalkylene, substituted or unsubstituted cycloalkylene, substituted or unsubstituted heterocycloalkylene, substituted or unsubstituted arylene, or substituted or unsubstituted heteroarylene;

wherein R 2A and R 2B may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl; and

R 4 and R 5 may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.

2. The compound of claim 1 , having the formula:

3. The compound of claim 1 , wherein R 3 , R 4 , or R 5 is hydrogen.

4. The compound of claim 1 , wherein R 8 is substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.

5. The compound of claim 1 , wherein R 8 is substituted or unsubstituted phenyl.

6. The compound of claim 1 , wherein L 9 is a bond, substituted or unsubstituted alkylene, or substituted or unsubstituted arylene.

7. The compound of claim 1 , wherein L 9 is an unsubstituted phenylene.

8. The compound of claim 1 , wherein R 9 is substituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.

9. The compound of claim 1 , wherein -L 9 -R 9 is

10. The compound of claim 1 , wherein R 2A is hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.

11. The compound of claim 1 , wherein R 2A is substituted or unsubstituted phenyl.

12. The compound of claim 1 , wherein R 2B is hydrogen.

13. The compound of claim 1 , wherein R 1A is hydrogen, —CX 1A 3 , —CHX 1A 2 , —CH 2 X 1A , or unsubstituted C 1 -C 3 alkyl.

14. A pharmaceutical composition comprising a compound, or a pharmaceutically acceptable salt thereof, of claim 1 and a pharmaceutically acceptable excipient.

15. A method of inhibiting an E1 enzyme, said method comprising contacting an E1 enzyme with a compound of claim 1 , thereby inhibiting said E1 enzyme.

16. The method of claim 15 , wherein said method comprises allowing said compound to covalently bind said E1 enzyme.

17. The method of claim 15 , further comprising administering to a cancer subject said compound.

18. The compound of claim 1 , having the formula:

19. The compound of claim 1 , having the formula: