Modulators of the eIF2alpha pathway
Provided herein, inter alia, are compounds and methods useful for modulating the translational effects of eIF2α phosphorylation, the Integrated Stress Response (ISR), and the unfolded protein response (UPR); for treating diseases; for increasing protein production, and for improving long-term memory.
1. A method of improving memory consolidation and long term memory in a patient, said method comprising administering a therapeutically effective amount of a compound, or a pharmaceutically acceptable salt thereof, to said patient, wherein said compound has the formula:
wherein
L 2 and L 4 are independently, —O—, —S—, —S(O)—, —S(O) 2 —, substituted or unsubstituted alkylene or substituted or unsubstituted heteroalkylene;
R 1 , R 3 , R 5 , R 6 and R 7 are independently hydrogen, halogen, —OCH 3 , —OCH 2 Ph, —C(O)Ph, —CH 3 , —CF 3 , —CCl 3 , —CN, —S(O)CH 3 , —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —C(O)CH 3 , —CH(CH 3 ) 2 , —CCSi(CH 3 ) 3 , —C(NN)CF 3 , —C(NH—NH)CF 3 , —CCH, —CH 2 CCH, —SH, —SO 2 Cl, —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, —OCF 3 , —OCHF 2 , —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 2 and R 4 are independently ═NR 7 , ═O, or ═S;
R 8 and R 9 are independently hydrogen, halogen, —OCH 3 , —OCH 2 Ph, —C(O)Ph, —CH 3 , —CF 3 , —CCl 3 , —CN, —S(O)CH 3 , —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —C(O)CH 3 , —CH(CH 3 ) 2 , —CCSi(CH 3 ) 3 , —CCH, —CH 2 CCH, —SH, —SO 2 Cl, —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, —OCF 3 , —OCHF 2 , 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;
b and d are independently 0 or 1; and
z5 and z6 are independently an integer from 0 to 5.
2. The method of claim 1 , wherein the compound has the formula:
wherein:
R 5.1 and R 6.1 are independently hydrogen, halogen, —CF 3 , —CN, —N 3 , substituted or unsubstituted C 1 -C 4 alkyl, substituted or unsubstituted 2 to 4 membered heteroalkyl, substituted or unsubstituted 5 to 6 membered heteroaryl,
R 5.2 and R 6.2 are independently hydrogen,
halogen, —CCSi(CH 3 ) 3 , —CF 3 , —NO 2 , —CN, —N 3 , substituted or unsubstituted C 1 -C 4 alkyl, substituted or unsubstituted 2 to 4 membered heteroalkyl, substituted or unsubstituted 5 to 6membered heteroaryl,
3. The method of claim 2 , wherein,
R 5.1 and R 6.1 are independently —Cl, —I, —CF 3 , —CH 3 , or —CCH; and
R 5.2 and R 6.2 are independently
hydrogen, —Cl, —F, —I, —CCSi(CH 3 ) 3 , —CF 3 , —NO 2 , —CH 3 , or —CCH.
4. The method of claim 1 , wherein the compound is
5. The method of claim 1 , wherein the compound is
6. The method of claim 1 , wherein the patient has traumatic brain injury.
7. A method of treating vanishing white matter disease in a patient, said method comprising administering a therapeutically effective amount of a compound, or a pharmaceutically acceptable salt thereof, to said patient, wherein said compound has the formula:
wherein
L 2 and L 4 are independently —O—, —S—, —S(O)—, —S(O) 2 —, substituted or unsubstituted alkylene or substituted or unsubstituted heteroalkylene;
R 1 , R 3 , R 5 , R 6 and R 7 are independently hydrogen,
halogen, —OCH 3 , —OCH 2 Ph, —C(O)Ph, —CH 3 , —CF 3 , —CCl 3 , —CN, —S(O)CH 3 , —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —C(O)CH 3 , —CH(CH 3 ) 2 , —CCSi(CH 3 ) 3 , —C(NN)CF 3 , —C(NH—NH)CF 3 , —CCH, —CH 2 CCH, —SH, —SO 2 Cl, —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, —OCF 3 , —OCHF 2 , —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 2 and R 4 are independently ═NR 7 , ═O, or ═S;
R 8 and R 9 are independently hydrogen, halogen, —OCH 3 , —OCH 3 , —OCH 2 Ph, —C(O)Ph, —CH 3 , —CF 3 , —CCl 3 , —CN, —S(O)CH 3 , —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —C(O)CH 3 , —CH(CH 3 ) 2 , —CCSi(CH 3 ) 3 , —CCH, —CH 2 CCH, —SH, —SO 2 Cl, —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, —OCF 3 , —OCHF 2 , 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;
and b and d are independently 0 or 1; and
z5 and z6 are independently an integer from 0 to 5.