Inhibitors of beta-secretase

1. A compound represented by the following Structural Formula:

or a pharmaceutically acceptable salt thereof, wherein:

ring Het is a 5 membered monocyclic heterocycle;

X is —C(R 3 R 4 )—;

each R 0 is independently selected from —H, ═O, ═S, ═NR 15 , (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, —CN, —NO 2 , halogen, —OR 5 , —NR 6 R 7 , —S(O) i R 5 , —S(O) i NR 12 R 13 , —NR 11 S(O) i R 5 , —C(═O)OR 5 , —OC(═O)OR 5 , —C(═S)OR 5 , —O(C═S)R 5 , —C(═O)NR 12 R 13 , —NR 11 C(═O)R 5 , —C(═S)NR 12 R 13 , —NR 11 C(═S)R 5 , —NR 11 (C═O)OR 5 , —O(C═O)NR 12 R 13 , —NR 11 (C═S)OR 5 , —O(C═S)NR 12 R 13 , —NR 11 (C═O)NR 12 R 13 , —C(═S)R 5 , —C(═O)R 5 , (C 3 -C 8 )cycloalkyl, (C 3 -C 8 )cycloalkyl(C 1 -C 3 )alkyl, (C 3 -C 9 )heterocycloalkyl, (C 3 -C 9 )heterocycloalkyl(C 1 -C 3 )alkyl, aryl, aryl(C 1 -C 6 )alkyl, heteroaryl or heteroaryl(C 1 -C 6 )alkyl, each of the (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 3 -C 8 )cycloalkyl, (C 3 -C 8 )cycloalkyl(C 1 -C 3 )alkyl, (C 3 -C 9 )heterocycloalkyl, (C 3 -C 9 )heterocycloalkyl(C 1 -C 3 )alkyl, aryl, aryl(C 1 -C 6 )alkyl, heteroaryl or heteroaryl(C 1 -C 6 )alkyl group represented by R 0 is optionally substituted with 1 to 5 substituents independently selected from the group consisting of -halogen, —CN, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy, (C 1 -C 3 )alkoxy(C 1 -C 3 )alkyl, (C 3 -C 8 )cycloalkyl, (C 3 -C 9 )heterocycloalkyl, aryl, heteroaryl, —NR 6 R 7 , —NR 11 S(O) i R 5 , —C(═O)NR 12 R 13 , —NR 11 C(═O)R 5 , —S(O) i R 5 —, —S(O) i NR 12 R 13 , —OR 5 , —C(═O)R 5 , —C(═S)NR 12 R 13 , —NR 11 C(═S)R 5 , —C(O)OR 5 , —OC(═O)OR 5 , —C(═S)OR 5 , —O(C═S)R 5 , —O(C═O)NR 12 R 13 , —NR 11 (C═O)OR 5 , —NR 11 (C═S)OR 5 , —O(C═S)NR 12 R 13 , —NR 11 (C═O)NR 12 R 13 , —NR 11 (C═S)NR 12 R 13 and —C(═S)R 5 , wherein the cycloalkyl, heterocycloalkyl, aryl and heteroaryl groups in the substituents on the groups represented by R 0 are each optionally substituted with 1 to 3 substituents independently selected from halogen, —CN, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy and (C 1 -C 3 )alkoxy(C 1 -C 6 )alkyl;

R 1 is —H, —OH, —(C 1 -C 4 )alkoxy, (C 1 -C 6 )alkyl, aryl(C 1 -C 6 )alkyl, or heteroaryl(C 1 -C 6 )alkyl; wherein each alkyl, aryl and heteroaryl is optionally substituted with 1 to 5 substituents independently selected from halogen, —CN, —OH, (C 1 -C 4 )alkyl, halo(C 1 -C 4 )alkyl, (C 1 -C 3 )alkoxy and halo(C 1 -C 3 )alkoxy;

each R 2 is independently selected from a) —H, -halogen, —CN, —NO 2 , —OR 5 , —NR 6 R 7 , —S(O) i R 5 , —NR 11 S(O) i R 5 , —S(O) i NR 12 R 13 , C(═O)OR 5 , —OC(═O)OR 5 , —C(═S)OR 5 , —O(C═S)R 5 , —C(═O)NR 12 R 13 , —NR 11 C(═O)R 5 , —C(═S)NR 12 R 13 , —NR 11 C(═S)R 5 , —NR 11 (C═O)OR 5 , —O(C═O)NR 12 R 13 , —NR 11 (C═S)OR 5 , —O(C═S)NR 12 R 13 , —NR 11 (C═O)NR 12 R 13 , —NR 11 (C═S)NR 12 R 13 , —C(═S)R 5 , and —C(═O)R 5 ; and b) (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, (C 3 -C 8 )cycloalkyl, (C 3 -C 8 )cycloalkyl(C 1 -C 6 )alkyl, (C 3 -C 8 )cycloalkyl(C 2 -C 6 )alkynyl, (C 4 -C 8 )cycloalkenyl, (C 3 -C 9 )heterocycloalkyl, (C 3 -C 9 )heterocycloalkyl(C 1 -C 6 )alkyl, (C 3 -C 9 )heterocycloalkyl(C 2 -C 6 )alkynyl, aryl, aryl(C 1 -C 6 )alkyl, aryl(C 2 -C 6 )alkynyl, heteroaryl, heteroaryl(C 1 -C 6 )alkyl, and heteroaryl(C 2 -C 6 )alkynyl, wherein each of the (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, (C 3 -C 8 )cycloalkyl, (C 3 -C 8 )cycloalkyl(C 1 -C 6 )alkyl, (C 3 -C 8 )cycloalkyl(C 2 -C 6 )alkynyl, (C 4 -C 8 )cycloalkenyl, (C 3 -C 9 )heterocycloalkyl, (C 3 -C 9 )heterocycloalkyl(C 1 -C 6 )alkyl, (C 3 -C 9 )heterocycloalkyl(C 2 -C 6 )alkynyl, aryl, aryl(C 1 -C 6 )alkyl, aryl(C 2 -C 6 )alkynyl, heteroaryl, heteroaryl(C 1 -C 6 )alkyl, and heteroaryl(C 2 -C 6 )alkynyl groups represented by R 2 is optionally substituted with 1 to 5 substituents independently selected from the group consisting of -halogen, —CN, —NO 2 , —OR 5 , —SR 5 , —NR 6 R 7 , —S(O) i R 5 , —NR 11 S(═O) i R 5 , —S(O) i NR 12 R 13 , —C(═O)OR 5 , —OC(═O)R 5 , —C(═S)OR 5 , —OC(═S)R 5 , —C(═O)NR 12 R 13 , —NR 11 C(═O)R 5 , —C(═S)NR 12 R 13 , —NR 11 C(═S)R 5 , —C(═O)R 5 , —C(═S)R 5 , —OC(═O)OR 5 , —O(C═O)NR 12 R 13 , —NR 11 (C═O)OR 5 , —NR 11 (C═S)OR 5 , —O(C═S)NR 12 R 13 , —NR 11 (C═O)NR 12 R 13 , —NR 11 (C═S)NR 12 R 13 , —C(═O)R 5 , —C(═S)R 5 , (C 1 -C 6 )alkyl, (C 2 -C 6 )alkynyl, (C 3 -C 8 )cycloalkyl, (C 4 -C 8 )cycloalkenyl, (C 3 -C 9 )heterocycloalkyl, (C 2 -C 6 )alkenyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylsulfonylaminoalkyl, hydroxy(C 1 -C 6 )alkyl, cyano(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylcarbonylamino(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy, (C 1 -C 6 )alkoxy(C 1 -C 3 )alkyl, aryl and heteroaryl, wherein the cycloalkyl, heterocycloalkyl, aryl and heteroaryl groups in the substituents on the groups represented by R 2 are each optionally substituted with 1 to 3 substituents independently selected from halogen, —CN, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy and (C 1 -C 3 )alkoxy(C 1 -C 6 )alkyl;

R 3 and R 4 are each independently —H, -halogen, —CN, —NO 2 , —OR 5 , —NR 6 R 7 , —S(O) i R 5 , —NR 11 S(O) i R 5 , —S(O) i NR 12 R 13 , —C(═O)OR 5 , —OC(═O)OR 5 , —C(═S)OR 5 , —O(C═S)R 5 , —C(═O)NR 12 R 13 , —NR 11 C(═O)R 5 , —C(═S)NR 12 R 13 , —NR 11 C(═S)R 5 , —NR 11 (C═O)OR 5 , —O(C═O)NR 12 R 13 , —NR 11 (C═S)OR 5 , —O(C═S)NR 12 R 13 , —NR 11 (C═O)NR 12 R 13 , —NR 11 (C═S)NR 12 R 13 , —C(═S)R 5 , —C(═O)R 5 , (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, (C 3 -C 8 )cycloalkyl, (C 3 -C 8 )cycloalkyl(C 1 -C 6 )alkyl, (C 3 -C 8 )cycloalkyl(C 2 -C 6 )alkynyl, (C 3 -C 9 )heterocycloalkyl, (C 3 -C 9 )heterocycloalkyl(C 1 -C 6 )alkyl, (C 3 -C 9 )heterocycloalkyl(C 2 -C 6 )alkynyl, aryl, aryl(C 1 -C 6 )alkyl, aryl(C 2 -C 6 )alkynyl, heteroaryl, heteroaryl(C 1 -C 6 )alkyl or heteroaryl(C 1 -C 6 )alkynyl, wherein each (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, (C 3 -C 8 )cycloalkyl, (C 3 -C 8 )cycloalkyl(C 1 -C 6 )alkyl, (C 3 -C 8 )cycloalkyl(C 2 -C 6 )alkynyl, (C 3 -C 9 )heterocycloalkyl, (C 3 -C 9 )heterocycloalkyl(C 1 -C 6 )alkyl, (C 3 -C 9 )heterocycloalkyl(C 2 -C 6 )alkynyl, aryl, aryl(C 1 -C 6 )alkyl, aryl(C 2 -C 6 )alkynyl, heteroaryl, heteroaryl(C 1 -C 6 )alkyl or heteroaryl(C 1 -C 6 )alkynyl represented by R 3 and R 4 is optionally substituted with 1 to 5 substituents independently selected from the group consisting of halogen, —OR 5 , —NR 6 R 7 , —S(O) i R 5 , —NR 11 S(O) i R 5 , —S(O) i NR 12 R 13 , —C(═O)OR 5 , —OC(═O)OR 5 , —C(═S)OR 5 , —O(C═S)R 5 , —C(═O)NR 12 R 13 , —NR 11 C(═O)R 5 , —C(═S)NR 12 R 13 , —NR 11 C(═S)R 5 , —NR 11 (C═O)OR 5 , —O(C═O)NR 12 R 13 , —NR 11 (C═S)OR 5 , —O(C═S)NR 12 R 13 , —NR 11 (C═O)NR 12 R 13 , —NR 11 (C═S)NR 12 R 13 , —C(═S)R 5 , —C(═O)R 5 , (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylsulfonylaminoalkyl, hydroxy(C 1 -C 6 )alkyl, cyano(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylcarbonylamino(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy, (C 1 -C 6 )alkoxy(C 1 -C 3 )alkyl, (C 3 -C 8 )cycloalkyl, (C 3 -C 9 )heterocycloalkyl, aryl and heteroaryl, wherein the cycloalkyl, heterocycloalkyl, aryl and heteroaryl groups in the substituents on the groups represented by R 3 and R 4 are each optionally substituted with 1 to 3 substituents independently selected from halogen, —CN, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy and (C 1 -C 3 )alkoxy(C 1 -C 6 )alkyl;

R 5 is —H, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, (C 1 -C 3 )alkoxy(C 1 -C 6 )alkyl, (C 3 -C 8 )cycloalkyl, (C 3 -C 8 )cycloalkyl(C 1 -C 6 )alkyl, (C 3 -C 9 )heterocycloalkyl, (C 3 -C 9 )heterocycloalkyl(C 1 -C 6 )alkyl, aryl, aryl(C 1 -C 6 )alkyl, heteroaryl or heteroaryl(C 1 -C 6 )alkyl, each of the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl and heteroaryl in the groups represented by R 5 is optionally substituted with 1 to 5 substituents independently selected from the group consisting of halogen, ═O, —NR 6 C(═NH)NR 6 R 7 , —C(═O)OR c , —OR c , —SR c , —C(═O)NR 6 R 7 , —C(═O)R c , —S(O) i R c , —NO 2 , —CN, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy and —NR 6 R 7 ;

R c is —H, (C 1 -C 3 )alkyl, halo(C 1 -C 3 )alkyl or (C 1 -C 3 )alkoxy(C 1 -C 3 )alkyl;

R 6 and R 7 are each independently —H, (C 1 -C 6 )alkyl, hydroxy(C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 3 -C 8 ) cycloalkyl, (C 3 -C 8 )cycloalkyl(C 1 -C 6 )alkyl, (C 3 -C 9 )heterocycloalkyl, (C 3 -C 9 )heterocycloalkyl(C 1 -C 6 )alkyl, aryl, aryl(C 1 -C 6 )alkyl, heteroaryl, or heteroaryl(C 1 -C 6 )alkyl, all of which are optionally substituted with 1 to 3 substituents independently selected from the group consisting of halogen, —CN, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy and (C 1 -C 3 )alkoxy(C 1 -C 6 )alkyl;

R 8 and R 9 , together with the carbon to which they are attached, form ring A, which is a 3-14 membered monocyclic ring, wherein ring A optionally contains 1 to 3 heteroatoms independently selected from O, N, and S and when the heteroatom is nitrogen, the nitrogen is substituted with —H, (C 1 -C 3 )alkyl or halo(C 1 -C 3 )alkyl, and when the heteroatom is sulfur, the sulfur is optionally mono or di-oxygenated; and ring A is optionally substituted with 1 to 4 substituents independently selected from the group consisting of halogen, —CN, —OR 5 , —NR 6 R 7 , —S(O) i R 5 , —NR 11 S(O) i R 5 , —S(O) i NR 12 R 13 , —C(═O)OR 5 , —OC(═O)OR 5 , —C(═S)OR 5 , —O(C═S)R 5 , —C(═O)NR 12 R 13 , —NR 11 C(═O)R 5 , —C(═S)NR 12 R 13 , —NR 11 C(═S)R 5 , —NR 11 (C═O)OR 5 , —O(C═O)NR 12 R 13 , —NR 11 (C═S)OR 5 , —O(C═S)NR 12 R 13 , —NR 11 (C═O)NR 12 R 13 , —NR 11 (C═S)NR 12 R 13 , —C(═S)R 5 , —C(═O)R 5 , (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylsulfonylamino(C 1 -C 6 )alkyl, hydroxy(C 1 -C 6 )alkyl, cyano(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylcarbonylamino(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy, (C 1 -C 6 )alkoxy(C 1 -C 3 )alkyl, (C 3 -C 8 )cycloalkyl, (C 3 -C 8 )cycloalkyl(C 1 -C 6 )alkyl, (C 3 -C 8 )cycloalkyl(C 2 -C 6 )alkynyl, (C 3 -C 9 )heterocycloalkyl, (C 3 -C 9 )heterocycloalkyl(C 1 -C 6 )alkyl, (C 3 -C 9 )heterocycloalkyl(C 2 -C 6 )alkynyl, aryl, aryl(C 1 -C 6 )alkyl, aryl(C 2 -C 6 )alkynyl, heteroaryl, heteroaryl(C 1 -C 6 )alkyl, and heteroaryl(C 2 -C 6 )alkynyl, wherein the cycloalkyl, heterocycloalkyl, aryl and heteroaryl groups in the substituents on ring A are each optionally substituted with 1 to 3 substituents independently selected from halogen, —CN, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy and (C 1 -C 3 )alkoxy(C 1 -C 6 )alkyl;

R 11 is —H or (C 1 -C 6 )alkyl, wherein (C 1 -C 6 )alkyl is optionally substituted with 1 to 5 substituents independently selected from halogen, CN, (C 1 -C 6 )alkoxy, (C 2 -C 6 )alkynyl, (C 3 -C 8 )cycloalkyl, (C 3 -C 9 )heterocycloalkyl, aryl and heteroaryl, wherein the (C 1 -C 6 )alkoxy, (C 2 -C 6 )alkynyl, (C 3 -C 8 )cycloalkyl, (C 3 -C 9 )heterocycloalkyl, aryl and heteroaryl groups are each optionally substituted with 1 to 3 substituents independently selected from the group consisting of halogen, —CN, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy and (C 1 -C 3 )alkoxy(C 1 -C 6 )alkyl;

R 12 and R 13 are each independently —H, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy(C 1 -C 6 )alkyl, hydroxy(C 1 -C 6 )alkyl, cyano(C 1 -C 6 )alkyl, amino(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylamino(C 1 -C 6 )alkyl, di(C 1 -C 3 )alkylamino(C 1 -C 6 )alkyl, (C 3 -C 8 )cycloalkyl, (C 3 -C 8 )cycloalkyl(C 1 -C 6 )alkyl, (C 3 -C 9 )heterocycloalkyl, (C 3 -C 9 )heterocycloalkyl(C 1 -C 6 )alkyl, aryl, aryl(C 1 -C 6 )alkyl, heteroaryl or heteroaryl(C 1 -C 6 )alkyl, wherein the (C 3 -C 8 )cycloalkyl, (C 3 -C 8 )cycloalkyl(C 1 -C 6 )alkyl, (C 3 -C 9 )heterocycloalkyl, (C 3 -C 9 )heterocycloalkyl(C 1 -C 6 )alkyl, aryl, aryl(C 1 -C 6 )alkyl, heteroaryl and heteroaryl(C 1 -C 6 )alkyl group is optionally substituted with 1 to 3 substituents independently selected from the group consisting of -halogen, —CN, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy and (C 1 -C 3 )alkoxy(C 1 -C 6 )alkyl;

or R 12 and R 13 , together with the nitrogen to which they are attached, form a 3-8 membered ring optionally substituted with 1 to 3 substituents independently selected from the group consisting of halogen, —CN, —OR 5 , —NR 6 R 7 , —S(O) i R 5 , —S(O) i NR 12 R 13 , —NR 11 S(O) i R 5 , —C(═O)OR 5 , —OC(═O)OR 5 , —C(═S)OR 5 , —O(C═S)R 5 , —C(═O)NR 6 R 7 , —NR 11 C(═O)R 5 , —C(═S)NR 6 R 7 , —NR 11 C(═S)R 5 , —NR (C═O)OR 5 , —O(C═O)NR 6 R 7 , —NR 11 (C═S)OR 5 , —O(C═S)NR 6 R 7 , —NR 11 (C═O)NR 6 R 7 , —NR 11 (C═S)NR 6 R 7 , —C(═S)R 5 , —C(═O)R 5 , (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylsulfonylaminoalkyl, hydroxy(C 1 -C 6 )alkyl, cyano(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylcarbonylamino(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy and (C 1 -C 6 )alkoxy(C 1 -C 3 )alkyl, wherein the 3-8 membered ring optionally contains 1 to 3 additional heteroatoms, which are independently selected from O, N and S, wherein when the additional heteroatom is nitrogen, the nitrogen is substituted with —H, (C 1 -C 3 )alkyl or halo(C 1 -C 3 )alkyl, and when the additional heteroatom is sulfur, the sulfur is optionally mono or di-oxygenated;

R 15 is —H or (C 1 -C 6 )alkyl optionally substituted with 1 to 5-F;

i is 0, 1 or 2;

p is 1, 2, 3 or 4; and

q is 1, 2 or 3.

2. The compound of claim 1 , wherein the compound is represented by the following Structural Formula:

or a pharmaceutically acceptable salt thereof, wherein:

X is —C(R 3 R 4 )—;

W is —N(R 14 )—, —S—, or —O—;

Z is —C(═O)—, —C(═S)—, —C(═NR 15 )—, —O—, —N(R 18 )—, or —(CR 16 R 17 ) m , provided when W is —S— or —O—, Z is not —O—;

R 1 is —H, (C 1 -C 6 )alkyl, aryl(C 1 -C 6 )alkyl, or heteroaryl(C 1 -C 6 )alkyl;

each R 2 is independently selected from a) —H, -halogen, —CN, —NO 2 , —OR 5 , —NR 6 R 7 , —S(O) i R 5 , —C(═O)OR 5 , —C(═O)NR 12 R 13 , and —C(═O)R 5 ; and b) (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, (C 3 -C 8 )cycloalkyl, aryl, heteroaryl, phenoxy, and benzyloxy, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —F, —Cl, —Br, —CN, —OR 5 , —SR 5 , —NR 6 R 7 , —S(O) i R 5 , —NR 11 S(═O) i R 5 , —C(═O)OR 5 , —C(═O)NR 12 R 13 , —NR 11 C(═O)R 5 , —C(═S)NR 12 R 13 , —C(═O)R 5 , (C 1 -C 6 )alkyl, (C 3 -C 8 )cycloalkyl, (C 2 -C 6 )alkenyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylsulfonylaminoalkyl, hydroxy(C 1 -C 6 )alkyl, cyano(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylcarbonylamino(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy, (C 1 -C 6 )alkoxy(C 1 -C 3 )alkyl, aryl and heteroaryl;

R 3 and R 4 are each independently —H, -halogen, —CN, —NO 2 , —OR 5 , —NR 6 R 7 , —S(O) i R 5 , —C(═O)OR 5 , —C(═O)NR 12 R 13 , —C(═O)R 5 , (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, (C 3 -C 8 )cycloalkyl, aryl, or heteroaryl, wherein each (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, (C 3 -C 8 )cycloalkyl, aryl, or heteroaryl is optionally substituted with 1 to 3 substituents independently selected from the group consisting of —F, —Cl, —Br, —CN, —OR 5 , —NR 6 R 7 , —S(O) i R 5 , —NR 11 S(═O) i R 5 , —C(═O)OR 5 , —C(═O)NR 12 R 13 , —NR 11 C(═O)R 5 , —C(═S)NR 12 R 13 , —C(═O)R 5 , (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylsulfonylaminoalkyl, hydroxy(C 1 -C 6 )alkyl, cyano(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylcarbonylamino(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy, (C 1 -C 6 )alkoxy(C 1 -C 3 )alkyl, aryl and heteroaryl;

R 5 is —H, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, (C 1 -C 3 )alkoxy(C 1 -C 6 )alkyl, (C 3 -C 8 )cycloalkyl, (C 3 -C 8 )cycloalkyl(C 1 -C 6 )alkyl, (C 3 -C 7 ) cycloheteroalkyl, aryl, heteroaryl or benzyl, each of which is optionally substituted with 1 to 3 substituents independently selected from the group consisting of —F, —Cl, —Br, —CN, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, and (C 1 -C 3 )alkoxy(C 1 -C 6 )alkyl;

R 6 and R 7 are each independently —H, (C 1 -C 6 )alkyl, hydroxy(C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 3 -C 8 ) cycloalkyl, (C 3 -C 8 )cycloalkyl(C 1 -C 6 )alkyl, each of which is optionally substituted with 1 to 3 substituents independently selected from the group consisting of —F, —Cl, —Br, —CN, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl and (C 1 -C 3 )alkoxy(C 1 -C 6 )alkyl;

R 8 and R 9 , together with the carbon to which they are attached, form ring A, which is a 3-14 membered monocyclic ring, wherein ring A is optionally substituted with 1 to 4 substituents independently selected from the group consisting of —F, —Cl, —Br, —CN, —OR 5 , —NR 6 R 7 , —S(O) i R 5 , —NR 11 S(═O) i R 5 , —C(═O)OR 5 , —NR 11 C(═O)NR 12 R 13 , —NR 11 C(═O)R 5 , —C(═S)NR 12 R 13 , —C(═O)R 5 , (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylsulfonylaminoalkyl, hydroxy(C 1 -C 6 )alkyl, cyano(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylcarbonylamino(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy, (C 1 -C 6 )alkoxy(C 1 -C 3 )alkyl, aryl and heteroaryl;

R 11 is —H, or (C 1 -C 6 )alkyl;

R 12 and R 13 are each independently —H, (C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy(C 1 -C 6 )alkyl, hydroxy(C 1 -C 6 )alkyl, cyano(C 1 -C 6 )alkyl, amino(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylamino(C 1 -C 6 )alkyl, or di(C 1 -C 3 )alkylamino(C 1 -C 6 )alkyl;

or R 12 and R 13 , together with the nitrogen to which they are attached, form a 3-8 membered ring optionally substituted with 1 to 3 substituents independently selected from the group consisting of —F, —Cl, —Br, —CN, —OR 5 , —NR 6 R 7 , —S(O) i R 5 , —NR 11 S(═O) i R 5 , —C(═O)OR 5 , —C(═O)NR 12 R 13 , —NR 11 C(═O)R 5 , —C(═S)NR 12 R 13 , —C(═O)R 5 , (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylsulfonylaminoalkyl, hydroxy(C 1 -C 6 )alkyl, cyano(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylcarbonylamino(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy and (C 1 -C 6 )alkoxy(C 1 -C 3 )alkyl, wherein the 3-8 membered ring optionally contains 1 to 3 additional heteroatoms, which are independently selected from O, N and S, wherein when the additional heteroatom is nitrogen, the nitrogen is substituted with —H, (C 1 -C 3 )alkyl or halo(C 1 -C 3 )alkyl, and when the additional heteroatom is sulfur, the sulfur is optionally mono or di-oxygenated;

R 14 is —H, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 3 -C 8 )cycloalkyl, cycloheteroalkyl(C 1 -C 3 )alkyl, (C 3 -C 8 )cycloalkyl(C 1 -C 3 )alkyl, aryl(C 1 -C 6 )alkyl, heteroaryl(C 1 -C 6 )alkyl, each of which is optionally substituted with 1 to 3 substituents independently selected from the group consisting of —F,−Cl, —CN, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl and (C 1 -C 3 )alkoxy;

R 15 is —H or (C 1 -C 6 )alkyl;

R 16 and R 17 are each independently —H or (C 1 -C 3 )alkyl;

R 18 is —H or (C 1 -C 3 )alkyl;

i is 0, 1 or 2;

p is 1 or 2; and

m is 1.

3. The compound of claim 1 , wherein the compound is represented by any one of the following Structural Formulas:

wherein R 14 is —H, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 3 -C 8 )cyclo alkyl, (C 3 -C 9 )cycloheteroalkyl(C 1 -C 3 )alkyl, (C 3 -C 8 )cycloalkyl(C 1 -C 3 )alkyl, aryl(C 1 -C 6 )alkyl, heteroaryl(C 1 -C 6 )alkyl, each of which is optionally substituted with 1 to 3 substituents independently selected from the group consisting of —F, —Cl, —CN, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl and (C 1 -C 3 )alkoxy, or a pharmaceutically acceptable salt thereof.

4. The compound of claim 1 , wherein the compound is represented by the following Structural Formulas:

wherein R 14 is —H, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 3 -C 8 )cycloalkyl, (C 3 -C 9 )cycloheteroalkyl(C 1 -C 3 )alkyl, (C 3 -C 8 )cycloalkyl(C 1 -C 3 )alkyl, aryl(C 1 -C 6 )alkyl, heteroaryl(C 1 -C 6 )alkyl, each of which is optionally substituted with 1 to 3 substituents independently selected from the group consisting of —F, —Cl, —CN, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl and (C 1 -C 3 )alkoxy, or a pharmaceutically acceptable salt thereof.

5. The compound of claim 3 , wherein ring A is a 5-7 membered monocyclic ring optionally substituted with 1 to 3 substituents independently selected from the group consisting of —F, —Cl, —Br, —CN, —OR 5 , —NR 6 R 7 , —S(O) i R 5 , —NR 11 S(═O) i R 5 , —C(═O)OR 5 , —C(═O)NR 12 R 13 , —NR 11 C(═O)R 5 , —C(═S)NR 12 R 13 , —C(═O)R 5 , (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylsulfonylaminoalkyl, hydroxy(C 1 -C 6 )alkyl, cyano(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylcarbonylamino(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy, (C 1 -C 6 )alkoxy(C 1 -C 3 )alkyl, aryl and heteroaryl, wherein ring A contains 0 to 2 heteroatoms, which are independently selected from O, N and S.

6. The compound of claim 5 , wherein ring A is selected from the group consisting of tetrahydrofuran, tetrahydropyran, cyclopentane, cyclohexane, cyclohexene, cycloheptane, oxepane, 1,3-dioxane, and piperidine, each of which is optionally substituted with 1 to 3 substituents independently selected from the group consisting of —F, —Cl, —Br, —CN, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, hydroxy(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy and phenyl.

7. The compound of claim 6 , wherein R 2 is a pyridinyl, thiophenyl, pyrrolyl or pyrimidinyl, each of which is optionally substituted with 1 to 3 substituents independently selected from the group consisting of halogen, —CN, (C 1 -C 6 )alkyl, (C 3 -C 8 )cycloalkyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy and (C 1 -C 6 )alkoxy(C 1 -C 3 )alkyl.

8. The compound of claim 3 , wherein the compound is represented by any one of the following Structural Formula:

or a pharmaceutically acceptable salt thereof, wherein R 10 is independently selected from the group consisting of -halogen, —CN, —NO 2 , —OR 5 , —SR 5 , —NR 6 R 7 , —S(O) i R 5 , —NR 11 S(═O) i R 5 , —S(O) i NR 12 R 13 , —C(═O)OR 5 , —OC(═O)R 5 , —C(═S)OR 5 , —OC(═S)R 5 , —C(═O)NR 12 R 13 , —NR 11 C(═O)R 5 , —C(═S)NR 12 R 13 , —NR 11 C(═S)R 5 , —C(═O)R 5 , —C(═S)R 5 , —OC(═O)OR 5 , —O(C═O)NR 12 R 13 , —NR 11 (C═O)OR 5 , —NR 11 (C═S)OR 5 , —O(C═S)NR 12 R 13 , —NR 11 (C═O)NR 12 R 13 , —NR 11 (C═S)NR 12 R 13 , —C(═O)R 5 , —C(═S)R 5 , (C 1 -C 6 )alkyl, (C 2 -C 6 )alkynyl, (C 3 -C 8 )cycloalkyl, (C 4 -C 8 )cycloalkenyl, (C 3 -C 9 )heterocycloalkyl, (C 2 -C 6 )alkenyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylsulfonylaminoalkyl, hydroxy(C 1 -C 6 )alkyl, cyano(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylcarbonylamino(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy, (C 1 -C 6 )alkoxy(C 1 -C 3 )alkyl, aryl and heteroaryl, wherein the cycloalkyl, heterocycloalkyl, aryl and heteroaryl groups in the groups represented by R 10 are each optionally substituted with 1 to 3 substituents independently selected from halogen, —CN, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy and (C 1 -C 3 )alkoxy(C 1 -C 6 )alkyl;

and s is 0, 1, 2 or 3.

9. The compound of claim 4 , wherein the compound is represented by the following Structural Formula:

or a pharmaceutically acceptable salt thereof, wherein R 10 is independently selected from the group consisting of -halogen, —CN, —NO 2 , —OR 5 , —SR 5 , —NR 6 R 7 , —S(O) i R 5 , —NR 11 S(═O) i R 5 , —S(O) i NR 12 R 13 , —C(═O)OR 5 , —OC(═O)R 5 , —C(═S)OR 5 , —OC(═S)R 5 , —C(═O)NR 12 R 13 , —NR 11 C(═O)R 5 , —C(═S)NR 12 R 13 , —NR 11 C(═S)R 5 , —C(═O)R 5 , —C(═S)R 5 , —OC(═O)OR 5 , —O(C═O)NR 12 R 13 , —NR 11 (C═O)OR 5 , —NR 11 (C═S)OR 5 , —O(C═S)NR 12 R 13 , —NR 11 (C═O)NR 12 R 13 , —C(═O)R 5 , —C(═S)R 5 , (C 1 -C 6 )alkyl, (C 2 -C 6 )alkynyl, (C 3 -C 8 )cycloalkyl, (C 4 -C 8 )cycloalkenyl, (C 3 -C 9 )heterocycloalkyl, (C 2 -C 6 )alkenyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylsulfonylaminoalkyl, hydroxy(C 1 -C 6 )alkyl, cyano(C 1 -C 6 )alkyl, (C 1 -C 3 )alkylcarbonylamino(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy, (C 1 -C 6 )alkoxy(C 1 -C 3 )alkyl, aryl and heteroaryl, wherein the cycloalkyl, heterocycloalkyl, aryl and heteroaryl groups in the groups represented by R 10 are each optionally substituted with 1 to 3 substituents independently selected from halogen, —CN, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy and (C 1 -C 3 )alkoxy(C 1 -C 6 )alkyl;

and s is 0, 1, 2 or 3.

10. The compound of claim 8 , wherein R 10 is independently selected from the group consisting of —F, —Cl, —CN, (C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy, halo(C 1 -C 6 )alkyl and halo(C 1 -C 6 )alkoxy.

11. The compound of claim 10 , wherein R 10 is independently selected from the group consisting of —F, —Cl, —CN, —Me, —Et, -OMe, —CF 3 and —OCF 3 .

12. The compound of claim 10 , wherein R 1 is —H and R 14 , when present, is -Me.

13. The compound of claim 12 , wherein ring A is represented by the following structural formula:

wherein:

R 19 and R 20 are each independently selected from —H, halogen, —CN, —OR 5 , —NR 6 R 7 , —S(O) i R 5 , —NR 11 S(═O) i R 5 , —C(═O)OR 5 , —C(═O)NR 12 R 13 , —NR 11 C(═O)R 5 , —C(═S)NR 12 R 13 , —C(═O)R 5 , (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, aryl, aryl(C 1 -C 6 )alkyl, heteroaryl and heteroaryl(C 1 -C 6 )alkyl, wherein each of the (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, aryl, aryl(C 1 -C 6 )alkyl, heteroaryl and heteroaryl(C 1 -C 6 )alkyl groups represented by R 19 and R 20 is optionally substituted with 1 to 3 substituents independently selected from the group consisting of halogen, —CN, —NR 11 SO 2 (C 1 -C 3 )alkyl, —NR 11 C(═O)—(C 1 -C 3 )alkyl, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy and (C 1 -C 3 )alkoxy(C 1 -C 6 )alkyl.

14. The compound of claim 13 , wherein:

R 20 is —H and R 19 is —OH, (C 1 -C 3 )alkoxy, halo(C 1 -C 3 )alkoxy or (C 1 -C 3 )alkoxy(C 1 -C 3 )alkoxy.

15. The compound of claim 1 , wherein:

R 1 is —H; and

R 2 is —H, halogen, —CN, —OR 5 , —C(═O)NR 12 R 13 , —C(═O)OR 5 , —C(O)R 5 , (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, (C 3 -C 6 )cycloalkyl, (C 3 -C 6 )cycloalkyl(C 1 -C 3 )alkyl, (C 4 -C 6 )cycloalkenyl, phenyl, phenyl(C 1 -C 3 )alkyl, heteroaryl, heteroaryl(C 1 -C 3 )alkyl, (C 5 -C 6 )heterocycloalkyl, (C 5 -C 6 )heterocycloalky(C 1 -C 3 )alkyl, wherein the heteroaryl is selected from pyridyl, pyridazinyl, pyridinonyl, pyridazinonyl, thiazolyl, oxazolyl, oxadiazolyl, pyrazinyl, pyrimidyl, indolyl, quinolyl, quinoxalinyl, triazole and thiophenyl, the heterocycloalkyl is selected from oxetanyl, tetrahydrofuran, tetrahydropyran, piperidine, pyrrolidinyl and pyrrolidinonyl, and each of (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, (C 3 -C 6 )cycloalkyl, (C 3 -C 6 )cycloalkyl(C 1 -C 3 )alkyl, (C 4 -C 6 )cycloalkenyl, phenyl, phenyl(C 1 -C 3 )alkyl, heteroaryl, heteroaryl(C 1 -C 3 )alkyl, (C 5 -C 6 )heterocycloalkyl and (C 5 -C 6 )heterocycloalky(C 1 -C 3 )alkyl groups represented by R 2 is optionally substituted with 1 to 5 substituents independently selected from halogen, —CN, (C 1 -C 3 )alkyl, halo(C 1 -C 3 )alkyl, (C 2 -C 6 )alkynyl, —NR 6 R 7 , —S(O) i R 5 , —C(O)R 5 , —OH, (C 3 -C 6 )cycloalkyl, (C 1 -C 3 )alkoxy and halo(C 1 -C 3 )alkoxy.

16. The compound of claim 15 , wherein:

R 5 is selected from the group consisting of —H, (C 1 -C 3 )alkyl, halo(C 1 -C 3 )alkyl, (C 1 -C 3 )alkoxy(C 1 -C 3 )alkyl, (C 3 -C 6 )cycloalkyl, (C 3 -C 6 )cycloalkyl(C 1 -C 3 )alkyl, phenyl and phenyl(C 1 -C 3 )alkyl, wherein the phenyl group in the groups represented by R 5 is optionally substituted with 1 to 3 substituents independently selected from —F, —Cl, —Br, —CN, ═O, —NR 6 R 7 , (C 1 -C 3 )alkyl, halo(C 1 -C 3 )alkyl and (C 1 -C 3 )alkoxy(C 1 -C 3 )alkyl;

R 6 is —H or (C 1 -C 3 )alkyl;

R 7 is —H, (C 1 -C 3 )alkyl, halo(C 1 -C 3 )alkyl, (C 3 -C 6 )cycloalkyl, (C 3 -C 6 )cycloalkyl(C 1 -C 3 )alkyl or (C 1 -C 3 )alkoxy(C 1 -C 3 )alkyl;

R 11 is —H or (C 1 -C 3 )alkyl;

R 12 is —H or (C 1 -C 3 )alkyl; and

R 13 is —H, (C 1 -C 3 )alkyl, halo(C 1 -C 3 )alkyl, (C 3 -C 6 )cycloalkyl(C 1 -C 3 )alkyl or (C 1 -C 3 )alkoxy(C 1 -C 3 )alkyl, or R 12 and R 13 together with the nitrogen atom to which they are attached form a pyrrolidine or piperidine ring.

17. A pharmaceutical composition comprising a pharmaceutically acceptable carrier or diluent and a compound of claim 1 or a pharmaceutically acceptable salt thereof.

18. A method for treating Alzheimer's disease in a subject comprising administering to the subject an effective amount of a compound of claim 1 or a pharmaceutically acceptable salt thereof, such that Alzheimer's disease is treated in the subject.

19. A method for treating cognitive impairment or cognitive decline in a subject comprising administering to the subject an effective amount of a compound of claim 1 or a pharmaceutically acceptable salt thereof, such that cognitive impairment or cognitive decline is treated in the subject.

20. A method for treating Down's Syndrome in a subject comprising administering to the subject an effective amount of a compound of claim 1 or a pharmaceutically acceptable salt thereof, such that Down's Syndrome is treated in the subject.

21. A method for treating HCHWA-D in a subject comprising administering to the subject an effective amount of a compound of claim 1 or a pharmaceutically acceptable salt thereof, such that HCHWA-D is treated in the subject.

22. A method for treating glaucoma in a subject comprising administering to the subject an effective amount of a compound of claim 1 or a pharmaceutically acceptable salt thereof, such that glaucoma is treated in the subject.

23. A compound represented by any one of the following structural formulas: