Enzyme modulators and treatments

1. A compound of the formula

wherein A2 is a bicyclic fused heteroaryl selected from the group consisting of

and wherein the symbol (**) is the point of attachment to the A1 ring of formula I;

and wherein  indicates either a saturated or an unsaturated bond;

wherein each Z3 and Z5 may be independently attached to either of the rings making up the foregoing bicyclic structures;

A1 is R2-substituted monocyclic 5-membered ring heteroaryl;

D is a moiety of the formula

wherein E1 is phenyl;

wherein the symbol (***) is the point of attachment to the Y group of formula I;

X1 is selected from the group consisting of O, S, NR3, —C(═O)—, —O—(CH 2 ) n —, —S—(CH 2 ) n —, —NR3-(CH 2 ) n —, —O—(CH 2 ) q —O—, —O—(CH 2 ) q —NR3-, —N(R3)-(CH 2 ) q —N(R3)-, —(CH 2 ) n —N(R4)-C(═O)—, —(CH 2 ) n —N(R4)-C(═O)(CH 2 ) n —, —(CH 2 ) n —CO—N(R4)-, —(CH 2 ) p —, C2-C5alkenyl, C2-C5alkynyl, C3-C6cycloalkyl, and a direct bond wherein the E1 ring and the E2 ring are directly linked by a covalent bond;

and wherein the carbon atoms of —(CH 2 ) n —, —(CH 2 ) q —, (CH 2 ) p , C2-C5alkenyl, and C2-C5alkynyl moieties of X1 may be further substituted by one or more C1-C6alkyl;

X2 is a direct bond wherein E1 is directly linked to the Y group of formula I;

and wherein the E2 ring is Z5- and/or Z6-substituted pyridinyl, pyrimidinyl;

each Z2 is independently and individually selected from the group consisting of hydroxyl, hydroxyC1-C6alkyl, cyano, (R3) 2 N—, (R4) 2 N—, (R4) 2 NC1-C6alkyl, (R4) 2 NC2-C6alkylN(R4)-(CH 2 ) n , (R4) 2 NC2-C6alkylO—(CH 2 ) n , (R3) 2 N—C(═O)—, (R4) 2 N—C(═O)—, (R4) 2 N—CO—C1-C6alkyl, carboxyl, carboxyC1-C6alkyl, C1-C6alkoxycarbonyl, C1-C6alkoxycarbonylC1-C6alkyl, (R3) 2 NSO 2 , (R4) 2 NSO 2 , —SO 2 R5-, —(CH 2 ) n N(R4)C(O)R8, ═O, ═NOH, ═N(OR6), heteroarylC1-C6alkyl, heterocyclylC1-C6alkyl, heteroaryloxyC1-C6alkyl, heterocyclyloxyC1-C6alkyl, arylaminoC1-C6alkyl, heteroarylaminoC1-C6alkyl, heterocyclylaminoC1-C6alkyl, and moieties of the formulae

wherein the symbol (#) indicates the point of attachment of the Z2 moiety to the A2 ring of formula I; in the event that Z2 contains an alkyl or alkylene moiety, such moieties may be further substituted with one or more C1-C6alkyls;

each Z3 is independently and individually selected from the group consisting of H, C1-C6alkyl, hydroxyl, hydroxyC1-C6alkyl, cyano, C1-C6alkoxy, C1-C6alkoxyC1-C6alkyl, halogen, CF 3 , (R3) 2 N—, (R4) 2 N—, (R4) 2 NC1-C6alkyl, (R4) 2 NC2-C6alkylN(R4)-CH 2 ) n , (R4) 2 NC2-C6alkylO—(CH 2 ) n , —R8C(═O)—, (R4) 2 N—CO—C1-C6alkyl, carboxyl, carboxyC1-C6alkyl, C1-C6alkoxycarbonyl, C1-C6alkoxycarbonylC1-C6alkyl, (R3) 2 NSO 2 , —SO 2 R3, SOR3, (R4) 2 NSO 2 , —SO 2 R4, —SOR4, —(CH 2 ) n N(R4)C(O)R8, —C═(NOH)R6, —C═(NOR3)R6, heteroaryl, heterocyclyl, heteroarylC1-C6alkyl, heterocyclylC1-C6alkyl, heteroaryloxy, heterocyclyloxy, heteroaryloxyC1-C6alkyl, heterocyclyloxyC1-C6alkyl, arylamino, heteroarylamino, heterocyclylamino, arylaminoC1-C6alkyl, heteroarylaminoC1-C6alkyl, heterocyclylaminoC1-C6alkyl, and moieties of the formulae

wherein the symbol (#) indicates the point of attachment of the Z3 moiety to the A2 ring of formula I;

in the event that Z3 contains an alkyl or alkylene moiety, such moieties may be further substituted with one or more C1-C6alkyls;

each Z4 is a substituent attached to a ring nitrogen and is independently and individually selected from the group consisting of H, C1-C6alkyl, hydroxyC2-C6alkyl, C1-C6alkoxyC2-C6alkyl, (R4) 2 N—C2-C6alkyl, (R4) 2 N—C2-C6alkylN(R4)-C2-C6alkyl, (R4) 2 N—C2-C6alkyl-O—C2-C6alkyl, (R4) 2 N—CO—C2-C6alkyl, carboxyC2-C6alkyl, C1-C6alkoxycarbonylC2-C6alkyl, —C2-C6alkylN(R4)C(O)R8, R8-C(═NR3)-, —SO 2 R8, —COR8, heteroaryl, heteroarylC1-C6alkyl, heterocyclyl, heterocyclylC1-C6alkyl, heteroaryloxyC2-C6alkyl, heterocyclyloxyC2-C6alkyl, arylaminoC2-C6alkyl, heteroarylaminoC2-C6alkyl, heterocyclylaminoC2-C6alkyl, and moieties of the formulae

wherein the symbol (#) indicates the point of attachment of the Z4 moiety to the A2 ring for formula I;

in the event that Z4 contains an alkyl or alkylene moiety, such moieties may be further substituted with one or more C1-C6alkyls;

each Z5 is independently and individually selected from the group consisting of H, C1-C6alkyl, branched C3-C7alkyl, halogen, fluoroalkyl, cyano, hydroxyl, alkoxy, oxo, aminocarbonyl, carbonylamino, aminosulfonyl, sulfonylamino, —N(R3) 2 , —O—(CH 2 ) q —N(R4) 2 , —N(R3)-(CH 2 ) q —N(R4) 2 , —R5, —O—(CH 2 ) q —O-Alkyl, —O—(CH 2 ) q —N(R4) 2 , —N(R3)-(CH 2 ) q —O-Alkyl, —N(R3)-(CH 2 ) q —N(R4) 2 , —O—(CH 2 ) q —R5, and —N(R3)-(CH 2 ) q —R5;

each Z6 is independently and individually selected from the group consisting of H, C1-C6alkyl, branched C3-C7alkyl, hydroxyl, C1-C6alkoxy, heteroaryl, heterocyclyl, heteroaryloxy, heterocyclyloxy, arylamino, heteroarylamino, and heterocyclylamino, (R3) 2 N—, —N(R3)COR8, (R4) 2 N—, —R5, —N(R4)COR8, —N(R3)SO 2 R6-, —CON(R3) 2 , —CON(R4) 2 , —COR5, and —SO 2 NHR4;

each R2 is selected from the group consisting of monocyclic heteroaryl, C1-C6alkyl, branched C3-C7alkyl, R19 substituted C3-C8-carbocyclyl wherein R19 is H or C1-C6alkyl, C1-C6-fluoroalkyl wherein the alkyl group is partially or fully fluorinated, phenyl wherein the phenyl group is optionally substituted by one or more fluorine substituents and chlorine;

each R3 is independently and individually selected from the group consisting of H, C1-C6alkyl, branched C3-C7alkyl, C3-C7-carbocyclyl, and phenyl;

each R4 is selected from the group consisting of H, C1-C6alkyl, hydroxyC1-C6alkyl, dihydroxyC1-C6alkyl, C1-C6alkoxyC1-C6alkyl, branched C3-C7alkyl, branched hydroxyC1-C6 alkyl, branched C1-C6alkoxyC1-C6alkyl, branched dihydroxyC1-C6alkyl, carbocyclyl, hydroxyl substituted carbocyclyl, alkoxy substituted carbocyclyl, dihydroxy substituted carbocyclyl, phenyl, heteroaryl, heterocyclyl, phenylC1-C6alkyl, heteroarylC1-C6alkyl, and heterocyclylC1-C6alkyl;

each R5 is independently and individually selected from the group consisting of

and wherein the symbol (##) is the point of attachment to respective R8, R10, Z2, or Z3 moieties containing a R5 moiety;

each R6 is independently and individually selected from the group consisting of C1-C6alkyl, branched C3-C7alkyl, carbocyclyl, phenyl, heteroaryl, and heterocyclyl;

each R8 is independently and individually selected from the group consisting of C1-C6alkyl, branched C3-C7alkyl, fluoroalkyl wherein the alkyl moiety is partially or fully fluorinated, carbocyclyl, phenyl, phenyC1-C6lalkyl, heteroaryl, heteroarylC1-C6alkyl, heterocyclyl, heterocyclylC1-C6alkyl, OH, C1-C6alkoxy, N(R3) 2 , N(R4) 2 , and R5;

each R10 is independently and individually selected from the group consisting of CO 2 H, CO 2 C1-C6alkyl, CO—N(R4) 2 , OH, C1-C6alkoxy, and —N(R4) 2 ;

each R13 is independently and individually selected from the group consisting of H, C1-C6alkyl, branched C3-C7alkyl, carbocyclyl, hydroxyC2-C7alkyl, C1-C6alkoxyC2-C7alkyl, (R4) 2 N—CO, (R4) 2 N—CO—C1-C6alkyl, carboxyC1-C6alkyl, C1-C6alkoxycarbonyl, C1-C6alkoxycarbonylC1-C6alkyl, (R4) 2 N—C2-C6alkyl, (R4) 2 N—C2-C6alkylN(R4)-(CH 2 ) q , R5-C2-C6alkylN(R4)-(CH 2 ) q , (R4) 2 N—C2-C6alkylO-(CH 2 ) q , R5-C2-C6alkyl-O—(CH 2 ) q , —(CH 2 ) q N(R4)C(O)R8, aryl, arylC1-C6alkyl, heteroaryl, heteroarylC1-C6alkyl, heterocyclyl, heterocyclylC1-C6alkyl, aryloxyC2-C6alkyl, heteroaryloxyC2-C6alkyl, heterocyclyloxyC2-C6alkyl, arylaminoC2-C6alkyl, heteroarylaminoC2-C6alkyl, and heterocyclylaminoC2-C6alkyl;

V, V1, and V2 are each independently O or represent two hydrogens connected to the methylene carbon to which the V, V1, or V2 is attached;

wherein two R3 or R4 moieties are independently and individually taken from the group consisting of C1-C6alkyl and branched C3-C6alkyl, hydroxyalkyl, and alkoxyalkyl and are attached to the same nitrogen atom, said moieties may cyclize to form a C3-C7 heterocyclyl ring;

n is 0-4; p is 1-4; q is 2-6; r is 1; and v is 1 or 2;

or a tautomer, diastereomer, geometric isomer, enantiomer, hydrate, or salt of any of the foregoing.

2. The compound of claim 1 wherein A2 is selected from the group consisting of

and wherein the symbol (**) is the point of attachment to the A1 ring of formula I;

wherein each Z3 and Z5 is independently attached to either aryl or heteroaryl ring of the A2 bicyclic ring.

3. The compound of claim 1 , wherein A1 is selected from the group consisting of

wherein the symbol (*) denotes the attachment to the W moiety of formula I and the symbol (**) denotes the attachment to the A2 moiety of formula I.

4. A compound of the formula

wherein A2 is selected from the group consisting of

wherein each Z3 and Z5 is independently attached to either aryl or heteroaryl ring of the A2 bicyclic ring;

wherein the symbol (**) denotes the attachment to the A1 moiety of formula I;

A1 is selected from the group consisting of

wherein the symbol (*) denotes the attachment to the NH moiety of formula I and the symbol (**) denotes the attachment to the A2 moiety of formula I;

D is selected from the group consisting of

wherein E1 is phenyl;

X1 is selected from the group consisting of O;

X2 is a direct bond wherein E1 is directly linked to the Y group of formula I;

each R2 is selected from the group consisting of monocyclic heteroaryl, C1-C6alkyl, branched C3-C7alkyl, R19 substituted C3-C8-carbocyclyl wherein R19 is H or C1-C6alkyl, C1-C6-fluoroalkyl wherein the alkyl group is partially or fully fluorinated, phenyl wherein the phenyl group is optionally substituted by one or more fluorine substituents and chlorine;

each R3 is independently and individually selected from the group consisting of H, C1-C6alkyl, branched C3-C7 alkyl, C3-C7-carbocyclyl, and phenyl;

each R4 is selected from the group consisting of H, C1-C6alkyl, hydroxyC1-C6 alkyl, dihydroxyC1-C6alkyl, C1-C6alkoxyC1-C6alkyl, branched C3-C7alkyl, branched hydroxyC1-C6 alkyl, branched C1-C6alkoxyC1-C6alkyl, branched dihydroxyC1-C6alkyl, carbocyclyl, hydroxyl substituted carbocyclyl, alkoxy substituted carbocyclyl, dihydroxy substituted carbocyclyl, phenyl, heteroaryl, heterocyclyl, phenylC1-C6alkyl, heteroarylC1-C6alkyl, and heterocyclylC1-C6alkyl;

each R5 is independently and individually selected from the group consisting of

and wherein the symbol (##) is the point of attachment to respective R8, R10, R13, Z2, Z3, Z4, Z5, or A2 ring moieties containing a R5 moiety;

wherein each R6 is independently and individually selected from the group consisting of C1-C6alkyl, branched C3-C7alkyl, carbocyclyl, phenyl, heteroaryl, and heterocyclyl;

each R8 is independently and individually selected from the group consisting of C1-C6alkyl, branched C3-C7alkyl, fluoroalkyl wherein the alkyl moiety is partially or fully fluorinated, carbocyclyl, phenyl, phenylC1-C6lalkyl, heteroaryl or heteroarylC1-C6alkyl, heterocyclyl, heterocyclylC1-C6alkyl, OH, C1-C6alkoxy, N(R3) 2 , N(R4) 2 , and R5;

each R10 is independently and individually selected from the group consisting of CO 2 H, CO 2 C1-C6alkyl, CO—N(R4) 2 , OH, C1-C6alkoxy, and —N(R4) 2 ;

each R13 is independently and individually selected from the group consisting of H, C1-C6alkyl, branched C3-C7alkyl, carbocyclyl, hydroxyC2-C7alkyl, C1-C6alkoxyC2-C7alkyl, (R4) 2 N—CO, (R4) 2 N—CO—C1-C6alkyl, carboxyC1-C6alkyl, C1-C6alkoxycarbonyl, C1-C6alkoxycarbonylC1-C6alkyl, (R4) 2 N—C2-C6alkyl, (R4) 2 N—C2-C6alkylN(R4)-(CH 2 ) q , R5-C2-C6alkylN(R4)-(CH 2 ) q , (R4) 2 N—C2-C6alkylO-(CH 2 ) q , R5-C2-C6alkyl-O—(CH 2 ) q , —(CH 2 ) q N(R4)C(O)R8, aryl, arylC1-C6alkyl, heteroaryl, heteroarylC1-C6alkyl, heterocyclyl, heterocyclylC1-C6alkyl, aryloxyC2-C6alkyl, heteroaryloxyC2-C6alkyl, heterocyclyloxyC2-C6alkyl, arylaminoC2-C6alkyl, heteroarylaminoC2-C6alkyl, and heterocyclylaminoC2-C6alkyl;

V, V1, and V2 are each independently or represent two hydrogens connected to the methylene carbon to which the V, V1, or V2 is attached;

each Z2 is independently and individually selected from the group consisting of hydroxyl, hydroxyC1-C6alkyl, cyano, (R3) 2 N—, (R4) 2 N—, (R4) 2 NC1-C6alkyl, (R4) 2 NC2-C6alkylN(R4)-(CH 2 ) n , (R4) 2 NC2-C6alkylO-(CH 2 ) n , (R3) 2 N—C(═O)—, (R4) 2 N—C(═O)—, (R4) 2 N—CO—C1-C6alkyl, carboxyl, carboxyC1-C6alkyl, C1-C6alkoxycarbonyl, C1-C6alkoxycarbonylC1-C6alkyl, (R3) 2 NSO 2 , (R4) 2 NSO 2 , —SO 2 R5-, —(CH 2 ) n N(R4)C(O)R8, ═O, ═NOH, ═N(OR6), heteroarylC1-C6alkyl, heterocyclylC1-C6alkyl, heteroaryloxyC1-C6alkyl, heterocyclyloxyC1-C6alkyl, arylaminoC1-C6alkyl, heteroarylaminoC1-C6alkyl, heterocyclylaminoC1-C6alkyl, and moieties of the formulae

wherein the symbol (#) indicates the point of attachment of the Z2 moiety to the A2 ring of formula I; in the event that Z2 contains an alkyl or alkylene moiety, such moieties may be further substituted with one or more C1-C6alkyls;

each Z3 is independently and individually selected from the group consisting of H, C1-C6alkyl, hydroxyl, hydroxyC1-C6alkyl, cyano, C1-C6alkoxy, C1-C6alkoxyC1-C6alkyl, halogen, CF 3 , (R3) 2 N—, (R4) 2 N—, (R4) 2 NC1-C6alkyl, (R4) 2 NC2-C6alkylN(R4)-CH 2 ) n , (R4) 2 NC2-C6alkylO—(CH 2 ) n , R8CO—, (R4) 2 N—CO—C1-C6alkyl, carboxyl, carboxyC1-C6alkyl, C1-C6alkoxycarbonyl, C1-C6alkoxycarbonylC1-C6alkyl, (R3) 2 NSO 2 , —SO 2 R3, SOR3, (R4) 2 NSO 2 , —SO 2 R4, —SOR4, —(CH 2 ) n N(R4)C(O)R8, —C═(NOH)R6, —C═(NOR3)R6, heteroaryl, heterocyclyl, heteroarylC1-C6alkyl, heterocyclylC1-C6alkyl, heteroaryloxy, heterocyclyloxy, heteroaryloxyC1-C6alkyl, heterocyclyloxyC1-C6alkyl, arylamino, heteroarylamino, heterocyclylamino, arylaminoC1-C6alkyl, heteroarylaminoC1-C6alkyl, heterocyclylaminoC1-C6alkyl, and moieties of the formulae

wherein the symbol (#) indicates the point of attachment of the Z3 moiety to the A2 ring of formula I;

in the event that Z3 contains an alkyl or alkylene moiety, such moieties may be further substituted with one or more C1-C6alkyls;

each Z4 is a substituent attached to a ring nitrogen and is independently and individually selected from the group consisting of H, C1-C6alkyl, hydroxyC2-C6alkyl, C1-C6alkoxyC2-C6alkyl, (R4) 2 N—C2-C6alkyl, (R4) 2 N—C2-C6alkylN(R4)-C2-C6alkyl, (R4) 2 N—C2-C6alkyl-O—C2-C6alkyl, (R4) 2 N—CO—C2-C6alkyl, carboxyC2-C6alkyl, C1-C6alkoxycarbonylC2-C6alkyl, —C2-C6alkylN(R4)C(O)R8, R8-C(═NR3)-, —SO 2 R8, —COR8, heteroaryl, heteroarylC1-C6alkyl, heterocyclyl, heterocyclylC1-C6alkyl, heteroaryloxyC2-C6alkyl, heterocyclyloxyC2-C6alkyl, arylaminoC2-C6alkyl, heteroarylaminoC2-C6alkyl, heterocyclylaminoC2-C6alkyl, and moieties of the formulae

wherein the symbol (#) indicates the point of attachment of the Z4 moiety to the A2 ring for formula I;

in the event that Z4 contains an alkyl or alkylene moiety, such moieties may be further substituted with one or more C1-C6alkyls;

Z5 is independently and individually selected from the group consisting of H, C1-C6alkyl, branched C3-C7alkyl, halogen, fluoroalkyl, cyano, hydroxyl, alkoxy, oxo, aminocarbonyl, carbonylamino, aminosulfonyl, sulfonylamino, —N(R3) 2 , —O—(CH 2 ) q —N(R4) 2 , —N(R3)-(CH 2 ) q —N(R4) 2 , —R5, —O—(CH 2 ) q —O-Alkyl, —O—(CH 2 ) q —N(R4) 2 , —N(R3)-(CH 2 ) q —O-Alkyl, —N(R3)-(CH 2 ) q —N(R4) 2 , —O—(CH 2 ) q —R5, and —N(R3)-(CH 2 ) q —R5;

each Z6 is independently and individually selected from the group consisting of H, C1-C6alkyl, branched C3-C7alkyl, hydroxyl, C1-C6alkoxy, heteroaryl, heterocyclyl, heteroaryloxy, heterocyclyloxy, arylamino, heteroarylamino, and heterocyclylamino, (R3) 2 N—, —N(R3)COR8, (R4) 2 N—, —R5, —N(R4)COR8, —N(R3)SO 2 R6-, —CON(R3) 2 , —CON(R4) 2 , —COR5, and —SO 2 NHR4;

wherein two R3 or R4 moieties are independently and individually taken from the group consisting of C1-C6alkyl and branched C3-C6alkyl, hydroxyalkyl, and alkoxyalkyl and are attached to the same nitrogen atom, said moieties may cyclize to form a C3-C7 heterocyclyl ring;

n is 0-4; p is 1-4; q is 2-6; and v is 1 or 2;

or a tautomer, diastereomer, geometric isomer, enantiomer, hydrate, or salt of any of the foregoing.

5. The compound of claim 4 having the formula If

wherein A2 is selected from the group consisting of

wherein the symbol (**) denotes the attachment to the A1 moiety of formula If;

wherein each Z3 and Z5 is independently attached to either aryl or heteroaryl ring of the A2 bicyclic ring;

wherein A1 is selected from the group consisting of

wherein the symbol (*) denotes the attachment to the NH moiety of formula If and the symbol (**) denotes the attachment to the A2 moiety of formula If;

wherein D is

wherein the symbol (***) denotes the attachment to the NH moiety of formula If;

wherein E1 is phenyl;

wherein X1 is selected from the group consisting of O;

wherein X2 is a direct bond.

6. Compounds of claim 4 having the formula If

wherein A2 is selected from the group consisting of

wherein the symbol (**) denotes the attachment to the A1 moiety of formula If;

wherein each Z3 and Z5 is independently attached to either aryl or heteroaryl ring of the A2 bicyclic ring;

wherein A1 is selected from the group consisting of

wherein the symbol (*) denotes the attachment to the NH moiety of formula If and the symbol (**) denotes the attachment to the A2 moiety of formula If;

wherein D is

wherein the symbol (***) denotes the attachment to the NH moiety of formula If;

wherein E1 is phenyl;

wherein X1 is selected from the group consisting of O; and

wherein X2 is a direct bond.

7. A compound selected from

1-(3-tert-butyl-1-(quinolin-6-yl)-1H-pyrazol-5-yl)-3-(3-(pyridin-3-yloxy)phenyl)urea,

1-(3-tert-butyl-1-(1H-indol-5-yl)-1H-pyrazol-5-yl)-3-(3-(pyridin-3-yloxy)phenyl)urea,

1-(3-tert-butyl-1-(indolin-5-yl)-1H-pyrazol-5-yl)-3-(3-(pyridin-3-yloxy)phenyl)urea,

1-(3-tert-butyl-1-(1,2,3,4-tetrahydroisoquinolin-6-yl)-1H-pyrazol-5-yl)-3-(3-(pyridin-3-yloxy)phenyl)urea,

1-(3-tert-butyl-1-(1,2,3,4-tetrahydroisoquinolin-6-yl)-1H-pyrazol-5-yl)-3-(4-(2-(methylcarbamoyl)pyridin-4-yloxy)phenyl)urea,

1-(3-tert-butyl-1-(1,2,3,4-tetrahydroisoquinolin-6-yl)-1H-pyrazol-5-yl)-3-(3-(5-chloropyridin-3-yloxy)phenyl)urea,

1-(3-tert-butyl-1-(2-oxo-1,2-dihydroquinolin-6-yl)-1H-pyrazol-5-yl)-3-(3-(pyridin-3-yloxy)phenyl)urea,

1-(3-tert-butyl-1-(2-oxo-1,2-dihydroquinolin-6-yl)-1H-pyrazol-5-yl)-3-(3-(2-(methylcarbamoyl)pyridin-4-yloxy)phenyl)urea,

1-(3-tert-butyl-1-(2-oxo-1,2-dihydroquinolin-6-yl)-1H-pyrazol-5-yl)-3-(4-(2-(methylcarbamoyl)pyridin-4-yloxy)phenyl)urea,

1-(3-cyclopentyl-1-(2-oxo-1,2-dihydroquinolin-6-yl)-1H-pyrazol-5-yl)-3-(4-(2-(methylcarbamoyl)pyridin-4-yloxy)phenyl)urea,

1-(3-cyclopentyl-1-(2-oxo-1,2-dihydroquinolin-6-yl)-1H-pyrazol-5-yl)-3-(3-(pyridin-3-yloxy)phenyl)urea,

1-(3-tert-butyl-1-(2-(piperazin-1-yl)quinolin-6-yl)-1H-pyrazol-5-yl)-3-(4-(2-(methylcarbamoyl)pyridin-4-yloxy)phenyl)urea,

1-(1-(2-(2-aminoethylamino)quinolin-6-yl)-3-tert-butyl-1H-pyrazol-5-yl)-3-(4-(2-(methylcarbamoyl)pyridin-4-yloxy)phenyl)urea,

1-(3-tert-butyl-1-(2-((R)-3-(dimethylamino)pyrrolidin-1-yl)quinolin-6-yl)-1H-pyrazol-5-yl)-3-(4-(2-(methylcarbamoyl)pyridin-4-yloxy)phenyl)urea,

1-(3-tert-butyl-1-(2-(methylamino)quinolin-6-yl)-1H-pyrazol-5-yl)-3-(4-(2-(methylcarbamoyl)pyridin-4-yloxy)phenyl)urea,

1-(3-tert-butyl-1-(2-(dimethylamino)quinolin-6-yl)-1H-pyrazol-5-yl)-3-(4-(2-(methylcarbamoyl)pyridin-4-yloxy)phenyl)urea,

1-(1-(2-aminoquinolin-6-yl)-3-tert-butyl-1H-pyrazol-5-yl)-3-(4-(2-(methylcarbamoyl)pyridin-4-yloxy)phenyl)urea,

1-(3-tert-butyl-1-(3-carbamoyl-1,2,3,4-tetrahydroisoquinolin-6-yl)-1H-pyrazol-5-yl)-3-(3-(pyridin-3-yloxy)phenyl)urea,

1-(3-tert-butyl-1-(1-(methylcarbamoyl)-1,2,3,4-tetrahydroisoquinolin-6-yl)-1H-pyrazol-5-yl)-3-(3-(pyridin-3-yloxy)phenyl)urea,

1-(1-(3-((2,3-dihydroxypropyl)carbamoyl)-1,2,3,4-tetrahydroisoquinolin-6-yl)-3-tert-butyl-1H-pyrazol-5-yl)-3-(3-(pyridin-3-yloxy)phenyl)urea,

6-(3-tert-butyl-5-(3-(3-(pyridin-3-yloxy)phenyl)ureido)-1H-pyrazol-1-yl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid,

1-(3-tert-butyl-1-(3-(methylcarbamoyl)-1,2,3,4-tetrahydroisoquinolin-6-yl)-1H-pyrazol-5-yl)-3-(3-(pyridin-3-yloxy)phenyl)urea, and

1-(1-(1-((2,3-dihydroxypropyl)carbamoyl)-1,2,3,4-tetrahydroisoquinolin-6-yl)-3-t-butyl-1H-pyrazol-5-yl)-3-(3-(pyridin-3-yloxy)phenyl)urea.

8. A pharmaceutical composition comprising a compound of claim 1 , 4 , or 7 , together with a pharmaceutically acceptable carrier, said carried including an additive selected from the group including adjuvants, excipients, diluents, and stablilizers.