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| US patent
number: |
6608048 |
| Title: |
Tricyclic protein kinase inhibitors |
| Inventor(s): |
Tsou; Hwei-Ru (New City, NY)
Overbeek-Klumpers; Elsebe Geraldine (Bergentheim,NL)
Wissner; Allan (Ardsley, NY)
|
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Owner:
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Wyeth Holdings (Madison, NJ)
|
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Agent/attorney/firm:
|
Goudie; Joy S.
|
| Filing date: |
March 28, 2001 |
| Application Number: |
09/820,132 |
| Issue date: |
August 19, 2003 |
|
Primary examiner:
|
Raymond; Richard L.
|
| Assistant
examiner:
|
McKenzie; Thomas
|
|
US classification code:
|
514/183; 514/151; 514/211.15; 514/218; 514/224.5; 514/230.2; 540/467; 540/470; 540/544; 540/553; 540/575; 544/101; 544/34; 544/60; 544/73 |
|
Examiner's field of search: |
514/183 514/211.15 514/218 514/224.5 514/229.1 540/467 540/470 540/544 540/553 540/575 544/34 544/60 544/73 544/101 |
| Parent case: |
CROSS REFERENCE TO RELATED APPLICATIONS
This application claims benefit of U.S. Provisional Application No. 60/304,206 which was converted from U.S. patent application Ser. No. 09/536,919 filed Mar. 28, 2000 pursuant to a petition filed under 37 C.F.R. 1.53 (c) (2) filed Jul. 11, 2000. |
| Priority data: |
|
| Claims: |
|
What is claimed is:
1. A compound of Formula (I) ##STR90##
wherein: Z is --NH--, --O--, --S(O).sub.a --, or --NR--; R is alkyl of 1 to 6 carbon atoms, or carboalkyl of 2 to 7 carbon atoms; X is cycloalkyl of 3 to 7 carbon atoms, which may be optionally substituted with one or more alkyl of 1 to 6 carbon atom groups; or X is pyridinyl, pyrimidinyl, or an aryl ring; wherein the pyridinyl, pyrimidinyl or aryl ring may be optionally mono-, di-, or tri-substituted with a substituent independently selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or X is a bicyclic aryl or bicyclic heteroaryl ring system of 8 to 12 atoms, where the bicyclic heteroaryl ring contains 1 to 4 heteroatoms independently selected from N, O, and S; wherein the bicyclic aryl or bicyclic heteroaryl ring may be optionally mono-, di-, tri-, or tetra-substituted with a substituent independently selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or X is the radical ##STR91## E is pyridinyl, pyrimidinyl, or an aryl ring; wherein the pyridinyl, pyrimidinyl or aryl ring may be optionally mono-, di-, or tri-substituted with a substituent selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; T is substituted on E at a carbon and is --NH(CH.sub.2).sub.m --, --O(CH.sub.2).sub.m --, --S(O).sub.a --(CH.sub.2).sub.m --, --NR(CH.sub.2).sub.m --, --(CH.sub.2).sub.m --, --(CH.sub.2).sub.m NH--, --(CH.sub.2).sub.m O--, --(CH.sub.2).sub.m S(O).sub.a --, or --(CH.sub.2).sub.m NR--; L is an aryl ring; that is optionally mono-, di, or tri-substituted with a substituent selected from the group consisting of halogen, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or L is a 5- or 6-membered heteroaryl ring where the heteroaryl ring contains 1 to 3 heteroatoms independently selected from N, O, and S; wherein the heteroaryl ring may be optionally mono- or di-substituted with a substituent selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 t o 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; A" is a moiety selected from the group ##STR92##
G.sub.1, G.sub.2, G.sub.3 and G.sub.4 are independently selected from the group consisting of hydrogen, and alkyl of 1 to 6 carbon atoms; R.sub.1 is --H, R.sub.11 --CH.sub.2 --, --R.sub.12, ##STR93## R.sub.11 is --H, alkyl of 1 to 5 carbon atoms, aryl, or R.sub.13 --(C(R.sub.6).sub.2).sub.k --; R.sub.13 is ##STR94## R.sub.7 --, R.sub.7 --(C(R.sub.6).sub.2).sub.p --M--, or Het-(C(R.sub.6).sub.2).sub.q --W--, R.sub.7 is --H, --NR.sub.6 R.sub.6, --OR.sub.6, --J, --N(R.sub.6).sub.3.sup.+, or --NR.sub.6 (OR.sub.6); ##STR95##
or a bond; Het is a heterocyclic radical selected from the group consisting of morpholine, thiomorpholine, thiomorpholine S-oxide, thiomorpholine S,S-dioxide, piperidine, pyrrolidine, aziridine, pyridine, imidazole, 1,2,3-triazole, 1,2,4-triazole, thiazole, thiazolidine, tetrazole, piperazine, furan, thiophene, tetrahydrothiophene, tetrahydrofuran, dioxane, 1,3-dioxolane, and tetrahydropyran, optionally mono- or di-substituted on carbon by --R.sub.6, hydroxy, --N(R.sub.6).sub.2, --OR.sub.6, --(C(R.sub.6).sub.2).sub.s OR.sub.6, or --(C(R.sub.6).sub.2).sub.s N(R.sub.6).sub.2 ; or optionally mono-substituted on nitrogen with --R.sub.6 ; and optionally mono or di-substituted on a saturated carbon with divalent radicals --O--, or --O(C(R.sub.6).sub.2).sub.s O--; R.sub.6 is independently selected from --H, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, cycloalkyl of 3 to 6 carbon atoms, carboalkyl of 2 to 7 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, phenyl, or phenyl optionally substituted with one or more halogen, alkoxy of 1 to 6 carbon atoms, trifluoromethyl, amino, alkylamino of 1 to 3 carbon atoms, dialkylamino of 2 to 6 carbon atoms, nitro, cyano, azido, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, carboxyl, carboalkoxy of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, and alkyl of 1 to 6 carbon atoms; R.sub.12 is alkylsulphonyl of 1 to 6 carbon atoms, carboalkoxy of 2 to 7 carbon atoms, or carboalkyl of 2 to 7 carbon atoms; R.sub.5 is hydrogen, alkyl of 1 to 6 carbon atoms, carboxy, carboalkoxy of 1 to 6 carbon atoms, aryl, carboalkyl of 2 to 7 carbon atoms, ##STR96## R.sub.7 --(C(R.sub.6).sub.2).sub.s --, R.sub.7 --(C(R.sub.6).sub.2).sub.p --M--(C(R.sub.6).sub.2).sub.r --, R.sub.8 R.sub.9 --CH--M--(C(R.sub.6).sub.2).sub.r --, or Het-(C(R.sub.6).sub.2).sub.q --W--(C(R.sub.6).sub.2).sub.r --; R.sub.8, and R.sub.9 are each, independently, --(C(R.sub.6).sub.2).sub.r NR.sub.6 R.sub.6, or --(C(R.sub.6)2).sub.r OR.sub.6 ; J is independently --H, --F, or --J'; J' is independently chlorine, bromine, iodine, tosylate (p-toluenesulfonate), or mesylate (methanesulfonate); Q is Q', alkoxy of 1 to 6 carbon atoms, hydroxy, or hydrogen; Q' is alkyl of 1 to 6 carbon atoms; R.sub.2 is selected from the group consisting of ##STR97## R.sub.3 is independently selected from --H, alkyl of 1 to 6 carbon atoms, carboxy, carboalkoxy of 1 to 6 carbon atoms, aryl, carboalkyl of 2 to 7 carbon atoms, and R.sub.3a --(C(R.sub.6).sub.2).sub.s --; R.sub.3a is ##STR98## R.sub.7 --, R.sub.7 --(C(R.sub.6).sub.2).sub.p --M--, R.sub.8 R.sub.9 --CH--M--, or Het-(C(R.sub.6).sub.2).sub.q --W--; a is 0 to 2; k is 1,3 to 5; n is 0 to 1; m is 0 to 3; p is 2 to 4; q is 0 to 4; r is 1 to 4; s is 1 to 6; u is 0 to 4 and v is 0 to 4, wherein the sum of u+v is 2 to 4; provided that: a. when --R.sub.6 is alkenyl of 2 to 7 carbon atoms or alkynyl of 2 to 7 carbon atoms, said alkenyl of 2 to 7 carbon atoms or alkynyl of 2 to 7 carbon atoms is bound to a nitrogen or oxygen atom through a saturated carbon atom; b. when R.sub.3 is bound to sulfur, R.sub.3 is not --H, carboxy, carboalkoxy, or carboalkyl; c. when M is --O--, and R.sub.7 is --OR.sub.6, then p is 1 to 4; d. when M is --O--, then k is 1 to 5; e. when W is --O--, then k is 1 to 5; f. when R.sub.7 is --OR.sub.6, then k is 1 to 5; g. when W is not a bond with Het bonded through a nitrogen atom, q is 2 to 4, and when W is a bond, q is 0;
or a pharmaceutically acceptable salt thereof.
2. A compound according to claim 1 wherein Z is --NH--, n is 0, X is aryl and A" is the moiety ##STR99##
or a pharmaceutically acceptable salt thereof.
3. A compound according to claim 1, wherein Z is --NH--, n is 0, X is aryl and A" is the moiety ##STR100##
or a pharmaceutically acceptable salt thereof.
4. A compound according to claim 1, wherein Z is --NH--, n is 0, X is aryl and A" is the moiety ##STR101##
or a pharmaceutically acceptable salt thereof.
5. A compound according to claim 1, wherein Z is --NH--, n is 0, X is aryl and A" is the moiety ##STR102##
or a pharmaceutically acceptable salt thereof.
6. A compound according to claim 1, wherein Z is --NH--, n is 0, X is aryl and A" is the moiety ##STR103## G.sub.1, G.sub.2, G.sub.3, and G.sub.4 are H;
or a pharmaceutically acceptable salt thereof.
7. A compound according to claim 1, wherein Z is --NH--, n is 0, X is aryl and A" is the moiety ##STR104##
G.sub.1, G.sub.2, G.sub.3, and G.sub.4 are H;
or a pharmaceutically acceptable salt thereof.
8. A compound according to claim 1 wherein Z is --NH--, n is 0, X is aryl and A" is the moiety ##STR105## G.sub.1, G.sub.2, G.sub.3, and G.sub.4 are H;
or a pharmaceutically acceptable salt thereof.
9. The compound according to claim 1, wherein Z is --NH--, n is 0, X is aryl and A" is the moiety ##STR106## G.sub.1, G.sub.2, G.sub.3, and G.sub.4 are H;
or a pharmaceutically acceptable salt thereof.
10. A compound according to claim 1, wherein Z is --NH--, n is 0, X is aryl and A" is the moiety ##STR107## R.sub.1 is selected from H, R.sub.2 C(O)-- and R.sub.11 -CH.sub.2 --;
or a pharmaceutically acceptable salt thereof.
11. A compound according to claim 1, wherein Z is --NH--, n is 0, X is aryl and A" is the moiety ##STR108## R.sub.1 is selected from H, R.sub.2 C(O)-- and R.sub.11 --CH.sub.2 --;
or a pharmaceutically acceptable salt thereof.
12. A compound according to claim 1, wherein Z is --NH--, n is 0, X is aryl and A" is the moiety ##STR109## R.sub.1 is selected from H, R.sub.2 C(O)-- and R.sub.11 --CH.sub.2 --;
or a pharmaceutically acceptable salt thereof.
13. A compound according to claim 1, wherein Z is --NH--, n is 0, X is aryl and A" is the moiety ##STR110## R.sub.1 is selected from H, R.sub.2 C(O)-- and R.sub.11 --CH.sub.2 --;
or a pharmaceutically acceptable salt thereof.
14. A compound according to claim 1, wherein Z is --NH--, n is 0, X is aryl and A" is the moiety ##STR111## R.sub.1 is selected from H, R.sub.2 C(O)-- and R.sub.11 --CH.sub.2 --; G.sub.1, G.sub.2, G.sub.3, and G.sub.4 are H;
or a pharmaceutically acceptable salt thereof.
15. A compound according to claim 1, wherein Z is --NH--, n is 0, X is aryl and A" is the moiety ##STR112## R.sub.1 is selected from H, R.sub.2 C(O)-- and R.sub.11 --CH.sub.2 --; G.sub.1, G.sub.2, G.sub.3, and G.sub.4 are H;
or a pharmaceutically acceptable salt thereof.
16. A compound according to claim 1, wherein Z is --NH--, n is 0, X is aryl and A" is the moiety ##STR113## R.sub.1 is selected from H, R.sub.2 C(O)-- and R.sub.11 --CH.sub.2 --; G.sub.1, G.sub.2, G.sub.3, and G.sub.4 are H;
or a pharmaceutically acceptable salt thereof.
17. A compound according to claim 1, wherein Z is --NH--, n is 0, X is aryl and A" is the moiety ##STR114## R.sub.1 is selected from H, R.sub.2 C(O)-- and R.sub.11 --CH.sub.2 --; G.sub.1, G.sub.2, G.sub.3, and G.sub.4 are H;
or a pharmaceutically acceptable salt thereof.
18. The compound of claim 1, which is 9-(3-Chloro-4-fluoroanilino)-2,3-dihydro-1H-[1,4]oxazino[3,2-g]quinoline-8 -carbonitrile or a pharmaceutically acceptable salt thereof.
19. The compound of claim 1, which is 1-[(2E)-4-Chloro-2-butenoyl]-9-(3-chloro-4-fluoroanilino)-2,3-dihydro-1H-[ 1,4]oxazino[3,2-g]quinoline-8-carbonitrile or a pharmaceutically acceptable salt thereof.
20. The compound according to claim 1, which is 1-[(2E)-4-Bromo-2-butenoyl]-9-(3-chloro-4-fluoroanilino)-2,3-dihydro-1H-[1 ,4]oxazino[3,2-g]quinoline-8-carbonitrile or a pharmaceutically acceptable salt thereof.
21. The compound according to claim 1, which is 9-(3-Chloro-4-fluoroanilino)-1-[(2E)-4-(dimethylamino)-2-butenoyl]-2,3-dih ydro-1H-[1,4]oxazino[3,2-g]quinoline-8-carbonitrile or a pharmaceutically acceptable salt thereof.
22. The compound according to claim 1, which is 9-(3-Chloro-4-fluoroanilino)-1-[4-(dimethylamino)butanoyl]-2,3-dihydro-1H- [1,4]oxazino[3,2-g]quinoline-8-carbonitrile or a pharmaceutically acceptable salt thereof.
23. The compound according to claim 1, which is 1-(4-Chlorobutyl)-9-(3-chloro-4-fluoroanilino)-2,3-dihydro-1H-[1,4]oxazino [3,2-g]quinoline-8-carbonitrile or a pharmaceutically acceptable salt thereof.
24. The compound according to claim 1, which is 9-(3-Chloro-4-fluoroanilino)-1-[4-(dimethylamino)butyl]-2,3-dihydro-1H-[1, 4]oxazino[3,2-g]quinoline-8-carbonitrile or a pharmaceutically acceptable salt thereof.
25. The compound according to claim 1, 9-(2,4-Dichloroanilino)-3,4-dihydro-2H-[1,4]oxazino[2,3-g]quinoline-8-carb onitrile or a pharmaceutically acceptable salt thereof.
26. The compound according to claim 1, 4-(4-Chlorobutyl)-9-(2,4-dichloroanilino)-3,4-dihydio-2H-[1,4]oxazino[2,3- g]quinoline-8-carbonitnile or a pharmaceutically acceptable salt thereof.
27. The compound of claim 1, which is 9-(2,4-Dichloroanilino)-4-[4-(4-ethyl-1-piperazinyl)butyl]-3,4-dihydro-2H- [1,4]oxazino[2,3-g]quinoline-8-carbonitnile, or a pharmaceutically acceptable salt thereof.
28. A pharmaceutical composition comprising a compound of Formula (I) ##STR115##
wherein: Z is --NH--, --O--, --S(O).sub.a --, or --NR--; R is alkyl of 1 to 6 carbon atoms, or carboalkyl of 2 to 7 carbon atoms; X is cycloalkyl of 3 to 7 carbon atoms, which may be optionally substituted with one or more alkyl of 1 to 6 carbon atom groups; or X is pyridinyl, pyrimidinyl, or an aryl ring; wherein the pyridinyl, pyrimidinyl or aryl ring may be optionally mono-, di-, or tri-substituted with a substituent independently selected from the group consisiting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or X is a bicyclic aryl or bicyclic heteroaryl ring system of 8 to 12 atoms, where the bicyclic heteroaryl ring contains 1 to 4 heteroatoms independently selected from N, O, and S; wherein the bicyclic aryl or bicyclic heteroaryl ring may be optionally mono-, di-, tri-, or tetra-substituted with a substituent independently selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or X is the radical ##STR116## E is pyridinyl, pyrimidinyl, or an aryl ring; wherein the pyridinyl, pyrimidinyl or aryl ring may be optionally mono-, di-, or tri-substituted with a substituent selected from the group consisiting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; T is substituted on E at a carbon and is --NH(CH.sub.2).sub.m --, --O(CH.sub.2).sub.m --, --S(O).sub.a --(CH.sub.2).sub.m --, NR(CH.sub.2).sub.m --, (CH.sub.2).sub.m --, --(CH.sub.2).sub.m NH --, --(CH.sub.2).sub.m O --, --(CH.sub.2).sub.m S(O).sub.a --, or --(CH.sub.2).sub.m NR--; L is an aryl ring; that is optionally mono-, di, or tri-substituted with a substituent selected from the group consisting of halogen, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or L is a 5- or 6-membered heteroaryl ring where the heteroaryl ring contains 1 to 3 heteroatoms independently selected from N, O, and S; wherein the heteroaryl ring may be optionally mono- or di-substituted with a substituent selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; A" is a moiety selected from the group ##STR117## G.sub.1, G.sub.2, G.sub.3 and G.sub.4 are independently selected from the group consisting of hydrogen, and alkyl of 1 to 6 carbon atoms; R.sub.1 is --H, R.sub.11 --CH.sub.2 --, --R.sub.12, ##STR118## R.sub.11 is --H, alkyl of 1 to 5 carbon atoms, aryl, or R.sub.13 --(C(R.sub.6).sub.2).sub.k --; R.sub.13 is ##STR119## R.sub.7 --R.sub.7 (C(R.sub.6).sub.2).sub.p --M-- or Het-(C(R.sub.6).sub.2).sub.q --W--; R.sub.7 is --H, --NR.sub.6 R.sub.6, --OR.sub.6, --J, --N(R.sub.6).sub.3.sup.+, or --NR.sub.6 (OR.sub.6); ##STR120## or a bond; Het is a heterocyclic radical selected from the group consisting of morpholine, thiomorpholine, thiomorpholine S-oxide, thiomorpholine S,S-dioxide, piperidine, pyrrolidine, aziridine, pyridine, imidazole, 1,2,3-triazole, 1,2,4-triazole, thiazole, thiazolidine, tetrazole, piperazine, furan, thiophene, tetrahydrothiophene, tetrahydrofuran, dioxane, 1,3-dioxolane, tetrahydropyran, optionally mono- or di-substituted on carbon by --R.sub.6, hydroxy, --N(R.sub.6).sub.2, --OR.sub.6 --(C(R.sub.6).sub.2).sub.s OR.sub.6, or --(C(R.sub.6).sub.2).sub.s N(R.sub.6).sub.2 ; or optionally mono-substituted on nitrogen with --R.sub.6 ; and optionally mono or di-substituted on a saturated carbon with divalent radicals --O--, or --O(C(R.sub.6).sub.2).sub.s O--; R.sub.6 is independently selected from --H, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, cycloalkyl of 3 to 6 carbon atoms, carboalkyl of 2 to 7 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, phenyl, or phenyl optionally substituted with one or more halogen, alkoxy of 1 to 6 carbon atoms, trifluoromethyl, amino, alkylamino of 1-3 carbon atoms, dialkylamino of 2 to 6 carbon atoms, nitro, cyano, azido, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, carboxyl, carboalkoxy of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, and alkyl of 1 to 6 carbon atoms; R.sub.12 is alkylsulphonyl of 1 to 6 carbon atoms, carboalkoxy of 2 to 7 carbon atoms, or carboalkyl of 2 to 7 carbon atoms; R.sub.5 is hydrogen, alkyl of 1 to 6 carbon atoms, carboxy, carboalkoxy of 1 to 6 carbon atoms, aryl, carboalkyl of 2 to 7 carbon atoms, ##STR121## R.sub.7 --(C(R.sub.6).sub.2).sub.s --, R.sub.7 --(C(R.sub.6).sub.2).sub.p --M--(C(R.sub.6).sub.2).sub.r --, R.sub.8 R.sub.9 --CH--M--(C(R.sub.6).sub.2).sub.r --, or Het-(C(R.sub.6).sub.2).sub.q --W--(C(R.sub.6).sub.2).sub.r --; R.sub.8, and R.sub.9 are each, independently, --(C(R.sub.6).sub.2).sub.r NR.sub.6 R.sub.6, or --(C(R.sub.6)2).sub.r OR.sub.6 ; J is independently --H, --F, or --J'; J' is independently chlorine, bromine, iodine, tosylate (p-toluenesulfonate), or mesylate (methanesulfonate); Q is Q', alkoxy of 1 to 6 carbon atoms, hydroxy, or hydrogen; Q' is alkyl of 1 to 6 carbon atoms; R.sub.2 is selected from the group consisting of ##STR122## R.sub.3 is independently selected from --H, alkyl of 1 to 6 carbon atoms, carboxy, carboalkoxy of 1 to 6 carbon atoms, aryl, carboalkyl of 2 to 7 carbon atoms, and R.sub.3a --(C(R.sub.6).sub.2).sub.s --; R.sub.3a is ##STR123## R.sub.7 --, R.sub.7 --(C(R.sub.6).sub.2).sub.p --M--, R.sub.8 R.sub.9 --CH--M--, or Het-(C(R.sub.6).sub.2).sub.q --W--, a is 0-2; k is 1, 3-5; n is 0-1; m is 0-3; p is 2-4; q is 0-4; r is 1-4; s is 1 to 6; u is 0-4 and v is 0-4, wherein the sum of u+v is 2-4; provided that: a. when --R.sub.6 is alkenyl of 2 to 7 carbon atoms or alkynyl of 2 to 7 carbon atoms, said alkenyl of 2 to 7 carbon atoms or alkynyl of 2 to 7 carbon atoms is bound to a nitrogen or oxygen atom through a saturated carbon atom; b. when R.sub.3 is bound to sulfur, R.sub.3 is not --H, carboxy, carboalkoxy, or carboalkyl; c. when M is --O--, and R.sub.7 is --OR.sub.6, then p is 1-4; d. when M is --O--, then k is 1 to 5; e. when W is --O--, then k is 1 to 5; f. when R.sub.7 is --OR.sub.6, then k is 1 to 5; g. when W is not a bond with Het bonded through a nitrogen atom, q is 2-4, and when W is a bond, q is 0;
or a pharmaceutically acceptable salt thereof and one or more pharmaceutically acceptable carriers or excipients.
29. A method of treating, inhibiting the growth of, or eradicating a neoplasm in a mammal in need thereof which comprises providing to said mammal an effective amount of a compound of Formula (I) ##STR124##
wherein: Z is --NH--, --O--, --S(O).sub.a --, or --NR--; R is alkyl of 1 to 6 carbon atoms, or carboalkyl of 2 to 7 carbon atoms; X is cycloalkyl of 3 to 7 carbon atoms, which may be optionally substituted with one or more alkyl of 1 to 6 carbon atom groups; or X is pyridinyl, pyrimidinyl, or an aryl ring; wherein the pyridinyl, pyrimidinyl or aryl ring may be optionally mono-, di-, or tri-substituted with a substituent independently selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or X is a bicyclic aryl or bicyclic heteroaryl ring system of 8 to 12 atoms, where the bicyclic heteroaryl ring contains 1 to 4 heteroatoms independently selected from N, O, and S; wherein the bicyclic aryl or bicyclic heteroaryl ring may be optionally mono-, di-, tri-, or tetra-substituted with a substituent independently selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, methylmercapto, and benzoylamino; or X is the radical ##STR125## E is pyridinyl, pyrimidinyl, or an aryl ring; wherein the pyridinyl, pyrimidinyl or aryl ring may be optionally mono-, di-, or tri-substituted with a substituent selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; T is substituted on E at a carbon and is --NH(CH.sub.2).sub.m --, --O(CH.sub.2).sub.m --, --S(O).sub.a --(CH.sub.2).sub.m --, --NR(CH.sub.2).sub.m --, --(CH.sub.2).sub.m --, --(CH.sub.2).sub.m NH--, --(CH.sub.2).sub.m O--, --(CH.sub.2).sub.m S(O).sub.a --, or --(CH.sub.2).sub.m NR--; L is an aryl ring; that is optionally mono-, di, or tri-substituted with a substituent selected from the group consisting of halogen, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or L is a 5- or 6-membered heteroaryl ring where the heteroaryl ring contains 1 to 3 heteroatoms independently selected from N, O, and S; wherein the heteroaryl ring may be optionally mono- or di-substituted with a substituent selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; A" is a moiety selected from the group ##STR126## G.sub.1, G.sub.2, G.sub.3 and G.sub.4 are independently selected from the group consisting of hydrogen, and alkyl of 1 to 6 carbon atoms; R.sub.1 is --H, R.sub.11 --CH.sub.2 --, --R.sub.12, ##STR127## R.sub.11, is --H, alkyl of 1 to 5 carbon atoms, aryl, or R.sub.13 --(C(R.sub.6).sub.2).sub.k --; R.sub.13 is ##STR128## R.sub.7 --, R.sub.7 --(C(R.sub.6).sub.2).sub.p --M--, or Het-(C(R.sub.6).sub.2).sub.q --W--; R.sub.7 is --H, --NR.sub.6 R.sub.6, --OR.sub.6, --J, --N(R.sub.6).sub.3.sup.+ or --NR.sub.6 (OR.sub.6); ##STR129## or a bond; Het is a heterocyclic radical selected from the group consisting of morpholine, thiomorpholine, thiomorpholine S-oxide, thiomorpholine S,S-dioxide, piperidine, pyrrolidine, aziridine, pyridine, imidazole, 1,2,3-triazole, 1,2,4-triazole, thiazole, thiazolidine, tetrazole, piperazine, furan, thiophene, tetrahydrothiophene, tetrahydrofuran, dioxane, 1,3-dioxolane, and tetrahydropyran, optionally mono- or di-substituted on carbon by --R.sub.6, hydroxy, --N(R.sub.6).sub.2, --OR.sub.6, --(C(R.sub.6).sub.2).sub.s OR.sub.6, or --(C(R.sub.6).sub.2).sub.s N(R.sub.6).sub.2 ; or optionally mono-substituted on nitrogen with --R.sub.6 ; and optionally mono or di-substituted on a saturated carbon with divalent radicals --O--, or --O(C(R.sub.6).sub.2).sub.s O--; R.sub.6 is independently selected from --H, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, cycloalkyl of 3 to 6 carbon atoms, carboalkyl of 2 to 7 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, phenyl, or phenyl optionally substituted with one or more halogen, alkoxy of 1 to 6 carbon atoms, trifluoromethyl, amino, alkylamino of 1 to 3 carbon atoms, dialkylamino of 2 to 6 carbon atoms, nitro, cyano, azido, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, carboxyl, carboalkoxy of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, and alkyl of 1 to 6 carbon atoms; R.sub.12 is alkylsulphonyl of 1 to 6 carbon atoms, carboalkoxy of 2 to 7 carbon atoms, or carboalkyl of 2 to 7 carbon atoms; R.sub.5 is hydrogen, alkyl of 1 to 6 carbon atoms, carboxy, carboalkoxy of 1 to 6 carbon atoms, aryl, carboalkyl of 2 to 7 carbon atoms, ##STR130## R.sub.7 --(C(R.sub.6).sub.2).sub.s --, R.sub.7 --(C(R.sub.6).sub.2).sub.p --M--(C(R.sub.6).sub.2).sub.r --, R.sub.8 R.sub.9 --CH--M--(C(R.sub.6).sub.2).sub.r --, or Het-(C(R.sub.6).sub.2).sub.q --W--(C(R.sub.6).sub.2).sub.r --; R.sub.8, and R.sub.9 are each, independently, --(C(R.sub.6).sub.2).sub.r NR.sub.6 R.sub.6, or --(C(R.sub.6).sub.2).sub.r OR.sub.6 ; J is independently --H, --F, or --J'; J' is independently chlorine, bromine, iodine, tosylate (p-toluenesulfonate), or mesylate (methanesulfonate); Q is Q', alkoxy of 1 to 6 carbon atoms, hydroxy, or hydrogen; Q' is alkyl of 1 to 6 carbon atoms; R.sub.2 is selected from the group consisting of ##STR131## R.sub.3 is independently selected from --H, alkyl of 1 to 6 carbon atoms, carboxy, carboalkoxy of 1 to 6 carbon atoms, aryl, carboalkyl of 2 to 7 carbon atoms, and R.sub.3a --(C(R.sub.6).sub.2).sub.s --; R.sub.3a is ##STR132## R.sub.7 --, R.sub.7 --(C(R.sub.6).sub.2).sub.p --M--, R.sub.8 R.sub.9 --CH--M--, or Het-(C(R.sub.6).sub.2).sub.q --W--; k is 1,3 to 5; n is 0 to; m is 0 to 3; p is 2 to 4; q is 0 to 4; r is 1 to 4; s is 1 to 6; u is 0 to 4 and v is 0 to 4, wherein the sum of u+v is 2 to 4; provided that: a. when --R.sub.6 is alkenyl of 2 to 7 carbon atoms or alkynyl of 2 to 7 carbon atoms, said alkenyl of 2 to 7 carbon atoms or alkynyl of 2 to 7 carbon atoms is bound to a nitrogen or oxygen atom through a saturated carbon atom; b. when R.sub.3 is bound to sulfur, R.sub.3 is not --H, carboxy, carboalkoxy, or carboalkyl; c. when M is --O--, and R.sub.7 is --OR.sub.6, then p is 1 to 4; d. when M is --O--, then k is 1 to 5; e. when W is --O--, then k is 1 to 5; f. when R.sub.7 is --OR.sub.6, then k is 1 to 5; g. when W is not a bond with Het bonded through a nitrogen atom, q is 2 to 4, and when W is a bond, q is 0;
or a pharmaceutically acceptable salt thereof, wherein the neoplasm is selected from the group consisting of breast, kidney, bladder, mouth, larynx, esophagus, stomach, colon, ovary, lung, pancreas, liver, prostate, brain, and skin.
30. A method of treating, inhibiting the progression of, or eradicating polycystic kidney disease in a mammal in need thereof which comprises providing to said mammal an effective amount of a compound of Formula (I) ##STR133##
wherein: Z is --NH--, --O--, --S(O).sub.a --, or --N--; R is alkyl of 1 to 6 carbon atoms, or carboalkyl of 2 to 7 carbon atoms; X is cycloalkyl of 3 to 7 carbon atoms, which may be optionally substituted with one or more alkyl of 1 to 6 carbon atom groups; or X is pyridinyl, pyrimidinyl, or an aryl ring; wherein the pyridinyl, pyrimidinyl or aryl ring may be optionally mono-, di-, or tri-substituted with a substituent independently selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or X is a bicyclic aryl or bicyclic heteroaryl ring system of 8 to 12 atoms, where the bicyclic heteroaryl ring contains 1 to 4 heteroatoms independently selected from N, 0, and S; wherein the bicyclic aryl or bicyclic heteroaryl ring may be optionally mono-, di-, tri-, or tetra-substituted with a substituent independently selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or X is the radical ##STR134## E is pyridinyl, pyrimidinyl, or an aryl ring; wherein the pyridinyl, pyrimidinyl or aryl ring may be optionally mono-, di-, or tri-substituted with a substituent selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; T is substituted on E at a carbon and is --NH(CH.sub.2).sub.m --, --O(CH.sub.2).sub.m --, --S(O).sub.a --(CH.sub.2).sub.m --, --NR(CH.sub.2).sub.m --, --(CH.sub.2).sub.m --; --(CH.sub.2).sub.m NH--, --(CH.sub.2).sub.m O--, --(CH.sub.2).sub.m S(O).sub.a --, or --(CH.sub.2).sub.m NR--; L is an aryl ring; that is optionally mono-, di, or tri-substituted with a substituent selected from the group consisting of halogen, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylaraino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or L is a 5- or 6-membered heteroaryl ring where the heteroaryl ring contains 1 to 3 heteroatoms independently selected from N, O, and S; wherein the heteroaryl ring may be optionally mono- or di-substituted with a substituent selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; A" is a moiety selected from the group ##STR135## G.sub.1, G.sub.2, G.sub.3 and G.sub.4 are independently selected from the group consisting of hydrogen, and alkyl of 1 to 6 carbon atoms; R.sub.1 is --H, R.sub.11 --CH.sub.2 --, --R.sub.12, ##STR136## R.sub.11 is --H, alkyl of 1 to 5 carbon atoms, aryl, or R.sub.13 --(C(R.sub.6).sub.2).sub.k --; R.sub.13 is ##STR137## R.sub.7 --, R.sub.7 --(C(R.sub.6).sub.2).sub.p --M--, or Het-(C(R.sub.6).sub.2).sub.q --W--; R.sub.7 is --H, --NR.sub.6 R.sub.6, --OR.sub.6, --J, --N(R.sub.6).sub.3.sup.+, or --NR.sub.6 (OR.sub.6); ##STR138## or a bond; Het is a heterocyclic radical selected from the group consisting of morpholine, thiomorpholine, thiomorpholine S-oxide, thiomorpholine S,S-dioxide, piperidine, pyrrolidine, aziridine, pyridine, imidazole, 1,2,3-triazole, 1,2,4-triazole, thiazole, thiazolidine, tetrazole, piperazine, furan, thiophene, tetrahydrothiophene, tetrahydrofuran, dioxane, 1,3-dioxolane, and tetrahydropyran, optionally mono- or di-substituted on carbon by --R.sub.6, hydroxy, --N(R.sub.6).sub.2, --OR.sub.6, --(C(R.sub.6).sub.2).sub.s OR.sub.6, or --(C(R.sub.6).sub.2).sub.s N(R.sub.6).sub.2 ; or optionally mono-substituted on nitrogen with --R.sub.6 ; and optionally mono or di-substituted on a saturated carbon with divalent radicals --O--, or --O(C(R.sub.6).sub.2).sub.s O--; R.sub.6 is independently selected from --H, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, cycloalkyl of 3 to 6 carbon atoms, carboalkyl of 2 to 7 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, phenyl, or phenyl optionally substituted with one or more halogen, alkoxy of 1 to 6 carbon atoms, trifluoromethyl, amino, alkylamino of 1 to 3 carbon atoms, dialkylamino of 2 to 6 carbon atoms, nitro, cyano, azido, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, carboxyl, carboalkoxy of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, and alkyl of 1 to 6 carbon atoms; R.sub.12 is alkylsulphonyl of 1 to 6 carbon atoms, carboalkoxy of 2 to 7 carbon atoms, or carboalkyl of 2 to 7 carbon atoms; R.sub.5 is hydrogen, alkyl of 1 to 6 carbon atoms, carboxy, carboalkoxy of 1 to 6 carbon atoms, aryl, carboalkyl of 2 to 7 carbon atoms, ##STR139## R.sub.7 --(C(R.sub.6).sub.2).sub.s --, R.sub.7 --(C(R.sub.6).sub.2).sub.p --M--(C(R.sub.6).sub.2).sub.r --, R.sub.8 R.sub.9 --CH--M--(C(R.sub.6).sub.2).sub.r --, or Het-(C(R.sub.6).sub.2).sub.q --W--(C(R.sub.6).sub.2).sub.r --; R.sub.8, and R.sub.9 are each, independently, --(C(R.sub.6).sub.2).sub.r NR.sub.6 R.sub.6, or --(C(R.sub.6).sub.2).sub.r OR.sub.6 ; J is independently --H, --F, or --J'; J' is independently chlorine, bromine, iodine, tosylate (p-toluenesulfonate), or mesylate (methanesulfonate); Q is Q', alkoxy of 1 to 6 carbon atoms, hydroxy, or hydrogen; Q' is alkyl of 1 to 6 carbon atoms; R.sub.2 is selected from the group consisting of ##STR140## R.sub.3 is independently selected from --H, alkyl of 1 to 6 carbon atoms, carboxy, carboalkoxy of 1 to 6 carbon atoms, aryl, carboalkyl of 2 to 7 carbon atoms, and R.sub.3a --(C(R.sub.6).sub.2).sub.s --; R.sub.3a is ##STR141## R.sub.7 --, R.sub.7 --(C(R.sub.6).sub.2).sub.p --M--, R.sub.8 R.sub.9 --CH--M--, or Het-(C(R.sub.6).sub.2) .sub.q --W--; a is 0 to 2; k is 1,3 to 5; n is 0 to 1; m is 0 to 3; p is 2 to 4; q is 0 to 4; r is 1 to 4; s is 1 to 6; u is 0 to 4 and v is 0 to 4, wherein the sum of u+v is 2 to 4; provided that: a. when --R.sub.6 is alkenyl of 2 to 7 carbon atoms or alkynyl of 2 to 7 carbon atoms, said alkenyl of 2 to 7 carbon atoms or alkynyl of 2 to 7 carbon atoms is bound to a nitrogen or oxygen atom through a saturated carbon atom; b. when R.sub.3 is bound to sulfur, R.sub.3 is not --H, carboxy, carboalkoxy, or carboalkyl; c. when M is --O--, and R.sub.7 is --OR.sub.6, then p is 1 to 4; d. when M is --O--, then k is 1 to 5; e. when W is --O--, then k is 1 to 5; f. when R.sub.7 is --OR.sub.6, then k is 1 to 5; g. when W is not a bond with Het bonded through a nitrogen atom, q is 2 to 4, and when W is a bond, q is 0;
or a pharmaceutically acceptable salt thereof.
31. A method of treating, inhibiting, or eradicating colonic polyps in a mammal in need thereof which comprises providing to said mammal an effective amount of a compound of Formula (I) ##STR142## wherein: Z is --NH--, --O--, --S(O).sub.a --, or --NR--; R is alkyl of 1 to 6 carbon atoms, or carboalkyl of 2 to 7 carbon atoms; X is cycloalkyl of 3 to 7 carbon atoms, which may be optionally substituted with one or more alkyl of 1 to 6 carbon atom groups; or X is pyridinyl, pyrimidinyl, or an aryl ring; wherein the pyridinyl, pyrimidinyl or aryl ring may be optionally mono-, di-, or tri-substituted with a substituent independently selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or X is a bicyclic aryl or bicyclic heteroaryl ring system of 8 to 12 atoms, where the bicyclic heteroaryl ring contains 1 to 4 heteroatoms independently selected from N, O, and S; wherein the bicyclic aryl or bicyclic heteroaryl ring may be optionally mono-, di-, tri-, or tetra-substituted with a substituent independently selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or X is the radical ##STR143## E is pyridinyl, pyrimidinyl, or an aryl ring; wherein the pyridinyl, pyrimidinyl or aryl ring may be optionally mono-, di-, or tri-substituted with a substituent selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; T is substituted on E at a carbon and is --NH(CH.sub.2).sub.m --, --O(CH.sub.2).sub.m, --S(O).sub.a --(CH.sub.2).sub.m --, --NR(CH.sub.2).sub.m --, --(CH.sub.2).sub.m --, --(CH.sub.2).sub.m NH--, --(CH.sub.2).sub.m O--, --(CH.sub.2).sub.m S(O).sub.a --, or --(CH.sub.2).sub.m NR--; L is an aryl ring; that is optionally mono-, di, or tri-substituted with a substituent selected from the group consisting of halogen, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or L is a 5- or 6-membered heteroaryl ring where the heteroaryl ring contains 1 to 3 heteroatoms independently selected from N, 0, and S; wherein the heteroaryl ring may be optionally mono- or di-substituted with a substituent selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; A' is a moiety selected from the group ##STR144## G.sub.1, G.sub.2, G.sub.3 and G.sub.4 are independently selected from the group consisting of hydrogen, and alkyl of 1 to 6 carbon atoms; R.sub.1 is --H, R.sub.11 --CH.sub.2 --, --R.sub.12, ##STR145## R.sub.11 is --H, alkyl of 1 to 5 carbon atoms, aryl, or R.sub.13 --(C(R.sub.6).sub.2).sub.k --; R.sub.13 is ##STR146## R.sub.7 --,R.sub.7 --(C(R.sub.7 (R.sub.6).sub.2).sub.p --M--, or Het-(C(R.sub.6).sub.2).sub.q --W--; R.sub.7 is --H, --NR.sub.6 R.sub.6, --OR.sub.6, --J, --N(R.sub.6).sub.3.sup.+, or --NR.sub.6 (OR.sub.6); ##STR147## or a bond; Het is a heterocyclic radical selected from the group consisting of morpholine, thiomorpholine, thiomorpholine S-oxide, thiomorpholine S,S-dioxide, piperidine, pyrrolidine, aziridine, pyridine, imidazole, 1,2,3-triazole, 1,2,4-triazole, thiazole, thiazolidine, tetrazole, piperazine, furan, thiophene, tetrahydrothiophene, tetrahydrofuran, dioxane, 1,3-dioxolane, tetrahydropyran, optionally mono- or di-substituted on carbon by --R.sub.6, hydroxy, --N(R.sub.6).sub.2, --OR.sub.6, --(C(R.sub.6).sub.2).sub.s OR.sub.6, or --(C(R.sub.6).sub.2).sub.s N(R.sub.6).sub.2 ; or optionally mono-substituted on nitrogen with --R.sub.6 ; and optionally mono or di-substituted on a saturated carbon with divalent radicals --O--, or --O(C(R.sub.6).sub.2).sub.s O--; R.sub.6 is independently selected from --H, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, cycloalkyl of 3 to 6 carbon atoms, carboalkyl of 2 to 7 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, phenyl, or phenyl optionally substituted with one or more halogen, alkoxy of 1 to 6 carbon atoms, trifluoromethyl, amino, alkylamino of 1 to 3 carbon atoms, dialkylamino of 2 to 6 carbon atoms, nitro, cyano, azido, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, carboxyl, carboalkoxy of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, and alkyl of 1 to 6 carbon atoms; R.sub.12 is alkylsulphonyl of 1 to 6 carbon atoms, carboalkoxy of 2 to 7 carbon atoms, or carboalkyl of 2 to 7 carbon atoms; R.sub.5 is hydrogen, alkyl of 1 to 6 carbon atoms, carboxy, carboalkoxy of 1 to 6 carbon atoms, aryl, carboalkyl of 2 to 7 carbon atoms, ##STR148## R.sub.7 --(C(R.sub.6).sub.2).sub.s --, R.sub.7 (C(R.sub.6).sub.2).sub.p --M--(C(R.sub.6).sub.2).sub.r --, R.sub.8 R.sub.9 --CH--M--(C(R.sub.6).sub.2).sub.r --, or Het-(C(R.sub.6).sub.2).sub.q --W--(C(R.sub.6).sub.2).sub.r --; R.sub.8, and R.sub.9 are each, independently, --(C(R.sub.6).sub.2).sub.r NR.sub.6 R.sub.6, or --(C(R.sub.6).sub.2).sub.r OR.sub.6 ; J is independently --H, --F, or --J'; J' is independently chlorine, bromine, iodine, tosylate (p-toluenesulfonate), or mesylate (methanesulfonate); Q is Q', alkoxy of 1 to 6 carbon atoms, hydroxy, or hydrogen; Q' is alkyl of 1 to 6 carbon atoms; R.sub.2 is selected from the group consisting of ##STR149## R.sub.3 is independently selected from --H, alkyl of 1 to 6 carbon atoms, carboxy, carboalkoxy of 1 to 6 carbon atoms, aryl, carboalkyl of 2 to 7 carbon atoms, and R.sub.3a --(C(R.sub.6).sub.2).sub.s --; R.sub.3a is ##STR150## R.sub.7 --, R.sub.7 --(C(R.sub.6).sub.2).sub.p --M--, R.sub.8 R.sub.9 --CH--M--, or Het-(C(R.sub.6).sub.2).sub.q --W--; a is 0 to 2; l is 1,3 to 5; n is 0 to 1; m is 0 to 3; p is 2 to 4; q is to 4; r is 1 to 4; s is 1 to 6; u is 0 to 4 and v is 0 to 4, wherein the sum of u+v is 2 to 4; provided that: a. when --R.sub.6 is alkenyl of 2 to 7 carbon atoms or alkynyl of 2 to 7 carbon atoms, said alkenyl of 2 to 7 carbon atoms or alkynyl of 2 to 7 carbon atoms is bound to a nitrogen or oxygen atom through a saturated carbon atom; b. when R.sub.3 is bound to sulfur, R.sub.3 is not --H, carboxy, carboalkoxy, or carboalkyl; c. when M is --O--, and R.sub.7 is --OR.sub.6, then p is 1 to 4; d. when M is --O--, then k is 1 to 5; e. when W is --O--, then k is 1 to 5; f. when R.sub.7 is --OR.sub.6, then k is 1 to 5; g. when W is not a bond with Het bonded through a nitrogen atom, q is 2 to 4, and when W is a bond, q is 0;
or a pharmaceutically acceptable salt thereof.
32. A method of treating or inhibiting the recurrence of stenopsis after corrective surgery on the heart valve in a mammal in need thereof which comprises providing to said mammal an effective amount of a PDGFr kinase inhibitor of Formula (1), ##STR151##
wherein: Z is --NH--, --O--, --S(O).sub.a --, or --NR--; R is alkyl of 1 to 6 carbon atoms, or carboalkyl of 2 to 7 carbon atoms; X is cycloalkyl of 3 to 7 carbon atoms, which may be optionally substituted with one or more alkyl of 1 to 6 carbon atom groups; or X is pyridinyl, pyrimidinyl, or an aryl ring; wherein the pyridinyl, pyrimidinyl or aryl ring may be optionally mono-, di-, or tri-substituted with a substituent independently selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or X is a bicyclic aryl or bicyclic heteroaryl ring system of 8 to 12 atoms, where the bicyclic heteroaryl ring contains 1 to 4 heteroatoms independently selected from N, O, and S; wherein the bicyclic aryl or bicyclic heteroaryl ring may be optionally mono-, di-, tri-, or tetra-substituted with a substituent independently selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or X is the radical ##STR152## E is pyridinyl, pyrimidinyl, or an aryl ring; wherein the pyridinyl, pyrimidinyl or aryl ring may be optionally mono-, di-, or tri-substituted with a substituent selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; T is substituted on E at a carbon and is --NH(CH.sub.2).sub.m --, --O(CH.sub.2).sub.m --, S(O).sub.a --(CH.sub.2).sub.a --, --NR(CH.sub.2).sub.m --, --(CH.sub.2).sub.m --, --(CH.sub.2).sub.m NH--, --(CH.sub.2).sub.m O--, --(CH.sub.2).sub.m S(O).sub.a --, or --(CH.sub.2).sub.m NR--; L is an aryl ring; that is optionally mono-, di, or tri-substituted with a substituent selected from the group consisting of halogen, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or L is a 5- or 6-membered heteroaryl ring where the heteroaryl ring contains 1 to 3 heteroatoms independently selected from N, O, and S; wherein the heteroaryl ring may be optionally mono- or di-substituted with a substituent selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoakyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; A' is a moiety selected from the group ##STR153## G.sub.1, G.sub.2, G.sub.3 and G.sub.4 are independently selected from the group consisting of hydrogen, and alkyl of 1 to 6 carbon atoms; R.sub.1 is --H, R.sub.11 --CH.sub.2 --, --R.sub.12, ##STR154## R.sub.11, is --H, alkyl of 1 to 5 carbon atoms, aryl, or R.sub.13 --(C(R.sub.6).sub.2).sub.k --; R.sub.13 is ##STR155## R.sub.7 --, R.sub.7 --(C(R.sub.6).sub.2).sub.p --M--, or Het-(C(R.sub.6).sub.2).sub.q --W--; R.sub.7 is --H, --NR.sub.6 R.sub.6, --OR.sub.6, --J, --N(R.sub.6).sub.3, or --NR.sub.6 (OR.sub.6); ##STR156## or a bond; Het is a heterocyclic radical selected from the group consisting of morpholine, thiomorpholine, thiomorpholine S-oxide, thiomorpholine S,S-dioxide, piperidine, pyrrolidine, aziridine, pyridine, imidazole, 1,2,3-triazole, 1,2,4-triazole, thiazole, thiazolidine, tetrazole, piperazine, furan, thiophene, tetrahydrothiophene, tetrahydrofuran, dioxane, 1,3-dioxolane, and tetrahydropyran, optionally mono- or di-substituted on carbon by --R.sub.6, hydroxy, --N(R.sub.6).sub.2, --OR.sub.6, --(C(R.sub.6).sub.2).sub.s OR.sub.6, or --(C(R.sub.6).sub.2).sub.s N(R.sub.6).sub.2 ; or optionally mono-substituted on nitrogen with --R.sub.6 ; and optionally mono or di-substituted on a saturated carbon with divalent radicals --O--, or --O(C(R.sub.6).sub.2).sub.s O--; R.sub.6 is independently selected from --H, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, cycloalkyl of 3 to 6 carbon atoms, carboalkyl of 2 to 7 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, phenyl, or phenyl optionally substituted with one or more halogen, alkoxy of 1 to 6 carbon atoms, trifluoromethyl, amino, alkylamino of 1 to 3 carbon atoms, dialkylamino of 2 to 6 carbon atoms, nitro, cyano, azido, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, carboxyl, carboalkoxy of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, and alkyl of 1 to 6 carbon atoms; R.sub.12 is alkylsulphonyl of 1 to 6 carbon atoms, carboalkoxy of 2 to 7 carbon atoms, or carboalkyl of 2 to 7 carbon atoms; R.sub.5 is hydrogen, alkyl of 1 to 6 carbon atoms, carboxy, carboalkoxy of 1 to 6 carbon atoms, aryl, carboalkyl of 2 to 7 carbon atoms, ##STR157## R.sub.7 --(C(R.sub.6).sub.2).sub.s --, R.sub.7 --(C(R.sub.6).sub.2).sub.p --M--(C(R.sub.6).sub.2).sub.r --, R.sub.8 R.sub.9 --CH--M--(C(R.sub.6).sub.2).sub.r --, or Het-(C(R.sub.6).sub.2).sub.q --W--(C(R.sub.6).sub.2).sub.r --; R.sub.8, and R.sub.9 are each, independently, --(C(R.sub.6).sub.2).sub.r --NR.sub.6 R.sub.6, or --(C(R.sub.6).sub.2).sub.r OR.sub.6 ; J is independently --H, --F, or --J'; J' is independently chlorine, bromine, iodine, tosylate (p-toluenesulfonate), or mesylate (methanesulfonate); Q is Q', alkoxy of 1 to 6 carbon atoms, hydroxy, or hydrogen; Q' is alkyl of 1 to 6 carbon atoms; R.sub.2 is selected from the group consisting of ##STR158## R.sub.3 is independently selected from --H, alkyl of 1 to 6 carbon atoms, carboxy, carboalkoxy of 1 to 6 carbon atoms, aryl, carboalkyl of 2 to 7 carbon atoms, and R.sub.3a --(C(R.sub.6).sub.2).sub.s --; R.sub.3a is ##STR159## R.sub.7 --, R.sub.7 --(C(R.sub.6).sub.2).sub.p --M--, R.sub.8 R.sub.9 --CH--M--, or Het-(C(R.sub.6).sub.2).sub.q --W--; a is 0 to 2; k is 1, 3 to 5; n is 0 to 1; m is 0 to 3; p is 2 to 4; q is 0 to 4; r is 1 to 4; s is 1 to 6; u is 0 to 4 and v is 0 to 4, wherein the sum of u+v is 2 to 4; provided that: a. when --R.sub.6 is alkenyl of 2 to 7 carbon atoms or alkynyl of 2 to 7 carbon atoms, said alkenyl of 2 to 7 carbon atoms or alkynyl of 2 to 7 carbon atoms is bound to a nitrogen or oxygen atom through a saturated carbon atom; b. when R.sub.3 is bound to sulfur, R.sub.3 is not --H, carboxy, carboalkoxy, or carboalkyl; c. when M is --O--, and R.sub.7 is --OR.sub.6, then p is 1 to 4; d. when M is --O--, then k is 1 to 5; e. when W is --O--, then k is 1 to 5; f. when R.sub.7 is --OR.sub.6, then k is 1 to 5; g. when W is not a bond with Het bonded through a nitrogen atom, q is 2 to 4, and when W is a bond, q is 0;
or a pharmaceutically acceptable salt thereof.
33. A method of treating, inhibiting or eradicating rheumatoid arthritis in a mammal in need thereof which comprises providing to said mammal an effective amount of a Zap-70 or Lck kinase inhibitor of Formula (I), ##STR160##
wherein: Z is --NH--, --O--, --S(O).sub.a --, or --NR--; R is alkyl of 1 to 6 carbon atoms, or carboalkyl of 2 to 7 carbon atoms; X is cycloalkyl of 3 to 7 carbon atoms, which may be optionally substituted with one or more alkyl of 1 to 6 carbon atom groups; or X is pyridinyl, pyrimidinyl, or an aryl ring; wherein the pyridinyl, pyrimidinyl or aryl ring may be optionally mono-, di-, or tri-substituted with a substituent independently selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or X is a bicyclic aryl or bicyclic heteroaryl ring system of 8 to 12 atoms, where the bicyclic heteroaryl ring contains 1 to 4 heteroatoms independently selected from N, O, and S; wherein the bicyclic aryl or bicyclic heteroaryl ring may be optionally mono-, di-, tri-, or tetra-substituted with a substituent independently selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or X is the radical ##STR161## E is pyridinyl, pyrimidinyl, or an aryl ring; wherein the pyridinyl, pyrimidinyl or aryl ring may be optionally mono-, di-, or tri-substituted with a substituent selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; T is substituted on E at a carbon and is --NH(CH.sub.2).sub.m --, --O(CH.sub.2).sub.m --, --S(O).sub.a --(CH.sub.2).sub.m --, --NR(CH.sub.2).sub.m --, --(CH.sub.2).sub.m --, --(CH.sub.2).sub.m NH--, --(CH.sub.2).sub.m O--, --(CH.sub.2).sub.m S(O).sub.a --, or --(CH.sub.2).sub.m NR--; L is an aryl ring; that is optionally mono-, di, or tri-substituted with a substituent selected from the group consisting of halogen, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or L is a 5- or 6-membered heteroaryl ring where the heteroaryl ring contains 1 to 3 heteroatoms independently selected from N, O, and S; wherein the heteroaryl ring may be optionally mono- or di-substituted with a substituent selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; A' is a moiety selected from the group ##STR162##
G.sub.1, G.sub.2, G.sub.3 and G.sub.4 are independently selected from the group consisting of hydrogen, and alkyl of 1 to 6 carbon atoms; R.sub.1 is --H, R.sub.11 --CH.sub.2 --, --R.sub.12, ##STR163## R.sub.11 is --H, alkyl of 1 to 5 carbon atoms, aryl, or R.sub.13 --(C(R.sub.6).sub.2).sub.k --; R.sub.13 is ##STR164## R.sub.7 --, R.sub.7 --(C(R.sub.6).sub.2).sub.p --M--, or Het-(C(R.sub.6).sub.2).sub.q --W--; R.sub.7 is --H, --NR.sub.6 R.sub.6, --OR.sub.6, --J, --N(R.sub.6).sub.3.sup.+, or --NR.sub.6 (OR.sub.6); ##STR165## or a bond Het is a heterocyclic radical selected from the group consisting of morpholine, thiomorpholine, thiomorpholine S-oxide, thiomorpholine S,S-dioxide, piperidine, pyrrolidine, aziridine, pyridine, imidazole, 1,2,3-triazole, 1,2,4-triazole, thiazole, thiazolidine , tetrazole, piperazine, furan, thiophene, tetrahydrothiophene, tetrahydrofuran, dioxane, 1,3-dioxolane, and tetrahydropyran, optionally mono- or di-substituted on carbon by --R.sub.6, hydroxy, --N(R.sub.6).sub.2, --OR.sub.6, --(C(R.sub.6).sub.2).sub.s OR.sub.6, or --(C(R.sub.6).sub.2).sub.s N(R.sub.6).sub.2 ; or optionally mono-substituted on nitrogen with --R.sub.6 ; and optionally mono or di-substituted on a saturated carbon with divalent radicals --O--, or --O(C(R.sub.6).sub.2).sub.s O--; R.sub.6 is independently selected from --H, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, cycloalkyl of 3 to 6 carbon atoms, carboalkyl of 2 to 7 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, phenyl, or phenyl optionally substituted with one or more halogen, alkoxy of 1 to 6 carbon atoms, trifluoromethyl, amino, alkylamino of 1 to 3 carbon atoms, dialkylamino of 2 to 6 carbon atoms, nitro, cyano, azido, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, carboxyl, carboalkoxy of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, and alkyl of 1 to 6 carbon atoms; R.sub.12 is alkylsulphonyl of 1 to 6 carbon atoms, carboalkoxy of 2 to 7 carbon atoms, or carboalkyl of 2 to 7 carbon atoms; R.sub.5 is hydrogen, alkyl of 1 to 6 carbon atoms, carboxy, carboalkoxy of 1 to 6 carbon atoms, aryl, carboalkyl of 2 to 7 carbon atoms, ##STR166## R.sub.7 --(C(R.sub.6).sub.2).sub.s --, R.sub.7 --(C(R.sub.6).sub.2).sub.p --M--(C(R.sub.6).sub.2).sub.r --, R.sub.8 R.sub.9 --CH--M--(C(R.sub.6).sub.2).sub.r --, or Het-(C(R.sub.6).sub.2).sub.q --W--(C(R.sub.6).sub.2).sub.r --; R.sub.8, and R.sub.9 are each, independently, --(C(R.sub.6).sub.2).sub.r NR.sub.6 R.sub.6, or --(C(R.sub.6).sub.2).sub.r OR.sub.6 ; J is independently --H, --F, or --J'; J' is independently chlorine, bromine, iodine, tosylate (p-toluenesulfonate), or mesylate (methanesulfonate); Q is Q', alkoxy of 1 to 6 carbon atoms, hydroxy, or hydrogen; Q' is alkyl of 1 to 6 carbon atoms; R.sub.2 is selected from the group consisting of ##STR167## R.sub.3 is independently selected from --H, alkyl of 1 to 6 carbon atoms, carboxy, carboalkoxy of 1 to 6 carbon atoms, aryl, carboalkyl of 2 to 7 carbon atoms, and R.sub.3a --(C(R.sub.6).sub.2).sub.s --; R.sub.3a is ##STR168## a is 0 to 2; k is 1, 3 to 5; n is 0 to 1; m is 0 to 3; p is 2to 4; q is 0 to 4; r is 1 to 4; s is 1 to 6; u is 0 to 4 and v is 0 to 4, wherein the sum of u+v is 2 to 4; provided that: a. when --R.sub.6 is alkenyl of 2 to 7 carbon atoms or alkynyl of 2 to 7 carbon atoms, said alkenyl of 2 to 7 carbon atoms or alkynyl of 2 to 7 carbon atoms is bound to a nitrogen or oxygen atom through a saturated carbon atom; b. when R.sub.3 is bound to sulfur, R.sub.3 is not --H, carboxy, carboalkoxy, or carboalkyl; c. when M is --O--, and R.sub.7 is --OR.sub.6, then p is 1 to 4; d. when M is --O--, then k is 1 to 5; e. when W is --O--, then k is 1 to 5; f. when R.sub.7 is --OR.sub.6, then k is 1 to 5; g. when W is not a bond with Het bonded through a nitrogen atom, q is 2 to 4, and when W is a bond, q is 0;
or a pharmaceutically acceptable salt thereof.
34. A method of treating or inhibiting the progression of osteoporosis in a mammal in need thereof which comprises providing to said mammal an effective amount of a Src kinase inhibitor of Formula (I), ##STR169##
wherein: Z is --NH--, --O--, --S(O).sub.a --, or --NR-- R is alkyl of 1 to 6 carbon atoms, or carboalkyl of 2 to 7 carbon atoms; X is cycloalkyl of 3 to 7 carbon atoms, which may be optionally substituted with one or more alkyl of 1 to 6 carbon atom groups; or X is pyridinyl, pyrimidinyl, or an aryl ring; wherein the pyridinyl, pyrimidinyl or aryl ring may be optionally mono-, di-, or tri-substituted with a substituent independently selected from the group consisiting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or X is a bicyclic aryl or bicyclic heteroaryl ring system of 8 to 12 atoms, where the bicyclic heteroaryl ring contains 1 to 4 heteroatoms independently selected from N, O, and S; wherein the bicyclic aryl or bicyclic heteroaryl ring may be optionally mono-, di-, tri-, or tetra-substituted with a substituent independently selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or X is the radical ##STR170## E is pyridinyl, pyrimidinyl, or an aryl ring; wherein the pyridinyl, pyrimidinyl or aryl ring may be optionally mono-, di-, or tri-substituted with a substituent selected from the group consisiting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; T is substituted on E at a carbon and is --NH(CH.sub.2).sub.m --, --O(CH.sub.2).sub.m --, --S(O).sub.a --(CH.sub.2).sub.m --, --NR(CH.sub.2).sub.m --, --(CH.sub.2).sub.m --, --(CH.sub.2).sub.m NH--, --(CH.sub.2).sub.m O--, --(CH.sub.2).sub.m S(O).sub.a --, or --(CH.sub.2).sub.m NR--; L is an aryl ring; that is optionally mono-, di, or tri-substituted with a substituent selected from the group consisting of halogen, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; or L is a 5- or 6-membered heteroaryl ring where the heteroaryl ring contains 1 to 3 heteroatoms independently selected from N, O, and S; wherein the heteroaryl ring may be optionally mono- or di-substituted with a substituent selected from the group consisting of halogen, oxo, thio, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2 to 6 carbon atoms, azido, hydroxyalkyl of 1 to 6 carbon atoms, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2 to 7 carbon atoms, carboalkyl of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, amino, alkylamino of 1 to 6 carbon atoms, dialkylamino of 2 to 12 carbon atoms, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, alkenoylamino of 3 to 8 carbon atoms, alkynoylamino of 3 to 8 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, carboalkoxyalkyl of 3 to 8 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, N-alkylaminoalkyl of 2 to 9 carbon atoms, N,N-dialkylaminoalkyl of 3 to 10 carbon atoms, N-alkylaminoalkoxy of 2 to 9 carbon atoms, N,N-dialkylaminoalkoxy of 3 to 10 carbon atoms, mercapto, and benzoylamino; A" is a moiety selected from the group ##STR171## G.sub.1, G.sub.2, G.sub.3 and G.sub.4 are independently selected from the group consisting of hydrogen, and alkyl of 1 to 6 carbon atoms; R.sub.1 is --H, R.sub.11 --CH.sub.2 --, --R.sub.12, ##STR172## R.sub.11 is --H, alkyl of 1 to 5 carbon atoms, aryl, or R.sub.13 --(C(R.sub.6).sub.2).sub.k --; R.sub.13 is ##STR173## R.sub.7 --, R.sub.7 --(C(R.sub.6).sub.2).sub.p --M--, or Het-(C(R.sub.6).sub.2).sub.q --W--; R.sub.7 is --H, --NR.sub.6 R.sub.6, --OR.sub.6, --J, --N(R.sub.6).sub.3.sup.+, or --NR.sub.6 (OR.sub.6); ##STR174## or a bond; Het is a heterocyclic radical selected from the group consisting of morpholine, thiomorpholine, thiomorpholine S-oxide, thiomorpholine S,S-dioxide, piperidine, pyrrolidine, aziridine, pyridine, imidazole, 1,2,3-triazole, 1,2,4-triazole, thiazole, thiazolidine, tetrazole, piperazine, furan, thiophene, tetrahydrothiophene, tetrahydrofuran, dioxane, 1,3-dioxolane, and tetrahydropyran, optionally mono- or di-substituted on carbon by --R.sub.6, hydroxy, --N(R.sub.6).sub.2, --OR.sub.6, --(C(R.sub.6).sub.2).sub.s OR.sub.6, or --(C(R.sub.6).sub.2).sub.s N(R.sub.6).sub.2 ; or optionally mono-substituted on nitrogen with --R.sub.6 ; and optionally mono or di-substituted on a saturated carbon with divalent radicals --O--, or --O(C(R.sub.6).sub.2).sub.s O--; R.sub.6 is independently selected from --H, alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms, alkynyl of 2- to carbon atoms, cycloalkyl of 3 to 6 carbon atoms, carboalkyl of 2 to 7 carbon atoms, carboxyalkyl of 2 to 7 carbon atoms, phenyl, or phenyl optionally substituted with one or more halogen, alkoxy of 1 to 6 carbon atoms, trifluoromethyl, amino, alkylamino of 1 to 3 carbon atoms, dialkylamino of 2 to 6 carbon atoms, nitro, cyano, azido, halomethyl, alkoxymethyl of 2 to 7 carbon atoms, alkanoyloxymethyl of 2 to 7 carbon atoms, alkylthio of 1 to 6 carbon atoms, hydroxy, carboxyl, carboalkoxy of 2 to 7 carbon atoms, phenoxy, phenyl, thiophenoxy, benzoyl, benzyl, phenylamino, benzylamino, alkanoylamino of 1 to 6 carbon atoms, and alkyl of 1 to 6 carbon atoms; R.sub.12 is alkylsulphonyl of 1 to 6 carbon atoms, carboalkoxy of 2 to 7 carbon atoms, or carboalkyl of 2 to 7 carbon atoms; R.sub.5 is hydrogen, alkyl of 1 to 6 carbon atoms, carboxy, carboalkoxy of 1 to 6 carbon atoms, aryl, carboalkyl of 2 to 7 carbon atoms, ##STR175## R.sub.7 --(C(R.sub.6).sub.2).sub.s --, R.sub.7 --(C(R.sub.6).sub.2).sub.p --M--(C(R.sub.6).sub.2).sub.r --, R.sub.8 R.sub.9 --CH--M--(C(R.sub.6).sub.2).sub.r --, or Het-(C(R.sub.6) .sub.2).sub.q --W--(C(R.sub.6).sub.2).sub.r --; R.sub.8, and R.sub.9 are each, independently, --(C(R.sub.6).sub.2).sub.r NR.sub.6 R.sub.6, or --(C(R.sub.6).sub.2).sub.r OR.sub.6 ; J is independently --H, --F, or --J'; J' is independently chlorine, bromine, iodine, tosylate (p-toluenesulfonate), or mesylate (methanesulfonate); Q is Q', alkoxy of 1 to 6 carbon atoms, hydroxy, or hydrogen; Q' is alkyl of 1 to 6 carbon atoms; R.sub.2 is selected from the group consisting of ##STR176## R.sub.3 is independently selected from --H, alkyl of 1 to 6 carbon atoms, carboxy, carboalkoxy of 1 to 6 carbon atoms, aryl, carboalkyl of 2 to 7 carbon atoms, and R.sub.3a --(C(R.sub.6).sub.2).sub.s --; R.sub.3a is ##STR177## R.sub.7 --,R.sub.7 --(C(R.sub.6).sub.2).sub.p --M--, R.sub.8 R.sub.9 --CH--M--, or Het-(C(R.sub.6).sub.2).sub.q--W--; a is 0 to 2; k is 1, 3 to 5; n is 0 to 1; m is 0 to 3; p is 2 to 4; q is 0 to 4; r is 1 to 4; s is 1 to 6; u is 0 to 4 and v is 0 to 4, wherein the sum of u+v is 2 to 4; provided that: a. when --R.sub.6 is alkenyl of 2 to 7 carbon atoms or alkynyl of 2 to 7 carbon atoms, said alkenyl of 2 to 7 carbon atoms or alkynyl of 2 to 7 carbon atoms is bound to a nitrogen or oxygen atom through a saturated carbon atom; b. when R.sub.3 is bound to sulfur, R.sub.3 is not --H, carboxy, carboalkoxy, or carboalkyl; c. when M is --O--, and R.sub.7 is --OR.sub.6, then p is 1 to 4; d. when M is --O--, then k is 1 to 5; e. when W is --O--, then k is 1 to 5; f. when R.sub.7 is --OR.sub.6, then k is 1 to 5; g. when W is not a bond with Het bonded through a nitrogen atom, q is 2 to 4, and when W is a bond, q is 0;
or a pharmaceutically acceptable salt thereof.
35. The method according to claim 29 wherein the neoplasm expresses EGFR or erbB2(Her2).
36. The method according to claim 29 wherein the neoplasm depends, on the MAPK pathway.
37. The method of claim 29 wherein the neoplasm depends, on the ECK/LERK-1 pathway.
38. The method according to claim 29 wherein the neoplasm depends, on the VEGF/KDR pathway.
39. The method of claim 29 wherein the neoplasm expresses Src or wherein the neoplasm depends on the Src pathway.
40. The method of claim 29 wherein the neoplasm expresses raf or wherein the neoplasm depends on the raf pathway.
41. The method of claim 29 wherein the neoplasm expresses EGFr, erbB-2, erbB-3 or erbB-4 or wherein the neoplasm depends on the EGFr, erbB-2, erbB-3 or erbB-4 pathway.
42. The method of claim 29 wherein the neoplasm expresses KDR or flt-1 or wherein the neoplasm depends on the KDR or flt-1 pathway.
43. The method of claim 29 wherein the neoplasm expresses PDGFr or wherein the neoplasm depends on the PDGFr pathway.
44. The method of claim 29 wherein the neoplasm expresses FGFr or wherein the neoplasm depends on the FGFr pathway.
45. The method of claim 29 wherein the neoplasm expresses tie-1 or tie-2 or wherein the neoplasm depends on the tie-1 or tie-2 pathway.
46. The method of claim 29 wherein the neoplasm expresses EPH or wherein the neoplasm depends on the EPH pathway.
47. The method of claim 29 wherein the neoplasm expresses a non-receptor tyrosine kinase including Abl, Jak, Fak, Syk or Csk or wherein the neoplasm depends on the Abl, Jak, Fak, Syk or Csk pathway.
48. The method of claim 29 wherein the neoplasm expresses mek or erk or wherein the neoplasm depends on the MAPK pathway.
49. The method of claim 29 wherein the neoplasm expresses a cyclin dependent kinase or wherein the neoplasm depends on a cyclin dependent kinase pathway.
50. The method of claim 29 wherein the neoplasm expresses a Src family kinase including Yes, Lck or Lyn or wherein the neoplasm depends on a Src family kinase pathway.
51. The method of claim 29 wherein the neoplasm expresses PKA, PKB or PKC or wherein the neoplasm depends on a PKA, PKB or PKC pathway.
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