Keratinocyte growth factor receptor—tyrosine specific inhibitors for the prevention of cancer metastatis
Compounds and methods for treating, inhibiting, or delaying the onset of cancer in a subject by administering a therapeutically effective amount of a keratinocyte growth factor receptor tyrosine kinase (KGFR TK) inhibitor to the subject in need of such treatment. Also provided are compounds and methods for the treating, inhibiting, or delaying the onset of metastasis in a subject with cancer by administering a therapeutically effective amount of a KGFR TK inhibitor to the subject in need of such treatment.
1. A compound of formula II:
wherein R 4 is a substituted phenyl; wherein the phenyl has at least one substituent selected from the group consisting of sulfonamide, para-hydroxy, meta-ethoxy, meta-propoxy and meta-butoxy;
R 2 and R 3 are selected from the group consisting of H, ester, alkoxy, hydroxyl, and sulfonamide;
and pharmaceutically acceptable salts and esters thereof.
2. The compound of claim 1 wherein the compound is a keratinocyte growth factor receptor-tyrosine specific kinase (KGFR-TK) inhibitor.
3. A compound of formula III:
wherein R 5 is H and R 6 is substituted phenyl, wherein the substituted phenyl has at least one substituent selected from the group consisting of hydroxy, sulfonamide, and —O(CH 2 ) n OH, wherein n is 1-4
R 2 is selected from the group consisting of H, amino, ester, carboxylic acid, alkoxy, hydroxyl, and sulfonamide;
R 3 is selected from the group consisting of amino, carboxylic acid, alkoxy, and sulfonamide;
and pharmaceutically acceptable salts thereof.
4. The compound of claim 3 wherein R 5 and R 6 form a heteroaryl ring.
5. The compound of claim 4 wherein the heteroaryl ring is fused to another aromatic ring.
6. The compound of claim 5 wherein R 5 and R 6 form a furyl ring, wherein the furyl ring is fused to a benzene ring.
7. The compound of claim 3 wherein the compound is a keratinocyte growth factor receptor-tyrosine specific kinase (KGFR-TK) inhibitor.
8. A compound of the formula:
wherein R 1 is selected from the group consisting of amino, amide, ester, carboxylic acid, alkoxy, hydroxyl, and sulfonamide;
wherein R 2 is selected from the group consisting of H, amino, amide, ester, carboxylic acid, alkyl, alkoxy, hydroxyl, and sulfonamide;
wherein R 3 is selected from the group consisting of H, phenyl, substituted aromatic, and phenoxy; wherein the substituted aromatic has at least one substituent selected from the group consisting of alkyl, hydroxy, alkoxy, sulfonamide, and O(CH 2 ) n OH, wherein n is 1-4; and
pharmaceutically acceptable salts and esters thereof.
9. The compound of claim 8 , wherein R 1 is selected from the group consisting of amide, ester, carboxylic acid, alkoxy, and hydroxyl; and
wherein R 2 and R 3 are H.
10. The compound of claim 8 , wherein R 1 is carboxyl, R 2 is H, and R 3 is H.
11. The compound of claim 8 , wherein R 1 is hydroxyl, R 2 is H, and R 3 is H.