3-3-di-substituted-oxindoles as inhibitors of translation initiation
Compositions and methods for inhibiting translation using 3-(5-tert-Butyl-2-Hydroxy-phenyl)-3-phenyl-1,3-dihydro-indol-2-one and/or its derivatives are provided. Compositions, methods and kits for treating (1) cellular proliferative disorders, (2) non-proliferative, degenerative disorders, (3) viral infections, and/or (4) disorders associated with viral infections, using 3-(5-tert-butyl-2-hydroxy-phenyl)-3-phenyl-1,3-dihydro-indol-2-one and/or its derivatives are described.
1. A method of treating cancer in a human or non-human mammal in need thereof, the method comprising administering to the human or non-human mammal a compound of formula III
wherein X is selected from the group consisting of oxygen, NH and CH 2 ; and
R is selected from the group consisting of 3′-CH 2 CH(CO 2 Me)NH 2 , 3′-CH 2 CH(CO 2 Me)NHFmoc, 3′-t-Bu, 3′-OH, 3′-O(CH 2 3 CHCH 2 , 3′-O(CH 2 ) 4 Br, 3 ′-O(CH 2 ) 4 NMe 2 , 3′-O(CH 2 ) 4 N 3 ,
3′-O(CH 2 ) 4 NH 2 , 3′-CF 3 , 3′-CH 3 , 3′-n-heptyl, 3′-n-nonyl, 3′-i-Bu, 3′-i-propyl, 3′-n-propyl, 3′-n-octyl, 3′-Et, 3′-n-pentyl, 3′-n-Bu, 3′-n-hexyl, 3′-n-cyclopentyl, 3′-n-cyclohexyl, 4-NHSO 2 (4-tBu)Ph and 3′-NHSO 2 (4-tBu)Ph, and
wherein the cancer is a member selected from the group consisting of breast cancer, lung cancer, melanoma, prostate cancer, leukemia, multiple myeloma, plasmocytoma, pancreatic cancer and colon cancer.
2. The method of claim 1 wherein the compound is 3-(5-tert-butyl-2-hydroxy-phenyl)-3-phenyl-1,3,-dihydro-indol-2-one.
3. The method of claim 1 , wherein the compound is administered by inhalation, transdermally, orally, rectally, transmucosally, intestinally, parenterally, intramuscularly, subcutaneously or intravenously.
4. A method of treating cancer in a human or non-human mammal in need thereof, the method comprising administering to the human or non-human mammal a compound of formula IV
wherein R is selected from the group consisting of 4-F, 4-O(CH 2 ) 3 CHCH 2 , 3-Cl, 3-F, 3-Me, 2-Me and 2-OMe, and
wherein the cancer is a member selected from the group consisting of breast cancer, lung cancer, melanoma, prostate cancer, leukemia, multiple myeloma, plasmocytoma, pancreatic cancer and colon cancer.
5. The method of claim 4 , wherein the compound is administered by inhalation, transdermally, orally, rectally, transmucosally, intestinally, parenterally, intramuscularly, subcutaneously or intravenously.
6. A method of treating cancer in a human or non-human mammal in need thereof, the method comprising administering to the human or non-human mammal a compound of formula VI
wherein R 1 is selected from the group consisting of 7-Br, 4-Cl, 5-Br, 5-NO 2 , 5-I, 5-OMe, 5-Cl, 7-CF 3 , 5-NH 2 , 4-Br, 6-Br, H, 7-OMe, 7-I, 5-Et, 7-Et, 4-Et, 6-Et, 5-F, 5-N 3 , 7-COOH, 7-CO 2 H, 4-Cl, 6-Cl and 5-NHSO 2 -1-napthyl; and R 2 is H or 7-CO 2 H, and
wherein the cancer is a member selected from the group consisting of breast cancer, lung cancer, melanoma, prostate cancer, leukemia, multiple myeloma, plasmocytoma, pancreatic cancer and colon cancer.
7. The method of claim 6 , wherein the compound is administered by inhalation, transdermally, orally, rectally, transmucosally, intestinally, parenterally, intramuscularly, subcutaneously or intravenously.
8. A method of treating cancer in a human or non-human mammal in need thereof, the method comprising administering to the human or non-human mammal a compound of formula VIII
wherein R 1 is selected from the group consisting of H and 7-CO 2 H;
R 2 is selected from the group consisting of H, 2-Me, 3′-Me, 3-F and 3-CF 3 ; and
R 3 is selected from the group consisting of H, 2-NHFmoc, 2-NHSO 2 CH 2 Ph, 2-NHSO 2 CH 3 , 2-NHSO 2 (4-tBu)Ph, 2-NHSO 2 (4-NHAc)Ph, 2-NHSO 2 (3-CF 3 )Ph, 2-NHSO 2 (4-NO 2 )Ph, 2-NHSO 2 (4-OMe)Ph, 2-NHSO 2 (4-Br)Ph, 2-NHSO 2 (4-I)Ph, 2-NHSO 2 (4-Ph)Ph, 2-NHSO 2 (4-OPh)Ph, 2-NHAc, 2-NHCO(4-tBu)Ph and 3′-NHSO 2 (4-tBu)Ph, and
wherein the cancer is a member selected from the group consisting of breast cancer, lung cancer, melanoma, prostate cancer, leukemia, multiple myeloma, plasmocytoma, pancreatic cancer and colon cancer.
9. The method of claim 8 , wherein the compound is administered by inhalation, transdermally, orally, rectally, transmucosally, intestinally, parenterally, intramuscularly, subcutaneously or intravenously.
10. The method of claim 8 wherein the compound is 4-tert-butyl-N-(5-hydroxy-4-methyl-2-(2-oxo-3-phenylindolin-3-yl)phenyl)benzenesulfonamide.
11. A method of treating breast cancer in a human or non-human mammal, the method comprising administering to the human or non-human mammal a compound of
wherein X is selected from the group consisting of oxygen, NH and CH 2 ; and
R is selected from the group consisting of 3′-CH 2 CH(CO 2 Me)NH 2 , 3′-CH 2 CH(CO 2 Me)NHFmoc, 3′-t-Bu, 3′-OH, 3′-O(CH 2 ) 3 CHCH 2 , 3′-O(CH 2 ) 4 Br, 3′-O(CH 2 ) 4 NMe 2 , 3′-O(CH 2 ) 4 N 3 ,
3′-O(CH 2 ) 4 NH 2 , 3′-CF 3 , 3′-CH 3 , 3′-n-heptyl, 3′-n-nonyl, 3′-i-Bu, 3′-i-propyl, 3′-n-propyl, 3′-n-octyl, 3′-Et, 3′-n-pentyl, 3′-n-Bu, 3′-n-hexyl, 3′-n-cyclopentyl, 3′-n-cyclohexyl, 4-NHSO 2 (4-tBu)Ph and 3′-NHSO 2 (4-tBu)Ph;
wherein R is selected from the group consisting of 4-F, 4-O(CH 2 ) 3 CHCH 2 , 3-Cl, 3-F, 3-Me, 2-Me and 2-OMe;
wherein R 1 is selected from the group consisting of 7-Br, 4-Cl, 5-Br, 5-NO 2 , 5-I, 5-OMe, 5-Cl, 7-CF 3 , 5-NH 2 , 4-Br, 6-Br, H, 7-OMe, 7-I, 5-Et, 7-Et, 4-Et, 6-Et, 5-F, 5-N 3 , 7-COOH, 7-CO 2 H, 4-Cl, 6-Cl and 5-NHSO 2 -1-napthyl; and R 2 is H or 7-CO 2 H;
R 2 is selected from the group consisting of 2-OH, 4-OH, 4-t-Bu and H with the proviso that R 1 and R 2 cannot both be H or 4-OH; or
wherein R 1 is selected from the group consisting of H and 7-CO 2 H;
R 2 is selected from the group consisting of H, 2-Me, 3′-Me, 3-F and 3-CF 3 ; and
R 3 is selected from the group consisting of H, 2-NHFmoc, 2-NHSO 2 CH 2 Ph, 2-NHSO 2 CH 3 , 2-NHSO 2 (4-tBu)Ph, 2-NHSO 2 (4-NHAc)Ph, 2-NHSO 2 (3-CF 3 )Ph, 2-NHSO 2 (4-NO 2 )Ph, 2-NHSO 2 (4-OMe)Ph, 2-NHSO 2 (4-Br)Ph, 2-NHSO 2 (4-I)Ph, 2-NHSO 2 (4-Ph)Ph, 2-NHSO 2 (4-OPh)Ph, 2-NHAc, 2-NHCO(4-tBu)Ph and 3′-NHSO 2 (4-tBu)Ph.
12. A method of treating lung cancer in a human or non-human mammal, the method comprising administering to the human or non-human mammal a compound of
wherein X is selected from the group consisting of oxygen, NH and CH 2 ; and
R is selected from the group consisting of 3′-CH 2 CH(CO 2 Me)NH 2 , 3′-CH 2 CH(CO 2 Me)NHFmoc, 3′-t-Bu, 3′-OH, 3′-O(CH 2 ) 3 CHCH 2 , 3′-O(CH 2 ) 4 Br, 3′-O(CH 2 ) 4 NMe 2 , 3′-O(CH 2 ) 4 N 3 ,
3′-O(CH 2 ) 4 NH 2 , 3′-CF 3 , 3′-CH 3 , 3′-n-heptyl, 3′-n-nonyl, 3′-i-Bu, 3′-i-propyl, 3′-n-propyl, 3′-n-octyl, 3′-Et, 3′-n-pentyl, 3′-n-Bu, 3′-n-hexyl, 3′-n-cyclopentyl, 3′-n-cyclohexyl, 4-NHSO 2 (4-tBu)Ph and 3-NHSO 2 (4-tBu)Ph;
wherein R is selected from the group consisting of 4-F, 4-O(CH 2 ) 3 CHCH 2 , 3-Cl, 3-F, 3-Me, 2-Me and 2-OMe;
wherein R 1 is selected from the group consisting of 7-Br, 4-Cl, 5-Br, 5-NO 2 , 5-I, 5-OMe, 5-Cl, 7-CF 3 , 5-NH 2 , 4-Br, 6-Br, H, 7-OMe, 7-I, 5-Et, 7-Et, 4-Et, 6-Et, 5-F, 5-N 3 , 7-COOH, 7-CO 2 H, 4-Cl, 6-Cl and 5-NHSO 2 -1-napthyl; and R 2 is H or 7-CO 2 H;
R 2 is selected from the group consisting of 2-OH, 4-OH, 4-t-Bu and H with the proviso that R 1 and R 2 cannot both be H or 4- 0 H; or
wherein R 1 is selected from the group consisting of H and 7-CO 2 H;
R 2 is selected from the group consisting of H, 2-Me, 3′-Me, 3-F and 3-CF 3 ; and
R 3 is selected from the group consisting of H, 2-NHFmoc, 2-NHSO 2 CH 2 Ph, 2-NHSO 2 CH 3 , 2-NHSO 2 (4-tBu)Ph, 2-NHSO 2 (4-NHAc)Ph, 2-NHSO 2 (3-CF 3 )Ph, 2-NHSO 2 (4-NO 2 )Ph, 2-NHSO 2 (4-OMe)Ph, 2-NHSO 2 (4-Br)Ph, 2-NHSO 2 (4-I)Ph, 2-NHSO 2 (4-Ph)Ph, 2-NHSO 2 (4-OPh)Ph, 2-NHAc, 2-NHCO(4-tBu)Ph and 3′-NHSO 2 (4-tBu)Ph.
13. A method of treating melanoma in a human or non-human mammal, the method comprising administering to the human or non-human mammal a compound of
wherein X is selected from the group consisting of oxygen, NH and CH 2 ; and
R is selected from the group consisting of 3′-CH 2 CH(CO 2 Me)NH 2 , 3′-CH 2 CH(CO 2 Me)NHFmoc, 3′-t-Bu, 3′-OH, 3′-O(CH 2 ) 3 CHCH 2 , 3′-O(CH 2 ) 4 Br, 3′-O(CH 2 ) 4 NMe 2 , 3-O(CH 2 ) 4 N 3 ,
3′-O(CH 2 ) 4 NH 2 , 3′-CF 3 , 3′-CH 3 , 3′-n-heptyl, 3′-n-nonyl, 3′-i-Bu, 3′-i-propyl, 3′-n-propyl, 3′-n-octyl, 3′-Et, 3′-n-pentyl, 3 40 -n-Bu, 3′-n-hexyl, 3′-n-cyclopentyl, 3 40 -n-cyclohexyl, 4-NHSO 2 (4-tBu)Ph and 3′-NHSO 2 (4-tBu)Ph;
wherein R is selected from the group consisting of 4-F, 4-O(CH 2 ) 3 CHCH 2 , 3-Cl, 3-F, 3-Me, 2-Me and 2-OMe;
wherein R 1 is selected from the group consisting of 7-Br, 4-Cl, 5-Br, 5-NO 2 , 5-I, 5-OMe, 5-Cl, 7-CF 3 , 5-NH 2 , 4-Br, 6-Br, H, 7-OMe, 7-I, 5-Et, 7-Et, 4-Et, 6-Et, 5-F, 5-N 3 , 7-COOH, 7-CO 2 H, 4-Cl, 6-Cl and 5-NHSO 2 -1-napthyl; and R 2 is H or 7-CO 2 H;
wherein R 1 is selected from the group consisting of H and 7-CO 2 H;
R 2 is selected from the group consisting of H, 2-Me, 3′-Me, 3-F and 3-CF 3 ; and
R 3 is selected from the group consisting of H, 2-NHFmoc, 2-NHSO 2 CH 2 Ph, 2-NHSO 2 CH 3 , 2-NHSO 2 (4-tBu)Ph, 2-NHSO 2 (4-NHAc)Ph, 2-NHSO 2 (3-CF 3 )Ph, 2-NHSO 2 (4-NO 2 )Ph, 2-NHSO 2 (4-OMe)Ph, 2-NHSO 2 (4-Br)Ph, 2-NHSO 2 (4-I)Ph, 2-NHSO 2 (4-Ph)Ph, 2-NHSO 2 (4-OPh)Ph, 2-NHAc, 2-NHCO(4-tBu)Ph and 3′-NHSO 2 (4-tBu)Ph.
14. A method of prostate cancer in a human or non-human mammal, the method comprising administering to the human or non-human mammal a compound of
wherein X is selected from the group consisting of oxygen, NH and CH 2 ; and
R is selected from the group consisting of 3′-CH 2 CH(CO 2 Me)NH 2 , 3′-CH 2 CH(CO 2 Me)NHFmoc, 3′-t-Bu, 3′-OH, 3′-O(CH 2 ) 3 CHCH 2 , 3′-O(CH 2 ) 4 Br, 3′-O(CH 2 ) 4 NMe 2 , 3′-O(CH 2 ) 4 N 3 ,
3′-O(CH 2 ) 4 NH 2 , 3′-CF 3 , 3′-CH 3 , 3′-n-heptyl, 3′-n-nonyl, 3′-i-Bu, 3′-i-propyl, 3′-n-propyl, 3′-n-octyl, 3′-Et, 3′-n-pentyl, 3′-n-Bu, 3′-n-hexyl, 3′-n-cyclopentyl, 3′-n-cyclohexyl, 4-NHSO 2 (4-tBu)Ph and 3′-NHSO 2 (4-tBu)Ph;
wherein R is selected from the group consisting of 4-F, 4-O(CH 2 ) 3 CHCH 2 , 3-Cl, 3-F, 3-Me, 2-Me and 2-OMe;
wherein R 1 is selected from the group consisting of 7-Br, 4-Cl, 5-Br, 5-NO 2 , 5-I, 5-OMe, 5-Cl, 7-CF 3 , 5-NH 2 , 4-Br, 6-Br, H, 7-OMe, 7-I, 5-Et, 7-Et, 4-Et, 6-Et, 5-F, 5-N 3 , 7-COOH, 7-CO 2 H, 4-Cl, 6-Cl and 5-NHSO 2 -1-napthyl; and R 2 is H or 7-CO 2 H; or
wherein R 1 is selected from the group consisting of H and 7-CO 2 H;
R 2 is selected from the group consisting of H, 2-Me, 3′-Me, 3-F and 3-CF 3 ; and
R 3 is selected from the group consisting of H, 2-NHFmoc, 2-NHSO 2 CH 2 Ph, 2-NHSO 2 CH 3 , 2-NHSO 2 (4-tBu)Ph, 2-NHSO 2 (4-NHAc)Ph, 2-NHSO 2 (3-CF 3 )Ph, 2-NHSO 2 (4-NO 2 )Ph, 2-NHSO 2 (4-OMe)Ph, 2-NHSO 2 (4-Br)Ph, 2-NHSO 2 (4-I)Ph, 2-NHSO 2 (4-Ph)Ph, 2-NHSO 2 (4-OPh)Ph, 2-NHAc, 2-NHCO(4-tBu)Ph and 3′-NHSO 2 (4-tBu)Ph.
15. A method of treating leukemia in a human or non-human mammal, the method comprising administering to the human or non-human mammal a compound of
wherein X is selected from the group consisting of oxygen, NH and CH 2 ; and
R is selected from the group consisting of 3′-CH 2 CH(CO 2 Me)NH 2 , 3′-CH 2 CH(CO 2 Me)NHFmoc, 3′-t-Bu, 3′-OH, 3′-O(CH 2 ) 3 CHCH 2 , 3′-O(CH 2 ) 4 Br, 3′-O(CH 2 ) 4 NMe 2 , 3′-O(CH 2 ) 4 N 3 ,
3′-O(CH 2 ) 4 NH 2 , 3′-CF 3 , 3′-CH 3 , 3′-n-heptyl, 3′-n-nonyl, 3′-i-Bu, 3′-i-propyl, 3′-n-propyl, 3′-n-octyl, 3′-Et, 3′-n-pentyl, 3′-n-Bu, 3′-n-hexyl, 3′-n-cyclopentyl, 3′-n-cyclohexyl, 4-NHSO 2 (4-tBu)Ph and 3′-NHSO 2 (4-tBu)Ph;
wherein R is selected from the group consisting of 4-F, 4-O(CH 2 ) 3 CHCH 2 , 3-Cl, 3-F, 3-Me, 2-Me and 2-OMe;
wherein R 1 is selected from the group consisting of 7-Br, 4-Cl, 5-Br, 5-NO 2 , 5-I, 5-OMe, 5-Cl, 7-CF 3 , 5-NH 2 , 4-Br, 6-Br, H, 7-OMe, 7-I, 5-Et, 7-Et, 4-Et, 6-Et, 5-F, 5-N 3 , 7-COOH, 7-CO 2 H, 4-Cl, 6-Cl and 5-NHSO 2 -1-napthyl; and R 2 is H or 7-CO 2 H;
wherein R 1 is selected from the group consisting of H and 7-CO 2 H;
R 2 is selected from the group consisting of H, 2-Me, 3′-Me, 3-F and 3-CF 3 ; and
R 3 is selected from the group consisting of H, 2-NHFmoc, 2-NHSO 2 CH 2 Ph, 2-NHSO 2 CH 3 , 2-NHSO 2 (4-tBu)Ph, 2-NHSO 2 (4-NHAc)Ph, 2-NHSO 2 (3-CF 3 )Ph, 2-NHSO 2 (4-NO 2 )Ph, 2-NHSO 2 (4-OMe)Ph, 2-NHSO 2 (4-Br)Ph, 2-NHSO 2 (4-I)Ph, 2-NHSO 2 (4-Ph)Ph, 2-NHSO 2 (4-OPh)Ph, 2-NHAc, 2-NHCO(4-tBu)Ph and 3′-NHSO 2 (4-tBu)Ph.
16. A method of treating multiple myeloma in a human or non-human mammal, the method comprising administering to the human or non-human mammal a compound of
wherein X is selected from the group consisting of oxygen, NH and CH 2 ; and
R is selected from the group consisting of 3′-CH 2 CH(CO 2 Me)NH 2 , 3′-CH 2 CH(CO 2 Me)NHFmoc, 3′-t-Bu, 3′-OH, 3′-O(CH 2 ) 3 CHCH 2 , 3′-O(CH 2 ) 4 Br, 3′-O(CH 2 ) 4 NMe 2 , 3′-O(CH 2 ) 4 N 3 ,
3′-O(CH 2 ) 4 NH 2 , 3′-CF 3 , 3′-CH 3 , 3′-n-heptyl, 3′-n-nonyl, 3′-i-Bu, 3′-i-propyl, 3′-n-propyl, 3′-n-octyl, 3′-Et, 3′-n-pentyl, 3′-n-Bu, 3′-n-hexyl, 3′-n-cyclopentyl, 3′-n-cyclohexyl, 4-NHSO 2 (4-tBu)Ph and 3′-NHSO 2 (4-tBu)Ph;
wherein R is selected from the group consisting of 4-F, 4-O(CH 2 ) 3 CHCH 2 , 3-Cl, 3-F, 3-Me, 2-Me and 2-OMe;
wherein R 1 is selected from the group consisting of 7-Br, 4-Cl, 5-Br, 5-NO 2 , 5-I, 5-OMe, 5-Cl, 7-CF 3 , 5-NH 2 , 4-Br, 6-Br, H, 7-OMe, 7-I, 5-Et, 7-Et, 4-Et, 6-Et, 5-F, 5-N 3 , 7-COOH, 7-CO 2 H, 4-Cl, 6-Cl and 5-NHSO 2 -1-napthyl; and R 2 is H or 7-CO 2 H;
wherein R 1 is selected from the group consisting of H and 7-CO 2 H;
R 2 is selected from the group consisting of H, 2-Me, 3′-Me, 3-F and 3-CF 3 ; and
R 3 is selected from the group consisting of H, 2-NHFmoc, 2-NHSO 2 CH 2 Ph, 2-NHSO 2 CH 3 , 2-NHSO 2 (4-tBu)Ph, 2-NHSO 2 (4-NHAc)Ph, 2-NHSO 2 (3-CF 3 )Ph, 2-NHSO 2 (4-NO 2 )Ph, 2-NHSO 2 (4-OMe)Ph, 2-NHSO 2 (4-Br)Ph, 2-NHSO 2 (4-I)Ph, 2-NHSO 2 (4-Ph)Ph, 2-NHSO 2 (4-OPh)Ph, 2-NHAc, 2-NHCO(4-tBu)Ph and 3′-NHSO 2 (4-tBu)Ph.
17. A method of treating plasmocytoma in a human or non-human mammal, the method comprising administering to the human or non-human mammal a compound of
wherein X is selected from the group consisting of oxygen, NH and CH 2 ; and
R is selected from the group consisting of 3′-CH 2 CH(CO 2 Me)NH 2 , 3′-CH 2 CH(CO 2 Me)NHFmoc, 3′-t-Bu, 3′-OH, 3′-O(CH 2 ) 3 CHCH 2 , 3′-O(CH 2 ) 4 Br, 3′-O(CH 2 ) 4 NMe 2 , 3′-O(CH 2 ) 4 N 3 ,
3′-O(CH 2 ) 4 NH 2 , 3′-CF 3 , 3′-CH 3 , 3′-n-heptyl, 3′-n-nonyl, 3′-i-Bu, 3′-i-propyl, 3′-n-propyl, 3′-n-octyl, 3′-Et, 3′-n-pentyl, 3′-n-Bu, 3′-n-hexyl, 3′-n-cyclopentyl, 3′-n-cyclohexyl, 4-NHSO 2 (4-tBu)Ph and 3′-NHSO 2 (4-tBu)Ph;
wherein R is selected from the group consisting of 4-F, 4-O(CH 2 ) 3 CHCH 2 , 3-Cl, 3-F, 3-Me, 2-Me and 2-OMe;
wherein R 1 is selected from the group consisting of 7-Br, 4-Cl, 5-Br, 5-NO 2 , 5-I, 5-OMe, 5-Cl, 7-CF 3 , 5-NH 2 , 4-Br, 6-Br, H, 7-OMe, 7-I, 5-Et, 7-Et, 4-Et, 6-Et, 5-F, 5-N 3 , 7-COOH, 7-CO 2 H, 4-Cl, 6-Cl and 5-NHSO 2 -1-napthyl; and R 2 is H or 7-CO 2 H;
wherein R 1 is selected from the group consisting of H and 7-CO 2 H;
R 2 is selected from the group consisting of H, 2-Me, 3′-Me, 3-F and 3-CF 3 ; and
R 3 is selected from the group consisting of H, 2-NHFmoc, 2-NHSO 2 CH 2 Ph, 2-NHSO 2 CH 3 , 2-NHSO 2 (4-tBu)Ph, 2-NHSO 2 (4-NHAc)Ph, 2-NHSO 2 (3-CF 3 )Ph, 2-NHSO 2 (4-NO 2 )Ph, 2-NHSO 2 (4-OMe)Ph, 2-NHSO 2 (4-Br)Ph, 2-NHSO 2 (4-I)Ph, 2-NHSO 2 (4-Ph)Ph, 2-NHSO 2 (4-OPh)Ph, 2-NHAc, 2-NHCO(4-tBu)Ph and 3′-NHSO 2 (4-tBu)Ph.
18. A method of treating pancreatic cancer in a human or non-human mammal, the method comprising administering to the human or non-human mammal a compound of
wherein X is selected from the group consisting of oxygen, NH and CH 2 ; and
R is selected from the group consisting of 3′-CH 2 CH(CO 2 Me)NH 2 , 3′-CH 2 CH(CO 2 Me)NHFmoc, 3′-t-Bu, 3′-OH, 3′-O(CH 2 ) 3 CHCH 2 , 3′-O(CH 2 ) 4 Br, 3′-O(CH 2 ) 4 NMe 2 , 3′-O(CH 2 ) 4 N 3 ,
3′-O(CH 2 ) 4 NH 2 , 3′-CF 3 , 3′-CH 3 , 3′-n-heptyl, 3′-n-nonyl, 3′-i-Bu, 3′-i-propyl, 3′-n-propyl, 3′-n-octyl, 3′-Et, 3′-n-pentyl, 3′-n-Bu, 3′-n-hexyl, 3′-n-cyclopentyl, 3′-n-cyclohexyl, 4-NHSO 2 (4-tBu)Ph and 3′-NHSO 2 (4-tBu)Ph;
wherein R is selected from the group consisting of 4-F, 4-O(CH 2 ) 3 CHCH 2 , 3-Cl, 3-F, 3-Me, 2-Me and 2-OMe;
wherein R 1 is selected from the group consisting of 7-Br, 4-Cl, 5-Br, 5-NO 2 , 5-I, 5-OMe, 5-Cl, 7-CF 3 , 5-NH 2 , 4-Br, 6-Br, H, 7-OMe, 7-I, 5-Et, 7-Et, 4-Et, 6-Et, 5-F, 5-N 3 , 7-COOH, 7-CO 2 H, 4-Cl, 6-Cl and 5-NHSO 2 -1-napthyl; and R 2 is H or 7-CO 2 H;
wherein R 1 is selected from the group consisting of H and 7-CO 2 H;
R 2 is selected from the group consisting of H, 2-Me, 3′-Me, 3-F and 3-CF 3 ; and
R 3 is selected from the group consisting of H, 2-NHFmoc, 2-NHSO 2 CH 2 Ph, 2-NHSO 2 CH 3 , 2-NHSO 2 (4-tBu)Ph, 2-NHSO 2 (4-NHAc)Ph, 2-NHSO 2 (3-CF 3 )Ph, 2-NHSO 2 (4-NO 2 )Ph, 2-NHSO 2 (4-OMe)Ph, 2-NHSO 2 (4-Br)Ph, 2-NHSO 2 (4-I)Ph, 2-NHSO 2 (4-Ph)Ph, 2-NHSO 2 (4-OPh)Ph, 2-NHAc, 2-NHCO(4-tBu)Ph and 3′-NHSO 2 (4-tBu)Ph.
19. A method of treating colon cancer in a human or non-human mammal, the method comprising administering to the human or non-human mammal a compound of
wherein X is selected from the group consisting of oxygen, NH and CH 2 ; and
R is selected from the group consisting of 3′-CH 2 CH(CO 2 Me)NH 2 , 3′-CH 2 CH(CO 2 Me)NHFmoc, 3′-t-Bu, 3′-OH, 3′-O(CH 2 ) 3 CHCH 2 , 3′-O(CH 2 ) 4 Br, 3′-O(CH 2 ) 4 NMe 2 , 3-O(CH 2 ) 4 N 3 ,
3-′-O(CH 2 ) 4 NH 2 , 3′-CF 3 , 3′-CH 3 , 3′-n-heptyl, 3′-n-nonyl, 3′-i-Bu, 3′-i-propyl, 3′-n-propyl, 3′-n-octyl, 3′-Et, 3′-n-pentyl, 3′-n-Bu, 3′-n-hexyl, 3′-n-cyclopentyl, 3′-n-cyclohexyl, 4-NHSO 2 (4-tBu)Ph and 3′-NHSO 2 (4-tBu)Ph;
wherein R is selected from the group consisting of 4-F, 4-O(CH 2 ) 3 CHCH 2 , 3-Cl, 3-F, 3-Me, 2-Me and 2-OMe;
wherein R 1 is selected from the group consisting of 7-Br, 4-Cl, 5-Br, 5-NO 2 , 5-I, 5-OMe, 5-Cl, 7-CF 3 , 5-NH 2 , 4-Br, 6-Br, H, 7-OMe, 7-I, 5-Et, 7-Et, 4-Et, 6-Et, 5-F, 5-N 3 , 7-COOH, 7-CO 2 H, 4-Cl, 6-Cl and 5-NHSO 2 -1-napthyl; and R 2 is H or 7-CO 2 H;
wherein R 1 is selected from the group consisting of H and 7-CO 2 H;
R 2 is selected from the group consisting of H, 2-Me, 3′-Me, 3-F and 3-CF 3 ; and
R 3 is selected from the group consisting of H, 2-NHFmoc, 2-NHSO 2 CH 2 Ph, 2-NHSO 2 CH 3 , 2-NHSO 2 (4-tBu)Ph, 2-NHSO 2 (4-NHAc)Ph, 2-NHSO 2 (3-CF 3 )Ph, 2-NHSO 2 (4-NO 2 )Ph, 2-NHSO 2 (4-OMe)Ph, 2-NHSO 2 (4-Br)Ph, 2-NHSO 2 (4-I)Ph, 2-NHSO 2 (4-Ph)Ph, 2-NHSO 2 (4-OPh)Ph, 2-NHAc, 2-NHCO(4-tBu)Ph and 3′-NHSO 2 (4-tBu)Ph.
20. The method of claim 11 wherein the compound is 3-(5-tert-butyl-2-hydroxy-phenyl)-3-phenyl-1,3,-dihydro-indol-2-one or 4-tert-butyl-N-(5-hydroxy-4-methyl-2-(2-oxo-3-phenylindolin-3-yl)phenyl)benzenesulfonamide.
21. The method of claim 12 wherein the compound is 3-(5-tert-butyl-2-hydroxy-phenyl)-3-phenyl-1,3,-dihydro-indol-2-one or 4-tert-butyl-N-(5-hydroxy-4-methyl-2-(2-oxo-3-phenylindolin-3-yl)phenyl)benzenesulfonamide.
22. The method of claim 13 wherein the compound is 3-(5-tert-butyl-2-hydroxy-phenyl)-3-phenyl-1,3,-dihydro-indol-2-one or 4-tert-butyl-N-(5-hydroxy-4-methyl-2-(2-oxo-3-phenylindolin-3-yl)phenyl)benzenesulfonamide.
23. The method of claim 14 wherein the compound is 3-(5-tert-butyl-2-hydroxy-phenyl)-3-phenyl-1,3,-dihydro-indol-2-one or 4-tert-butyl-N-(5-hydroxy-4-methyl-2-(2-oxo-3-phenylindolin-3-yl)phenyl)benzenesulfonamide.
24. The method of claim 15 wherein the compound is 3-(5-tert-butyl-2-hydroxy-phenyl)-3-phenyl-1,3,-dihydro-indol-2-one or 4-tert-butyl-N-(5-hydroxy-4-methyl-2-(2-oxo-3-phenylindolin-3-yl)phenyl)benzenesulfonamide.
25. The method of claim 16 wherein the compound is 3-(5-tert-butyl-2-hydroxy-phenyl)-3-phenyl-1,3,-dihydro-indol-2-one or 4-tert-butyl-N-(5-hydroxy-4-methyl-2-(2-oxo-3-phenylindolin-3-yl)phenyl)benzenesulfonamide.
26. The method of claim 17 wherein the compound is 3-(5-tert-butyl-2-hydroxy-phenyl)-3-phenyl-1,3,-dihydro-indol-2-one or 4-tert-butyl-N-(5-hydroxy-4-methyl-2-(2-oxo-3-phenylindolin-3-yl)phenyl)benzenesulfonamide.
27. The method of claim 18 wherein the compound is 3-(5-tert-butyl-2-hydroxy-phenyl)-3-phenyl-1,3,-dihydro-indol-2-one or 4-tert-butyl-N-(5-hydroxy-4-methyl-2-(2-oxo-3-phenylindolin-3-yl)phenyl)benzenesulfonamide.
28. The method of claim 19 wherein the compound is 3-(5-tert-butyl-2-hydroxy-phenyl)-3-phenyl-1,3,-dihydro-indol-2-one or 4-tert-butyl-N-(5-hydroxy-4-methyl-2-(2-oxo-3-phenylindolin-3-yl)phenyl)benzenesulfonamide.
29. A method of treating cancer in a human or non-human mammal in need thereof, the method comprising administering to the human or non-human mammal 3-(5-tert-butyl-2-hydroxy-phenyl)-3-phenyl-1,3,-dihydro-indol-2-one or 4-tert-butyl-N-(5-hydroxy-4-methyl-2-(2-oxo-3-phenylindolin-3-yl)phenyl)benzenesulfonamide wherein the cancer is a member selected from the group consisting of breast cancer, lung cancer, melanoma, prostate cancer, leukemia, multiple myeloma, plasmocytoma, pancreatic cancer and colon cancer.
30. The method of claim 29 comprising administering 3-(5-tert-butyl-2-hydroxy-phenyl)-3-phenyl-1,3,-dihydro-indol-2-one.