Thiazolidinone amides, thiazolidine carboxylic acid amides, and serine amides, including polyamine conjugates thereof, as selective anti-cancer agents
Substituted thiazolidinone carboxylic acid amides and substituted thiazolidine carboxylic acid amides according to formulae (I) and (II) are disclosed where the various substituent groups are as defined in the specification. Methods of making these compounds, pharmaceutical compositions containing the compounds, and their use, particularly for treating or preventing cancer, are also disclosed.
1. A method of destroying a melanoma cell comprising:
providing a compound according to formula (II)
wherein
X 1 and X 2 are each optional, and each can be oxygen;
X 3 is oxygen or sulfur;
R 1 is
where m is an integer from 0 to 10;
R 2 is an aliphatic straight- or branched-chain C1 to C30 hydrocarbon;
R 3 is hydrogen or an aliphatic straight- or branched-chain C1 to C10 hydrocarbon;
R 4 is optional, or can be hydrogen or an aliphatic or non-aliphatic straight- or branched-chain C1 to C10 hydrocarbon; and
R 5 , R 6 , R 7 , R 8 , and R 9 are independently selected from the group of hydrogen, hydroxyl, an aliphatic or non-aliphatic straight- or branched-chain C1 to C10 hydrocarbon, alkoxy, aryloxy, nitro, cyano, chloro, fluoro, bromo, iodo, haloalkyl, dihaloalkyl, trihaloalkyl, amino, alkylamino, dialkylamino, acylamino, arylamino, amido, alkylamido, dialkylamido, arylamido, aryl, C5 to C7 cycloalkyl, and arylalkyl; and
contacting the melanoma cell with the compound under conditions effective to kill the melanoma cell.
2. The method according to claim 1 wherein R 1 is benzyl, phenyl, or a substituted phenyl.
3. The method according to claim 1 wherein R 2 is an aliphatic straight- or branched-chain C8 to C24 hydrocarbon.
4. The method according to claim 1 wherein R 2 is an aliphatic straight- or branched-chain C14 to C18 alkyl.
5. The method according to claim 1 wherein the compound is
(4S)-N-octadecyl-2-phenylthiazolidine-4-carboxamide;
(4R)-N-tetradecyl-2-phenylthiazolidine-4-carboxamide hydrochloride;
(4S)-N-tetradecyl-2-phenylthiazolidine-4-carboxamide hydrochloride;
(4R)-2-(4-methoxyphenyl)-N-octadecylthiazolidine-4-carboxamide;
(4S)-2-(4-methoxyphenyl)-N-octadecylthiazolidine-4-carboxamide;
(4R)-2-(2,4,6-trimethoxyphenyl)-N-octadecylthiazolidine-4-carboxamide;
(4S)-2-(2,4,6-trimethoxyphenyl)-N-octadecylthiazolidine-4-carboxamide;
(4R)-2-(3,4,5-trimethoxyphenyl)-N-octadecylthiazolidine-4-carboxamide;
(4S)-2-(3,4,5-trimethoxyphenyl)-N-octadecylthiazolidine-4-carboxamide;
(4R)-2-(3,4-dimethoxyphenyl)-N-octadecylthiazolidine-4-carboxamide;
(4S)-2-(3,4-dimethoxyphenyl)-N-octadecylthiazolidine-4-carboxamide
(4R)-2-(4-acetamidophenyl)-N-octadecylthiazolidine-4-carboxamide;
(4S)-2-(4-acetamidophenyl)-N-octadecylthiazolidine-4-carboxamide;
(4R)-2-(4-methoxyphenyl)-N-tetradecylthiazolidine-4-carboxamide;
(4S)-2-(4-methoxyphenyl)-N-tetradecylthiazolidine-4-carboxamide;
(4R)-2-(2,4,6-trimethoxyphenyl)-N-tetradecylthiazolidine-4-carboxamide;
(4S)-2-(2,4,6-trimethoxyphenyl)-N-tetradecylthiazolidine-4-carboxamide;
(4R)-2-(3,4,5-trimethoxyphenyl)-N-tetradecylthiazolidine-4-carboxamide;
(4S)-2-(3,4,5-trimethoxyphenyl)-N-tetradecylthiazolidine-4-carboxamide;
(4R)-2-(3,4-dimethoxyphenyl)-N-tetradecylthiazolidine-4-carboxamide;
(4S)-2-(3,4-dimethoxyphenyl)-N-tetradecylthiazolidine-4-carboxamide
(4R)-2-(4-acetamidophenyl)-N-tetradecylthiazolidine-4-carboxamide; or
(4S)-2-(4-acetamidophenyl)-N-tetradecylthiazolidine-4-carboxamide; and salts thereof.
6. A method of treating melanoma comprising:
providing a compound according to formula (II)
wherein
X 1 and X 2 are each optional, and each can be oxygen;
X 3 is oxygen or sulfur;
R 1 is
where m is an integer from 0 to 10;
R 2 is an aliphatic straight- or branched-chain C1 to C30 hydrocarbon,
R 3 is hydrogen or an aliphatic straight- or branched-chain C1 to C10 hydrocarbon;
R 4 is optional, or can be hydrogen or an aliphatic or non-aliphatic straight- or branched-chain C1 to C10 hydrocarbon;
R 5 , R 6 , R 7 , R 8 , and R 9 are independently selected from the group of hydrogen, hydroxyl, an aliphatic or non-aliphatic straight- or branched-chain C1 to C10 hydrocarbon, alkoxy, aryloxy, nitro, cyano, chloro, fluoro, bromo, iodo, haloalkyl, dihaloalkyl, trihaloalkyl, amino, alkylamino, dialkylamino, acylamino, arylamino, amido, alkylamido, dialkylamido, arylamido, aryl, C5 to C7 cycloalkyl, and arylalkyl; and
administering the compound to a patient having melanoma, wherein said administering is effective to kill melanoma cells and thereby treat the melanoma.
7. The method according to claim 6 wherein R 1 is benzyl, phenyl, or a substituted phenyl.
8. The method according to claim 6 wherein R 2 is an aliphatic straight- or branched-chain C8 to C24 hydrocarbon.
9. The method according to claim 6 wherein R 2 is an aliphatic straight- or branched-chain C14 to C18 alkyl.
10. The method according to claim 6 wherein the compound is
(4S)-N-octadecyl-2-phenylthiazolidine-4-carboxamide;
(4R)-N-tetradecyl-2-phenylthiazolidine-4-carboxamide hydrochloride;
(4S)-N-tetradecyl-2-phenylthiazolidine-4-carboxamide hydrochloride;
(4R)-2-(4-methoxyphenyl)-N-octadecylthiazolidine-4-carboxamide;
(4S)-2-(4-methoxyphenyl)-N-octadecylthiazolidine-4-carboxamide;
(4R)-2-(2,4,6-trimethoxyphenyl)-N-octadecylthiazolidine-4-carboxamide;
(4S)-2-(2,4,6-trimethoxyphenyl)-N-octadecylthiazolidine-4-carboxamide;
(4R)-2-(3,4,5-trimethoxyphenyl)-N-octadecylthiazolidine-4-carboxamide;
(4S)-2-(3,4,5-trimethoxyphenyl)-N-octadecylthiazolidine-4-carboxamide;
(4R)-2-(3,4-dimethoxyphenyl)-N-octadecylthiazolidine-4-carboxamide;
(4S)-2-(3,4-dimethoxyphenyl)-N-octadecylthiazolidine-4-carboxamide (4R)-2-(4-acetamidophenyl)-N-octadecylthiazolidine-4-carboxamide;
(4S)-2-(4-acetamidophenyl)-N-octadecylthiazolidine-4-carboxamide;
(4R)-2-(4-methoxyphenyl)-N-tetradecylthiazolidine-4-carboxamide;
(4S)-2-(4-methoxyphenyl)-N-tetradecylthiazolidine-4-carboxamide;
(4R)-2-(2,4,6-trimethoxyphenyl)-N-tetradecylthiazolidine-4-carboxamide;
(4S)-2-(2,4,6-trimethoxyphenyl)-N-tetradecylthiazolidine-4-carboxamide;
(4R)-2-(3,4,5-trimethoxyphenyl)-N-tetradecylthiazolidine-4-carboxamide;
(4S)-2-(3,4,5-trimethoxyphenyl)-N-tetradecylthiazolidine-4-carboxamide;
(4R)-2-(3,4-dimethoxyphenyl)-N-tetradecylthiazolidine-4-carboxamide;
(4S)-2-(3,4-dimethoxyphenyl)-N-tetradecylthiazolidine-4-carboxamide
(4R)-2-(4-acetamidophenyl)-N-tetradecylthiazolidine-4-carboxamide; or
(4S)-2-(4-acetamidophenyl)-N-tetradecylthiazolidine-4-carboxamide; and salts thereof.
11. The method according to claim 6 , wherein said administering is carried out systemically.
12. The method according to claim 6 , wherein said administering is carried out directly to a site where melanoma cells are present.
13. The method according to claim 6 , wherein said administering is carried out orally, topically, transdermally, parenterally, subcutaneously, intravenously, intramuscularly, intraperitoneally, by intranasal instillation, by intracavitary or intravesical instillation, intraocularly, intraarterially, intralesionally, or by application to mucous membranes.
14. The method according to claim 6 wherein the melanoma is malignant melanoma.
15. The method according to claim 6 wherein the melanoma is non-malignant melanoma.
16. The method according to claim 6 , wherein the compound is administered at a dosage rate of about 0.01 to about 100 mg/kg·body weight.
17. The method according to claim 6 , wherein said administering is repeated periodically.
18. The method according to claim 6 , wherein said administering is carried out in combination with another melanoma therapy.
19. The method according to claim 18 , wherein the other melanoma therapy is selected from the group of radiation therapy, chemotherapy, surgical intervention, and combinations thereof.
20. The method according to claim 1 , wherein R 2 is a C10 to C20 alkyl group.
21. The method according to claim 1 , wherein R 2 is a C2 to C30 alkenyl group.
22. The method according to claim 1 , wherein R 1 is 4-methoxyphenyl, 4-ethoxyphenyl, 3,5-difluorophenyl, 4-cyanophenyl, p-tolyl,4-hydroxyphenyl, 3-hydroxyphenyl, 2,4,6-trimethoxyphenyl, 3,4-dimethoxyphenyl, 3,4,5-trimethoxyphenyl, 4-acetamidophenyl, 4-fluorophenyl, 2,6-dichiorophenyl, 4-bromophenyl, 4-nitrophenyl, 4-(dimethylamino)phenyl, or 3-bromo-4-fluorophenyl.
23. The method according to claim 1 , wherein R 5 , R 6 , R 7 , R 8 , and R 9 are independently selected from the group of hydrogen, hydroxyl, alkoxy, amino, alkylamino, dialkylamino, acylamino, amido, alkylamido, and dialkylamido.
24. The method according to claim 6 , wherein R 2 is a C10 to C20 alkyl group.
25. The method according to claim 6 , wherein R 2 is a C2 to C30 alkenyl group.
26. The method according to claim 6 , wherein R 1 is 4-methoxyphenyl, 4-ethoxyphenyl, 3,5-difluorophenyl, 4-cyanophenyl, p-tolyl,4-hydroxyphenyl, 3-hydroxyphenyl, 2,4,6-trimethoxyphenyl, 3,4-dimethoxyphenyl, 3,4,5-trimethoxyphenyl, 4-acetamidophenyl, 4-fluorophenyl, 2,6-dichiorophenyl, 4-bromophenyl, 4-nitrophenyl, 4-(dimethylamino)phenyl, or 3-bromo-4-fluorophenyl.
27. The method according to claim 6 , wherein R 5 , R 6 , R 7 , R 8 , and R 9 are independently selected from the group of hydrogen, hydroxyl, alkoxy, amino, alkylamino, dialkylamino, acylamino, amido, alkylamido, and dialkylamido.