Antitumor agents
The invention provides compounds of formula I: wherein Y is F, Cl, Br, methyl or methoxy; and pharmaceutically acceptable salts thereof. The compounds are effective antitumor agent. The invention also provides pharmaceutical compositions comprising a compound of formula I or a salt thereof, intermediates useful for preparing a compound of formula I, and therapeutic methods comprising administering a compound of formula I or a salt thereof to a mammal in need thereof.
1. A therapeutic method to inhibit tumor cell growth in a mammal, comprising administering to a mammal in need of such therapy an effective amount of a composition comprising a compound of formula I:
wherein
Y is F, Cl, Br, methyl or methoxy; and
Z is an alkali metal cation or alkaline earth metal cation;
and a pharmaceutically acceptable diluent or carrier.
2. The method of claim 1 wherein the composition is formulated for oral, parenteral, intravenous, intramuscular, subcutaneous, or topical administration.
3. The method of claim 2 wherein Y is Cl or Br.
4. The method of claim 3 wherein Z of formula I is a Li cation, Na cation, K cation, Rb cation, Cs cation, Ca cation, Mg cation, or Ba cation.
5. The method of claim 4 wherein the composition is formulated for oral administration and is in the form of a tablet, buccal tablet, troche, capsule, elixir, suspension, syrup, or wafer.
6. The method of claim 5 wherein the composition comprises at least 0.1 weight % of the compound of formula I.
7. The method of claim 6 wherein the composition comprises between about 2 weight % to about 60 weight % of the compound of formula I.
8. The method of claim 2 wherein the composition is formulated for administration by infusion or injection, and the pharmaceutically acceptable diluent or carrier comprises water.
9. The method of claim 8 wherein the composition comprises at least 0.1 weight % of the compound of formula I.
10. The method of claim 9 wherein the composition comprises between about 2 weight % to about 60 weight % of the compound of formula I.
11. The method of claim 8 wherein the compound of formula I is encapsulated in a liposome.
12. The method of claim 2 wherein the configuration of the carbon indicated by the asterisk in formula I is the (R) configuration.
13. The method of claim 12 wherein the cancer is colon cancer, breast cancer, melanoma, pancreatic cancer, or leukemia.
14. The method of claim 13 wherein the cancer is pancreatic ductal adenocarcinoma, mammary adenocarcinoma, or colon carcinoma.
15. The method of claim 12 wherein the compound of formula I is (R) 2[4-(7-chloroquinolin-2-yloxy)phenoxy]propionic acid sodium salt or (R) 2[4-(7-bromoquinolin-2-yloxy)phenoxy]propionic acid sodium salt.
16. A therapeutic method to inhibit tumor cell growth in a mammal, comprising administering to a mammal in need of such therapy an effective amount of a composition comprising a compound of formula I:
wherein
Y is F, Cl, Br, methyl or methoxy;
Z is an alkali metal cation or alkaline earth metal cation; and
the configuration of the carbon indicated by the asterisk in formula I is the (R) configuration; and
a pharmaceutically acceptable diluent or carrier comprising water.
17. The method of claim 16 wherein the compound of formula I is (R) 2[4-(7-chloroquinolin-2-yloxy)phenoxy]propionic acid sodium salt or (R) 2[4-(7-bromoquinolin-2-yloxy)phenoxy]propionic acid sodium salt.
18. The method of claim 17 wherein the composition is formulated for oral, parenteral, intravenous, intramuscular, subcutaneous, or topical administration.
19. The method of claim 18 wherein the cancer is colon cancer, breast cancer, melanoma, pancreatic cancer, or leukemia.
20. The method of claim 19 wherein the cancer is pancreatic ductal adenocarcinoma, mammary adenocarcinoma, or colon carcinoma.