Prodrugs of glutamine analogs
The disclosure provides compounds having formula (I): and the pharmaceutically acceptable salts thereof, wherein R 1 , R 2 , R 2 ′, and X are as defined as set forth in the specification. Compounds having formula (I) are prodrugs that release glutamine analogs, e.g., 6-diazo-5-oxo-L-norleucine (DON). The disclosure also provides compounds having formula (I) for use in treating cancer.
1. A method of treating cancer in a subject, the method comprising administering to the subject in need thereof a compound having formula (I):
or a pharmaceutically acceptable salt thereof, wherein:
X is —(CH 2 ) n —, wherein n is 1;
R 1 is selected from the group consisting of H, C 1-6 alkyl, substituted C 1-6 alkyl, C 3 -C 10 cycloalkyl, substituted C 3 -C 10 cycloalkyl, C 2 -C 6 alkenyl, and substituted C 2 -C 6 alkenyl;
R 2 is an amino acid or an N-substituted amino acid; and
R 2 ′ is selected from the group consisting of H, C 1 -C 6 alkyl, and substituted C 1 -C 6 alkyl;
wherein the cancer is hepatocellular cancer, brain cancer, lung cancer, breast cancer, head and neck cancer, pancreatic cancer, prostate cancer, melanoma, colorectal cancer, acute lymphoblastic leukemia, acute myelogenous leukemia, or chronic myelocytic leukemia.
2. The method of claim 1 , wherein R 1 is selected from the group consisting of methyl, ethyl, isopropyl, cyclopentyl, and cyclohexyl.
3. The method of claim 1 , wherein R 2 is a N-acyl amino acid.
4. The method of claim 3 , wherein the amino acid is tryptophan.
5. The method of claim 1 , wherein the compound of formula (I) is selected from the group consisting of:
6. The method of claim 5 , wherein the compound of formula (I) is:
7. A method of treating cancer in a subject, the method comprising administering to the subject in need thereof a compound having formula (IIA):
or a pharmaceutically acceptable salt thereof, wherein:
R 1 is selected from the group consisting of H and C 1-6 alkyl;
R 11 is selected from the group consisting of H, methyl, isopropyl, sec-butyl, CH 2 CH(CH 3 ) 2 , benzyl, p-hydroxybenzyl CH 2 OH, CH(OH)CH 3 , CH 2 -3-indoyl, CH 2 COOH, CH 2 CH 2 COOH, —CH 2 C(O)NH 2 , CH 2 CH 2 C(O)NH 2 , CH 2 SH, CH 2 CH 2 SCH 3 , (CH 2 ) 4 NH 2 , (CH 2 ) 3 NHC(═NH)NH 2 , and CH 2 -3-imidazoyl;
R 12 is selected from the group consisting of H, C 1-4 alkyl, and —C(═O)R 13 ; and
R 13 is C 1-4 alkyl,
wherein the cancer is hepatocellular cancer, brain cancer, lung cancer, breast cancer, head and neck cancer, pancreatic cancer, prostate cancer, melanoma, colorectal cancer, acute lymphoblastic leukemia, acute myelogenous leukemia, or chronic myelocytic leukemia.
8. The method of claim 7 , wherein the cancer is hepatocellular cancer.
9. The method of claim 7 , wherein the cancer is brain cancer.
10. The method of claim 7 , wherein the cancer is lung cancer.
11. The method of claim 7 , wherein the cancer is breast cancer.
12. The method of claim 7 , wherein the cancer is head and neck cancer.
13. The method of claim 7 , wherein the cancer is pancreatic cancer.
14. The method of claim 7 , wherein the cancer is prostate cancer.
15. The method of claim 7 , wherein the cancer is melanoma.
16. The method of claim 7 , wherein the cancer is colorectal cancer.
17. The method of claim 7 , wherein the cancer is acute lymphoblastic leukemia.
18. The method of claim 7 , wherein the cancer is acute myelogenous leukemia.
19. The method of claim 7 , wherein the cancer is chronic myelocytic leukemia.