Anthracycline antibiotics and methods of treating cancer using the same
The present invention discloses new and novel substituted anthracyclines with modified alkyl-aromatic ring substitutions on the C-3′ of the sugar moiety or modified or unmodified alkyl-aromatic ring substitutions at the C-4′ of the sugar moiety. It also discloses novel methods for the preparation of sugar substrates and methods for the preparation of anthracycline antibiotics. These anthracycline analogs show high cytotoxicity in vitro against several tumor cell lines.
1. A method of treating cancer comprising administering to a patient a DNA damaging agent and a substituted anthracycline having the formula:
wherein R is a H or OCH 3 .
2. The method of claim 1 , wherein R is H.
3. The method of claim 1 , wherein R is OCH 3 .
4. The method of claim 1 , wherein the DNA damaging agent is a chemotherapeutic agent.
5. The method of claim 4 , wherein the chemotherapeutic agent is selected from the group consisting of 5-fluorouracil (5FU), etoposide (VP-16), camptothecin, actinomycin-D, mitomycin, cisplatin (CDDP), hydrogen peroxide, carboplatin, procarbazine, mechlorethamine, cyclophosphamide, ifosfamide, melphalan, chlorambucil, bisulfan, nitrosurea, dactinomycin, bleomycin, plicomycin, tamoxifen, taxol, transplatinum, vincristine, vinblastine, and methotrexate.
6. The method of claim 1 , wherein the DNA damaging agent is a radiotherapeutic agent.
7. The method of claim 6 , wherein the radiotherapeutic agent is radiation.
8. The method of claim 7 , wherein the radiation is selected from the group consisting of γ-irradiation, X-rays, UV-irradiation, microwaves, electronic emissions, and radioisotopes.
9. The method of claim 1 , wherein the cancer is breast cancer, lung cancer, ovarian cancer, Hodgkin's disease, non-Hodgkin's lymphoma, acute leukemia, or carcinoma of the testes.
10. The method of claim 1 , wherein the substituted anthracycline is formulated for parenteral administration.
11. The method of claim 1 , wherein the substituted anthracycline is formulated for oral administration.
12. The method of claim 1 , wherein the DNA damaging agent is formulated for parenteral administration.
13. The method of claim 1 , wherein the DNA damaging agent is formulated for oral administration.
14. The method of claim 1 , wherein the substituted anthracycline is administered before the DNA damaging agent is administered to the patient.
15. The method of claim 1 , wherein the substituted anthracycline is administered at the same time the DNA damaging agent is administered to the patient.
16. The method of claim 1 , wherein the substituted anthracycline is administered after the DNA damaging agent is administered to the patient.
17. The method of claim 1 , wherein the DNA damaging agent is administered before the substituted anthracycline is administered to the patient.
18. The method of claim 1 , wherein the DNA damaging agent is administered at the same time the substituted anthracycline is administered to the patient.
19. The method of claim 1 , wherein the DNA damaging agent is administered after the substituted anthracycline is administered to the patient.
20. The method of claim 1 , wherein the substituted anthracycline and the DNA damaging agent are formulated into a single composition.
21. A pharmaceutically acceptable composition comprising a DNA damaging agent and a substituted anthracycline having the formula:
wherein R is a H or OCH 3 .
22. The pharmaceutically acceptable composition of claim 21 , wherein R is H.
23. The pharmaceutically acceptable composition of claim 21 , wherein R is OCH 3 .
24. The pharmaceutically acceptable composition of claim 21 , wherein the DNA damaging agent is a chemotherapeutic agent.
25. The pharmaceutically acceptable composition of claim 24 , wherein the chemotherapeutic agent is selected from the group consisting of 5-fluorouracil (5FU), etoposide (VP-16), camptothecin, actinomycin-D, mitomycin, cisplatin (CDDP), hydrogen peroxide, carboplatin, procarbazine, mechlorethamine, cyclophosphamide, ifosfamide, melphalan, chlorambucil, bisulfan, nitrosurea, doxorubicin, bleomycin, plicomycin, tamoxifen, taxol, transplatinum, vincristine, vinblastine, and methotrexate.
26. The pharmaceutically acceptable composition of claim 21 , wherein the composition is formulated for parenteral administration.
27. The pharmaceutically acceptable composition of claim 21 , wherein the composition is formulated for oral administration.
28. A method of treating cancer comprising administering to a patient a DNA damaging agent and a substituted anthracycline having the formula:
wherein, R 1 is an alkyl chain, a (—COCH 2 R 13 ) group, or a (C(OH)—CH 2 R 13 ) group;
wherein, R 13 is a hydrogen (—H) group, a hydroxyl group (—OH), a methoxy group (—OCH 3 ), an alkoxy group comprising 1-20 carbon atoms, an alkyl group comprising 1-20 carbon atoms, an aryl group comprising 1-20 carbon atoms, a fatty acyl group comprising the general structure —O—CO(CH 2 ) n CH 3 , wherein n=an integer from 1 to about 20, a fatty acyl group comprising the general structure —O—CO(CH 2 ) l (CH═CH) m (CH 2 ) n CH 3 , a —OCO—(CH 2 ) n —CH 2 NH 2 group, or a —OCO—(CH 2 ) n —CO 2 H group, wherein 1 is an integer between 1 to 3, m is an integer between 1 and 6, and n is an integer between 1 and 9;
wherein R 2 and R 3 are, independently of the other, a hydrogen (—H), a hydroxyl group (—OH), or a methoxy group (—OCH 3 );
wherein R 4 is a hydrogen (—H) group, a methoxy group (—OCH 3 ), a hydroxyl group (—OH), or a halide;
wherein Y 1 and Y 2 are, independently of the other, a double bonded oxygen, sulphur, or nitrogen atom;
wherein Z is a —H, —OH, a —CO 2 H, or a —CO 2 R group;
wherein R 5 and R 6 , are, independently, —H, —OH, a halide, —OR 19 , —SH, —SR 19 , —NH 2 , —NHR 19 , —N(R 19 ) 2 or —CH 3 , and R 5 can additionally be an alkylating moiety, wherein R 19 is an alkyl chain, an alkylating moiety, a cycloalkyl chain, a cyclic ring, or a hydrogen;
wherein R 9 is an —H, —CH 3 , alkyl, aryl, CH 2 OH, or CH 2 F group;
wherein R 10 , R 11 , and R 12 are, independently, —H, —OH, a halide, —OR, —SH, —SR, —NH 2 , —NHR, —N(R) 2 or —CH 3 ;
wherein one of R 7 and R 8 is an —H and wherein one of R 7 and R 8 is a X-alkyl aromatic-ring (—XAAR) substituent, wherein, A is an alkyl group and wherein, AR is an unsubstituted phenyl ring, a substituted phenyl ring, a substituted five-member ring or a heteroatomic five-member ring, of the general form:
wherein, R 14 -R 18 are independently a (—H) group, a hydroxyl group (—OH), a methoxy group (—OCH 3 ), a nitro group (—NO 2 ), an amine group (—NH 2 ), a halide, an alkoxy group having 1-20 carbon atoms, an alkyl group having 1-20 carbon atoms, an aryl group having 1-20 carbon atoms, an alkyl-amino group, an alkyl-thio group, a cyano group (CN, SCN), an —CO 2 H group, or a —CO 2 R group; and
X is a —O, —N, —S, —SO, or a —SO 2 group; and
A is (CH 2 ) n , where n=0-10;
wherein if R 7 is a XAAR substituent R 8 is not and if R 8 is a XAAR substituent R 7 is not.
29. The method of claim 28 , wherein the aromatic ring of the —XAAR substituent is disubstituted, trisubstituted, tetrasubstituted, or pentasubstituted.
30. The method of claim 28 , wherein the DNA damaging agent is a chemotherapeutic agent.
31. The method of claim 30 , wherein the chemotherapeutic agent is selected from the group consisting of 5-fluorouracil (5FU), etoposide (VP-16), camptothecin, actinomycin-D, mitomycin, cisplatin (CDDP), hydrogen peroxide, carboplatin, procarbazine, mechlorethamine, cyclophosphamide, ifosfamide, melphalan, chlorambucil, bisulfan, nitrosurea, dactinomycin, bleomycin, plicomycin, tamoxifen, taxol, transplatinum, vincristine, vinblastine, and methotrexate.
32. The method of claim 28 , wherein the DNA damaging agent is a radiotherapeutic agent.
33. The method of claim 28 , wherein the radiotherapeutic agent is radiation.
34. The method of claim 33 , wherein the radiation is selected from the group consisting of γ-irradiation, X-rays, UV-irradiation, microwaves, electronic emissions, and radioisotopes.