Cytotoxic agents comprising taxanes and their therapeutic use
A cytotoxic agent comprising one or more taxanes linked to a cell binding agent. A therapeutic composition for killing selected cell populations comprising: (A) a cytotoxic amount of one or more taxanes covalently bonded to a cell binding agent through a linking group, and (B) a pharmaceutically acceptable carrier, diluent or excipient. A method for killing selected cell populations comprising contacting target cells or tissue containing target cells with an effective amount of a cytotoxic agent comprising one or more taxanes linked to a cell binding agent. Novel sulfur-containing taxanes.
1. A cytotoxic agent comprising one or more taxanes covalently bonded to a cell binding agent through a linking group, wherein at least one of said taxanes is a compound represented by formula (I):
wherein:
R 1 , R 1 ′ and R 1 ″ are the same or different and are H, —F, —NO 2 , —CN, —Cl, —CHF 2 , —CF 3 , —NR 7 R 8 or —OR 9 , wherein R 7 and R 8 are the same or different and are linear alkyl having 1 to 10 carbon atoms, branched or cyclic alkyl having 3 to 10 carbon atoms, or simple or substituted phenyl or naphthyl, and R 9 is linear alkyl having 1 to 10 carbon atoms, or branched or cyclic alkyl having 3 to 10 carbon atoms;
R 2 together with the oxygen atom at the C-10 position forms a linear ester having from 1 to 10 carbon atoms, or a branched or cyclic ester having from 3 to 10 carbon atoms;
R 3 is aryl, linear alkyl having 1 to 10 carbon atoms, or branched or cyclic alkyl having 3 to 10 carbon atoms;
R 4 is —OC(CH 3 ) 3 or phenyl;
R 5 is H; and
R 6 is —(CH 2 ) n SZ, —CO(CH 2 ) n SZ, —(CH 2 ) n CH(CH 3 )SZ, —CO(CH 2 ) n CH(CH 3 )SZ,
—(CH 2 ) n C(CH 3 ) 2 SZ, —CO(CH 2 ) n C(CH 3 ) 2 SZ, —CONR 12 (CH 2 ) n SZ, —CONR 12 (CH 2 ) n CH(CH 3 )SZ, —CONR 12 (CH 2 ) n C(CH 3 ) 2 SZ, —CO-morpholino-XSZ, —CO-piperazino-XSZ, —CO-piperidino-XSZ, or —CO—N-methylpiperazino-XSZ, wherein Z is H or SR, wherein R and R 12 are the same or different and are linear alkyl having 1 to 10 carbon atoms, branched or cyclic alkyl having 3 to 10 carbon atoms, or simple or substituted phenyl, naphthyl or heterocyclic, and R 12 in addition can be H, X is linear alkyl having 1-10 carbon atoms or branched alkyl having 3-10 carbon atoms, and n is an integer of 1 to 10.
2. The cytotoxic agent of claim 1 , wherein R 7 and R 8 each has 1 to 4 carbon atoms.
3. The cytotoxic agent of claim 1 , wherein R 7 and R 8 are the same.
4. The cytotoxic agent of claim 1 , wherein R 1 is in the meta position.
5. The cytotoxic agent of claim 1 , wherein R 1 ′ and R 1 ″ are H.
6. The cytotoxic agent of claim 1 , wherein R 1 is —OCH 3 , R 1 ′ is —OCH 3 , and R 1 ″ is H.
7. The cytotoxic agent of claim 1 , wherein the cell binding agent is selected from the group consisting of antibodies, an antigen specific antibody fragment, interferons, lymphokines, hormones, vitamins, growth factors, colony stimulating factors, and nutrient-transport molecules.
8. The cytotoxic agent of claim 7 , wherein the cell binding agent is an antibody or an antigen specific antibody fragment thereof.
9. The cytotoxic agent of claim 7 , wherein the cell binding agent is a monoclonal antibody or an antigen specific antibody fragment thereof.
10. The cytotoxic agent of claim 9 , wherein the cell binding agent is specific for Common Acute Lymphoblastic Leukemia Antigen (CALLA) or CD19 antigen.
11. The cytotoxic agent of claim 9 , wherein the monoclonal antibody is monoclonal antibody J5 or an anti-B4 monoclonal antibody.
12. The cytotoxic agent of claim 9 , wherein the antigen specific antibody fragment is selected from the group consisting of sFV, Fab, Fab′, and F(ab′) 2 .
13. The cytotoxic agent of claim 1 , wherein the cell-binding agent binds to human cancer cells, wherein the human cancer cells are lung, breast, colon, prostate, kidney, pancreas, ovary, or lymphatic cancer cells.
14. The cytotoxic agent of claim 13 , wherein the cancer cells are solid tumor cells.
15. A therapeutic composition comprising a therapeutically effective amount of the cytotoxic agent of any one of claims 1 - 14 , and a pharmaceutically acceptable carrier.
16. A method of inducing cell death in selected cell populations comprising contacting target cells or tissue containing target cells with an effective amount of the cytotoxic agent of claim 1 , wherein the target cells express a marker that binds to the cell binding agent, and wherein the target cells are human cancer cells selected from the group consisting of lung, breast, colon, prostate, kidney, pancreas, ovary, and lymphatic cancer cells.
17. The method of claim 16 , wherein R 7 and R 8 each has 1 to 4 carbon atoms.
18. The method of claim 16 , wherein R 7 and R 8 are the same.
19. The method of claim 16 , wherein R 1 is in the meta position.
20. The method of claim 16 , wherein R 1 ′ and R 1 ″ are H.
21. The method of claim 16 , wherein R 1 is —OCH 3 , R 1 ′ is —OCH 3 , and R 1 ″ is H.
22. The method of claim 16 , wherein the cell binding agent is selected from the group consisting of antibodies, an antigen specific antibody fragment, interferons, lymphokines, hormones, vitamins, growth factors, colony stimulating factors, and nutrient-transport molecules.
23. The method of claim 16 , wherein the cell binding agent is an antibody or an antigen specific antibody fragment thereof.
24. The method of claim 16 , wherein the cell binding agent is a monoclonal antibody or an antigen specific antibody fragment thereof.
25. The method of claim 24 , wherein the cell binding agent is specific for Common Acute Lymphoblastic Leukemia Antigen (CALLA) or CD19 antigen.
26. The method of claim 25 , wherein the monoclonal antibody is monoclonal antibody J5 or an anti-B4 monoclonal antibody.
27. The method of claim 24 , wherein the antigen specific antibody fragment is selected from the group consisting of sFV, Fab, Fab′, and F(ab′) 2 .
28. The method of claim 16 , wherein the cancer cells are solid tumor cells.