Methods for inhibiting angiogenesis
View Patent ↗Novel methods for inhibiting angiogenesis and treating diseases associated with angiogenesis are described. The methods may comprise administering to a patient an effective amount of a 1,2-dithiol-3-thione derivative or metabolite thereof. Preferred compounds for use in the methods include 5-(2-pyrazinyl)-4methyl-1,2-dithiol-3-thione (Oltipraz) and its metabolites.
1. A method for inhibiting angiogenesis in a patient comprising administering to said patient an anti-angiogenically effective amount of a 1,2-dithiol-3-thione derivative selected from the group consisting of 5-(2-pyrazinyl)-1,2-diothiol-3-thione (ADT), and 5-(2-pyrazinyl)-4-methyl-1,2-diothiol-3-thione or a metabolite thereof and determining the anti-angiogenic effect on said patient produced by said derivative or metabolite thereof.
2. The method according to claim 1 wherein said 1,2-dithiol-3-thione derivative is 5-(2-pyrazinyl)-4-methyl-1,2-dithiol-3-thione.
3. A method for inhibiting the growth or metastasis of an angiogenesis-dependent tumor in a patient comprising administering to said patient an effective amount of an anti-angiogenic agent, wherein said anti-angiogenic agent comprises a compound of the following formula (I):
wherein:
Ar is a monocyclic or bicyclic aryl group or a monocyclic or bicyclic heteroaryl group containing 1 to 3 —O—, —S— or N(R 2 ) m heteroatoms, wherein m is 0 or 1; and
R 1 and R 2 are independently hydrogen or an alkyl group; or a steroisomer, prodrug, metabolite, or pharmaceutically acceptable salt, hydrate or N-oxide thereof and determining the anti-angiogenic effect on said tumor produced by said compound.
4. The method according to claim 3 wherein Ar is a monocyclic or bicyclic heteroaryl group containing 1 to 3 oxygen, sulfur or nitrogen heteroatoms.
5. The method according to claim 4 wherein Ar is a monocylic heteroaryl group containing 1 to 2 nitrogen atoms.
6. The method according to claim 5 wherein Ar is selected from the group consisting of pyridyl, pyridazinyl, pyrimidinyl and pyrazinyl.
7. The method according to claim 6 wherein Ar is pyrazinyl.
8. The method according to claim 3 wherein R 1 is hydrogen.
9. The method according to claim 3 comprising administering to said patient a metabolite of the compound of formula (I).
10. The method according to claim 9 wherein said metabolite has the following formula (II):
wherein:
X 1 is C(R 6 ) y or N(R 7 ) n in which y is an integer 1 or 2, and n is an integer 0 or 1;
X 2 and X 3 are each independently —O—, —S(O) x — where x is an integer 0, 1 or 2, or —N(R 8 );
X 4 is C(R 6 ) y or C(═O), in which y is an integer 1 or 2;
R 3 is hydrogen, alkyl, the residue of glucuronic acid, or the radical
R 4 , R 5 and R 6 are each independently hydrogen or alkyl;
R 7 is hydrogen or the residue of glucuronic acid;
R 8 is hydrogen or alkyl; and X 1 , X 2 , X 3 and X 4 are as previously defined.
11. The method according to claim 10 wherein:
X 1 is N;
X 2 and X 3 are —S—; and
R 3 , R 4 and R 5 are methyl.
12. The method according to claim 3 , wherein said anti-angiogenic effect is determined by measuring the tumor burden in said patient.
13. A method for inhibiting the growth or metastasis of an angiogenesis-dependent tumor in a patient comprising administering to said patient an effective amount of an anti-angiogenic agent, wherein said anti-angiogenic agent comprises a 1,2-dithiol-3-thione derivative selected from the group consisting of 5-(2-pyrazinyl)-1,2-diothiol-3-thione (ADT), and 5-(2-pyrazinyl)-4-methyl-1,2-diothiol-3-thione or a metabolite thereof and determining the anti-angiogenic effect on said tumor produced by said 1,2-diothiol-3-thione derivative or metabolite thereof.
14. The method according to claim 13 wherein said 1,2-dithiol-3-thione derivative is 5-(2-pyrazinyl)-4-methyl-1,2-dithiol-3-thione.
15. The method according to claim 13 , wherein said anti-angiogenic effect is determined by measuring the tumor burden in said patient.
16. A method for treating a disease or disorder associated with angiogensesis in a patient, said disease or disorder being selected from the group consisting neoplastic diseases, restenosis, rheumatoid arthritis, Crohn's disease, diabetic retinopathy, psoriasis, endometriosis, macular degeneration, neovascular glaucoma, and adiposity, comprising administering to said patient an effective amount of an anti-angiogenic agent, wherein said anti-angiogenic agent comprises a compound of the following formula (I):
wherein:
Ar is a monocyclic or bicyclic aryl group or a monocyclic or bicyclic heteroaryl group containing 1 to 3 —O—, —S— or —N(R2)m heteroatoms, wherein m is 0 or 1; and
R1 and R2 are independently hydrogen or an alkyl group; or a steroisomer, prodrug, metabolite, or pharmaceutically acceptable salt, hydrate or N-oxide thereof and determining the anti-angiogenic effect on said patient produced by said compound.
17. The method according to claim 16 wherein Ar is a monocyclic or bicyclic heteroaryl group containing 1 to 3 oxygen, sulfur or nitrogen heteroatoms.
18. The method according to claim 17 wherein Ar is a monocylic heteroaryl group containing 1 to 2 nitrogen atoms.
19. The method according to claim 18 wherein Ar is selected from the group consisting of pyridyl, pyridazinyl, pyrimidinyl and pyrazinyl.
20. The method according to claim 19 wherein Ar is pyrazinyl.
21. The method according to claim 16 wherein R 1 is hydrogen.
22. The method according to claim 16 comprising administering to said patient a metabolite of the compound of formula (I).
23. The method according to claim 22 wherein said metabolite has the following formula (II):
wherein:
X 1 is C(R 6 ) y or N(R 7 ) n in which y is an integer 1 or 2, and n is an integer 0 or 1;
X 2 and X 3 are each independently —O—, —S(O) x — where x is an integer 0, 1 or 2, or —N(R 8 );
X 4 is C(R 6 ) y or C(═O), in which y is an integer 1 or 2;
R 3 is hydrogen, alkyl, the residue of glucuronic acid, or the radical
R 4 , R 5 and R 6 are each independently hydrogen or alkyl;
R 7 is hydrogen or the residue of glucuronic acid;
R 8 is hydrogen or alkyl and X 1 , X 2 , X 3 and X 4 are as previously defined.
24. The method according to claim 23 wherein:
X 1 is N;
X 2 and X 3 are —S—; and
R 3 , R 4 and R 5 are methyl.
25. The method according to claim 16 , wherein said disease or disorder is a neoplastic disease.
26. The method according to claim 25 , wherein said neoplastic disease is cancer.
27. The method according to claim 25 , wherein said an anti-angiogenic effect is determined on the basis of neoplasm regression.
28. The method according to claim 27 , wherein neoplasm regression is demonstrated by reduced size.
29. The method according to claim 27 , wherein neoplasm regression is demonstrated by reduced neoplasm number.
30. The method according to claim 25 , wherein said anti-angiogenic effect is determined on the basis of reduced neovascularization.
31. A method for treating a disease or disorder associated with angiogenesis in a patient, said disease or disorder being selected from the group consisting of neoplastic diseases, restenosis, rheumatoid arthritis, Crohn's disease, diabetic retinopathy, psoriasis, endometriosis, macular degeneration, neovascular glaucoma, and adiposity, comprising administering to said patient an effective amount of an anti-angiogenic agent, wherein said anti-angiogenic agent comprises a 1,2-dithiol-3-thione derivative selected from the group consisting of 5-(2-pyrazinyl)1,2-diothiol-3-thione (APT), and 5-(2-pyrazinyl)-4-methyl-1,2-diothiol-3-thione or a metabolite thereof and determining the anti-angiogenic effect on said patient produced by said 1,2-dithiol-3-thione derivative or metabolize thereof.
32. The method according to claim 31 wherein said 1,2-dithiol-3-thione derivative is 5-(2-pyrazinyl)-4-methyl-1,2-dithiol-3-thione.