Compositions for modulating a kinase cascade and methods of use thereof
The invention relates to compositions comprising 2-(5-(4-(2-morpholinoethoxy)phenyl)pyridin-2-yl)-N-benzylacetamide and its mesylate and dihydrochloride salts. The invention provides an efficient process for the synthesis of 2-(5-(4-(2-morpholinoethoxy)phenyl)pyridin-2-yl)-N-benzylacetamide and its mesylate and dihydrochloride salts and methods for modulating one or more components of a kinase cascade using the compositions of the invention. The present invention also provides a novel polymorph of the mesylate salt of 2-(5-(4-(2-morpholinoethoxy)phenyl)pyridin-2-yl)-N-benzylacetamide (Form A), characterized by a unique X-ray diffraction pattern and Differential Scanning Calorimetry profile, as well as a unique crystalline structure.
1. A composition comprising KX2-391 MSA, Form A, wherein the KX2-391 MSA, Form A has a purity greater than 98.0% as determined by HPLC.
2. The composition of claim 1 , wherein the KX2-391 MSA, Form A has a purity of 99.0%.
3. The composition of claim 1 , wherein the KX2-391 MSA, Form A has a purity of 99.5%.
4. The composition of claim 1 , wherein the KX2-391 MSA, Form A has a purity of 99.6%.
5. The composition of claim 1 , wherein the KX2-391 MSA, Form A has a purity of 99.7%.
6. The composition of claim 1 , wherein the composition contains less than 2% of an impurity selected from ethyl chloride, ethanol, ethyl acetate, heptane, anisole, palladium, and combinations thereof.
7. The composition of claim 1 further comprising a pharmaceutically acceptable carrier or excipient.
8. A method of treating a disease or disorder in a subject in need thereof comprising administering a composition of claim 1 to said subject, wherein the disease or disorder is selected from proliferative disorders, osteoporosis, cardiovascular disorders, immune system dysfunction, type II diabetes, obesity, hearing loss, stroke, ophthalmic disease, atherosclerosis, neuropathic pain, hepatitis B, autoimmune disease, and transplant rejection.
9. The method of claim 8 , wherein the disorder is proliferative disorder.
10. The method of claim 9 , wherein the proliferative disorder is colon cancer, lung cancer, or prostate cancer.
11. The method of claim 8 , wherein the disease is ophthalmic disease.
12. The method of claim 11 , wherein the ophthalmic disease is macular degeneration, retinopathy, or macular edema.
13. The method of claim 8 , wherein the disease is autoimmune disease.
14. The method of claim 13 , wherein the autoimmune disease is rheumatoid arthritis, multiple sclerosis, or lupus.
15. The method of claim 8 , wherein the composition is administered orally.
16. The method of claim 8 , wherein the composition is administered topically.
17. The method of claim 9 , wherein the proliferative disorder is psoriasis, acute myelocytic leukemia, chronic myelocytic leukemia, gastric cancer, breast cancer, or ovarian cancer.
18. The method of claim 9 , wherein the proliferative disorder is malignant melanoma, non-melanoma skin cancer, epidermic or dermoid cyst, lipoma, adenoma, capillary or cutaneous hemangioma, lymphangioma, nevi lesion, teratoma, nephroma, myofibromatosis, osteoplastic tumor, dysplastic mass, or dysplasia.
19. The method of claim 9 , wherein the proliferative disorder is brain cancer, liver cancer, pancreatic cancer, hematologic tumor, childhood leukemia, lymphoma, multiple myeloma, Hodgkin's disease, lymphoma of lymphocytic or cutaneous origin, acute or chronic leukemia, acute lymphoblastic leukemia, plasma cell neoplasm, lymphoid neoplasm, or cancer associated with AIDS.