| abstract |
The invention is directed to compounds of Formula (I): wherein Z,X,J,R2 and W are set forth in the specification, as well as solvates, hydrates, tautomers and phannaceutically acceptable salts thereof, that inhibit protein tyrosine kinases, especially c-fins kinase. Methods of treating autoimmune diseases; and disease with an inflammatory component; treating metastasis from ovarian cancer, uterine cancer, breast cancer, prostate cancer, lung cancer, colon cancer, stomach cancer, hairy cell leukemia; and treating pain, including skeletal pain caused by tumor metastasis or osteoarthritis, or visceral, inflammatory, and neurogenic pain; as well as osteoporosis, Paget's disease, and other diseases in which bone resorption mediates morbidity including rheumatoid arthritis, and other forms of inflammatory arthritis, osteoarthritis, prosthesis failure, osteolytic sarcoma, myeloma, and tumor metastasis to bone with the compounds of Formula (I), are also provided. |