Aminopyrimidine kinase inhibitors
Disclosed are compounds, pharmaceutical compositions containing those compounds, and uses of the compounds and compositions as modulators of CK1, CK1γ1, CK1γ2, CK1γ3, CK2, Pim 1, Pim2, Pim3, the TGFβ pathway, the Wnt pathway, the JAK/STAT pathway, the AKT pathway, and/or the mTOR pathway. Uses are also disclosed for the treatment or prevention of a range of therapeutic indications due at least in part to aberrant physiological activity of CK1, CK1γ1, CK1γ2, CK1γ3, CK2, Pim 1, Pim2, Pim3, the TGFβ pathway, the Wnt pathway, the JAK/STAT pathway, the AKT pathway, and/or the mTOR pathway.
1. A method of treating cancer, comprising administering to a mammal in need thereof a therapeutically effective amount of a compound of formula 1 or a pharmaceutically acceptable salt thereof:
wherein independently for each occurrence:
X is —N(R 7 ) 2 , —N(R 7 )(R 2 ), or —N(H)—R 3 —R 6 ;
R′ is H, methyl, (C 2 -C 4 )alkyl, or benzyl;
R 2 is H, —CH 2 OP(═O)(OH) 2 , —CH 2 O(P═O)(OR 8 ) 2 , —(C═O)OCHR 8 O(C═O)CH 3 , or —(C═O)OCH 2 O(P═O)(OH) 2 ;
R 3 is —C(═NR)— or —(C(R) 2 ) n —;
R 5 is selected from the group consisting of 1,4-cyclohexanediyl, 1,4-phenylene, 1,4-cycloheptanediyl, 1,4-cyclooctanediyl, 1,5-cyclooctanediyl, bicyclo[2.2.1]heptanediyl, 1,4-bicyclo[2.2.2]octanediyl, and 1,5-bicyclo[3.3.1]nonanediyl;
R 6 is selected from the group consisting of alkyl, alkylaryl, aryl, alkylheteroaryl, alkylheteroalkyl, and heteroaryl, any of which is optionally mono or di-substituted, and the substituents, if present, are independently selected from the group consisting of alkyl, alkylaryl, aralkyl, aryl, heteroaryl, alkoxy, hydroxy, perfluoroalkyl, trifluoromethoxy, and halide, wherein the optional aryl or heteroaryl substituent may be optionally substituted with alkyl, halide, alkoxy, perfluoroalkyl, or dioxolanyl;
R 7 is selected from the group consisting of H, —C(═NR)R, —(C(R) 2 ) n R, alkyl, alkylaryl, aryl, alkylheteroaryl, alkylheteroalkyl, and heteroaryl, any of which is optionally mono or di-substituted, and the substituents, if present, are independently selected from the group consisting of alkyl, alkylaryl, aralkyl, aryl, heteroaryl, alkoxy, hydroxy, perfluoroalkyl, trifluoromethoxy, and halide, wherein the optional aryl or heteroaryl substituent may be optionally substituted with alkyl, halide, alkoxy, perfluoroalkyl, or dioxolanyl, or
two instances of R 7 and the nitrogen to which they are bonded taken together represent a nitrogen-containing heterocyclyl, optionally containing one additional heteroatom in the ring, wherein said additional heteroatom is selected from the group consisting of —O—, —N(R)—, and —S—;
R 8 is H, alkyl, benzyl, t-butyl, aryl, or heteroaryl;
R is H or (C 1 -C 4 )alkyl; and
n is 1, 2 or 3;
wherein the cancer is selected from the group consisting of:
adrenocortical carcinoma; anal cancer; basal cell carcinoma; bladder cancer; breast cancer; bronchial adenomas/carcinoids; cervical cancer; colon cancer; colorectal cancer; endometrial cancer; esophageal cancer; extrahepatic bile duct cancer; gallbladder cancer; gastric (stomach) cancer; gastrointestinal carcinoid tumor; gestational trophoblastic tumor; head and neck cancer, hepatocellular (liver) cancer; hypopharyngeal cancer; kidney (renal cell) cancer; laryngeal cancer; lip and oral cavity cancer; metastatic squamous neck cancer with occult primary; multiple endocrine neoplasia syndrome; nasal cavity and paranasal sinus cancer; nasopharyngeal cancer; Non-Small Cell Lung cancer; oral cancer; oropharyngeal cancer; pancreatic cancer; parathyroid cancer; penile cancer; pituitary tumor; prostate cancer; rectal cancer; salivary gland cancer; skin carcinoma, Merkel Cell; small cell lung cancer; small intestine cancer; squamous cell carcinoma; thymoma; thymoma and thymic carcinoma; thyroid cancer; transitional cell cancer of the renal pelvis and ureter; urethral cancer; uterine cancer, endometrial; vaginal cancer; vulvar cancer; Wilms' Tumor;
acute lymphoblastic leukemia; acute myeloid leukemia; AIDS-related lymphoma; Burkitt's lymphoma; chronic lymphocytic leukemia; chronic myelogenous leukemia; chronic myeloproliferative disorders; cutaneous T-cell lymphoma; hairy cell leukemia; hematologic (blood) cancer; Hodgkin's lymphoma; multiple myeloma/plasma cell neoplasm' mycosis fungoides; myelodysplastic syndromes; myelodysplastic/myeloproliferative diseases; multiple myeloma; Non-Hodgkin's lymphoma; primary central nervous system lymphoma; Sezary Syndrome; Waldenstrom's Macroglobulinemia;
Ewing's sarcoma; Kaposi's Sarcoma; osteosarcoma/malignant fibrous histiocytoma of bone; soft tissue sarcoma; uterine sarcoma;
extracranial germ cell tumor; extragonadal germ cell tumor; ovarian cancer; ovarian epithelial cancer; ovarian germ cell tumor; and testicular cancer.
2. A method of increasing the rate of apoptosis in cancerous cells in a mammal, comprising administering to a mammal in need thereof a therapeutically effective amount of a compound of formula 1 or a pharmaceutically acceptable salt thereof:
wherein independently for each occurrence:
X is —N(R 7 ) 2 , —N(R 7 )(R 2 ), or —N(H)—R 3 —R 6 ;
R′ is H, methyl, (C 2 -C 4 )alkyl, or benzyl;
R 2 is H, —CH 2 OP(═O)(OH) 2 , —CH 2 O(P═O)(OR 8 ) 2 , —(C═O)OCHR 8 O(C═O)CH 3 , or —(C═O)OCH 2 O(P═O)(OH) 2 ;
R 3 is —C(═NR)— or —(C(R) 2 ) n —;
R 5 is selected from the group consisting of 1,4-cyclohexanediyl, 1,4-phenylene, 1,4-cycloheptanediyl, 1,4-cyclooctanediyl, 1,5-cyclooctanediyl, 1,4-bicyclo[2.2.1]heptanediyl, 1,4-bicyclo[2.2.2]octanediyl, and 1,5-bicyclo[3.3.1]nonanediyl;
R 6 is selected from the group consisting of alkyl, alkylaryl, aryl, alkylheteroaryl, alkylheteroalkyl, and heteroaryl, any of which is optionally mono or di-substituted, and the substituents, if present, are independently selected from the group consisting of alkyl, alkylaryl, aralkyl, aryl, heteroaryl, alkoxy, hydroxy, perfluoroalkyl, trifluoromethoxy, and halide, wherein the optional aryl or heteroaryl substituent may be optionally substituted with alkyl, halide, alkoxy, perfluoroalkyl, or dioxolanyl;
R 7 is selected from the group consisting of H, —C(═NR)R, —(C(R) 2 ) n R, alkyl, alkylaryl, aryl, alkylheteroaryl, alkylheteroalkyl, and heteroaryl, any of which is optionally mono or di-substituted, and the substituents, if present, are independently selected from the group consisting of alkyl, alkylaryl, aralkyl, aryl, heteroaryl, alkoxy, hydroxy, perfluoroalkyl, trifluoromethoxy, and halide, wherein the optional aryl or heteroaryl substituent may be optionally substituted with alkyl, halide, alkoxy, perfluoroalkyl, or dioxolanyl, or
two instances of R 7 and the nitrogen to which they are bonded taken together represent a nitrogen-containing heterocyclyl, optionally containing one additional heteroatom in the ring, wherein said additional heteroatom is selected from the group consisting of —O—, —N(R)—, and —S—;
R 8 is H, alkyl, benzyl, t-butyl, aryl, or heteroaryl;
R is H or (C 1 -C 4 )alkyl; and
n is 1, 2 or 3;
wherein the cancerous cells are cells of a cancer is selected from the group consisting of:
adrenocortical carcinoma; anal cancer; basal cell carcinoma; bladder cancer; breast cancer; bronchial adenomas/carcinoids; cervical cancer; colon cancer; colorectal cancer; endometrial cancer; esophageal cancer; extrahepatic bile duct cancer; gallbladder cancer; gastric (stomach) cancer; gastrointestinal carcinoid tumor; gestational trophoblastic tumor; head and neck cancer, hepatocellular (liver) cancer; hypopharyngeal cancer; kidney (renal cell) cancer; laryngeal cancer; lip and oral cavity cancer; metastatic squamous neck cancer with occult primary; multiple endocrine neoplasia syndrome; nasal cavity and paranasal sinus cancer; nasopharyngeal cancer; Non-Small Cell Lung cancer; oral cancer; oropharyngeal cancer; pancreatic cancer; parathyroid cancer; penile cancer; pituitary tumor; prostate cancer; rectal cancer; salivary gland cancer; skin carcinoma, Merkel Cell; small cell lung cancer; small intestine cancer; squamous cell carcinoma; thymoma; thymoma and thymic carcinoma; thyroid cancer; transitional cell cancer of the renal pelvis and ureter; urethral cancer; uterine cancer, endometrial; vaginal cancer; vulvar cancer; Wilms' Tumor;
acute lymphoblastic leukemia; acute myeloid leukemia; AIDS-related lymphoma; Burkitt's lymphoma; chronic lymphocytic leukemia; chronic myelogenous leukemia; chronic myeloproliferative disorders; cutaneous T-cell lymphoma; hairy cell leukemia; hematologic (blood) cancer; Hodgkin's lymphoma; multiple myeloma/plasma cell neoplasm' mycosis fungoides; myelodysplastic syndromes; myelodysplastic/myeloproliferative diseases; multiple myeloma; Non-Hodgkin's lymphoma; primary central nervous system lymphoma; Sezary Syndrome; Waldenstrom's Macroglobulinemia;
Ewing's sarcoma; Kaposi's Sarcoma; osteosarcoma/malignant fibrous histiocytoma of bone; soft tissue sarcoma; uterine sarcoma;
extracranial germ cell tumor; extragonadal germ cell tumor; ovarian cancer; ovarian epithelial cancer; ovarian germ cell tumor; and testicular cancer.
3. The method of claim 1 , wherein the cancer is selected from the group consisting of acute lymphoblastic leukemia; acute myeloid leukemia; AIDS-related lymphoma; breast cancer; Burkitt's lymphoma; chronic lymphocytic leukemia; chronic myelogenous leukemia; chronic myeloproliferative disorders; colon cancer; colorectal cancer; cutaneous T-cell lymphoma; Ewing's sarcoma; gastric (stomach) cancer; gastrointestinal carcinoid tumor; hairy cell leukemia; head and neck cancer; hematologic (blood) cancer, hepatocellular (liver) cancer; Hodgkin's lymphoma; lip and oral cavity cancer; metastatic squamous neck cancer with occult primary; multiple myeloma/plasma cell neoplasm' mycosis fungoides; myelodysplastic syndromes; myelodysplastic/myeloproliferative diseases; multiple myeloma; nasal cavity and paranasal sinus cancer; nasopharyngeal cancer; Non-Hodgkin's lymphoma; Non-Small Cell Lung cancer; oral cancer; oropharyngeal cancer; ovarian cancer; ovarian germ cell tumor; pancreatic cancer; primary central nervous system lymphoma; prostate cancer; small intestine cancer; squamous cell carcinoma; and Waldenstrom's Macroglobulinemia.
4. The method of claim 3 , wherein the cancer is selected from the group consisting of acute lymphoblastic leukemia; acute myeloid leukemia; breast cancer; chronic lymphocytic leukemia; colon cancer; colorectal cancer; cutaneous T-cell lymphoma; Ewing's sarcoma; gastric (stomach) cancer; head and neck cancer; hepatocellular (liver) cancer; Hodgkin's lymphoma; multiple myeloma; nasopharyngeal cancer; Non-Hodgkin's lymphoma; Non-Small Cell Lung cancer; oral cancer; ovarian cancer; pancreatic cancer; squamous cell carcinoma; and prostate cancer.
5. The method of claim 3 , wherein the cancer is selected from the group consisting of breast cancer; colon cancer; colorectal cancer; head and neck cancer; hepatocellular (liver) cancer; multiple myeloma; Non-Small Cell Lung cancer; ovarian cancer; squamous cell carcinoma; and prostate cancer.
6. The method of claim 3 , wherein the cancer is selected from the group consisting of adrenocortical carcinoma; anal cancer; basal cell carcinoma; bladder cancer; breast cancer; bronchial adenomas/carcinoids; cervical cancer; colon cancer; colorectal cancer; endometrial cancer; esophageal cancer; extrahepatic bile duct cancer; gallbladder cancer; gastric (stomach) cancer; gastrointestinal carcinoid tumor; gestational trophoblastic tumor; head and neck cancer, hepatocellular (liver) cancer; hypopharyngeal cancer; kidney (renal cell) cancer; laryngeal cancer; lip and oral cavity cancer; metastatic squamous neck cancer with occult primary; multiple endocrine neoplasia syndrome; nasal cavity and paranasal sinus cancer; nasopharyngeal cancer; Non-Small Cell Lung cancer; oral cancer; oropharyngeal cancer; pancreatic cancer; parathyroid cancer; penile cancer; pituitary tumor; prostate cancer; rectal cancer; salivary gland cancer; skin carcinoma, Merkel Cell; small cell lung cancer; small intestine cancer; squamous cell carcinoma; thymoma; thymoma and thymic carcinoma; thyroid cancer; transitional cell cancer of the renal pelvis and ureter; urethral cancer; uterine cancer, endometrial; vaginal cancer; vulvar cancer; and Wilms' Tumor.
7. The method of claim 6 , wherein the cancer is selected from the group consisting of breast cancer; colon cancer; colorectal cancer; gastric (stomach) cancer; head and neck cancer, hepatocellular (liver) cancer; metastatic squamous neck cancer with occult primary; nasopharyngeal cancer; Non-Small Cell lung cancer; oral cancer; pancreatic cancer; prostate cancer; and squamous cell carcinoma.
8. The method of claim 1 , wherein the cancer is selected from the group consisting of acute lymphoblastic leukemia; acute myeloid leukemia; AIDS-related lymphoma; Burkitt's lymphoma; chronic lymphocytic leukemia; chronic myelogenous leukemia; chronic myeloproliferative disorders; cutaneous T-cell lymphoma; hairy cell leukemia; hematologic (blood) cancer; Hodgkin's lymphoma; multiple myeloma/plasma cell neoplasm' mycosis fungoides; myelodysplastic syndromes; myelodysplastic/myeloproliferative diseases; multiple myeloma; Non-Hodgkin's lymphoma; primary central nervous system lymphoma; Sezary Syndrome; and Waldenstrom's Macroglobulinemia.
9. The method of claim 8 , wherein the cancer is selected from the group consisting of acute lymphoblastic leukemia; acute myeloid leukemia; chronic lymphocytic leukemia; cutaneous T-cell lymphoma; hematologic (blood) cancer; Hodgkin's lymphoma; multiple myeloma; and Non-Hodgkin's lymphoma.
10. The method of claim 8 , wherein the cancer is multiple myeloma.
11. The method of claim 1 , wherein the cancer is selected from the group consisting of Ewing's sarcoma; Kaposi's Sarcoma; osteosarcoma/malignant fibrous histiocytoma of bone; soft tissue sarcoma; and uterine sarcoma.
12. The method of claim 11 , wherein the cancer is Ewing's sarcoma.
13. The method of claim 1 , wherein the cancer is selected from the group consisting of extracranial germ cell tumor; extragonadal germ cell tumor; ovarian cancer; ovarian epithelial cancer; ovarian germ cell tumor; and testicular cancer.
14. The method of claim 13 , wherein the cancer is ovarian cancer.
15. The method of claim 1 , wherein R′ is H.
16. The method of claim 1 , wherein R 2 is H.
17. The method of claim 1 , wherein R 5 is 1,4-cyclohexanediyl.
18. The method of claim 1 , wherein R 5 is 1,4-phenylene.
19. The method of claim 1 , wherein R 6 is selected from the group consisting of alkyl, aryl, and heteroaryl.
20. The method of claim 1 , wherein R 6 is selected from the group consisting of phenyl, biphenyl, pyridyl, pyrimidyl, naphthyl, quinolinyl, furanyl, and thienyl.
21. The method of claim 1 , wherein the compound of formula 1 has the following structure:
22. The method of claim 2 , wherein the compound of formula 1 has the following structure: