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公开(公告)号:US07795279B2
公开(公告)日:2010-09-14
申请号:US11550077
申请日:2006-10-17
申请人: Shelley K. Ballentine , Christian Andrew Baumann , Jinsheng Chen , Carl R. Illig , Sanath K. Meegalla , M. Jonathan Rudolph , Robert W. Tuman , Mark J. Wall , Kenneth Wilson , Dana L. Johnson
发明人: Shelley K. Ballentine , Christian Andrew Baumann , Jinsheng Chen , Carl R. Illig , Sanath K. Meegalla , M. Jonathan Rudolph , Robert W. Tuman , Mark J. Wall , Kenneth Wilson , Dana L. Johnson
IPC分类号: A61K31/445 , C07D293/10
CPC分类号: A61K31/4439 , A61K31/454 , A61K31/497 , A61K31/5355 , Y10S514/908
摘要: A method of reducing or inhibiting kinase activity of FLT3 in a cell or a subject, and the use of such compounds for preventing or treating in a subject a cell proliferative disorder and/or disorders related to FLT3 using a compound of the present invention: or a solvate, hydrate, tautomer or pharmaceutically acceptable salt thereof. The present invention is further directed to methods for treating conditions such as cancers and other cell proliferative disorders.
摘要翻译: 降低或抑制细胞或受试者中FLT3的激酶活性的方法,以及使用本发明的化合物,在受试者中预防或治疗细胞增殖性病症和/或与FLT3有关的病症的用途:或 其溶剂合物,水合物,互变异构体或其药学上可接受的盐。 本发明还涉及治疗诸如癌症和其它细胞增殖性疾病的病症的方法。
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公开(公告)号:US07662837B2
公开(公告)日:2010-02-16
申请号:US11254276
申请日:2005-10-20
申请人: Carl R. Illig , Shelley K. Ballentine , Jinsheng Chen , Sanath K. Meegalla , M. Jonathan Rudolph , Mark J. Wall , Kenneth J. Wilson , Renee L. Desjarlais , Carl L. Manthey , Christopher Flores , Christopher J. Molloy
发明人: Carl R. Illig , Shelley K. Ballentine , Jinsheng Chen , Sanath K. Meegalla , M. Jonathan Rudolph , Mark J. Wall , Kenneth J. Wilson , Renee L. Desjarlais , Carl L. Manthey , Christopher Flores , Christopher J. Molloy
IPC分类号: A61K31/454 , C07D401/02
CPC分类号: C07D307/71 , C07D401/12 , C07D401/14 , C07D407/12 , C07D409/12 , C07D409/14
摘要: The invention is directed to compounds of Formula I: wherein A, X, R2 and W are set forth in the specification, as well as solvates, hydrates, tautomers and pharmaceutically acceptable salts thereof, that inhibit protein tyrosine kinases, especially c-fms kinase. Methods of treating autoimmune diseases; and diseases with an inflammatory component; treating metastasis from ovarian cancer, uterine cancer, breast cancer, colon cancer, stomach cancer, hairy cell leukemia and non-small lung carcinoma; 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 arthritis, prosthesis failure, osteolytic sarcoma, myeloma, and tumor metastasis to bone with the compounds of Formula I, are also provided.
摘要翻译: 本发明涉及式I化合物:其中A,X,R 2和W在本说明书中阐述,以及其抑制蛋白酪氨酸激酶,特别是c-fms激酶的溶剂合物,水合物,互变异构体及其药学上可接受的盐 。 治疗自身免疫性疾病的方法 和具有炎症成分的疾病; 治疗卵巢癌,子宫癌,乳腺癌,结肠癌,胃癌,毛细胞白血病和非小细胞肺癌的转移; 并治疗疼痛,包括由肿瘤转移或骨关节炎引起的骨骼疼痛,或内脏,炎症和神经源性疼痛; 还提供了骨质疏松症,佩吉特氏病和其它骨吸收介导包括关节炎,假体失败,溶骨性骨肉瘤,骨髓瘤以及与式I化合物对骨的肿瘤转移的其它疾病。
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公开(公告)号:US07645755B2
公开(公告)日:2010-01-12
申请号:US11408096
申请日:2006-04-20
申请人: Carl R. Illig , Shelley K. Ballentine , Jinsheng Chen , Sanath K. Meegalla , M. Jonathan Rudolph , Mark J. Wall , Kenneth J. Wilson , Renee L. Desjarlais , Carl L. Manthey , Christopher Flores , Christopher J. Molloy
发明人: Carl R. Illig , Shelley K. Ballentine , Jinsheng Chen , Sanath K. Meegalla , M. Jonathan Rudolph , Mark J. Wall , Kenneth J. Wilson , Renee L. Desjarlais , Carl L. Manthey , Christopher Flores , Christopher J. Molloy
IPC分类号: A61K31/5377 , A61K31/454 , C07D413/14 , C07D401/02
CPC分类号: C07D307/71 , A61K45/06 , C07D401/12 , C07D401/14 , C07D407/12 , C07D409/12 , C07D409/14
摘要: The invention is directed to compounds of Formula I: wherein A, X, R2 and W are set forth in the specification, as well as solvates, hydrates, tautomers and pharmaceutically acceptable salts thereof, that inhibit protein tyrosine kinases, especially c-fms kinase. Methods of treating autoimmune diseases; and diseases with an inflammatory component; treating metastasis from ovarian cancer, uterine cancer, breast cancer, colon cancer, stomach cancer, hairy cell leukemia and non-small lung carcinoma; 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 arthritis, prosthesis failure, osteolytic sarcoma, myeloma, and tumor metastasis to bone with the compounds of Formula I, are also provided.
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公开(公告)号:US08674100B2
公开(公告)日:2014-03-18
申请号:US11736635
申请日:2007-04-18
申请人: Carl R. Illig , Shelley K. Ballentine , Jinsheng Chen , Renee Louise DesJariais , Sanath K. Meegalla , Mark Wall , Kenneth Wilson
发明人: Carl R. Illig , Shelley K. Ballentine , Jinsheng Chen , Renee Louise DesJariais , Sanath K. Meegalla , Mark Wall , Kenneth Wilson
IPC分类号: C07D417/12 , C07D279/12 , C07D413/12 , C07D403/12 , C07D233/22 , C07D405/12 , A61K31/535 , A61K31/54 , A61K31/497 , A61K31/445 , A61K31/415
CPC分类号: C07D401/12 , C07C53/18 , C07D233/90 , C07D235/24 , C07D307/68 , C07D401/14 , C07D403/12 , C07D405/12 , C07D491/056
摘要: The invention is directed to compounds of Formula I: wherein Z, X, J, R2 and W are as set forth in the specification, as well as solvates, hydrates, tautomers and pharmaceutically acceptable salts thereof, that inhibit protein tyrosine kinases, especially c-fms kinase. The compounds of formula I are useful for treating a variety of disorders including autoimmune diseases such as rheumatoid arthritis, multiple sclerosis and psoriasis.
摘要翻译: 本发明涉及式I化合物:其中Z,X,J,R 2和W如说明书中所述,以及其抑制蛋白酪氨酸激酶的溶剂合物,水合物,互变异构体和药学上可接受的盐,特别是c -fms激酶。 式I的化合物可用于治疗各种疾病,包括自身免疫性疾病如类风湿性关节炎,多发性硬化和牛皮癣。
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公开(公告)号:US20070249593A1
公开(公告)日:2007-10-25
申请号:US11736617
申请日:2007-04-18
申请人: Carl R. Illig , Shelley K. Ballentine , Jinsheng Chen , Renee Louise DesJarlais , Sanath K. Meegalla , Mark Wall , Kenneth Wilson
发明人: Carl R. Illig , Shelley K. Ballentine , Jinsheng Chen , Renee Louise DesJarlais , Sanath K. Meegalla , Mark Wall , Kenneth Wilson
IPC分类号: A61K31/54 , C07D285/16
CPC分类号: C07D403/12 , C07D401/12 , C07D401/14 , C07D403/14 , C07D405/12 , C07D405/14 , C07D417/12 , C07D417/14
摘要: 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 pharmaceutically acceptable salts thereof, that inhibit protein tyrosine kinases, especially c-fms kinase. Methods of treating autoimmune diseases; and diseases 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.
摘要翻译: 本发明涉及式I化合物:其中Z,X,J,R 2和W在本说明书中列出,以及溶剂合物,水合物,互变异构体及其药学上可接受的盐,其中 抑制蛋白酪氨酸激酶,特别是c-fms激酶。 治疗自身免疫性疾病的方法 和具有炎症成分的疾病; 治疗卵巢癌,子宫癌,乳腺癌,前列腺癌,肺癌,结肠癌,胃癌,毛细胞白血病的转移; 并治疗疼痛,包括由肿瘤转移或骨关节炎引起的骨骼疼痛,或内脏,炎症和神经源性疼痛; 骨质疏松症,佩吉特氏病和其他疾病,其中骨吸收介导包括类风湿性关节炎和其它形式的炎症性关节炎,骨关节炎,假体衰竭,溶骨性肉瘤,骨髓瘤和肿瘤转移至骨骼的发病率与式I化合物, 也提供。
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公开(公告)号:US08859602B2
公开(公告)日:2014-10-14
申请号:US11736644
申请日:2007-04-18
申请人: Carl R. Illig , Shelley K. Ballentine , Jinsheng Chen , Renee Louise DesJarlais , Sanath K. Meegalla , Bruce E. Tomczuk , Mark Wall , Kenneth Wilson
发明人: Carl R. Illig , Shelley K. Ballentine , Jinsheng Chen , Renee Louise DesJarlais , Sanath K. Meegalla , Bruce E. Tomczuk , Mark Wall , Kenneth Wilson
IPC分类号: A61K31/4178 , C07D405/12 , C07D207/34 , C07D413/14 , C07D401/12 , C07D233/90 , C07D405/14 , C07D401/14 , C07D493/08 , C07D413/12 , C07D409/12
CPC分类号: C07D409/12 , C07D207/34 , C07D233/90 , C07D401/12 , C07D401/14 , C07D403/12 , C07D405/12 , C07D405/14 , C07D413/12 , C07D413/14 , C07D493/08 , C12N9/99
摘要: 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 pharmaceutically acceptable salts thereof, that inhibit protein tyrosine kinases, especially c-fms kinase. Methods of treating autoimmune diseases; and diseases 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.
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公开(公告)号:US08481564B2
公开(公告)日:2013-07-09
申请号:US13080861
申请日:2011-04-06
申请人: Carl R. Illig , Shelley K. Ballentine , Jinsheng Chen , Renee Louise DesJarlais , Sanath K. Meegalla , Mark Wall , Kenneth Wilson
发明人: Carl R. Illig , Shelley K. Ballentine , Jinsheng Chen , Renee Louise DesJarlais , Sanath K. Meegalla , Mark Wall , Kenneth Wilson
IPC分类号: C07D401/12 , C07D401/14 , C07D403/12 , C07D403/14 , A61K31/549 , A61K31/506 , A61K31/4545 , A61K31/444
CPC分类号: C07D403/12 , C07D401/12 , C07D401/14 , C07D403/14 , C07D405/12 , C07D405/14 , C07D417/12 , C07D417/14
摘要: 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 pharmaceutically acceptable salts thereof, that inhibit protein tyrosine kinases, especially c-fms kinase. Methods of treating autoimmune diseases; and diseases 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.
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公开(公告)号:US20110195960A1
公开(公告)日:2011-08-11
申请号:US13080861
申请日:2011-04-06
申请人: Carl R. Illig , Shelley K. Ballentine , Jinsheng Chen , Renee Louise DesJarlais , Sanath K. Meegalla , Mark Wall , Kenneth Wilson
发明人: Carl R. Illig , Shelley K. Ballentine , Jinsheng Chen , Renee Louise DesJarlais , Sanath K. Meegalla , Mark Wall , Kenneth Wilson
IPC分类号: A61K31/549 , C07D403/12 , A61K31/506 , C07D417/14 , C07D401/14 , A61K31/4545 , A61K31/444 , C07D401/12 , A61K31/443 , A61K31/4178 , A61P35/00 , A61P29/00 , A61P9/00 , A61P1/00 , A61P11/00 , A61P25/28 , A61P25/18 , A61P19/00 , C12N9/99
CPC分类号: C07D403/12 , C07D401/12 , C07D401/14 , C07D403/14 , C07D405/12 , C07D405/14 , C07D417/12 , C07D417/14
摘要: 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 pharmaceutically acceptable salts thereof, that inhibit protein tyrosine kinases, especially c-fms kinase. Methods of treating autoimmune diseases; and diseases 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.
摘要翻译: 本发明涉及式I化合物:其中Z,X,J,R 2和W在本说明书中列出,以及其抑制蛋白酪氨酸激酶,特别是c-型的溶剂化物,水合物,互变异构体和药学上可接受的盐, fms激酶。 治疗自身免疫性疾病的方法 和具有炎症成分的疾病; 治疗卵巢癌,子宫癌,乳腺癌,前列腺癌,肺癌,结肠癌,胃癌,毛细胞白血病的转移; 并治疗疼痛,包括由肿瘤转移或骨关节炎引起的骨骼疼痛,或内脏,炎症和神经源性疼痛; 骨质疏松症,佩吉特氏病和其他疾病,其中骨吸收介导包括类风湿性关节炎和其它形式的炎症性关节炎,骨关节炎,假体衰竭,溶骨性肉瘤,骨髓瘤和肿瘤转移至骨骼的发病率与式I化合物, 也提供。
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公开(公告)号:US07973035B2
公开(公告)日:2011-07-05
申请号:US12139876
申请日:2008-06-16
申请人: Carl R. Illig , Shelley K. Ballentine , Jinsheng Chen , Renee Louise DesJarlais , Sanath K. Meegalla , Mark Wall , Kenneth Wilson
发明人: Carl R. Illig , Shelley K. Ballentine , Jinsheng Chen , Renee Louise DesJarlais , Sanath K. Meegalla , Mark Wall , Kenneth Wilson
IPC分类号: A61K31/54 , A61K31/505 , C07D285/16 , C07D239/02
CPC分类号: C07D403/12 , C07D401/12 , C07D401/14 , C07D403/14 , C07D405/12 , C07D405/14 , C07D417/12 , C07D417/14
摘要: 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 pharmaceutically acceptable salts thereof, that inhibit protein tyrosine kinases, especially c-fms kinase. Methods of treating autoimmune diseases; and diseases 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.
摘要翻译: 本发明涉及式I化合物:其中Z,X,J,R 2和W在本说明书中列出,以及其抑制蛋白酪氨酸激酶,特别是c-型的溶剂化物,水合物,互变异构体和药学上可接受的盐, fms激酶。 治疗自身免疫性疾病的方法 和具有炎症成分的疾病; 治疗卵巢癌,子宫癌,乳腺癌,前列腺癌,肺癌,结肠癌,胃癌,毛细胞白血病的转移; 并治疗疼痛,包括由肿瘤转移或骨关节炎引起的骨骼疼痛,或内脏,炎症和神经源性疼痛; 骨质疏松症,佩吉特氏病和其他疾病,其中骨吸收介导包括类风湿性关节炎和其它形式的炎症性关节炎,骨关节炎,假体衰竭,溶骨性肉瘤,骨髓瘤和肿瘤转移至骨骼的发病率与式I化合物, 也提供。
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公开(公告)号:US20080275031A1
公开(公告)日:2008-11-06
申请号:US12139876
申请日:2008-06-16
申请人: Carl R. Illig , Shelley K. Ballentine , Jinsheng Chen , Renee Louise DesJarlais , Sanath K. Meegalla , Mark Wall , Kenneth Wilson
发明人: Carl R. Illig , Shelley K. Ballentine , Jinsheng Chen , Renee Louise DesJarlais , Sanath K. Meegalla , Mark Wall , Kenneth Wilson
IPC分类号: A61K31/549 , C07D401/12 , C07D285/16 , A61K31/506 , A61P35/00 , A61P25/00 , A61P37/00 , A61P35/04 , A61P9/00 , A61P29/00 , C07D239/04 , A61K31/454
CPC分类号: C07D403/12 , C07D401/12 , C07D401/14 , C07D403/14 , C07D405/12 , C07D405/14 , C07D417/12 , C07D417/14
摘要: 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 pharmaceutically acceptable salts thereof, that inhibit protein tyrosine kinases, especially c-fms kinase. Methods of treating autoimmune diseases; and diseases 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.
摘要翻译: 本发明涉及式I化合物:其中Z,X,J,R 2和W在本说明书中列出,以及溶剂合物,水合物,互变异构体及其药学上可接受的盐,其中 抑制蛋白酪氨酸激酶,特别是c-fms激酶。 治疗自身免疫性疾病的方法 和具有炎症成分的疾病; 治疗卵巢癌,子宫癌,乳腺癌,前列腺癌,肺癌,结肠癌,胃癌,毛细胞白血病的转移; 并治疗疼痛,包括由肿瘤转移或骨关节炎引起的骨骼疼痛,或内脏,炎症和神经源性疼痛; 骨质疏松症,佩吉特氏病和其他疾病,其中骨吸收介导包括类风湿性关节炎和其它形式的炎症性关节炎,骨关节炎,假体衰竭,溶骨性肉瘤,骨髓瘤和肿瘤转移至骨骼的发病率与式I化合物, 也提供。
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