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公开(公告)号:EP1318978A2
公开(公告)日:2003-06-18
申请号:EP01971244.7
申请日:2001-09-20
申请人: Abbott Laboratories
发明人: MCCLELLAN, William , OOST, Thorsten , BRUNCKO, Milan , WANG, Xilu , AUGERI, David, J. , BAUMEISTER, Steven, A. , DICKMAN, Daniel, A. , DING, Hong , DINGES, Jurgen , FESIK, Stephen, W. , HAJDUK, Philip, J. , KUNZER, Aaron, R. , NETTESHEIM, David, G. , PETROS, Andrew, M. , ROSENBERG, Saul, H. , SHEN, Wang , THOMAS, Sheela, A. , WENDT, Michael, D.
IPC分类号: C07C311/51 , C07C317/28 , C07C323/12 , C07C323/17 , C07C323/25 , C07C323/30 , C07C323/37 , C07C323/58 , C07C323/60
CPC分类号: C07D207/404 , C07C311/51 , C07C317/28 , C07C323/12 , C07C323/17 , C07C323/25 , C07C323/30 , C07C323/37 , C07C323/58 , C07C323/60 , C07C2601/08 , C07C2601/14 , C07C2601/16 , C07C2601/18 , C07C2602/08 , C07C2602/10 , C07C2602/28 , C07C2602/42 , C07C2602/44 , C07C2603/74 , C07D203/10 , C07D205/12 , C07D207/24 , C07D209/08 , C07D209/96 , C07D211/44 , C07D211/70 , C07D211/74 , C07D213/61 , C07D213/70 , C07D213/71 , C07D215/14 , C07D215/227 , C07D215/48 , C07D217/04 , C07D221/20 , C07D231/12 , C07D235/08 , C07D235/26 , C07D241/16 , C07D249/04 , C07D263/56 , C07D263/58 , C07D277/62 , C07D277/64 , C07D295/13 , C07D295/155 , C07D295/185 , C07D295/205 , C07D295/215 , C07D295/26 , C07D307/14 , C07D317/54 , C07D333/28 , C07D333/68 , C07D401/06 , C07D401/12 , C07D405/04 , C07D417/12 , C07D451/02
摘要: N-Benzoyl arylsulfonamides having the formula (I) are BCL-Xl inhibitors and are useful for promoting apoptosis. Also disclosed are BCL-Xl inhibiting compositions and methods of promoting apoptosis in a mammal.
摘要翻译: 具有式(I)的N-苯甲酰基芳基磺酰胺是BCL-X1抑制剂,可用于促进凋亡。 还公开了BCL-X1抑制组合物和促进哺乳动物细胞凋亡的方法。
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2.CYCLOBUTANE DERIVATIVES AS INHIBITORS OF SQUALENE SYNTHETASE AND PROTEIN FARNESYLTRANSFERASE 失效
标题翻译: CYCLOBUTAN-DERIVATE ALS INHIBITOREN DER SQUALEN-SYNTHETASE UND DER PROTEIN-FARNESYLTRANSFERASE公开(公告)号:EP0677039B1
公开(公告)日:1999-03-10
申请号:EP94931987.5
申请日:1994-10-20
申请人: Abbott Laboratories
发明人: BAKER, William, R. , ROCKWAY, Todd, W. , DONNER, B., Gregory , SHEN, Wang , ROSENBERG, Saul, H. , FAKHOURY, Stephen, A. , O'CONNOR, Stephen, J. , STOUT, David, M. , FUNG, Anthony, K., L. , GARVEY, David, S. , PRASAD, Rajnandan , SULLIVAN, Gerard, M.
IPC分类号: C07C233/60 , C07C323/40 , C07D257/04 , A61K31/16 , A61K31/41
CPC分类号: C07C233/61 , C07C69/74 , C07C233/19 , C07C233/58 , C07C233/59 , C07C233/60 , C07C233/62 , C07C233/63 , C07C235/36 , C07C235/40 , C07C237/24 , C07C245/14 , C07C251/42 , C07C259/08 , C07C311/51 , C07C323/40 , C07C323/46 , C07C2601/02 , C07C2601/04 , C07C2601/14 , C07D309/32 , C07D319/06 , C07D333/58
摘要: The present invention provides a compound of formula (I) processes for the preparation of the compounds of the invention in addition to intermediates useful in these processes, a pharmaceutical composition, and a method of treating disorders resulting from an excess of cholesterol or cancer or a fungal infection.
摘要翻译: 本发明提供式(I)化合物,除了可用于这些方法的中间体以外,还可用于制备本发明化合物的方法,药物组合物和治疗由过量胆固醇或癌症引起的病症的方法或 真菌感染。
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3.CYCLOBUTANE DERIVATIVES AS INHIBITORS OF SQUALENE SYNTHASE AND PROTEIN FARNESYLTRANSFERASE 失效
标题翻译: 环丁烷衍生物作为抑制剂鲨烯合酶和蛋白质法尼基转移公开(公告)号:EP0821665A1
公开(公告)日:1998-02-04
申请号:EP96912978.0
申请日:1996-04-18
申请人: Abbott Laboratories
发明人: ARENDSEN, David, L. , BAKER, William, R. , FAKHOURY, Stephen, A. , FUNG, K., L., Anthony , GARVEY, David, S. , MCCLELLAN, William, J. , O'CONNOR, Stephen, J. , PRASAD, Rajnandan, N. , ROCKWAY, Todd, W. , ROSENBERG, Saul, H. , STEIN, Herman, H. , SHEN, Wang , STOUT, David, M. , SULLIVAN, Gerard, M. , AUGERI, David, J.
IPC分类号: A61K31 , A61P3 , A61P9 , A61P31 , A61P35 , A61P43 , C07C233 , C07C235 , C07D271 , C07D285 , C07D333
CPC分类号: C07C235/82 , C07C233/58 , C07C233/59 , C07C233/60 , C07C235/40 , C07C2601/04 , C07D333/20
摘要: The present invention provides a compound of formula (I) or (II) or a pharmaceutically acceptable salt thereof, which is useful for inhibiting protein farnesyltransferase and the farnesylation of the oncogene protein Ras or inhibiting de novo squalene production resulting in the inhibition of cholesterol biosynthesis, processes for the preparation of the compounds of the invention in addition to intermediates useful in these processes, a pharmaceutical composition, and to methods of using such compounds.
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公开(公告)号:EP1318978B1
公开(公告)日:2006-02-08
申请号:EP01971244.7
申请日:2001-09-20
申请人: ABBOTT LABORATORIES
发明人: MCCLELLAN, William , OOST, Thorsten , BRUNCKO, Milan , WANG, Xilu , AUGERI, David, J. , BAUMEISTER, Steven, A. , DICKMAN, Daniel, A. , DING, Hong , DINGES, Jurgen , FESIK, Stephen, W. , HAJDUK, Philip, J. , KUNZER, Aaron, R. , NETTESHEIM, David, G. , PETROS, Andrew, M. , ROSENBERG, Saul, H. , SHEN, Wang , THOMAS, Sheela, A. , WENDT, Michael, D.
IPC分类号: C07C311/51 , C07C317/28 , C07C323/12 , C07C323/17 , C07C323/25 , C07C323/30 , C07C323/37 , C07C323/58 , C07C323/60 , C07D209/08 , C07D209/96 , C07D213/61 , C07D213/70 , C07D215/48 , C07D221/20 , C07D263/56 , C07D277/62 , C07D277/64 , C07D295/14 , C07D295/20 , C07D333/28
CPC分类号: C07D207/404 , C07C311/51 , C07C317/28 , C07C323/12 , C07C323/17 , C07C323/25 , C07C323/30 , C07C323/37 , C07C323/58 , C07C323/60 , C07C2601/08 , C07C2601/14 , C07C2601/16 , C07C2601/18 , C07C2602/08 , C07C2602/10 , C07C2602/28 , C07C2602/42 , C07C2602/44 , C07C2603/74 , C07D203/10 , C07D205/12 , C07D207/24 , C07D209/08 , C07D209/96 , C07D211/44 , C07D211/70 , C07D211/74 , C07D213/61 , C07D213/70 , C07D213/71 , C07D215/14 , C07D215/227 , C07D215/48 , C07D217/04 , C07D221/20 , C07D231/12 , C07D235/08 , C07D235/26 , C07D241/16 , C07D249/04 , C07D263/56 , C07D263/58 , C07D277/62 , C07D277/64 , C07D295/13 , C07D295/155 , C07D295/185 , C07D295/205 , C07D295/215 , C07D295/26 , C07D307/14 , C07D317/54 , C07D333/28 , C07D333/68 , C07D401/06 , C07D401/12 , C07D405/04 , C07D417/12 , C07D451/02
摘要: N-Benzoyl arylsulfonamides having the formula (I) are BCL-Xl inhibitors and are useful for promoting apoptosis. Also disclosed are BCL-Xl inhibiting compositions and methods of promoting apoptosis in a mammal.
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5.CYCLOBUTANE DERIVATIVES AS INHIBITORS OF SQUALENE SYNTHASE AND PROTEIN FARNESYLTRANSFERASE 失效
标题翻译: CYCLOBUTAN-DERIVATE ALS INHIBITOREN DER SQUALEN-SYNTHASE UND DER PROTEIN FARNESYLTRANSFERASE公开(公告)号:EP0821665B1
公开(公告)日:2001-10-04
申请号:EP96912978.2
申请日:1996-04-18
申请人: Abbott Laboratories
发明人: ARENDSEN, David, L. , BAKER, William, R. , FAKHOURY, Stephen, A. , FUNG, K., L., Anthony , GARVEY, David, S. , MCCLELLAN, William, J. , O'CONNOR, Stephen, J. , PRASAD, Rajnandan, N. , ROCKWAY, Todd, W. , ROSENBERG, Saul, H. , STEIN, Herman, H. , SHEN, Wang , STOUT, David, M. , SULLIVAN, Gerard, M. , AUGERI, David, J.
IPC分类号: C07C233/60 , C07D333/20 , C07C233/58 , C07C233/59 , C07C235/40 , A61K31/19 , A61K31/215 , A61K31/38 , A61K31/16
CPC分类号: C07C235/82 , C07C233/58 , C07C233/59 , C07C233/60 , C07C235/40 , C07C2601/04 , C07D333/20
摘要: The present invention provides a compound of formula (I) or (II) or a pharmaceutically acceptable salt thereof, which is useful for inhibiting protein farnesyltransferase and the farnesylation of the oncogene protein Ras or inhibiting de novo squalene production resulting in the inhibition of cholesterol biosynthesis, processes for the preparation of the compounds of the invention in addition to intermediates useful in these processes, a pharmaceutical composition, and to methods of using such compounds.
摘要翻译: 本发明提供式(II)化合物或其药学上可接受的盐,其可用于抑制蛋白质法呢基转移酶和癌基因蛋白Ras的法呢基化,制备本发明化合物的方法除了可用于 这些方法,药物组合物,以及使用这些化合物的方法。
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6.CYCLOBUTANE DERIVATIVES AS INHIBITORS OF SQUALENE SYNTHETASE AND PROTEIN FARNESYLTRANSFERASE 失效
标题翻译: CYCLOBUTAN-DERIVATE ALS INHIBITOREN DER SQUALEN-SYNTHETASE UND DER PROTEIN-FARNESYLTRANSFERASE。公开(公告)号:EP0677039A1
公开(公告)日:1995-10-18
申请号:EP94931987.0
申请日:1994-10-20
申请人: Abbott Laboratories
发明人: BAKER, William, R. , ROCKWAY, Todd, W. , DONNER, B., Gregory , SHEN, Wang , ROSENBERG, Saul, H. , FAKHOURY, Stephen, A. , O'CONNOR, Stephen, J. , STOUT, David, M. , FUNG, Anthony, K., L. , GARVEY, David, S. , PRASAD, Rajnandan , SULLIVAN, Gerard, M.
IPC分类号: C12N9 , A61K31 , A61P3 , A61P7 , A61P9 , A61P31 , A61P43 , C07C69 , C07C231 , C07C233 , C07C235 , C07C237 , C07C245 , C07C251 , C07C259 , C07C275 , C07C311 , C07C323 , C07C327 , C07D207 , C07D213 , C07D257 , C07D263 , C07D271 , C07D277 , C07D285 , C07D307 , C07D309 , C07D317 , C07D319 , C07D333
CPC分类号: C07C233/61 , C07C69/74 , C07C233/19 , C07C233/58 , C07C233/59 , C07C233/60 , C07C233/62 , C07C233/63 , C07C235/36 , C07C235/40 , C07C237/24 , C07C245/14 , C07C251/42 , C07C259/08 , C07C311/51 , C07C323/40 , C07C323/46 , C07C2601/02 , C07C2601/04 , C07C2601/14 , C07D309/32 , C07D319/06 , C07D333/58
摘要: The present invention provides a compound of formula (I) processes for the preparation of the compounds of the invention in addition to intermediates useful in these processes, a pharmaceutical composition, and a method of treating disorders resulting from an excess of cholesterol or cancer or a fungal infection.
摘要翻译: 本发明提供式(I)化合物,除了可用于这些方法的中间体以外,还可用于制备本发明化合物的方法,药物组合物和治疗由过量胆固醇或癌症引起的病症的方法或 真菌感染。
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公开(公告)号:EP1904047A2
公开(公告)日:2008-04-02
申请号:EP06774553.9
申请日:2006-07-07
申请人: ABBOTT LABORATORIES
发明人: WENDT, Michael, D. , SHEN, Wang , DICKMAN, Daniel, A. , DING, Hong , THOMAS, Sheela, A. , AUGERI, David , ELMORE, Steven, W.
IPC分类号: A61K31/192 , C07C15/12 , A61P35/00
CPC分类号: C07C311/41 , C07C63/48 , C07C63/49 , C07C65/26 , C07C65/28 , C07C205/58 , C07C229/52 , C07C229/56 , C07C233/81 , C07C311/13 , C07C311/18 , C07C311/21 , C07C311/37 , C07C311/44 , C07C323/20 , C07C323/25 , C07C323/62 , C07C2601/08 , C07C2601/14 , C07C2601/18 , C07C2602/10 , C07C2603/18 , C07C2603/74 , C07D207/30 , C07D213/53 , C07D215/12 , C07D215/48 , C07D333/34
摘要: Compounds which inhibit the activity of anti-apoptotic Mcl-I protein, compositions containing the compounds and methods of treating diseases during which are expressed the Mcl- 1 protein are disclosed.
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公开(公告)号:EP1904047B1
公开(公告)日:2013-01-02
申请号:EP06774553.9
申请日:2006-07-07
申请人: ABBOTT LABORATORIES
发明人: WENDT, Michael, D. , SHEN, Wang , DICKMAN, Daniel, A. , DING, Hong , THOMAS, Sheela, A. , AUGERI, David , ELMORE, Steven, W.
IPC分类号: A61K31/192 , C07C15/12 , A61P35/00
CPC分类号: C07C311/41 , C07C63/48 , C07C63/49 , C07C65/26 , C07C65/28 , C07C205/58 , C07C229/52 , C07C229/56 , C07C233/81 , C07C311/13 , C07C311/18 , C07C311/21 , C07C311/37 , C07C311/44 , C07C323/20 , C07C323/25 , C07C323/62 , C07C2601/08 , C07C2601/14 , C07C2601/18 , C07C2602/10 , C07C2603/18 , C07C2603/74 , C07D207/30 , C07D213/53 , C07D215/12 , C07D215/48 , C07D333/34
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