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公开(公告)号:WO2007084728A3
公开(公告)日:2007-07-26
申请号:PCT/US2007/001548
申请日:2007-01-19
Applicant: ABBOTT LABORATORIES , ROTH, Gregory P. , WALLACE, Grier A. , GEORGE, Dawn M. , GRONGSAARD, Pintipa , HAYES, Martin , BREINLINGER, Eric C.
Inventor: ROTH, Gregory P. , WALLACE, Grier A. , GEORGE, Dawn M. , GRONGSAARD, Pintipa , HAYES, Martin , BREINLINGER, Eric C.
IPC: A61K31/496
Abstract: Novel compounds of Formula (I) or pharmaceutically acceptable salts, prodrugs and biologically active metabolites thereof of Formula (I), wherein the substituents are as defined herein, which are useful as therapeutic agents.
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2.SMIPS: SMALL MOLECULE INHIBITORS OF P27 DEPLETION IN CANCERS AND OTHER PROLIFERATIVE DISEASES 审中-公开
Title translation: SMIPS:小分子抑制剂P27在癌症和其他增殖性疾病中的消除公开(公告)号:WO2009025854A1
公开(公告)日:2009-02-26
申请号:PCT/US2008/010000
申请日:2008-08-22
Inventor: WOLF, Dieter, A. , ROTH, Gregory, P.
IPC: G01N33/53
CPC classification number: G01N33/5011 , G01N2333/4739
Abstract: Methods are provided for screening for SMIPs (small molecule inhibitors of p 27 depletion). The SMIPs thus identified are useful for treating cancers and other proliferative diseases.
Abstract translation: 提供了筛选SMIPs(p27耗尽的小分子抑制剂)的方法。 如此确定的SMIPs可用于治疗癌症和其他增殖性疾病。
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公开(公告)号:WO2007084728A2
公开(公告)日:2007-07-26
申请号:PCT/US2007001548
申请日:2007-01-19
Applicant: ABBOTT LAB , ROTH GREGORY P , WALLACE GRIER A , GEORGE DAWN M , GRONGSAARD PINTIPA , HAYES MARTIN , BREINLINGER ERIC C
Inventor: ROTH GREGORY P , WALLACE GRIER A , GEORGE DAWN M , GRONGSAARD PINTIPA , HAYES MARTIN , BREINLINGER ERIC C
IPC: A61K31/4184
CPC classification number: C07D401/06 , C07D401/12 , C07D403/04 , C07D403/06 , C07D403/12 , C07D405/06 , C07D405/12 , C07D409/12 , C07D413/06 , C07D417/06 , C07D417/12 , C07D471/04 , C07D487/04
Abstract: Novel compounds of Formula (I) or pharmaceutically acceptable salts, prodrugs and biologically active metabolites thereof of Formula (I), wherein the substituents are as defined herein, which are useful as therapeutic agents.
Abstract translation: 式(I)的新型化合物或其药学上可接受的盐,前药和其生物活性代谢物,其中取代基如本文所定义,其可用作治疗剂。
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公开(公告)号:WO2005110410A3
公开(公告)日:2007-03-29
申请号:PCT/US2005016903
申请日:2005-05-13
Applicant: ABBOTT LAB , CUSACK KEVIN , SALMERON-GARCIA JOSE-ANDRES , GORDON THOMAS D , BARBERIS CLAUDE E , ALLEN HAMISH J , BISCHOFF AGNIESZKA K , ERICSSON ANNA M , FRIEDMAN MICHAEL M , GEORGE DAWN M , ROTH GREGORY P , TALANIAN ROBERT V , THOMAS CHRISTINE , WALLACE GRIER A , WISHART NEIL , YU ZHENGTIAN
Inventor: CUSACK KEVIN , SALMERON-GARCIA JOSE-ANDRES , GORDON THOMAS D , BARBERIS CLAUDE E , ALLEN HAMISH J , BISCHOFF AGNIESZKA K , ERICSSON ANNA M , FRIEDMAN MICHAEL M , GEORGE DAWN M , ROTH GREGORY P , TALANIAN ROBERT V , THOMAS CHRISTINE , WALLACE GRIER A , WISHART NEIL , YU ZHENGTIAN
IPC: C07D471/02 , A61K31/4743 , C07D471/04 , C07D491/04 , C07D495/04 , C07D498/02
CPC classification number: C07D471/04 , A61K31/4743 , C07D487/04 , C07D491/04 , C07D495/04
Abstract: A compound or pharmaceutically acceptable salts thereof of Formula (I) wherein the substituents are as defined herein, which are useful as kinase inhibitors.
Abstract translation: 式(I)的化合物或其药学上可接受的盐,其中取代基如本文所定义,其可用作激酶抑制剂。
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公开(公告)号:WO2005110410A2
公开(公告)日:2005-11-24
申请号:PCT/US2005/016903
申请日:2005-05-13
Applicant: ABBOTT LABORATORIES , CUSACK, Kevin , SALMERON-GARCIA, Jose-Andres , GORDON, Thomas D. , BARBERIS, Claude E. , ALLEN, Hamish J. , BISCHOFF, Agniezka K. , ERICSSON, Anna M. , FRIEDMAN, Michael M. , GEORGE, Dawn M. , ROTH, Gregory P. , TALANIAN, Robert V. , THOMAS, Christine , WALLACE, Grier A. , WISHART, Neil , YU, Zhengtian
Inventor: CUSACK, Kevin , SALMERON-GARCIA, Jose-Andres , GORDON, Thomas D. , BARBERIS, Claude E. , ALLEN, Hamish J. , BISCHOFF, Agniezka K. , ERICSSON, Anna M. , FRIEDMAN, Michael M. , GEORGE, Dawn M. , ROTH, Gregory P. , TALANIAN, Robert V. , THOMAS, Christine , WALLACE, Grier A. , WISHART, Neil , YU, Zhengtian
IPC: A61K31/4743
CPC classification number: C07D471/04 , A61K31/4743 , C07D487/04 , C07D491/04 , C07D495/04 , Y02A50/481
Abstract: A compound or pharmaceutically acceptable salts thereof of Formula (I) wherein the substituents are as defined herein, which are useful as kinase inhibitors.
Abstract translation: 式(I)的化合物或其药学上可接受的盐,其中取代基如本文所定义,其可用作激酶抑制剂。
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