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公开(公告)号:WO2011068899A1
公开(公告)日:2011-06-09
申请号:PCT/US2010/058598
申请日:2010-12-01
Applicant: ABBOTT LABORATORIES , WISHART, Neil , ARGIRIADI, Maria A. , BREINLINGER, Eric C. , CALDERWOOD, David J. , ERICSSON, Anna M. , FIAMENGO, Bryan A. , FRANK, Kristine E. , FRIEDMAN, Michael , GEORGE, Dawn M. , GOEDKEN, Eric R. , JOSEPHSOHN, Nathan S. , LI, Biqin C. , MORYTKO, Michael J. , MULLEN, Kelly D. , SOMAL, Gagandeep , STEWART, Kent D. , VOSS, Jeffrey W. , WALLACE, Grier A. , WANG, Lu , WOLLER, Kevin R.
Inventor: WISHART, Neil , ARGIRIADI, Maria A. , BREINLINGER, Eric C. , CALDERWOOD, David J. , ERICSSON, Anna M. , FIAMENGO, Bryan A. , FRANK, Kristine E. , FRIEDMAN, Michael , GEORGE, Dawn M. , GOEDKEN, Eric R. , JOSEPHSOHN, Nathan S. , LI, Biqin C. , MORYTKO, Michael J. , MULLEN, Kelly D. , SOMAL, Gagandeep , STEWART, Kent D. , VOSS, Jeffrey W. , WALLACE, Grier A. , WANG, Lu , WOLLER, Kevin R.
CPC classification number: C07F9/06 , C07D471/14 , C07D487/14 , C07D498/14 , C07D513/14
Abstract: The invention provides a compound of Formula (Ia), (Ib), (Ic), (Id), (Ie), (If), (Ig), (Ih), (Ii), (Ij), (Ik), or (Il) as defined herein, pharmaceutically acceptable salts, pro-drugs, biologically active metabolites, stereoisomers and isomers thereof wherein the variable are defined herein. The compounds of the invention are useful for treating immunological and oncological conditions.
Abstract translation: 本发明提供了式(Ia),(Ib),(Ic),(Id),(Ie),(If),(Ig),(Ih),(Ii),(Ij),(Ik) ,或(II),其药学上可接受的盐,前药,生物活性代谢物,立体异构体和异构体,其中变量在本文中定义。 本发明的化合物可用于治疗免疫学和肿瘤学病症。
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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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3.SPHINGOSINE-1 -PHOSPHATE RECEPTOR AGONIST AND ANTAGONIST COMPOUNDS 审中-公开
Title translation: SPHINGOSINE-1-磷酸酯受体激动剂和拮抗剂化合物公开(公告)号:WO2008079382A1
公开(公告)日:2008-07-03
申请号:PCT/US2007/026263
申请日:2007-12-21
Applicant: ABBOTT LABORATORIES , WALLACE, Grier A. , BREINLINGER, Eric C. , CUSACK, Kevin P. , FIX-STENZEL, Shannon R. , GORDON, Thomas D. , HOBSON, Adrian D. , HAYES, Martin E. , ANSELL, Graham K. , GRONGSAARD, Pintipa
Inventor: WALLACE, Grier A. , BREINLINGER, Eric C. , CUSACK, Kevin P. , FIX-STENZEL, Shannon R. , GORDON, Thomas D. , HOBSON, Adrian D. , HAYES, Martin E. , ANSELL, Graham K. , GRONGSAARD, Pintipa
IPC: A01N43/50 , A61K31/415
CPC classification number: C07D413/04 , C07C215/38 , C07C215/42 , C07C217/52 , C07C217/74 , C07C229/14 , C07C229/48 , C07C2601/02 , C07C2601/08 , C07D205/04 , C07D207/12 , C07D207/14 , C07D213/30 , C07D263/32 , C07D263/52 , C07D271/06 , C07D307/22 , C07D307/24 , C07D333/16 , C07D491/107 , C07F9/091 , C07F9/301 , C07F9/3808 , C07F9/3826 , C07F9/4006 , C07F9/653 , C07F9/65515 , C07F9/655345
Abstract: The present invention is directed to novel, potent, and selective agents, which are agonists or antagonists of the one or more of the individual receptors of the S1P receptor family. The compounds of the invention are useful as therapeutics for treating medical conditions associated with agonism or antagonism of the individual receptors of the S1P receptor family.
Abstract translation: 本发明涉及作为S1P受体家族的一种或多种单独受体的激动剂或拮抗剂的新颖的,有效的和选择性的药剂。 本发明的化合物可用作治疗与S1P受体家族的各个受体的激动作用或拮抗作用相关的医学病症的治疗剂。
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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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公开(公告)号:EP1753428A2
公开(公告)日:2007-02-21
申请号:EP05778736.8
申请日:2005-05-13
Applicant: ABBOTT LABORATORIES
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: A61K31/4743 , C07D498/02
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.
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公开(公告)号:EP1983992A2
公开(公告)日:2008-10-29
申请号:EP07717989.3
申请日:2007-01-19
Applicant: ABBOTT LABORATORIES
Inventor: ROTH, Gregory P. , WALLACE, Grier A. , GEORGE, Dawn M. , GRONGSAARD, Pintipa , HAYES, Martin , BREINLINGER, Eric C.
IPC: A61K31/496
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.
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7.SPHINGOSINE-1 -PHOSPHATE RECEPTOR AGONIST AND ANTAGONIST COMPOUNDS 审中-公开
Title translation: SPHINGOSINE-1 -PHOSPHATE受体激动剂和拮抗剂化合物公开(公告)号:EP2120575A1
公开(公告)日:2009-11-25
申请号:EP07863237.9
申请日:2007-12-21
Applicant: ABBOTT LABORATORIES
Inventor: WALLACE, Grier A. , BREINLINGER, Eric C. , CUSACK, Kevin P. , FIX-STENZEL, Shannon R. , GORDON, Thomas D. , HOBSON, Adrian D. , HAYES, Martin E. , ANSELL, Graham K. , GRONGSAARD, Pintipa
IPC: A01N43/50 , A61K31/415
CPC classification number: C07D413/04 , C07C215/38 , C07C215/42 , C07C217/52 , C07C217/74 , C07C229/14 , C07C229/48 , C07C2601/02 , C07C2601/08 , C07D205/04 , C07D207/12 , C07D207/14 , C07D213/30 , C07D263/32 , C07D263/52 , C07D271/06 , C07D307/22 , C07D307/24 , C07D333/16 , C07D491/107 , C07F9/091 , C07F9/301 , C07F9/3808 , C07F9/3826 , C07F9/4006 , C07F9/653 , C07F9/65515 , C07F9/655345
Abstract: The present invention is directed to novel, potent, and selective agents, which are agonists or antagonists of the one or more of the individual receptors of the S1P receptor family. The compounds of the invention are useful as therapeutics for treating medical conditions associated with agonism or antagonism of the individual receptors of the S1P receptor family.
Abstract translation: 本发明涉及作为S1P受体家族的一种或多种个体受体的激动剂或拮抗剂的新型,有效和选择性的药剂。 本发明的化合物可用作治疗剂,用于治疗与S1P受体家族的个体受体的激动或拮抗相关的医学病症。
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8.PROCESS FOR THE PREPARATION AND ISOLATION OF THE INDIVIDUAL STEREOISOMERS OF 1-AMINO, 3-SUBSTITUTED PHENYLCYCLOPENTANE CARBOXYLATES 审中-公开
Title translation: 用于产生和的每个异构体提取方法的1-氨基-3-取代PHENYLCYCLOPENTANCARBOXYLATEN公开(公告)号:EP2102145A1
公开(公告)日:2009-09-23
申请号:EP07863231.2
申请日:2007-12-21
Applicant: ABBOTT LABORATORIES
Inventor: GORDON, Thomas D. , WALLACE, Grier A. , HAYES, Martin E. , LUKIN, Kirill A. , WANG, Lei , FERNANDO, Dilinie, P.
IPC: C07C69/74
CPC classification number: C07D235/02 , C07B2200/07 , C07C45/69 , C07C227/18 , C07C227/24 , C07C227/26 , C07C227/34 , C07C253/00 , C07C253/34 , C07C2601/08 , C07C49/697 , C07C49/753 , C07C229/48 , C07C255/46
Abstract: The present invention discloses processes for the preparation and isolation of the individual stereoisomers of 1-amino, 3-substituted phenylcyclopentane-carboxylates.
Abstract translation: 为1-氨基,3- substituiertem苯基环戊烷羧酸盐的单个立体异构体的制备和分离本发明的分类盘的过程。
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