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1.Indazole, benzisoxazole, and benzisothiazole kinase inhibitor 有权
Title translation: 吲哚,苯唑唑和苯并噻唑激酶抑制剂公开(公告)号:JP2011088918A
公开(公告)日:2011-05-06
申请号:JP2010282815
申请日:2010-12-20
Applicant: Abbott Lab , アボット・ラボラトリーズAbbott Laboratories
Inventor: DAI YUJIA , DAVIDSEN STEVEN K , ERICSSON ANNA M , HARTANDI KRESNA , JI ZHIQIN , MICHAELIDES MICHAEL R
IPC: C07D231/56 , A61K31/416 , A61K31/4178 , A61K31/42 , A61K31/423 , A61K31/428 , A61K31/4439 , A61K31/454 , A61K31/4709 , A61K31/496 , A61K31/5377 , A61P9/10 , A61P17/06 , A61P19/02 , A61P27/02 , A61P35/00 , A61P37/06 , A61P43/00 , C07D261/20 , C07D275/04 , C07D401/04 , C07D401/12 , C07D403/04 , C07D403/12 , C07D409/04 , C07D409/12 , C07D409/14 , C07D413/02 , C07D413/12
CPC classification number: C07D231/56 , C07D261/20 , C07D275/04 , C07D401/04 , C07D401/12 , C07D403/04 , C07D403/12 , C07D405/12 , C07D409/04 , Y02P20/582
Abstract: PROBLEM TO BE SOLVED: To provide a compound useful for inhibiting a protein tyrosine kinase, a method for producing the compound, a composition containing the compound and a therapeutic method using the compound. SOLUTION: The compound is expressed by formula (I), wherein A is selected from the group consisting of indolye, phenyl, pyrazinyl, pyridazinyl, pyridinyl, pyrimidinyl and thienyl; X is selected from the group consisting of O, S, N and the like; and R 1 , R 2 , R 3 , R 4 and R 5 are each selected from hydrogen, alkoxy, alkoxyalkoxy, haloalkyl, heterocyclyl, heterocyclylalkenyl and the like. COPYRIGHT: (C)2011,JPO&INPIT
Abstract translation: 待解决的问题:提供一种可用于抑制蛋白质酪氨酸激酶的化合物,该化合物的制备方法,含该化合物的组合物和使用该化合物的治疗方法。 解决方案:化合物由式(I)表示,其中A选自取代基,苯基,吡嗪基,哒嗪基,吡啶基,嘧啶基和噻吩基; X选自O,S,N等; 和R
1 SP>,R 2 SP>,R 3 SP>,R 4 SP>和R 5 SP> 各自选自氢,烷氧基,烷氧基烷氧基,卤代烷基,杂环基,杂环基烯基等。 版权所有(C)2011,JPO&INPIT -
公开(公告)号:WO2008005368A2
公开(公告)日:2008-01-10
申请号:PCT/US2007015192
申请日:2007-06-29
Applicant: ABBOTT LAB , BETSCHMANN PATRICK , CARROLL WILLIAM A , ERICSSON ANNA M , FIX-STENZEL SHANNON R , FRIEDMAN MICHAEL , HIRST GAVIN C , JOSEPHSOHN NATHAN S , LI BIQIN , PEREZ-MEDRANO ARTURO , MORYTKO MICHAEL J , RAFFERTY PAUL , CHEN HAIPENG
Inventor: BETSCHMANN PATRICK , CARROLL WILLIAM A , ERICSSON ANNA M , FIX-STENZEL SHANNON R , FRIEDMAN MICHAEL , HIRST GAVIN C , JOSEPHSOHN NATHAN S , LI BIQIN , PEREZ-MEDRANO ARTURO , MORYTKO MICHAEL J , RAFFERTY PAUL , CHEN HAIPENG
IPC: A61K31/496
CPC classification number: C07D241/04 , C07D241/36 , C07D295/215 , C07D401/06 , C07D401/12 , C07D401/14 , C07D403/04 , C07D403/06 , C07D403/12 , C07D403/14 , C07D405/06 , C07D405/12 , C07D405/14 , C07D409/06 , C07D409/12 , C07D409/14 , C07D413/04 , C07D413/06 , C07D413/12 , C07D413/14 , C07D417/04 , C07D417/06 , C07D417/12 , C07D417/14 , C07D471/04 , C07D487/04 , C07D495/04 , C07D498/04 , C07D513/04
Abstract: Novel compounds of Formula (I) or pharmaceutically acceptable salts thereof, metabolites thereof, isomers thereof, enantiomers thereof or prodrugs 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,其代谢物,其异构体,其对映异构体或其前体药物,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:WO2007117465A3
公开(公告)日:2008-08-28
申请号:PCT/US2007008307
申请日:2007-04-02
Applicant: ABBOTT LAB , ERICSSON ANNA M , BURCHAT ANDREW , FRANK KRISTINE E , CALDERWOOD DAVID J , ABBOTT LILY K , ARGIRIADI MARIA A , BORHANI DAVID W , CUSACK KEVIN P , DIXON RICHARD W , GORDON THOMAS D , MULLEN KELLY D , TALANIAN ROBERT V , WU XIAOYUN , ZHANG XIAOLEI , WANG LU X , LI BIQIN , BARBERIS CLAUDE E , WISHART NEIL
Inventor: ERICSSON ANNA M , BURCHAT ANDREW , FRANK KRISTINE E , CALDERWOOD DAVID J , ABBOTT LILY K , ARGIRIADI MARIA A , BORHANI DAVID W , CUSACK KEVIN P , DIXON RICHARD W , GORDON THOMAS D , MULLEN KELLY D , TALANIAN ROBERT V , WU XIAOYUN , ZHANG XIAOLEI , WANG LU X , LI BIQIN , BARBERIS CLAUDE E , WISHART NEIL
IPC: A61K31/5377
CPC classification number: C07D487/04 , C07D403/12 , C07D403/14 , C07D409/04 , C07D409/14
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,前体药物和式(I)的生物活性代谢物,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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5.OCTAHYDROPENTALENE COMPOUNDS AS CHEMOKINE RECEPTOR ANTAGONISTS 审中-公开
Title translation: OCTAHYDROPENTALENVERBINDUNGEN ALS趋化因子受体拮抗剂公开(公告)号:EP2203051A4
公开(公告)日:2011-09-07
申请号:EP08834489
申请日:2008-09-25
Applicant: ABBOTT LAB
Inventor: GEORGE DAWN M , WANG LU , LI BIQIN , ERICSSON ANNA M , ANSELL GRAHAM K
IPC: A01N37/18 , A61K31/165 , C07D211/14 , C07D295/185 , C07D309/14 , C07D405/12 , C07D471/04
CPC classification number: C07D471/04 , C07D211/14 , C07D295/185 , C07D309/14 , C07D405/12
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公开(公告)号:EP2299821A4
公开(公告)日:2012-02-08
申请号:EP09763424
申请日:2009-06-09
Applicant: ABBOTT LAB
Inventor: WISHART NEIL , ARGIRIADI MARIA A , 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 , STEWART KENT D , VOSS JEFFREY W , WALLACE GRIER A , WANG LU , WOLLER KEVIN R
IPC: A01N43/42 , C07D487/14 , C07D498/14 , C07D513/14
CPC classification number: C07D487/14 , C07D498/14 , C07D513/14
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公开(公告)号:EP1753428A4
公开(公告)日:2010-09-15
申请号:EP05778736
申请日:2005-05-13
Applicant: ABBOTT LAB
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.
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公开(公告)号:EP2506716A4
公开(公告)日:2013-05-29
申请号:EP10835061
申请日:2010-12-01
Applicant: ABBOTT LAB
Inventor: WISHART NEIL , ARGIRIADI MARIA A , 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 , STEWART KENT D , VOSS JEFFREY W , WALLACE GRIER A , WANG LU , WOLLER KEVIN R
IPC: C07D487/14 , A61K31/437 , A61K31/4985 , A61P19/00 , C07D471/14 , C07D498/14 , C07D513/14
CPC classification number: C07D487/14 , A61K31/437 , A61K31/4985 , A61K45/06 , C07D471/14 , C07D498/14 , C07D513/14
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公开(公告)号:EP2001480A4
公开(公告)日:2011-06-15
申请号:EP07754773
申请日:2007-04-02
Applicant: ABBOTT LAB
Inventor: ERICSSON ANNA M , BURCHAT ANDREW , FRANK KRISTINE E , CALDERWOOD DAVID J , ABBOTT LILY K , ARGIRIADI MARIA A , BORHANI DAVID W , CUSACK KEVIN P , DIXON RICHARD W , GORDON THOMAS D , MULLEN KELLY D , TALANIAN ROBERT V , WU XIAOYUN , ZHANG XIAOLEI , WANG LU X , LI BIQIN , BARBERIS CLAUDE E , WISHART NEIL
IPC: A61K31/196 , A61P35/00 , C07D403/12
CPC classification number: C07D487/04 , C07D403/12 , C07D403/14 , C07D409/04 , C07D409/14
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公开(公告)号:CY1110742T1
公开(公告)日:2015-06-10
申请号:CY101100768
申请日:2010-08-19
Applicant: ABBOTT LAB
Inventor: DAI YUJIA , DAVIDSEN STEVEN K , ERICSSON ANNA M , HARTANDI KRESNA , JI ZHIQIN , MICHAELIDES MICHAEL R
IPC: C07D231/56 , A61K31/416 , A61K31/42 , A61K31/423 , A61K31/428 , A61K31/4709 , A61P35/00 , C07D261/20 , C07D275/04 , C07D401/04 , C07D401/12 , C07D403/04 , C07D403/12 , C07D405/12 , C07D409/04 , C07D413/02
Abstract: Ενώσειςπουέχουντοντύπο (I) είναιχρήσιμεςγιατηναναστολήτωνκινασώνπρωτεΐνηςτυροσίνης. Ηπαρούσαεφεύρεσηαποκαλύπτειεπίσηςμεθόδουςκατασκευήςτωνενώσεων, τωνσυνθέσεωνπουπεριέχουντιςενώσεις, καιμεθόδουςθεραπείαςχρησιμοποιώνταςτιςενώσεις.
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