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公开(公告)号:BRPI0810086A2
公开(公告)日:2016-07-26
申请号:BRPI0810086
申请日:2008-03-27
Applicant: PHARMACYCLICS INC
Inventor: LOURY DAVID , VERNER ERIK , BUGGY JOSEPH J , HONIGBERG LEE , CHEN WEI
IPC: A61K31/52 , A61K31/519 , A61P29/00 , A61P35/00 , C07D253/06 , C07D473/34 , C07D487/04
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公开(公告)号:IN3012DEN2012A
公开(公告)日:2015-07-31
申请号:IN3012DEN2012
申请日:2012-04-09
Applicant: PHARMACYCLICS INC
Inventor: CHEN WEI , LOURY DAVID J , MODY TARAK D , VERNER ERIK , SMYTH MARK STEPHEN , LUO WENCHEN
IPC: A61K20060101
Abstract: Described herein are kinase inhibitor compounds, methods for synthesizing such inhibitors, and methods for using such inhibitors in the treatment of diseases. Further described herein are methods, assays and systems for determining an appropriate inhibitor of a protein, including a kinase.
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公开(公告)号:CA2721218C
公开(公告)日:2015-03-24
申请号:CA2721218
申请日:2009-04-15
Applicant: PHARMACYCLICS INC
Inventor: VERNER ERIK , BALASUBRAMANIAN SRIRAM , BUGGY JOSEPH J
IPC: C07D235/06 , A61K31/395 , A61P35/00 , A61P35/02 , C07D235/08 , C07D235/10 , C07D235/12 , C07D235/14
Abstract: Described herein are compounds and pharmaceutical compositions containing such compounds, which inhibit the acitivy of histone deacetylase 8 (HDAC8). Also described herein are methods of using such HDAC8 inhibitors, alone and in combination with other compounds, for treating diseases or conditions that would benefit from inhibition of HDAC8 activity.
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公开(公告)号:NZ599396A
公开(公告)日:2014-03-28
申请号:NZ59939610
申请日:2010-10-12
Applicant: PHARMACYCLICS INC
Inventor: CHEN WEI , MODY TARAK D , LOURY DAVID J , VERNER ERIK , LUO WENCHEN , SMYTH MARK STEPHEN
IPC: C07D487/04 , A61K31/519 , A61P19/02 , A61P19/10 , C07D401/04 , C07D401/14
Abstract: NZ 599396 The disclosure relates to pyrazolo-pyrimidine derivatives of formula (II) that are inhibitors of bruton’s tyrosine kinase (Btk), wherein the variables are as defined in the specification. The disclosure also relates to methods for synthesizing such inhibitors, and methods, assays and systems for determining an appropriate inhibitor of a protein, including a kinase. These compounds are suitable for treating an autoimmune disease or condition, a heteroimmune disease or condition, cancers including B-cell proliferative disorder is diffuse large B cell lymphoma, follicular lymphoma or chronic lymphocytic leukemia, mastocytosis, osteoporosis, and an inflammatory disease or condition.
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公开(公告)号:ES2403546T3
公开(公告)日:2013-05-20
申请号:ES07867362
申请日:2007-11-05
Applicant: PHARMACYCLICS INC
Inventor: PAN ZHENGYING , LI SHYR , SCHEREENS HELEEN , HONIGBERG LEE , VERNER ERIK
IPC: C07D487/00 , C07D487/04 , G01N33/573
Abstract: Sonda de actividad de la Btk que comprende un resto inhibidor de la Btk que se une covalentemente a un residuode cisteína de una enzima Btk, un fluoróforo y un resto conector que une el resto inhibidor al fluoróforo, en la que elresto inhibidor es el siguiente: **Fórmula**
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公开(公告)号:CO6531429A2
公开(公告)日:2012-09-28
申请号:CO12057551
申请日:2012-04-09
Applicant: PHARMACYCLICS INC
Inventor: CHEN WEI , LOURY DAVID J , MODY TARAK D , VERNER ERIK , SMYTH MARK STEPHEN , LUO WEWNCHEN
IPC: C07D487/04
Abstract: Se describen aquí compuestos inhibidores de quinasa, métodos para sintetizar tales inhibidores y métodos para utilizar tales inhibidores en el tratamiento de enfermedades. Se describen aquí adicionalmente métodos, ensayos y sistemas para determinar un inhibidor apropiado de una proteína, incluyendo una quinasa.
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公开(公告)号:AU2012205166A1
公开(公告)日:2012-08-02
申请号:AU2012205166
申请日:2012-07-16
Applicant: PHARMACYCLICS INC
Inventor: VERNER ERIK , PAN ZHENGYING , HONIBERG LEE
IPC: C07D471/04 , A01N43/90 , A61K31/519 , A61K31/52 , A61P29/00 , A61P35/00 , A61P35/02
Abstract: INHIBITORS OF BRUTON'S TYROSINE KINASE Abstract Disclosed herein are compounds that form covalent bonds with Bruton's tyrosine kinase (Btk). Also described are irreversible inhibitors of Btk. Methods for the preparation of the compounds are disclosed. Also disclosed are pharmaceutical compositions that include the compounds. Methods of using the Btk inhibitors are disclosed, alone or in combination with other therapeutic agents, for the treatment of autoimmune diseases or conditions, heteroimmune diseases or conditions, cancer, including lymphoma, and inflammatory diseases or conditions. (64408731 ):KZA
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公开(公告)号:AU2006348662B2
公开(公告)日:2012-04-19
申请号:AU2006348662
申请日:2006-12-28
Applicant: PHARMACYCLICS INC
Inventor: HONIGBERG LEE , PAN ZHENGYING , VERNER ERIK
IPC: C07D471/04 , A01N43/90 , A61K31/519 , A61K31/52 , A61P29/00 , A61P35/00 , A61P35/02
Abstract: Disclosed herein are compounds that form covalent bonds with Bruton's tyrosine kinase (Btk). Also described are irreversible inhibitors of Btk. Methods for the preparation of the compounds are disclosed. Also disclosed are pharmaceutical compositions that include the compounds. Methods of using the Btk inhibitors are disclosed, alone or in combination with other therapeutic agents, for the treatment of autoimmune diseases or conditions, heteroimmune diseases or conditions, cancer, including lymphoma, and inflammatory diseases or conditions.
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公开(公告)号:ES2376424T3
公开(公告)日:2012-03-13
申请号:ES10155834
申请日:2006-12-28
Applicant: PHARMACYCLICS INC
Inventor: HONIGBERG LEE , VERNER ERIK , PAN ZHENGYING
IPC: A01N43/90 , A61K31/519 , A61P35/00 , C07D487/04
Abstract: Un compuesto de fórmula (D) que tiene la estructura: en la que: La es CH2, O, NH o S; Ar es un arilo sustituido o no sustituido, o un heteroarilo sustituido o no sustituido; Y es un grupo opcionalmente sustituido seleccionado de entre alquilo, heteroalquilo, cicloalquilo, heterocicloalquilo, arilo y heteroarilo; Z es C(=O), OC(=O), NHC(=O), C(=S), S(=O)x, OS(=O)x, NHS(=O)x, donde x es 1 o 2; R es H o alquilo C1-C6; y R7 y R8 son H o tomados conjuntamente forman un enlace; R6 es H, o una sal farmacéuticamente aceptable del mismo.
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公开(公告)号:CA2681756A1
公开(公告)日:2008-10-09
申请号:CA2681756
申请日:2008-03-27
Applicant: PHARMACYCLICS INC
Inventor: HONIGBERG LEE , CHEN WEI , VERNER ERIK , LOURY DAVID , BUGGY JOSEPH J
IPC: A61K31/52 , A61K31/519 , A61P29/00 , A61P35/00 , C07D253/06
Abstract: Described herein are irreversible kinase inhibitor compounds, methods for synthesizing such irreversible inhibitors, and methods for using such irrev ersible inhibitors in the treatment of diseases. Further described herein ar e methods, assays and systems for determining an appropriate irreversible in hibitor of a protein, including a kinase.
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