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公开(公告)号:EA018573B1
公开(公告)日:2013-09-30
申请号:EA200900351
申请日:2006-12-28
Applicant: PHARMACYCLICS INC
Inventor: HONIGBERG LEE , VERNER ERIK , PAN ZHENGYING
IPC: A01N43/90 , A61K31/519
Abstract: Визобретенииприведеныописаниясоединений, образующихковалентныесвязис тирозинкиназойБрутона (Btk). Крометого, описанынеобратимыеингибиторы Btk, атакжеспособыполучениятакихсоединений. Такжеописаныфармацевтическиекомпозиции, содержащиетакиесоединения, атакжеспособыпримененияингибиторов Btk отдельноилив комбинациис другимитерапевтическимиагентамидлялеченияаутоиммунныхзаболеванийилисостояний, гетероиммунныхзаболеванийилисостояний, рака, включаялимфому, ивоспалительныхзаболеванийилисостояний.
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公开(公告)号:CA2862259A1
公开(公告)日:2013-07-04
申请号:CA2862259
申请日:2012-12-19
Applicant: PHARMACYCLICS INC
Inventor: VERNER ERIK , CHEN WEI , BALASUBRAMANIAN SRIRAM
IPC: C07C259/06 , A61K31/165 , A61K31/18 , A61K31/4406 , A61K31/4409 , A61K31/445 , A61K31/4525 , A61K31/4545 , A61K31/455 , A61P35/00 , A61P35/02 , C07D211/40 , C07D213/30 , C07D213/38 , C07D213/63 , C07D213/81 , C07D295/088 , C07D401/06 , C07D405/06
Abstract: Described herein are compounds and pharmaceutical compositions containing such compounds, which inhibit the activy 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:AU2012205166A8
公开(公告)日:2013-06-27
申请号:AU2012205166
申请日:2012-07-16
Applicant: PHARMACYCLICS INC
Inventor: VERNER ERIK , PAN ZHENGYING , HONIGBERG 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:NZ595230A
公开(公告)日:2013-02-22
申请号:NZ59523006
申请日:2006-12-28
Applicant: PHARMACYCLICS INC
Inventor: HONIGBERG LEE , VERNER ERIK , PAN ZHENGYING
IPC: A01N43/90 , A61K31/519
Abstract: Disclosed are pyrazolo-pyrimidin derivatives of formula (D) that form covalent bonds with Bruton's tyrosine kinase (Btk), which is a member of the Tec family of non-receptor tyrosrne kinaces, and is a key signaling enzyme expressed in all hematopoietic cell types except T lymphocytes and natural killer cells, wherein the variables shown in the structure of formula (D) are as defined in the specification. Also described are irreversible inhibitors of Btk; methods for the preparation of these compounds; and pharmaceutical compositions that include the compounds. These Btk inhibitors are suitable 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:CL2012000917A1
公开(公告)日:2012-07-13
申请号:CL2012000917
申请日:2012-04-11
Applicant: PHARMACYCLICS INC
Inventor: CHEN WEI , LOURY DAVID J , MODY TARAK D , VERNER ERIK , SMYTH MARK STEPHEN , LUO WENCHEN
IPC: A61K31/519 , A61P19/02 , A61P19/10 , A61P35/00 , C07D487/04
Abstract: Compuestos derivados de pirazolo[3,4-D]pirimidina y sus sales, inhibidores de la tirosina quinasa de Bruton; composición farmacéutica que los comprende, útil para tratar una enfermedad o condición autoinmune tal como artritis reumatoide o lupus, para el tratamiento del cáncer, mastocitosis osteoporosis, entre otras enfermedades.
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公开(公告)号:PL2201840T3
公开(公告)日:2012-03-30
申请号:PL10155834
申请日:2006-12-28
Applicant: PHARMACYCLICS INC
Inventor: HONIGBERG LEE , VERNER ERIK , PAN ZHENGYING
IPC: A61K31/519 , A01N43/90 , A61P35/00 , C07D487/04
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公开(公告)号:MX2010011168A
公开(公告)日:2010-12-21
申请号:MX2010011168
申请日:2009-04-15
Applicant: PHARMACYCLICS INC
Inventor: BUGGY JOSEPH J , VERNER ERIK , BALASUBRAMANIAN SRIRAM
IPC: C07D235/06 , C07D235/08 , C07D235/10 , C07D235/12 , C07D235/14
Abstract: Se describen en la presente compuestos y composición farmacéuticas que contienen estos compuestos, que inhiben la actividad de histona-desacetilasa 8 (HDAC8). También se describen métodos para usar estos inhibidores de HDAC8, solos o en combinación con otros compuestos, para tratar enfermedades o condiciones que se beneficiarían de la inhibición de la actividad de HDAC8.
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公开(公告)号:HK1140107A1
公开(公告)日:2010-10-08
申请号:HK10106827
申请日:2009-09-14
Applicant: PHARMACYCLICS INC
Inventor: HONIGBERG LEE , VERNER ERIK , PAN ZHENGYING
IPC: A01N20060101 , A61K20060101 , A61P20060101 , C07D20060101
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:HK1132744A1
公开(公告)日:2010-03-05
申请号:HK10100318
申请日:2010-01-12
Applicant: PHARMACYCLICS INC
Inventor: PAN ZHENGYING , LI SHYR JIANN , SCHEREENS HELEEN , HONIGBERG LEE , VERNER ERIK
IPC: C07D20060101 , G01N20060101
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公开(公告)号:MX2009010284A
公开(公告)日:2010-01-29
申请号:MX2009010284
申请日:2008-03-27
Applicant: PHARMACYCLICS INC
Inventor: HONIGBERG LEE , VERNER ERIK , BUGGY JOSEPH J , LOURY DAVID , CHEN WEI
IPC: A61K31/52 , A61K31/519 , A61P29/00 , A61P35/00 , C07D253/06 , C07D473/34 , C07D487/04
Abstract: En la presente se describen compuestos inhibidores de cinasa irreversibles, métodos para sintetizar dichos inhibidores irreversibles, y métodos para usar dichos inhibidores irreversibles en el tratamiento de enfermedades. En la presente se describen también métodos, ensayos y sistemas para determinar un inhibidor irreversible apropiado de una proteína, que incluye una cinasa.
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