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公开(公告)号:US20140171407A1
公开(公告)日:2014-06-19
申请号:US14182190
申请日:2014-02-17
Applicant: Genentech, Inc.
Inventor: Hazel Joan Dyke , Lewis Gazzard , Karen Williams , Huifen Chen , Samuel Kintz , Joy Drobnick , Joseph P. Lyssikatos , Simon Goodacre , Calum Macleod , Charles Ellwood
IPC: C07D471/14 , A61K31/4375 , C07D453/02 , A61K45/06 , A61K31/4545 , A61K31/439 , A61K31/55 , A61K31/5377 , A61K31/496
CPC classification number: C07D471/14 , A61K31/4375 , A61K31/439 , A61K31/4545 , A61K31/496 , A61K31/5377 , A61K31/55 , A61K45/06 , C07D453/02 , C07D519/00
Abstract: The invention relates to 1,7-diazacarbazole compounds of Formula (I), (I-a) and (I-b) which are useful as kinase inhibitors, more specifically useful as checkpoint kinase 1 (chk1) inhibitors, thus useful as cancer therapeutics. The invention also relates to compositions, more specifically pharmaceutical compositions comprising these compounds and methods of using the same to treat various forms of cancer and hyperproliferative disorders, as well as methods of using the compounds for in vitro, in situ, and in vivo diagnosis or treatment of mammalian cells, or associated pathological conditions.
Abstract translation: 本发明涉及可用作激酶抑制剂的式(I),(I-a)和(I-b)的1,7-二氮杂咔唑化合物,更具体地用作检查点激酶1(chk1)抑制剂,因此可用作癌症治疗剂。 本发明还涉及包含这些化合物的组合物,更具体地是包含这些化合物的药物组合物以及使用该组合物治疗各种形式的癌症和过度增殖性疾病的方法,以及将该化合物用于体外,原位和体内诊断或 治疗哺乳动物细胞或相关病理状况。
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公开(公告)号:US11612606B2
公开(公告)日:2023-03-28
申请号:US16592502
申请日:2019-10-03
Applicant: Genentech, Inc.
Inventor: Jun Liang , Rohan V. Mendonca , Michael Siu , John Tellis , Weiru Wang , BinQing Wei , Bryan Chan , Edna F. Choo , Joy Drobnick , Lewis J. Gazzard , Timothy Heffron
IPC: A61K31/5383 , A61K31/4725 , C07D498/04 , C07D498/08 , A61K31/4375 , C07D491/052 , A61K31/436 , A61K31/551 , C07D471/04 , A61K31/439
Abstract: 3-Carbonylamino-8-aminoisoquinoline compounds of formula (I): variations thereof, and their use as inhibitors of HPK1 (hematopoietic kinase 1) are described. The compounds are useful in treating HPK1-dependent disorders and enhancing an immune response. Also described are methods of inhibiting HPK1, methods of treating HPK1-dependent disorders, methods for enhancing an immune response, and methods for preparing the 3-carbonylamino-8-aminoisoquinoline compounds.
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公开(公告)号:US20210163417A1
公开(公告)日:2021-06-03
申请号:US16921297
申请日:2020-07-06
Applicant: Genentech, Inc.
Inventor: Bryan Chan , Joy Drobnick , Lewis Gazzard , Timothy Heffron , Jun Liang , Sushant Malhotra , Rohan Mendonca , Naomi Rajapaksa , Craig Stivala , John Tellis , Weiru Wang , BinQing Wei , Aihe Zhou , Matthew W. Cartwright , Michael Lainchbury , Emanuela Gancia , Eileen Seward , Andrew Madin , David Favor , Kin Chiu Fong , Yonghan Hu , Andrew Good
IPC: C07D217/22 , A61K31/549 , A61P35/00 , A61K45/06 , C07D401/04 , A61K31/4725 , A61K31/506 , A61K31/501 , C07D471/04 , C07D413/04 , C07D413/14 , A61K31/5377 , C07D417/04 , A61K31/4985 , C07D401/14 , C07D487/04 , A61K31/551 , C07D498/04 , A61K31/5383 , C07D405/14 , C07D519/00 , C07D498/14 , C07D513/04 , A61K31/554 , A61K31/55 , A61K31/472 , C07D409/14 , C07D491/04 , C07D487/14
Abstract: Isoquinoline compounds and their use as inhibitors of HPK1 (hematopoietic kinase 1) are described. The compounds are useful in treating HPK1-dependent disorders and enhancing an immune response. Also described are methods of inhibiting HPK1, methods of treating HPK1-dependent disorders, methods for enhancing an immune response, and methods for preparing the isoquinoline compounds.
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公开(公告)号:US10899774B2
公开(公告)日:2021-01-26
申请号:US16715959
申请日:2019-12-16
Applicant: Genentech, Inc.
Inventor: Marian C. Bryan , Joy Drobnick , Alberto Gobbi , Tamiko Katsumoto , Naomi S. Rajapaksa , James Richard Kiefer, Jr.
IPC: C07D498/04 , C07D413/14 , C07D417/14 , C07D471/04 , C07D487/04 , C07D491/048 , C07D495/04 , C07D513/04
Abstract: Compounds of Formula 0, and stereoisomers and pharmaceutically acceptable salts thereof, as well as methods of use as Interleukin-1 Receptor Associated Kinase (IRAK4) inhibitors are described herein.
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公开(公告)号:US20180298015A1
公开(公告)日:2018-10-18
申请号:US16014231
申请日:2018-06-21
Applicant: Genentech, Inc.
Inventor: Marian C. Bryan , Alberto Gobbi , James Richard Kiefer, JR. , Aleksandr Kolesnikov , Alan G. Olivero , Joy Drobnick , Jun Liang , Naomi Rajapaksa , Chudi Ndubaku , Jianwen Feng
IPC: C07D487/04 , C07D519/00 , A61P29/00 , A61P35/00 , A61P37/02
Abstract: Compounds of Formula 0, Formula I, and Formula II and methods of use as Interleukin-1 Receptor Associated Kinase (IRAK4) inhibitors are described herein.
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公开(公告)号:US20180282328A1
公开(公告)日:2018-10-04
申请号:US15942321
申请日:2018-03-30
Applicant: Genentech, Inc.
Inventor: Bryan Chan , Blake Daniels , Joy Drobnick , Lewis Gazzard , Timothy Heffron , Malcolm Huestis , Jun Liang , Sushant Malhotra , Rohan Mendonca , Naomi Rajapaksa , Michael Siu , Craig Stivala , John Tellis , Weiru Wang , BinQing Wei , Aihe Zhou , Matthew W. Cartwright , Emanuela Gancia , Graham Jones , Michael Lainchbury , Andrew Madin , Eileen Seward , David Favor , Kin Chiu Fong , Andrew Good , Yonghan Hu , Baihua Hu , Aijun Lu
IPC: C07D471/04 , A61K45/06 , A61P35/00 , A61K31/444 , A61K31/4375 , A61K31/506 , C07D519/00 , A61K31/4545 , A61K31/4725 , A61K31/5383 , A61K31/496 , A61K31/5377 , A61K31/5025 , A61K31/551 , A61K31/55
CPC classification number: C07D471/04 , A61K31/4375 , A61K31/444 , A61K31/4545 , A61K31/4725 , A61K31/496 , A61K31/5025 , A61K31/506 , A61K31/5377 , A61K31/5383 , A61K31/55 , A61K31/551 , A61K45/06 , A61P35/00 , C07D519/00
Abstract: Naphthyridine compounds and their use as inhibitors of HPK1 are described. The compounds are useful in treating HPK1-dependent disorders and enhancing an immune response. Also described are methods of inhibiting HPK1, methods of treating HPK1-dependent disorders, methods for enhancing an immune response, and methods for preparing the naphthyridine compounds.
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公开(公告)号:US20180282282A1
公开(公告)日:2018-10-04
申请号:US15942333
申请日:2018-03-30
Applicant: Genentech, Inc.
Inventor: Bryan Chan , Joy Drobnick , Lewis Gazzard , Timothy Heffron , Jun Liang , Sushant Malhotra , Rohan Mendonca , Naomi Rajapaksa , Craig Stivala , John Tellis , Weiru Wang , BinQing Wei , Aihe Zhou , Matthew W. Cartwright , Michael Lainchbury , Emanuela Gancia , Eileen Seward , Andrew Madin , David Favor , Kin Chiu Fong , Yonghan Hu , Andrew Good
IPC: C07D217/22 , A61K31/472 , A61P35/00 , A61K45/06 , C07D401/04 , A61K31/4725 , A61K31/506 , A61K31/501 , C07D471/04 , C07D413/04 , C07D413/14 , A61K31/5377 , C07D417/04 , A61K31/4985 , C07D401/14 , C07D487/04 , A61K31/551 , C07D498/04 , A61K31/5383 , C07D405/14 , C07D519/00 , C07D498/14 , C07D513/04 , A61K31/554 , A61K31/55 , A61K31/549
Abstract: Isoquinoline compounds and their use as inhibitors of HPK1 (hematopoietic kinase 1) are described. The compounds are useful in treating HPK1-dependent disorders and enhancing an immune response. Also described are methods of inhibitng HPK1, methods of treating HPK1-dependent disorders, methods for enhancing an immune response, and methods for preparing the isoquinoline compounds.
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公开(公告)号:US20150328195A1
公开(公告)日:2015-11-19
申请号:US14743835
申请日:2015-06-18
Applicant: GENENTECH, INC.
Inventor: Hazel Joan Dyke , Lewis Gazzard , Karen Williams , Huifen Chen , Samuel Kintz , Joy Drobnick , Joseph P. Lyssikatos , Simon Goodacre , Calum Macleod , Charles Ellwood
IPC: A61K31/4375 , C07D471/14 , A61K31/496 , A61K45/06 , C07D453/02 , C07D519/00 , A61K31/55 , A61K31/5377 , A61K31/439
CPC classification number: C07D471/14 , A61K31/4375 , A61K31/439 , A61K31/4545 , A61K31/496 , A61K31/5377 , A61K31/55 , A61K45/06 , C07D453/02 , C07D519/00
Abstract: The invention relates to 1,7-diazacarbazole compounds of Formula (I), (I-a) and (I-b) which are useful as kinase inhibitors, more specifically useful as checkpoint kinase 1 (chk1) inhibitors, thus useful as cancer therapeutics. The invention also relates to compositions, more specifically pharmaceutical compositions comprising these compounds and methods of using the same to treat various forms of cancer and hyperproliferative disorders, as well as methods of using the compounds for in vitro, in situ, and in vivo diagnosis or treatment of mammalian cells, or associated pathological conditions.
Abstract translation: 本发明涉及可用作激酶抑制剂的式(I),(I-a)和(I-b)的1,7-二氮杂咔唑化合物,更具体地用作检查点激酶1(chk1)抑制剂,因此可用作癌症治疗剂。 本发明还涉及包含这些化合物的组合物,更具体地是包含这些化合物的药物组合物以及使用该组合物治疗各种形式的癌症和过度增殖性疾病的方法,以及将该化合物用于体外,原位和体内诊断或 治疗哺乳动物细胞或相关病理状况。
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