CO2021003074A2 - Derivados de 6-(4-amino-3-metil-2-oxa-8-azaespiro[4.5]decan-8-il)-3-(2,3-diclorofenil)-2-metilpirimidin-4(3h)-ona y compuestos relacionados como inhibidores de ptpn11 (shp2) para el tratamiento del cáncer - Google Patents

Derivados de 6-(4-amino-3-metil-2-oxa-8-azaespiro[4.5]decan-8-il)-3-(2,3-diclorofenil)-2-metilpirimidin-4(3h)-ona y compuestos relacionados como inhibidores de ptpn11 (shp2) para el tratamiento del cáncer

Info

Publication number
CO2021003074A2
CO2021003074A2 CONC2021/0003074A CO2021003074A CO2021003074A2 CO 2021003074 A2 CO2021003074 A2 CO 2021003074A2 CO 2021003074 A CO2021003074 A CO 2021003074A CO 2021003074 A2 CO2021003074 A2 CO 2021003074A2
Authority
CO
Colombia
Prior art keywords
treatment
cancer
ptpn11
inhibitors
shp2
Prior art date
Application number
CONC2021/0003074A
Other languages
English (en)
Inventor
Philip Jones
Barbara Czako
Christopher L Carroll
Pijus Mandal
Jason Cross
Original Assignee
Navire Pharma Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Navire Pharma Inc filed Critical Navire Pharma Inc
Publication of CO2021003074A2 publication Critical patent/CO2021003074A2/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/10Spiro-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/10Spiro-condensed systems
    • C07D491/107Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

La presente invención se refiere a compuestos que son útiles como inhibidores de PTPN11 para el tratamiento o la prevención del cáncer y otras enfermedades mediadas por PTP. En el presente documento se divulgan compuestos nuevos y compuestos a base de pirazolopirazinas y su aplicación como productos farmacéuticos para el tratamiento de enfermedades.
CONC2021/0003074A 2018-08-10 2021-03-09 Derivados de 6-(4-amino-3-metil-2-oxa-8-azaespiro[4.5]decan-8-il)-3-(2,3-diclorofenil)-2-metilpirimidin-4(3h)-ona y compuestos relacionados como inhibidores de ptpn11 (shp2) para el tratamiento del cáncer CO2021003074A2 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201862717588P 2018-08-10 2018-08-10
US201862773921P 2018-11-30 2018-11-30
PCT/US2019/045903 WO2020033828A1 (en) 2018-08-10 2019-08-09 6-(4-amino-3-methyl-2-oxa-8-azaspiro[4.5]decan-8-yl)-3-(2,3-dichlorophenyl)-2-methylpyrimidin-4(3h)-one derivatives and related compounds as ptpn11 (shp2) inhibitors for treating cancer

Publications (1)

Publication Number Publication Date
CO2021003074A2 true CO2021003074A2 (es) 2021-06-10

Family

ID=67766350

Family Applications (1)

Application Number Title Priority Date Filing Date
CONC2021/0003074A CO2021003074A2 (es) 2018-08-10 2021-03-09 Derivados de 6-(4-amino-3-metil-2-oxa-8-azaespiro[4.5]decan-8-il)-3-(2,3-diclorofenil)-2-metilpirimidin-4(3h)-ona y compuestos relacionados como inhibidores de ptpn11 (shp2) para el tratamiento del cáncer

Country Status (29)

Country Link
US (2) US11104675B2 (es)
EP (2) EP3833670B1 (es)
JP (2) JP2021534124A (es)
KR (1) KR102707409B1 (es)
CN (1) CN112601750B (es)
AU (1) AU2019319971A1 (es)
BR (1) BR112021002327A2 (es)
CA (1) CA3109181A1 (es)
CL (1) CL2021000355A1 (es)
CO (1) CO2021003074A2 (es)
CR (1) CR20210132A (es)
DK (1) DK3833670T3 (es)
ES (1) ES2981592T3 (es)
FI (1) FI3833670T3 (es)
HR (1) HRP20240861T1 (es)
IL (2) IL280701B2 (es)
LT (1) LT3833670T (es)
MX (2) MX2021001608A (es)
PE (1) PE20211050A1 (es)
PH (1) PH12021550268A1 (es)
PL (1) PL3833670T3 (es)
PT (1) PT3833670T (es)
RS (1) RS65728B1 (es)
SG (1) SG11202100199UA (es)
SI (1) SI3833670T1 (es)
TW (1) TWI827646B (es)
UA (1) UA128559C2 (es)
WO (1) WO2020033828A1 (es)
ZA (1) ZA202101449B (es)

Families Citing this family (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11466017B2 (en) 2011-03-10 2022-10-11 Board Of Regents, The University Of Texas System Heterocyclic inhibitors of PTPN11
AU2017274199B2 (en) 2016-05-31 2021-09-23 Board Of Regents, The University Of Texas System Heterocyclic inhibitors of PTPN11
EP3515916B1 (en) 2016-09-22 2023-06-07 Relay Therapeutics, Inc. Shp2 phosphatase inhibitors and methods of use thereof
TWI848901B (zh) 2016-10-24 2024-07-21 美商傳達治療有限公司 Shp2磷酸酶抑制劑及其使用方法
EP3630770B1 (en) 2017-05-26 2024-08-28 Relay Therapeutics, Inc. Pyrazolo[3,4-b]pyrazine derivatives as shp2 phosphatase inhibitors
WO2019067843A1 (en) 2017-09-29 2019-04-04 Relay Therapeutics, Inc. PYRAZOLO [3,4-B] PYRAZINE DERIVATIVES AS INHIBITORS OF PHOSPHATASE SHP2
IL301106A (en) 2018-03-21 2023-05-01 Relay Therapeutics Inc SHP2 phosphatase inhibitors and methods of using them
AU2019263294B2 (en) 2018-05-02 2024-03-21 Navire Pharma, Inc. Substituted heterocyclic inhibitors of PTPN11
WO2020033828A1 (en) 2018-08-10 2020-02-13 Board Of Regents, The University Of Texas System 6-(4-amino-3-methyl-2-oxa-8-azaspiro[4.5]decan-8-yl)-3-(2,3-dichlorophenyl)-2-methylpyrimidin-4(3h)-one derivatives and related compounds as ptpn11 (shp2) inhibitors for treating cancer
CA3113234A1 (en) 2018-09-18 2020-03-26 Nikang Therapeutics, Inc. Tri-substituted heteroaryl derivatives as src homology-2 phosphatase inhibitors
EA202191498A1 (ru) 2018-11-30 2021-08-20 Мерк Шарп энд Доум Корп. 9-замещенные производные аминотриазолохиназолина в качестве антагонистов аденозиновых рецепторов, фармацевтические композиции и их применение
JP2022511469A (ja) 2018-11-30 2022-01-31 コメット セラピューティクス インコーポレイテッド 環状パンテテイン誘導体及びその使用
MA55511A (fr) 2019-04-02 2022-02-09 Array Biopharma Inc Inhibiteurs de protéine tyrosine phosphatase
CA3127475A1 (en) 2019-04-08 2020-10-15 Merck Patent Gmbh Pyrimidinone derivatives as shp2 antagonists
WO2021061706A1 (en) 2019-09-24 2021-04-01 Relay Therapeutics, Inc. Shp2 phosphatase inhibitors and methods of making and using the same
JP2023500328A (ja) 2019-11-08 2023-01-05 レボリューション メディシンズ インコーポレイテッド 二環式ヘテロアリール化合物及びその使用
CN115916194A (zh) 2020-06-18 2023-04-04 锐新医药公司 用于延迟、预防和治疗针对ras抑制剂的获得性抗性的方法
WO2022060583A1 (en) 2020-09-03 2022-03-24 Revolution Medicines, Inc. Use of sos1 inhibitors to treat malignancies with shp2 mutations
AU2021345111A1 (en) 2020-09-15 2023-04-06 Revolution Medicines, Inc. Indole derivatives as Ras inhibitors in the treatment of cancer
WO2022235866A1 (en) 2021-05-05 2022-11-10 Revolution Medicines, Inc. Covalent ras inhibitors and uses thereof
WO2022235864A1 (en) 2021-05-05 2022-11-10 Revolution Medicines, Inc. Ras inhibitors
CN117616031A (zh) 2021-05-05 2024-02-27 锐新医药公司 用于治疗癌症的ras抑制剂
TW202313041A (zh) 2021-06-09 2023-04-01 瑞士商諾華公司 包含達拉菲尼、曲美替尼和shp2抑制劑之三重藥物組合
TW202317100A (zh) 2021-06-23 2023-05-01 瑞士商諾華公司 包含kras g12c抑制劑的藥物組合及其用於治療癌症之用途
WO2023031781A1 (en) 2021-09-01 2023-03-09 Novartis Ag Pharmaceutical combinations comprising a tead inhibitor and uses thereof for the treatment of cancers
WO2023056037A1 (en) * 2021-09-30 2023-04-06 Navire Pharma, Inc. Combination therapy using substituted pyrimidin-4(3h)-ones and sotorasib
JP2024536338A (ja) 2021-09-30 2024-10-04 ナビール ファーマ,インコーポレイティド Ptpn11阻害剤とegfr阻害剤を用いた併用療法
AU2022360835A1 (en) * 2021-10-06 2024-05-16 Navire Pharma, Inc. Substituted pyrimidin-4(3h)-ones for use in treating cancer
AR127308A1 (es) 2021-10-08 2024-01-10 Revolution Medicines Inc Inhibidores ras
WO2023172940A1 (en) 2022-03-08 2023-09-14 Revolution Medicines, Inc. Methods for treating immune refractory lung cancer
WO2023205794A1 (en) 2022-04-22 2023-10-26 Bristol-Myers Squibb Company Combination therapy using a pyrimidone derivative as ptpn11 inhibitor and a pd-1/pd-l1 inhibitor and its use in the treatment of cancer
TW202404599A (zh) * 2022-04-22 2024-02-01 美商必治妥美雅史谷比公司 使用經取代之嘧啶-4(3h)-酮及納武單抗(nivolumab)之組合療法
WO2023240263A1 (en) 2022-06-10 2023-12-14 Revolution Medicines, Inc. Macrocyclic ras inhibitors
WO2024206858A1 (en) 2023-03-30 2024-10-03 Revolution Medicines, Inc. Compositions for inducing ras gtp hydrolysis and uses thereof
WO2024211712A1 (en) 2023-04-07 2024-10-10 Revolution Medicines, Inc. Condensed macrocyclic compounds as ras inhibitors
WO2024211663A1 (en) 2023-04-07 2024-10-10 Revolution Medicines, Inc. Condensed macrocyclic compounds as ras inhibitors

Family Cites Families (67)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007504243A (ja) 2003-09-03 2007-03-01 ニューロジェン・コーポレーション 5−アリール−ピラゾロ[4,3−d]ピリミジン類、ピリジン類、ピラジン類及び関連化合物
MXPA06009462A (es) 2004-02-27 2007-03-15 Hoffmann La Roche Derivados pirazolo heteroaril fusionados.
US7897607B2 (en) 2004-04-07 2011-03-01 Takeda Pharmaceutical Company Limited Cyclic compounds
JP2008520738A (ja) 2004-11-22 2008-06-19 バーテックス ファーマシューティカルズ インコーポレイテッド プロテインキナーゼの阻害剤として有用なピロロピラジンおよびピラゾロピラジン
GB0427604D0 (en) 2004-12-16 2005-01-19 Novartis Ag Organic compounds
GB0506147D0 (en) 2005-03-24 2005-05-04 Merck Sharp & Dohme Therapeutic agents
WO2008061109A2 (en) 2006-11-15 2008-05-22 Forest Laboratories Holdings Limited Indazole derivatives useful as melanin concentrating receptor ligands
KR20090110913A (ko) * 2007-02-15 2009-10-23 노파르티스 아게 Lbh589와 암을 치료하기 위한 다른 치료제와의 조합물
EP2350020B1 (en) 2008-10-03 2014-08-13 Merck Sharp & Dohme Corp. Spiro-imidazolone derivatives as glucagon receptor antagonists
JP2010111624A (ja) 2008-11-06 2010-05-20 Shionogi & Co Ltd Ttk阻害作用を有するインダゾール誘導体
KR20110049217A (ko) 2009-11-04 2011-05-12 다우어드밴스드디스플레이머티리얼 유한회사 신규한 유기 발광 화합물 및 이를 채용하고 있는 유기 전계 발광 소자
JP2011246389A (ja) 2010-05-26 2011-12-08 Oncotherapy Science Ltd Ttk阻害作用を有する縮環ピラゾール誘導体
JPWO2012011592A1 (ja) * 2010-07-23 2013-09-09 武田薬品工業株式会社 複素環化合物およびその用途
EP2670733B1 (en) 2011-02-01 2019-04-10 The Board of Trustees of the University of Illionis N-hydroxybenzamide derivatives as hdac inhibitors and therapeutic methods using the same
WO2013052263A2 (en) 2011-09-16 2013-04-11 Microbiotix, Inc. Antifungal compounds
WO2013040527A1 (en) 2011-09-16 2013-03-21 Microbiotix, Inc. Antimicrobial compounds
WO2014047662A2 (en) 2012-09-24 2014-03-27 Whitehead Institute For Biomedical Research Indazole derivatives and uses thereof
CN110423212B (zh) 2013-04-26 2023-05-09 美国印第安纳大学研究和技术公司 Shp2的基于羟基吲哚羧酸的抑制剂
WO2014200682A1 (en) 2013-05-24 2014-12-18 The Scripps Research Institute Bidentate-binding modulators of lrrk2 and jnk kinases
WO2015099481A1 (ko) 2013-12-27 2015-07-02 주식회사 두산 유기 전계 발광 소자
CN105899493B (zh) 2014-01-17 2019-03-29 诺华股份有限公司 用于抑制shp2活性的1-(三嗪-3-基/哒嗪-3-基)-哌(-嗪)啶衍生物及其组合物
ES2699351T3 (es) 2014-01-17 2019-02-08 Novartis Ag Derivados de 1-piridazin/triazin-3-il-piper(-azina)/idina/pirolidina y composiciones de las mismas para inhibir la actividad de SHP2
JO3517B1 (ar) 2014-01-17 2020-07-05 Novartis Ag ان-ازاسبيرو الكان حلقي كبديل مركبات اريل-ان مغايرة وتركيبات لتثبيط نشاط shp2
KR101998435B1 (ko) 2014-06-09 2019-07-09 주식회사 두산 유기 전계 발광 소자
US9902719B2 (en) * 2014-07-03 2018-02-27 Celgene Quanticel Research, Inc. Inhibitors of lysine specific demethylase-1
KR101708097B1 (ko) 2014-10-22 2017-02-17 주식회사 두산 유기 전계 발광 소자
EP3273959A1 (en) 2015-03-25 2018-01-31 Novartis Ag Pharmaceutical combinations
JP6878316B2 (ja) * 2015-06-19 2021-05-26 ノバルティス アーゲー Shp2の活性を阻害するための化合物および組成物
WO2016203404A1 (en) 2015-06-19 2016-12-22 Novartis Ag Compounds and compositions for inhibiting the activity of shp2
JP6718889B2 (ja) 2015-06-19 2020-07-08 ノバルティス アーゲー Shp2の活性を阻害するための化合物および組成物
WO2017156397A1 (en) 2016-03-11 2017-09-14 Board Of Regents, The University Of Texas Sysytem Heterocyclic inhibitors of ptpn11
CN107286150B (zh) 2016-04-11 2020-07-07 中国科学院上海有机化学研究所 N-杂环类化合物、其中间体、制备方法、药物组合物和应用
AU2017274199B2 (en) 2016-05-31 2021-09-23 Board Of Regents, The University Of Texas System Heterocyclic inhibitors of PTPN11
MA45189A (fr) 2016-06-07 2019-04-10 Jacobio Pharmaceuticals Co Ltd Nouveaux dérivés hétérocycliques utiles en tant qu'inhibiteurs de shp2
CA3023216A1 (en) 2016-06-14 2017-12-21 Novartis Ag Compounds and compositions for inhibiting the activity of shp2
JP6916279B2 (ja) 2016-07-12 2021-08-11 レヴォリューション・メディスンズ,インコーポレイテッド アロステリックshp2阻害剤としての2,5−二置換3−メチルピラジンおよび2,5,6−三置換3−メチルピラジン
EP3515916B1 (en) 2016-09-22 2023-06-07 Relay Therapeutics, Inc. Shp2 phosphatase inhibitors and methods of use thereof
TWI848901B (zh) 2016-10-24 2024-07-21 美商傳達治療有限公司 Shp2磷酸酶抑制劑及其使用方法
WO2018130928A1 (en) 2017-01-10 2018-07-19 Novartis Ag Pharmaceutical combination comprising an alk inhibitor and a shp2 inhibitor
EP4230623A3 (en) 2017-01-23 2023-10-11 Revolution Medicines, Inc. Pyridine compounds as allosteric shp2 inhibitors
WO2018136265A1 (en) 2017-01-23 2018-07-26 Revolution Medicines, Inc. Bicyclic compounds as allosteric shp2 inhibitors
KR20220113545A (ko) 2017-03-23 2022-08-12 자코바이오 파마슈티칼스 컴퍼니 리미티드 Shp2 억제제로서 유용한 신규한 헤테로환형 유도체
EP3630770B1 (en) 2017-05-26 2024-08-28 Relay Therapeutics, Inc. Pyrazolo[3,4-b]pyrazine derivatives as shp2 phosphatase inhibitors
EP3678703A1 (en) 2017-09-07 2020-07-15 Revolution Medicines, Inc. Shp2 inhibitor compositions and methods for treating cancer
CN111201223B (zh) 2017-09-11 2024-07-09 克鲁松制药公司 SHP2的八氢环戊二烯并[c]吡咯别构抑制剂
WO2019067843A1 (en) 2017-09-29 2019-04-04 Relay Therapeutics, Inc. PYRAZOLO [3,4-B] PYRAZINE DERIVATIVES AS INHIBITORS OF PHOSPHATASE SHP2
CA3078565A1 (en) 2017-10-12 2019-04-18 Revolution Medicines, Inc. Pyridine, pyrazine, and triazine compounds as allosteric shp2 inhibitors
EP3724189B1 (en) 2017-12-15 2023-10-04 Revolution Medicines, Inc. Polycyclic compounds as allosteric shp2 inhibitors
WO2019152454A1 (en) 2018-01-30 2019-08-08 Research Development Foundation Shp2 inhibitors and methods of use thereof
MA51845A (fr) 2018-02-13 2020-12-23 Shanghai Blueray Biopharma Co Ltd Composé cyclique fusionné à une pyrimidine, son procédé de préparation et son application
EP3755699A1 (en) 2018-02-21 2020-12-30 Relay Therapeutics, Inc. Shp2 phosphatase inhibitors and methods of use thereof
CA3092011A1 (en) 2018-03-02 2019-09-06 Otsuka Pharmaceutical Co., Ltd. Pharmaceutical compounds
IL301106A (en) 2018-03-21 2023-05-01 Relay Therapeutics Inc SHP2 phosphatase inhibitors and methods of using them
CA3097709A1 (en) 2018-03-21 2019-09-26 Synblia Therapeutics, Inc. Shp2 inhibitors and uses thereof
US20210069188A1 (en) 2018-03-21 2021-03-11 Relay Therapeutics, Inc. Pyrazolo[3,4-b]pyrazine shp2 phosphatase inhibitors and methods of use thereof
WO2019199792A1 (en) 2018-04-10 2019-10-17 Revolution Medicines, Inc. Shp2 inhibitor compositions, methods for treating cancer and methods for identifying a subject with shp2 mutations
AU2019263294B2 (en) 2018-05-02 2024-03-21 Navire Pharma, Inc. Substituted heterocyclic inhibitors of PTPN11
CN115969853A (zh) 2018-05-09 2023-04-18 北京加科思新药研发有限公司 可用作shp2抑制剂的新型杂环衍生物
US20210230300A1 (en) 2018-06-04 2021-07-29 Bayer Aktiengesellschaft Inhibitors of shp2
BR112021001292A2 (pt) 2018-07-24 2021-05-11 Otsuka Pharmaceutical Co., Ltd compostos heterobicíclicos para inibir a atividade de shp2
TWI825144B (zh) 2018-08-10 2023-12-11 美商思達利醫藥公司 第二型轉麩醯胺酸酶(tg2)抑制劑
WO2020033828A1 (en) 2018-08-10 2020-02-13 Board Of Regents, The University Of Texas System 6-(4-amino-3-methyl-2-oxa-8-azaspiro[4.5]decan-8-yl)-3-(2,3-dichlorophenyl)-2-methylpyrimidin-4(3h)-one derivatives and related compounds as ptpn11 (shp2) inhibitors for treating cancer
AR117200A1 (es) 2018-11-30 2021-07-21 Syngenta Participations Ag Derivados de tiazol microbiocidas
EA202191498A1 (ru) 2018-11-30 2021-08-20 Мерк Шарп энд Доум Корп. 9-замещенные производные аминотриазолохиназолина в качестве антагонистов аденозиновых рецепторов, фармацевтические композиции и их применение
JP2022511469A (ja) 2018-11-30 2022-01-31 コメット セラピューティクス インコーポレイテッド 環状パンテテイン誘導体及びその使用
KR20210097154A (ko) 2018-11-30 2021-08-06 글락소스미스클라인 인털렉츄얼 프로퍼티 디벨로프먼트 리미티드 Hiv 요법에 유용한 화합물
AR117183A1 (es) 2018-11-30 2021-07-14 Syngenta Crop Protection Ag Derivados de tiazol microbiocidas

Also Published As

Publication number Publication date
CN112601750B (zh) 2023-10-31
FI3833670T3 (fi) 2024-05-21
EP4356973A3 (en) 2024-06-26
WO2020033828A1 (en) 2020-02-13
CA3109181A1 (en) 2020-02-13
ZA202101449B (en) 2024-08-28
US11104675B2 (en) 2021-08-31
IL307361A (en) 2023-11-01
IL307361B1 (en) 2024-08-01
EP3833670A1 (en) 2021-06-16
JP2023144075A (ja) 2023-10-06
IL280701B1 (en) 2023-11-01
IL280701A (en) 2021-03-25
TW202019900A (zh) 2020-06-01
US20220041594A1 (en) 2022-02-10
HRP20240861T1 (hr) 2024-10-11
SG11202100199UA (en) 2021-02-25
EP3833670B1 (en) 2024-04-17
US11945815B2 (en) 2024-04-02
KR20210043569A (ko) 2021-04-21
PE20211050A1 (es) 2021-06-04
CN112601750A (zh) 2021-04-02
PH12021550268A1 (en) 2021-11-03
KR102707409B1 (ko) 2024-09-13
JP2021534124A (ja) 2021-12-09
MX2024001249A (es) 2024-02-14
RS65728B1 (sr) 2024-08-30
US20200048249A1 (en) 2020-02-13
UA128559C2 (uk) 2024-08-14
PT3833670T (pt) 2024-05-22
ES2981592T3 (es) 2024-10-09
DK3833670T3 (da) 2024-05-13
IL280701B2 (en) 2024-03-01
TWI827646B (zh) 2024-01-01
PL3833670T3 (pl) 2024-08-19
CR20210132A (es) 2021-07-20
AU2019319971A1 (en) 2021-03-25
BR112021002327A2 (pt) 2021-05-04
LT3833670T (lt) 2024-06-25
MX2021001608A (es) 2021-07-15
EP4356973A2 (en) 2024-04-24
CL2021000355A1 (es) 2021-08-27
SI3833670T1 (sl) 2024-07-31

Similar Documents

Publication Publication Date Title
CO2021003074A2 (es) Derivados de 6-(4-amino-3-metil-2-oxa-8-azaespiro[4.5]decan-8-il)-3-(2,3-diclorofenil)-2-metilpirimidin-4(3h)-ona y compuestos relacionados como inhibidores de ptpn11 (shp2) para el tratamiento del cáncer
MX2020011528A (es) Inhibidores heterociclicos sustituidos de ptpn11.
SA518400547B1 (ar) مشتقات بيرازولو بيريميدين كمثبط كيناز
ECSP17070706A (es) Inhibidores de bromodominio
CO2018001268A2 (es) Derivados de heteroarilo como inhibidores de parp
CL2020001576A1 (es) Componentes heterocíclicos bicíclicos sustituidos como inhibidores de prmt5.
CR20150517A (es) Inhibidores de la phd de 6-(5-hidroxi-1h-pirazol-1-il) nicotinamida
CL2020001754A1 (es) Derivado de amino-fluoropiperidina como inhibidor de quinasa.
ECSP20061378A (es) COMPUESTOS DIÓLICOS DE AMINOPIRAZINA COMO INHIBIDORES DE PI3K-gamma
BR112019006987A2 (pt) inibidores de receptor de glicocorticoide
CO2019002517A2 (es) Inhibidores de dopamina–β–hidroxilasa
CO2017000011A2 (es) Derivados de quinolizinona como inhibidores de pi3k
DOP2018000238A (es) Inhibidores del potenciador del homólogo zeste 2
CO2018004572A2 (es) Inhibidores de calicreína plasmática humana
MX2023008677A (es) Derivados de urolitinas y métodos para su uso.
CL2020001093A1 (es) Proceso para preparar el benzotiofen-2-il boronato.
CO2019013254A2 (es) Compuestos bicíclicos 5,6-fusionados y composiciones para el tratamiento de enfermedades parasitarias
DOP2019000194A (es) Derivados de pirrolotriazina como inhibidor de cinasas
CL2021001944A1 (es) Derivados de aminoácidos para el tratamiento de enfermedades inflamatorias
EA201892698A1 (ru) Производные пиразолиламинобензимидазола в качестве ингибиторов jak
CY1124087T1 (el) Παραγωγα πυριδοκιναζολινης χρησιμα ως αναστολεις πρωτεϊνικων κινασων
CO2024009144A2 (es) Inhibidores de cinasa met
PH12017501063A1 (en) Compounds for the treatment of cancer
CR20190110A (es) Compuestos de tiazolo-piridina sustituida como inhibidores de malt1
ES2548927A1 (es) Derivados de purina como inhibidores de Dapk-1