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 cáncerInfo
- 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
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 206010028980 Neoplasm Diseases 0.000 title abstract 2
- 201000011510 cancer Diseases 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title abstract 2
- WYUIJDCKOPRFJO-UHFFFAOYSA-N 6-(4-amino-3-methyl-2-oxa-8-azaspiro[4.5]decan-8-yl)-3-(2,3-dichlorophenyl)-2-methylpyrimidin-4-one Chemical class NC1C(OCC11CCN(CC1)C1=CC(N(C(=N1)C)C1=C(C(=CC=C1)Cl)Cl)=O)C WYUIJDCKOPRFJO-UHFFFAOYSA-N 0.000 title 1
- 201000010099 disease Diseases 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- DDZGQYREBDXECY-UHFFFAOYSA-N 1h-pyrazolo[3,4-b]pyrazine Chemical class C1=CN=C2C=NNC2=N1 DDZGQYREBDXECY-UHFFFAOYSA-N 0.000 abstract 1
- 101001087416 Homo sapiens Tyrosine-protein phosphatase non-receptor type 11 Proteins 0.000 abstract 1
- 102100028516 Receptor-type tyrosine-protein phosphatase U Human genes 0.000 abstract 1
- 102100033019 Tyrosine-protein phosphatase non-receptor type 11 Human genes 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic 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
- C07D491/02—Heterocyclic 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
- C07D491/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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
- C07D401/04—Heterocyclic 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic 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
- C07D471/02—Heterocyclic 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
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic 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
- C07D491/02—Heterocyclic 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
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-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.
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)
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)
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 |
-
2019
- 2019-08-09 WO PCT/US2019/045903 patent/WO2020033828A1/en active Application Filing
- 2019-08-09 MX MX2021001608A patent/MX2021001608A/es unknown
- 2019-08-09 SG SG11202100199UA patent/SG11202100199UA/en unknown
- 2019-08-09 BR BR112021002327-5A patent/BR112021002327A2/pt unknown
- 2019-08-09 SI SI201930743T patent/SI3833670T1/sl unknown
- 2019-08-09 EP EP19759185.2A patent/EP3833670B1/en active Active
- 2019-08-09 PE PE2021000191A patent/PE20211050A1/es unknown
- 2019-08-09 HR HRP20240861TT patent/HRP20240861T1/hr unknown
- 2019-08-09 CR CR20210132A patent/CR20210132A/es unknown
- 2019-08-09 UA UAA202101174A patent/UA128559C2/uk unknown
- 2019-08-09 JP JP2021506929A patent/JP2021534124A/ja not_active Ceased
- 2019-08-09 US US16/536,923 patent/US11104675B2/en active Active
- 2019-08-09 DK DK19759185.2T patent/DK3833670T3/da active
- 2019-08-09 PT PT197591852T patent/PT3833670T/pt unknown
- 2019-08-09 FI FIEP19759185.2T patent/FI3833670T3/fi active
- 2019-08-09 CN CN201980046071.6A patent/CN112601750B/zh active Active
- 2019-08-09 AU AU2019319971A patent/AU2019319971A1/en active Pending
- 2019-08-09 RS RS20240780A patent/RS65728B1/sr unknown
- 2019-08-09 ES ES19759185T patent/ES2981592T3/es active Active
- 2019-08-09 LT LTEPPCT/US2019/045903T patent/LT3833670T/lt unknown
- 2019-08-09 EP EP24161326.4A patent/EP4356973A3/en active Pending
- 2019-08-09 KR KR1020217003134A patent/KR102707409B1/ko active IP Right Grant
- 2019-08-09 IL IL280701A patent/IL280701B2/en unknown
- 2019-08-09 PL PL19759185.2T patent/PL3833670T3/pl unknown
- 2019-08-09 CA CA3109181A patent/CA3109181A1/en active Pending
- 2019-08-09 IL IL307361A patent/IL307361B1/en unknown
- 2019-08-12 TW TW108128631A patent/TWI827646B/zh active
-
2021
- 2021-02-04 PH PH12021550268A patent/PH12021550268A1/en unknown
- 2021-02-09 MX MX2024001249A patent/MX2024001249A/es unknown
- 2021-02-10 CL CL2021000355A patent/CL2021000355A1/es unknown
- 2021-03-03 ZA ZA2021/01449A patent/ZA202101449B/en unknown
- 2021-03-09 CO CONC2021/0003074A patent/CO2021003074A2/es unknown
- 2021-07-20 US US17/380,943 patent/US11945815B2/en active Active
-
2023
- 2023-08-17 JP JP2023132960A patent/JP2023144075A/ja active Pending
Also Published As
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 |