+

PE20220141A1 - Inhibidores de la proteina tirosina fosfatasa - Google Patents

Inhibidores de la proteina tirosina fosfatasa

Info

Publication number
PE20220141A1
PE20220141A1 PE2021001646A PE2021001646A PE20220141A1 PE 20220141 A1 PE20220141 A1 PE 20220141A1 PE 2021001646 A PE2021001646 A PE 2021001646A PE 2021001646 A PE2021001646 A PE 2021001646A PE 20220141 A1 PE20220141 A1 PE 20220141A1
Authority
PE
Peru
Prior art keywords
bicyclic
membered
heteroaryl
heterocycle
cyano
Prior art date
Application number
PE2021001646A
Other languages
English (en)
Inventor
James F Blake
Mark Laurence Boys
Mark Joseph Chicarelli
Adam W Cook
Mohamed S A Elsayed
Jay Bradford Fell
John P Fischer
Ronald Jay Hinklin
Yutong Jiang
Oren T Mcnulty
Macedonio J Mejia
Martha E Rodriguez
Christina E Wong
Original Assignee
Array Biopharma 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 Array Biopharma Inc filed Critical Array Biopharma Inc
Publication of PE20220141A1 publication Critical patent/PE20220141A1/es

Links

Classifications

    • 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • 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
    • 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
    • A61K31/53Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D451/00Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
    • C07D451/02Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
    • C07D451/04Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
    • 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
    • C07D471/10Spiro-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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/10Spiro-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (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)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

Se refiere a compuestos de Formula I o una sal farmaceuticamente aceptable del mismo, donde: L1 se selecciona de un enlace directo, S, CH2, O, NH y Se; R1 se selecciona de hidrogeno y metilo; R2 se selecciona de fenilo, un heteroarilo de 5 a 6 miembros en donde el heteroarilo contiene 1 a 4 heteroatomos seleccionados del grupo que consiste en N, O y S, en donde un heteroatomo de N se puede sustituir con O para formar un oxido, un cicloalquilo biciclico de 8-10 miembros, un arilo biciclico de 10 miembros, un heterociclo biciclico de 9-10 miembros, en donde el heterociclo contiene 1 a 3 heteroatomos seleccionados del grupo que consiste en N, O y S, y un heteroarilo biciclico de 9-10 miembros, en donde el heteroarilo biciclico contiene 1 a 3 heteroatomos seleccionados del grupo que consiste en N, O y S, en donde el fenilo, heteroarilo, cicloalquilo biciclico, arilo biciclico, heterociclo biciclico y heteroarilo biciclico se sustituyen opcionalmente con halogeno, ciano, oxo, C1-C3 alquilo opcionalmente sustituido con 1 a 3 grupos seleccionados de halogeno, ciano y OH, C3-C6 cicloalquilo, C1-C3 alcoxi opcionalmente sustituido con 1 a 3 grupos seleccionados de halogeno, ciano y OH, NHRa, y un heterociclo de 3 a 6 miembros opcionalmente sustituido con 1 a 3 grupos seleccionados de halogeno, ciano y OH, en donde el heterociclo contiene 1 o 2 heteroatomos seleccionados de N, O y S. R2 se puede seleccionar del grupo de fenilo, 2-clorofenilo, 3-clorofenilo, 2,3-diclorofenilo, 2-amino-3-cloropiridin-4-ilo, 2,3-dicloropiridin-4-ilo, entre otros. Tambien se refiere a composiciones farmaceuticas. Dichos compuestos son utiles en el tratamiento de enfermedades hiperproliferativas y neoplasicas al inhibir la proteina SHP2 necesaria para la activacion completa de la via de Ras/ERK1/2, una cascada de senalizacion clave en la biologia del cancer.
PE2021001646A 2019-04-02 2020-03-30 Inhibidores de la proteina tirosina fosfatasa PE20220141A1 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201962828356P 2019-04-02 2019-04-02
US202062992558P 2020-03-20 2020-03-20
PCT/IB2020/053019 WO2020201991A1 (en) 2019-04-02 2020-03-30 Protein tyrosine phosphatase inhibitors

Publications (1)

Publication Number Publication Date
PE20220141A1 true PE20220141A1 (es) 2022-01-27

Family

ID=70277430

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2021001646A PE20220141A1 (es) 2019-04-02 2020-03-30 Inhibidores de la proteina tirosina fosfatasa

Country Status (25)

Country Link
US (3) US11634417B2 (es)
EP (1) EP3947367A1 (es)
JP (2) JP7284830B2 (es)
KR (1) KR102698608B1 (es)
CN (1) CN113874363B (es)
AU (1) AU2020251841B2 (es)
BR (1) BR112021018664A2 (es)
CA (1) CA3135555C (es)
CL (2) CL2021002542A1 (es)
CO (1) CO2021013030A2 (es)
CR (1) CR20210501A (es)
CU (1) CU20210080A7 (es)
DO (1) DOP2021000206A (es)
EC (1) ECSP21072994A (es)
GE (1) GEP20237561B (es)
IL (2) IL286462A (es)
MA (1) MA55511A (es)
MX (1) MX2021012122A (es)
PE (1) PE20220141A1 (es)
PH (1) PH12021552227A1 (es)
SG (1) SG11202110502PA (es)
TW (1) TWI766261B (es)
UY (1) UY38628A (es)
WO (1) WO2020201991A1 (es)
ZA (1) ZA202108443B (es)

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020072656A1 (en) 2018-10-03 2020-04-09 Gilead Sciences, Inc. Imidozopyrimidine derivatives
WO2020081848A1 (en) 2018-10-17 2020-04-23 Array Biopharma Inc. Protein tyrosine phosphatase inhibitors
PE20220141A1 (es) * 2019-04-02 2022-01-27 Array Biopharma Inc Inhibidores de la proteina tirosina fosfatasa
IL299131A (en) 2020-06-18 2023-02-01 Revolution Medicines Inc Methods for delaying, preventing and treating acquired resistance to RAS inhibitors
CN116209438A (zh) 2020-09-03 2023-06-02 锐新医药公司 使用sos1抑制剂治疗具有shp2突变的恶性疾病
CN116457358A (zh) 2020-09-15 2023-07-18 锐新医药公司 作为ras抑制剂以治疗癌症的吲哚衍生物
US20240025924A1 (en) * 2021-03-23 2024-01-25 Shanghai Haiyan Pharmaceutical Technology Co., Ltd. Heterocycle substituted ketone derivative, and composition and medicinal use thereof
TWI825637B (zh) 2021-03-31 2023-12-11 美商輝瑞股份有限公司 啶-1,6(2h,7h)-二酮
WO2022206684A1 (zh) * 2021-03-31 2022-10-06 南京明德新药研发有限公司 一系列含Se的吡嗪类化合物及其应用
CA3215295A1 (en) 2021-04-01 2022-10-06 Array Biopharma Inc. Crystalline form of a shp2 inhibitor
WO2022235870A1 (en) 2021-05-05 2022-11-10 Revolution Medicines, Inc. Ras inhibitors for the treatment of cancer
CN117500811A (zh) 2021-05-05 2024-02-02 锐新医药公司 共价ras抑制剂及其用途
AR125782A1 (es) 2021-05-05 2023-08-16 Revolution Medicines Inc Inhibidores de ras
CN115960109B (zh) * 2021-05-31 2024-06-25 药雅科技(上海)有限公司 稠环类shp2磷酸酶抑制剂的制备及其应用
TW202244049A (zh) * 2021-05-12 2022-11-16 大陸商藥雅科技(上海)有限公司 Shp2磷酸酶抑制劑的製備及其應用
JP2024527535A (ja) 2021-07-09 2024-07-25 カナプ セラピューティクス インコーポレイテッド Shp2阻害剤及びその使用
AR127308A1 (es) 2021-10-08 2024-01-10 Revolution Medicines Inc Inhibidores ras
EP4417600A4 (en) * 2021-10-14 2025-02-19 Beijing Tide Pharmaceutical Co., Ltd. SHP2 INHIBITOR, PHARMACEUTICAL COMPOSITION THEREOF AND USE THEREOF
CN119136806A (zh) 2022-03-08 2024-12-13 锐新医药公司 用于治疗免疫难治性肺癌的方法
EP4496629A1 (en) 2022-03-23 2025-01-29 Array BioPharma Inc. Crystalline salt form of a shp2 inhibitor
KR20250022133A (ko) 2022-06-10 2025-02-14 레볼루션 메디슨즈, 인크. 거대고리 ras 억제제
CN115177622B (zh) * 2022-07-19 2024-09-17 中南大学湘雅二医院 多个化合物在制备治疗骨髓增殖性肿瘤的药物中的应用
TW202504611A (zh) 2023-03-30 2025-02-01 美商銳新醫藥公司 用於誘導ras gtp水解之組合物及其用途
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
WO2024216048A1 (en) 2023-04-14 2024-10-17 Revolution Medicines, Inc. Crystalline forms of ras inhibitors, compositions containing the same, and methods of use thereof
WO2024216016A1 (en) 2023-04-14 2024-10-17 Revolution Medicines, Inc. Crystalline forms of a ras inhibitor
WO2024218632A1 (en) 2023-04-17 2024-10-24 Array Biopharma Inc. Erk protein kinase inhibitors
TW202508595A (zh) 2023-05-04 2025-03-01 美商銳新醫藥公司 用於ras相關疾病或病症之組合療法
WO2025006753A2 (en) 2023-06-30 2025-01-02 Merck Patent Gmbh Heterobifunctional compounds for the degradation of kras protein
WO2025034702A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Rmc-6291 for use in the treatment of ras protein-related disease or disorder
US20250154171A1 (en) 2023-10-12 2025-05-15 Revolution Medicines, Inc. Ras inhibitors
WO2025171296A1 (en) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Ras inhibitors

Family Cites Families (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3773919A (en) 1969-10-23 1973-11-20 Du Pont Polylactide-drug mixtures
US4485045A (en) 1981-07-06 1984-11-27 Research Corporation Synthetic phosphatidyl cholines useful in forming liposomes
US4544545A (en) 1983-06-20 1985-10-01 Trustees University Of Massachusetts Liposomes containing modified cholesterol for organ targeting
US5013556A (en) 1989-10-20 1991-05-07 Liposome Technology, Inc. Liposomes with enhanced circulation time
US5543523A (en) 1994-11-15 1996-08-06 Regents Of The University Of Minnesota Method and intermediates for the synthesis of korupensamines
US7834178B2 (en) 2006-03-01 2010-11-16 Bristol-Myers Squibb Company Triazine 11-beta hydroxysteroid dehydrogenase type 1 inhibitors
SG11201401460PA (en) 2011-10-14 2014-09-26 Array Biopharma Inc POLYMORPHS OF ARRY-380, A SELECTIVE ErbB2 (HER2) INHIBITOR AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
TW201408658A (zh) 2012-08-27 2014-03-01 Array Biopharma Inc 絲胺酸/酥胺酸激酶抑制劑
CN104703988B (zh) 2013-09-30 2017-04-12 韩国化学研究院 新的三唑并吡嗪衍生物及其用途
JP6473457B2 (ja) * 2014-01-17 2019-02-20 ノバルティス アーゲー Shp2の活性を阻害するための1−(トリアジン−3−イル/ピリダジン−3−イル)−ピペリジン/ピペラジン誘導体およびその組成物
JO3517B1 (ar) 2014-01-17 2020-07-05 Novartis Ag ان-ازاسبيرو الكان حلقي كبديل مركبات اريل-ان مغايرة وتركيبات لتثبيط نشاط shp2
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
US10308660B2 (en) 2015-06-19 2019-06-04 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
WO2016203404A1 (en) 2015-06-19 2016-12-22 Novartis Ag Compounds and compositions for inhibiting the activity of shp2
EP3463343B1 (en) 2016-05-31 2022-03-23 Board of Regents, The University of Texas System Heterocyclic inhibitors of ptpn11
PT3464272T (pt) 2016-06-07 2022-03-11 Jacobio Pharmaceuticals Co Ltd Novos derivados heterocíclicos úteis como inibidores de shp2
RU2021106500A (ru) 2016-06-14 2021-04-16 Новартис Аг Соединения и композиции для подавления активности shp2
WO2018013597A1 (en) * 2016-07-12 2018-01-18 Revolution Medicines, Inc. 2,5-disubstituted 3-methyl pyrazines and 2,5,6-trisubstituted 3-methyl pyrazines as allosteric shp2 inhibitors
WO2018057884A1 (en) 2016-09-22 2018-03-29 Relay Therapeutics, Inc. Shp2 phosphatase inhibitors and methods of use thereof
TW202500565A (zh) 2016-10-24 2025-01-01 美商傳達治療有限公司 Shp2磷酸酶抑制劑及其使用方法
CA3051054A1 (en) 2017-01-23 2018-07-26 Revolution Medicines, Inc. Pyridine compounds as allosteric shp2 inhibitors
SG11201906209SA (en) 2017-01-23 2019-08-27 Revolution Medicines Inc Bicyclic compounds as allosteric shp2 inhibitors
HUE068568T2 (hu) * 2017-03-23 2025-01-28 Jacobio Pharmaceuticals Co Ltd Új heterociklusos származékok, amelyek SHP2 inhibitorként hasznosíthatóak
US11591336B2 (en) 2017-05-26 2023-02-28 D. E. Shaw Research, Llc Substituted pyrazolo[3,4-b]pyrazines as SHP2 phosphatase inhibitors
MX2020002608A (es) 2017-09-07 2020-09-18 Revolution Medicines Inc Composiciones que comprenden inhibidores de shp2 y metodos para tratar el cáncer.
US10435389B2 (en) 2017-09-11 2019-10-08 Krouzon Pharmaccuticals, Inc. Octahydrocyclopenta[c]pyrrole allosteric inhibitors of SHP2
US11701354B2 (en) 2017-09-29 2023-07-18 D. E. Shaw Research, Llc Pyrazolo[3,4-b]pyrazine derivatives as SHP2 phosphatase inhibitors
BR112020007058A2 (pt) 2017-10-12 2020-10-06 Revolution Medicines, Inc. compostos de piridina, pirazina, e triazina como inibidores de shp2 alostéricos
AU2018385713A1 (en) 2017-12-15 2020-06-18 Revolution Medicines, Inc. Polycyclic compounds as allosteric SHP2 inhibitors
US11426422B2 (en) 2018-01-30 2022-08-30 Research Development Foundation SHP2 inhibitors and methods of use thereof
CA3097709A1 (en) 2018-03-21 2019-09-26 Synblia Therapeutics, Inc. Shp2 inhibitors and uses thereof
WO2019183364A1 (en) 2018-03-21 2019-09-26 Relay Therapeutics, Inc. Pyrazolo[3,4-b]pyrazine shp2 phosphatase inhibitors and methods of use thereof
JP7418395B2 (ja) 2018-03-21 2024-01-19 リレー セラピューティクス, インコーポレイテッド Shp2ホスファターゼ阻害剤およびこれらの使用方法
CN112601750B (zh) 2018-08-10 2023-10-31 纳维尔制药有限公司 Ptpn11(shp2)抑制剂
CN112839935A (zh) * 2018-09-26 2021-05-25 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
WO2020081848A1 (en) 2018-10-17 2020-04-23 Array Biopharma Inc. Protein tyrosine phosphatase inhibitors
PE20220141A1 (es) * 2019-04-02 2022-01-27 Array Biopharma Inc Inhibidores de la proteina tirosina fosfatasa

Also Published As

Publication number Publication date
AU2020251841B2 (en) 2025-01-30
CN113874363A (zh) 2021-12-31
US11634417B2 (en) 2023-04-25
CA3135555A1 (en) 2020-10-08
CR20210501A (es) 2021-11-02
CA3135555C (en) 2023-09-19
MA55511A (fr) 2022-02-09
CL2021002542A1 (es) 2022-06-24
US20240124453A1 (en) 2024-04-18
US11884664B2 (en) 2024-01-30
BR112021018664A2 (pt) 2021-11-23
CU20210080A7 (es) 2022-05-11
PH12021552227A1 (en) 2022-05-30
KR102698608B1 (ko) 2024-08-27
DOP2021000206A (es) 2021-11-21
SG11202110502PA (en) 2021-10-28
ECSP21072994A (es) 2021-11-18
CO2021013030A2 (es) 2021-10-20
US20200317665A1 (en) 2020-10-08
ZA202108443B (en) 2023-04-26
UY38628A (es) 2020-10-30
JP2023078421A (ja) 2023-06-06
WO2020201991A1 (en) 2020-10-08
CL2024000183A1 (es) 2024-06-07
CN113874363B (zh) 2024-11-12
IL320682A (en) 2025-07-01
GEP20237561B (en) 2023-10-25
JP7284830B2 (ja) 2023-05-31
TWI766261B (zh) 2022-06-01
KR20210146389A (ko) 2021-12-03
JP2022527796A (ja) 2022-06-06
TW202102490A (zh) 2021-01-16
US20220251083A1 (en) 2022-08-11
IL286462A (en) 2021-10-31
AU2020251841A1 (en) 2021-10-07
EP3947367A1 (en) 2022-02-09
MX2021012122A (es) 2021-11-03

Similar Documents

Publication Publication Date Title
PE20220141A1 (es) Inhibidores de la proteina tirosina fosfatasa
PE20220931A1 (es) Inhibidores de shp2 fosfatasa de tipo pirazolo[3,4-b]pirazina
PE20241063A1 (es) Composiciones y metodos para la inhibicion de ras
PE20220592A1 (es) Inhibidores de la autofagia de heteroarilaminopirimidina amida y metodos de uso de estos
PE20191755A1 (es) Derivados de pirazol como inhibidores de malt 1
CR20220312A (es) Compuestos tricíclicos sustituidos
MX2024001824A (es) Compuestos heterociclicos y metodos de uso.
SA522433155B1 (ar) مركبات ثلاثية الحلقة مستبدلة
PE20210004A1 (es) Inhibidores de mcl-1
PE20200796A1 (es) Compuestos derivados de 3-(1-oxoisoindolin-2-il)piperidina-2,6-diona y composiciones que los comprenden
EA201991894A1 (ru) ПИПЕРИДИН-ЗАМЕЩЕННЫЕ ИНГИБИТОРЫ Mnk И СВЯЗАННЫЕ С НИМИ СПОСОБЫ
PE20190395A1 (es) Pirimidin-2-ilamino-1h-pirazoles como inhibidores de lrrk2 para el uso en el tratamiento de trastornos neurodegenerativos
CY1120325T1 (el) Τρικυκλικες ετεροκυκλικες ενωσεις ως αναστολεις φωσφοϊνοσιτιδιου 3-κινασης
PE20231986A1 (es) Compuesto de heteroarilcarboxamida
AR054560A1 (es) Espiropiperidina como inhibidores de beta-secretasa para el tratamiento de la enfermedad de alzheimer
BRPI0510177A (pt) heterociclos monocìclicos como inibidores de cinase
PE20090435A1 (es) Inhibidores de tetrahidropiranocromeno de gamma secretasa
EA202091475A1 (ru) ПРОИЗВОДНЫЕ 5-(2-(2,5-ДИФТОРФЕНИЛ)ПИРРОЛИДИН-1-ИЛ)-3-(1H-ПИРАЗОЛ-1-ИЛ)ПИРАЗОЛО[1,5-а]ПИРИМИДИНА И РОДСТВЕННЫЕ СОЕДИНЕНИЯ В КАЧЕСТВЕ ИНГИБИТОРОВ Trk КИНАЗЫ ДЛЯ ЛЕЧЕНИЯ РАКА
CL2020002157A1 (es) Derivados de triazina para el tratamiento de enfermedades relacionadas con neurotrofinas.
MX2024002391A (es) Inhibidores de indolina de kif18a.
PE20240879A1 (es) Inhibidor sos1 y uso del mismo
PE20200445A1 (es) Inhibidores pirazolicos de magl
PE20211770A1 (es) 3,3-difluoroalilaminas o sales de las mismas y composiciones farmaceuticas que las comprenden
PE20211769A1 (es) Compuestos heteroaromaticos como inhibidores de vanina
PE20241934A1 (es) Inhibidores de raf quinasa y metodos de uso de los mismos
点击 这是indexloc提供的php浏览器服务,不要输入任何密码和下载