MA53675A - Composés substitués de pyrazolo[1,5-a]pyridine en tant qu'inhibiteurs de la kinase ret - Google Patents

Composés substitués de pyrazolo[1,5-a]pyridine en tant qu'inhibiteurs de la kinase ret

Info

Publication number
MA53675A
MA53675A MA053675A MA53675A MA53675A MA 53675 A MA53675 A MA 53675A MA 053675 A MA053675 A MA 053675A MA 53675 A MA53675 A MA 53675A MA 53675 A MA53675 A MA 53675A
Authority
MA
Morocco
Prior art keywords
pyrazolo
kinase inhibitors
substituted compounds
ret kinase
pyridine substituted
Prior art date
Application number
MA053675A
Other languages
English (en)
Inventor
Steven W Andrews
Sean Aronow
James F Blake
Barbara J Brandhuber
Adam Cook
Julia Haas
Yutong Jiang
Gabrielle R Kolakowski
Elizabeth A Mcfaddin
Megan L Mckenney
Oren T Mcnulty
Andrew T Metcalf
David A Moreno
Li Ren
Tony P Tang
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 MA53675A publication Critical patent/MA53675A/fr

Links

Classifications

    • 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
    • A61K31/4985Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • 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
    • A61K31/4995Pyrazines or piperazines forming part of bridged ring 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
    • A61K31/495Heterocyclic 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
    • 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
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • 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
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • 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
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/12Antidiarrhoeals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
    • 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
    • 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

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Organic Chemistry (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Oncology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Pyridine Compounds (AREA)
MA053675A 2016-10-10 2017-10-10 Composés substitués de pyrazolo[1,5-a]pyridine en tant qu'inhibiteurs de la kinase ret MA53675A (fr)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201662406252P 2016-10-10 2016-10-10
US201762447850P 2017-01-18 2017-01-18
US201762491164P 2017-04-27 2017-04-27
US201762554817P 2017-09-06 2017-09-06
US201762566093P 2017-09-29 2017-09-29

Publications (1)

Publication Number Publication Date
MA53675A true MA53675A (fr) 2021-11-17

Family

ID=60153575

Family Applications (1)

Application Number Title Priority Date Filing Date
MA053675A MA53675A (fr) 2016-10-10 2017-10-10 Composés substitués de pyrazolo[1,5-a]pyridine en tant qu'inhibiteurs de la kinase ret

Country Status (39)

Country Link
US (8) US10112942B2 (fr)
EP (2) EP3753939A1 (fr)
JP (6) JP6776446B2 (fr)
KR (1) KR102143899B1 (fr)
CN (2) CN114163437B (fr)
AU (1) AU2017342022B2 (fr)
BR (1) BR112019007144B8 (fr)
CA (1) CA3039760C (fr)
CL (1) CL2019000941A1 (fr)
CO (1) CO2019004650A2 (fr)
CR (1) CR20190218A (fr)
CY (1) CY1123201T1 (fr)
DK (1) DK3523301T3 (fr)
DO (1) DOP2019000090A (fr)
EC (1) ECSP19032676A (fr)
ES (1) ES2805087T3 (fr)
HR (1) HRP20201008T1 (fr)
HU (1) HUE051424T2 (fr)
IL (2) IL265916B (fr)
JO (1) JOP20190076B1 (fr)
LT (1) LT3523301T (fr)
MA (1) MA53675A (fr)
MD (1) MD3523301T2 (fr)
MX (2) MX376465B (fr)
MY (1) MY195573A (fr)
NZ (1) NZ752793A (fr)
PE (1) PE20190918A1 (fr)
PH (1) PH12019500775A1 (fr)
PL (1) PL3523301T3 (fr)
PT (1) PT3523301T (fr)
RS (1) RS60536B1 (fr)
SA (1) SA519401541B1 (fr)
SG (1) SG11201903144PA (fr)
SI (1) SI3523301T1 (fr)
TN (1) TN2019000110A1 (fr)
TW (1) TWI704148B (fr)
UA (1) UA125030C2 (fr)
WO (1) WO2018071447A1 (fr)
ZA (1) ZA202004040B (fr)

Families Citing this family (87)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL2918588T3 (pl) 2010-05-20 2017-10-31 Array Biopharma Inc Związki makrocykliczne jako inhibitory kinazy TRK
US10202365B2 (en) 2015-02-06 2019-02-12 Blueprint Medicines Corporation 2-(pyridin-3-yl)-pyrimidine derivatives as RET inhibitors
WO2017011776A1 (fr) 2015-07-16 2017-01-19 Array Biopharma, Inc. Composés substitués de pyrazolo[1,5-a]pyridines comme inhibiteurs de la kinase ret
MX384884B (es) 2015-11-02 2025-03-14 Blueprint Medicines Corp Inhibidores de ret.
TWI704148B (zh) * 2016-10-10 2020-09-11 美商亞雷生物製藥股份有限公司 作為ret激酶抑制劑之經取代吡唑并[1,5-a]吡啶化合物
JOP20190077A1 (ar) 2016-10-10 2019-04-09 Array Biopharma Inc مركبات بيرازولو [1، 5-a]بيريدين بها استبدال كمثبطات كيناز ret
JP6888101B2 (ja) 2017-01-18 2021-06-16 アレイ バイオファーマ インコーポレイテッド RETキナーゼ阻害剤としての置換ピラゾロ[1,5−a]ピラジン化合物
JOP20190213A1 (ar) 2017-03-16 2019-09-16 Array Biopharma Inc مركبات حلقية ضخمة كمثبطات لكيناز ros1
TWI783057B (zh) * 2017-10-10 2022-11-11 美商絡速藥業公司 製備6-(2-羥基-2-甲基丙氧基)-4-(6-(6-((6-甲氧基吡啶-3-基)甲基)-3,6-二氮雜雙環[3.1.1]庚-3-基)吡啶-3-基)吡唑并[1,5-a]吡啶-3-甲腈的方法
TWI791053B (zh) * 2017-10-10 2023-02-01 美商亞雷生物製藥股份有限公司 6-(2-羥基-2-甲基丙氧基)-4-(6-(6-((6-甲氧基吡啶-3-基)甲基)-3,6-二氮雜雙環[3.1.1]庚-3-基)吡啶-3-基)吡唑并[1,5-a]吡啶-3-甲腈之結晶形式及其醫藥組合物
TWI876442B (zh) * 2017-10-10 2025-03-11 美商絡速藥業公司 6-(2-羥基-2-甲基丙氧基)-4-(6-(6-((6-甲氧基吡啶-3-基)甲基)-3,6-二氮雜雙環[3.1.1]庚-3-基)吡啶-3-基)吡唑并[1,5-a]吡啶-3-甲腈之調配物
US11472802B2 (en) 2018-01-18 2022-10-18 Array Biopharma Inc. Substituted pyrazolyl[4,3-c]pyridine compounds as RET kinase inhibitors
EP3740491A1 (fr) * 2018-01-18 2020-11-25 Array Biopharma, Inc. Composés de pyrrolo[2,3-d]pyrimidines substitués utilisés en tant qu'inhibiteurs de la kinase ret
US11524963B2 (en) 2018-01-18 2022-12-13 Array Biopharma Inc. Substituted pyrazolo[3,4-d]pyrimidines as RET kinase inhibitors
EP3773589B1 (fr) 2018-04-03 2023-11-01 Blueprint Medicines Corporation Inhibiteur de ret destiné à être utilisé dans le traitement du cancer présentant une altération du ret
CN108658981A (zh) * 2018-06-01 2018-10-16 成都福柯斯医药技术有限公司 一种6-溴-4-甲氧基氢-吡唑[1,5-a]吡啶-3-甲腈的合成方法
EP3849986B1 (fr) 2018-09-10 2022-06-08 Array Biopharma, Inc. Composés hétérocycliques condensés comme inhibiteurs de kinases ret
EP3856743A4 (fr) * 2018-09-27 2022-06-15 Fochon Pharmaceuticals, Ltd. Composés imidazo [1, 2-a] pyridine et [1, 2, 4] triazolo [1, 5-a] pyridine substitués en tant qu'inhibiteurs de kinase ret
US20210379056A1 (en) * 2018-09-30 2021-12-09 Applied Pharmaceutical Science, Inc. Substituted pyrazole fused ring derivative, preparation method therefor, and application thereof
WO2020114388A1 (fr) 2018-12-06 2020-06-11 深圳市塔吉瑞生物医药有限公司 Composé pyrazolo[1,5-a]pyridine substitué, composition le contenant et utilisation associée
SG11202104686QA (en) * 2018-12-07 2021-06-29 Sunshine Lake Pharma Co Ltd Ret inhibitors, pharmaceutical compositions and uses thereof
EP3891149A4 (fr) * 2018-12-07 2022-09-07 Sunshine Lake Pharma Co., Ltd. Inhibiteurs de ret, compositions pharmaceutiques et utilisations associées
CA3130245A1 (fr) * 2019-02-19 2020-08-27 Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. Compose heterocyclique, composition pharmaceutique le comprenant, son procede de preparation et son utilisation
CN111635400A (zh) * 2019-03-02 2020-09-08 察略盛医药科技(上海)有限公司 吡唑并[1,5-a]吡啶类衍生物、及其制备方法和用途
US20220143049A1 (en) 2019-03-21 2022-05-12 Onxeo A dbait molecule in combination with kinase inhibitor for the treatment of cancer
JP7291243B2 (ja) * 2019-04-03 2023-06-14 広州白雲山医薬集団股分有限公司白雲山制薬総廠 Ret阻害剤としてのピラゾロピリジン系化合物及びその使用
WO2020207941A1 (fr) * 2019-04-09 2020-10-15 F. Hoffmann-La Roche Ag Composés hétérocycliques en tant qu'inhibiteurs de la monoacylglycérol lipase (magl)
CN112368283B (zh) * 2019-05-14 2023-02-17 上海翰森生物医药科技有限公司 含二并环类衍生物抑制剂、其制备方法和应用
CN111961034A (zh) * 2019-05-20 2020-11-20 浙江同源康医药股份有限公司 用作ret激酶抑制剂的化合物及其应用
US20220220128A1 (en) * 2019-06-10 2022-07-14 Js Innopharm (Shanghai) Ltd Heterocyclic compounds as kinase inhibitors, compositions comprising the heterocyclic compound, and methods of use thereof
GB201908511D0 (en) 2019-06-13 2019-07-31 Adorx Therapeutics Ltd Hydroxamate compounds
US11666570B2 (en) * 2019-07-11 2023-06-06 The Board Of Trustees Of The Leland Stanford Junior University Diagnosis and regulation of epidermal differentiation and cancer cell activity
US20220289740A1 (en) * 2019-07-12 2022-09-15 Shouyao Holdings (beijing) Co., Ltd. Ret selective inhibitor, preparation method therefor and use thereof
JP7732668B2 (ja) * 2019-08-05 2025-09-02 北京志健金瑞生物医▲薬▼科技有限公司 窒素含有多環式縮合環系化合物、その薬学的組成物、製造方法及び用途
WO2021043209A1 (fr) * 2019-09-04 2021-03-11 广东东阳光药业有限公司 Inhibiteur de ret, composition pharmaceutique et utilisation associée
WO2021057970A1 (fr) * 2019-09-29 2021-04-01 广东东阳光药业有限公司 Inhibiteur de ret, composition pharmaceutique associée et utilisation associée
CN112574235B (zh) * 2019-09-29 2024-01-16 广东东阳光药业股份有限公司 一种ret抑制剂、其药物组合物及其用途
WO2021088911A1 (fr) * 2019-11-08 2021-05-14 杭州邦顺制药有限公司 Dérivé de 3,6-diazabicyclo[3.1.1]heptane utilisé en tant qu'inhibiteur de kinase ret
EP4054579A1 (fr) 2019-11-08 2022-09-14 Institut National de la Santé et de la Recherche Médicale (INSERM) Méthodes pour le traitement de cancers qui ont acquis une résistance aux inhibiteurs de kinase
CN112851664B (zh) * 2019-11-12 2024-03-29 浙江海正药业股份有限公司 吡唑[1,5-a]吡啶-3-腈化合物及其在医药上的用途
CN112939967B (zh) * 2019-12-11 2024-08-27 深圳众格生物科技有限公司 吡唑并[1,5-a]吡啶类化合物及其制备方法和应用
CN111004257B (zh) * 2019-12-24 2021-06-29 武汉九州钰民医药科技有限公司 制备RET抑制剂Selpercatinib的方法
CN113045569B (zh) * 2019-12-27 2022-04-19 浙江同源康医药股份有限公司 用作ret激酶抑制剂的化合物及其应用
CN113121524B (zh) * 2019-12-31 2023-04-25 南京创济生物医药有限公司 杂环亚砜亚胺化合物及其中间体、制备方法和应用
WO2021148581A1 (fr) 2020-01-22 2021-07-29 Onxeo Nouvelle molécule dbait et son utilisation
CN111285887B (zh) * 2020-03-27 2020-11-17 苏州信诺维医药科技有限公司 一种螺环化合物
CN111269229B (zh) * 2020-03-27 2021-02-12 苏州信诺维医药科技有限公司 一种治疗癌症的化合物
CN111410662B (zh) * 2020-03-27 2020-12-29 苏州信诺维医药科技有限公司 一种酪氨酸激酶抑制剂
CN111233899B (zh) * 2020-03-27 2020-12-29 苏州信诺维医药科技有限公司 一种ret抑制剂
CN113527292B (zh) * 2020-04-13 2025-07-22 广东东阳光药业股份有限公司 一种ret抑制剂、其药物组合物及其用途
CN113527291B (zh) * 2020-04-13 2025-07-22 广东东阳光药业股份有限公司 Ret抑制剂、其药物组合物及其用途
CN113527290B (zh) * 2020-04-13 2025-07-22 广东东阳光药业股份有限公司 一种ret抑制剂、其药物组合物及其用途
TWI865765B (zh) * 2020-04-17 2024-12-11 美商絡速藥業公司 結晶ret抑制劑
CN113620945B (zh) * 2020-05-07 2024-08-23 广东东阳光药业股份有限公司 Ret抑制剂、其药物组合物及其在药物中的应用
KR20230017234A (ko) 2020-05-29 2023-02-03 블루프린트 메디신즈 코포레이션 프랄세티닙의 고체 형태
CN113880865A (zh) * 2020-07-01 2022-01-04 上海艾力斯医药科技股份有限公司 吡唑[1,5-a]吡啶类化合物及其制备方法与应用
WO2022020279A1 (fr) 2020-07-21 2022-01-27 Teva Pharmaceuticals International Gmbh Formes à l'état solide de selpercatinib et leur procédé de préparation
WO2022032026A1 (fr) 2020-08-05 2022-02-10 C4 Therapeutics, Inc. Composés pour la dégradation ciblée de ret
JP7564942B2 (ja) * 2020-08-20 2024-10-09 チャンスー チア タイ フェンハイ ファーマシューティカル カンパニー リミテッド Retキナーゼ阻害剤としてのヘテロ芳香族環化合物及びその製造と使用
US20230321098A1 (en) 2020-08-25 2023-10-12 Loxo Oncology, Inc. Osimertinib and selpercatinib combinations for the treatment of egfr- and ret-associated cancers
CN114249724B (zh) * 2020-09-25 2023-05-26 鲁南制药集团股份有限公司 一种唑吡坦中间体的制备方法
WO2022069357A1 (fr) 2020-10-01 2022-04-07 Sandoz Ag Forme cristalline du selpercatinib
AU2021377952A1 (en) * 2020-11-13 2023-06-29 Jiangsu Hansoh Pharmaceutical Group Co., Ltd. Crystal form of free base of inhibitor containing bicyclic ring derivative and preparation method and application of crystal form
CN114478586A (zh) * 2020-11-13 2022-05-13 上海翰森生物医药科技有限公司 一种含二并环类衍生物抑制剂盐或晶型及其制备方法和应用
CN114621256A (zh) * 2020-12-11 2022-06-14 深圳众格生物科技有限公司 吡唑并[1,5-a]吡啶类化合物及其制备方法和应用
TW202237118A (zh) 2020-12-14 2022-10-01 美商絡速藥業公司 用於預防腦轉移之組合物及方法
WO2022132683A1 (fr) 2020-12-18 2022-06-23 Loxo Oncology, Inc. Polythérapie à base d'inhibiteurs de ret pour le traitement du cancer
TW202237086A (zh) 2020-12-18 2022-10-01 美商絡速藥業公司 以ret抑制劑及鉑劑治療癌症之方法
TWI818424B (zh) * 2021-02-08 2023-10-11 大陸商北京志健金瑞生物醫藥科技有限公司 含氮多環稠環類化合物,其藥物組合物、製備方法和用途
CN113321668A (zh) * 2021-06-21 2021-08-31 江苏慧聚药业有限公司 塞尔帕替尼的合成
CN115594678B (zh) * 2021-07-09 2024-11-15 北京志健金瑞生物医药科技有限公司 含氮多环稠环类化合物的制备方法及其中间体和用途
CN113387947B (zh) * 2021-07-12 2022-07-01 中国科学院成都生物研究所 调节雌激素受体合成活性的吡唑并吡啶衍生物
WO2023239422A2 (fr) 2021-10-22 2023-12-14 University Of Houston System Méthodes et compositions pour traiter une lésion inflammatoire chronique, une métaplasie, une dysplasie et des cancers des tissus épithéliaux
KR20240101659A (ko) 2021-12-13 2024-07-02 록쏘 온콜로지, 인코포레이티드 셀페르카티닙 ret 억제제의 결정질 형태 a 및 그의 제조 방법
KR20250055538A (ko) * 2022-08-03 2025-04-24 브리스톨-마이어스 스큅 컴퍼니 Ret 단백질을 조정하기 위한 화합물
WO2024043257A1 (fr) 2022-08-24 2024-02-29 東レ株式会社 Médicament pour traitement et/ou prévention du cancer
CN117229292B (zh) * 2022-10-18 2025-08-15 药雅科技(上海)有限公司 Ret抑制剂的制备及其应用
WO2024206858A1 (fr) 2023-03-30 2024-10-03 Revolution Medicines, Inc. Compositions pour induire une hydrolyse de ras gtp et leurs utilisations
AU2024265078A1 (en) 2023-05-04 2025-12-11 Revolution Medicines, Inc. Combination therapy for a ras related disease or disorder
US20250049810A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
US20250154171A1 (en) 2023-10-12 2025-05-15 Revolution Medicines, Inc. Ras inhibitors
WO2025171296A1 (fr) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Inhibiteurs de ras
WO2025240847A1 (fr) 2024-05-17 2025-11-20 Revolution Medicines, Inc. Inhibiteurs de ras
US20250375445A1 (en) 2024-06-07 2025-12-11 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
WO2025265060A1 (fr) 2024-06-21 2025-12-26 Revolution Medicines, Inc. Compositions thérapeutiques et procédés de gestion d'effets liés au traitement
WO2026006747A1 (fr) 2024-06-28 2026-01-02 Revolution Medicines, Inc. Inhibiteurs de ras
CN119504796A (zh) * 2024-11-20 2025-02-25 南通大学附属医院 一种具有抗肿瘤活性的化合物及其应用

Family Cites Families (262)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4783443A (en) 1986-03-03 1988-11-08 The University Of Chicago Amino acyl cephalosporin derivatives
US5877016A (en) 1994-03-18 1999-03-02 Genentech, Inc. Human trk receptors and neurotrophic factor inhibitors
US5844092A (en) 1994-03-18 1998-12-01 Genentech, Inc. Human TRK receptors and neurotrophic factor inhibitors
US6677135B1 (en) 1996-05-08 2004-01-13 Biogen, Inc. Ret ligand (RetL) for stimulating neutral and renal growth
BR9710665A (pt) 1996-05-08 1999-08-17 Biogen Inc Compostos que promovem o desenvolvimento do tecido
US6682921B1 (en) 1996-08-21 2004-01-27 New York University Crystals of the tyrosine kinase domain of non-insulin receptor tyrosine kinases
US6531152B1 (en) 1998-09-30 2003-03-11 Dexcel Pharma Technologies Ltd. Immediate release gastrointestinal drug delivery system
AU7103900A (en) 1999-09-01 2001-03-26 Biogen, Inc. Ret ligand 5 (retl5) compositions and uses thereof
FI20000403A0 (fi) 2000-02-22 2000-02-22 Hannu Sariola GDNF perhesukuisten yhdisteiden käyttö kivessyövän hoitoon tarkoitettujen tuotteiden valmistamiseksi
DK1292680T3 (da) 2000-06-22 2010-03-08 Genentech Inc Agonist-anti-TrkC monoklonale antistoffer
WO2003020698A2 (fr) 2001-09-06 2003-03-13 Prochon Biotech Ltd. Inhibiteurs de la tyrosine kinase
US7466344B2 (en) 2002-06-07 2008-12-16 Scimeasure Analytical Systems, Inc. High-speed low noise CCD controller
ITMI20021620A1 (it) 2002-07-23 2004-01-23 Novuspharma Spa Composto ad ativita' antitumorale
JP2005535675A (ja) 2002-07-24 2005-11-24 ユニバーシティ・オブ・シンシナティ 変異型retキナーゼ関連疾患を処置するための4−(4−メチルピペラジン−1−イルメチル)−n−[4−メチル−3−(4−ピリジン−3−イル)ピリミジン−2−イルアミノ]フェニル]−ベンズアミド
EP1597251B1 (fr) 2003-02-20 2009-06-10 SmithKline Beecham Corporation Composes de pyrimidine
JP2005106669A (ja) 2003-09-30 2005-04-21 Olympus Corp 生体関連物質の反応・測定システム
US20090143399A1 (en) 2003-10-14 2009-06-04 Arizona Board Of Regents On Behalf Of The University Of Arizona Protein Kinase Inhibitors
WO2005044835A1 (fr) 2003-10-27 2005-05-19 Genelabs Technologies, Inc. Procedes de preparation de derives 7-(2'-$g(b)-d-ribofuranosyl substitue)-4-(nr2r3)-5-(ethyn-1-yl substitue)-pyrrolo[2,3-d]pyrimidine
MY141220A (en) 2003-11-17 2010-03-31 Astrazeneca Ab Pyrazole derivatives as inhibitors of receptor tyrosine kinases
WO2005054237A1 (fr) 2003-11-21 2005-06-16 Novartis Ag Derives d'1h-imidazoquinoline en tant qu'inhibiteurs de la proteine kinase
AR047496A1 (es) 2003-11-28 2006-01-25 Novartis Ag Derivados de diaril-urea en el tratamiento de enfermedades dependientes de la quinasa de proteina
ES2527118T3 (es) 2003-12-19 2015-01-20 Plexxikon Inc. Compuestos y procedimientos de desarrollo de moduladores de Ret
GB0330042D0 (en) 2003-12-24 2004-01-28 Pharmacia Italia Spa Pyrrolo [2,3-b] pyridine derivatives active as kinase inhibitors process for their preparation and pharmaceutical compositions them
GB0330043D0 (en) 2003-12-24 2004-01-28 Pharmacia Italia Spa Pyrrolo [2,3-b] pyridine derivatives active as kinase inhibitors process for their preparation and pharmaceutical compositions comprising them
WO2005068424A1 (fr) 2004-01-20 2005-07-28 Cell Therapeutics Europe S.R.L. Derives d'indolinone en tant qu'inhibiteurs de tyrosine kinase de recepteurs
AR049769A1 (es) 2004-01-22 2006-09-06 Novartis Ag Derivados de pirazolo(1,5-a)pirimidin 7-il-amina para utilizarse en el tratamiento de enfermedades dependientes de la quinasa de proteina
US20050222171A1 (en) 2004-01-22 2005-10-06 Guido Bold Organic compounds
WO2005099363A2 (fr) 2004-03-26 2005-10-27 Whitehead Institute For Biomedical Research Methodes de diagnostic, de prevention et de traitement de metastases cancereuses
GB0512324D0 (en) 2005-06-16 2005-07-27 Novartis Ag Organic compounds
US7465726B2 (en) 2004-08-02 2008-12-16 Osi Pharmaceuticals, Inc. Substituted pyrrolo[2.3-B]pyridines
PE20060664A1 (es) 2004-09-15 2006-08-04 Novartis Ag Amidas biciclicas como inhibidores de cinasa
US7855205B2 (en) 2004-10-29 2010-12-21 Janssen Pharmaceutica Nv Pyrimidinyl substituted fused-pyrrolyl compounds useful in treating kinase disorders
DE102005003687A1 (de) 2005-01-26 2006-07-27 Sphingo Tec Gmbh Immunoassay zur Bestimmung der Freisetzung von Neurotensin in die Zirkulation
GB0501999D0 (en) 2005-02-01 2005-03-09 Sentinel Oncology Ltd Pharmaceutical compounds
EP1848506A2 (fr) 2005-02-18 2007-10-31 Attenuon, LLC Derives de diazepine fusionnes pyrimidine et pteridines fusionnees indole
GB0507575D0 (en) * 2005-04-14 2005-05-18 Novartis Ag Organic compounds
US7402579B2 (en) 2005-04-15 2008-07-22 Cylene Pharmaceuticals, Inc. Quinobenzoxazine analogs and compositions
WO2006123113A2 (fr) 2005-05-16 2006-11-23 Astrazeneca Ab Composes chimiques
WO2006128042A2 (fr) 2005-05-26 2006-11-30 The Johns Hopkins University Procedes d'identification de mutations dans un acide nucleique
US7541367B2 (en) 2005-05-31 2009-06-02 Janssen Pharmaceutica, N.V. 3-benzoimidazolyl-pyrazolopyridines useful in treating kinase disorders
WO2006130613A2 (fr) 2005-05-31 2006-12-07 The Pfahl Family Trust (Dated 9 July 1996) Derives de biarylheterocycle substitues utilises comme inhibiteurs de la proteine kinase pour le traitement du cancer et d'autres maladies
ITRM20050290A1 (it) 2005-06-07 2006-12-08 Lay Line Genomics Spa Uso di molecole in grado di inibire il legame tra ngf e il suo recettore trka come analgesici ad effetto prolungato.
PT1893612E (pt) * 2005-06-22 2011-11-21 Plexxikon Inc Derivados de pirrolo [2,3-b]piridina como inibidores de proteína quinase
GB0515026D0 (en) 2005-07-21 2005-08-31 Novartis Ag Organic compounds
MX2008002524A (es) 2005-08-25 2008-03-14 Creabilis Therapeutics Spa Conjugados polimericos de k-252a y sus derivados.
EP1948647A1 (fr) 2005-11-03 2008-07-30 SGX Pharmaceuticals, Inc. Modulateurs de kinase de type pyrimidinylthiophène
US20070149523A1 (en) 2005-11-14 2007-06-28 Jan Ehlert Thiazole Analogues and Uses Thereof
EP1785420A1 (fr) 2005-11-14 2007-05-16 4Sc Ag Analogues de thiazole et leurs utilisation
WO2007057397A1 (fr) 2005-11-15 2007-05-24 Boehringer Ingelheim International Gmbh Traitement du cancer
WO2007057399A2 (fr) 2005-11-15 2007-05-24 Boehringer Ingelheim International Gmbh Traitement du cancer
GB0524436D0 (en) 2005-11-30 2006-01-11 Novartis Ag Organic compounds
AU2006322187A1 (en) 2005-12-08 2007-06-14 Novartis Ag Pyrazolo[1,5-a]pyridine-3-carboxylic acids as EphB and VEGFR2 kinase inhibitors
EP1968579A1 (fr) 2005-12-30 2008-09-17 Astex Therapeutics Limited Composes pharmaceutiques
EP1978958A4 (fr) 2006-01-24 2009-12-02 Merck & Co Inc Inhibition de la tyrosine kinase ret
PL1973910T3 (pl) 2006-01-27 2013-11-29 Shanghai hengrui pharmaceutical co ltd Pirolo[3,2-c]pirydyn-4-onowo-2-indolinonowe inhibitory kinazy białkowej
EP2001864A1 (fr) 2006-03-16 2008-12-17 Novartis Pharma AG Composes organiques
BRPI0708823B1 (pt) 2006-03-17 2022-01-18 Ambit Biosciences Corporation Composto, e, composição
ZA200808966B (en) 2006-03-27 2010-03-31 Nerviano Medical Sciences Srl Pyridyl- and pyrimidinyl-substituted pyrrole-, thiophene- and furane-derivatives as kinase inhibitors
MX2008014618A (es) 2006-05-15 2008-11-28 Irm Llc Composiciones y metodos para inhibidores de cinasas del receptor fgf.
CA2652442C (fr) 2006-05-18 2014-12-09 Eisai R & D Management Co., Ltd. Agent antitumoral destine au cancer de la thyroide
US8063225B2 (en) 2006-08-14 2011-11-22 Chembridge Corporation Tricyclic compound derivatives useful in the treatment of neoplastic diseases, inflammatory disorders and immunomodulatory disorders
WO2008031551A2 (fr) 2006-09-12 2008-03-20 Novartis Forschungsstiftung, Zweigniederlassung Traitement du cancer non neuroendocrinien
KR101507375B1 (ko) 2006-09-15 2015-04-07 엑스커버리 홀딩 컴퍼니 엘엘씨 키나아제 억제제 화합물
US20120225057A1 (en) 2006-10-11 2012-09-06 Deciphera Pharmaceuticals, Llc Methods and compositions for the treatment of myeloproliferative diseases and other proliferative diseases
EP1918291A1 (fr) 2006-10-30 2008-05-07 Novartis AG Dérives de pyrazole fusionnes substitués de 3-aminocarbonyle comme modulateurs de protéine kinase
HUE035868T2 (en) 2006-11-15 2018-05-28 Ym Biosciences Australia Pty Inhibitors of kinase activity
PE20121126A1 (es) 2006-12-21 2012-08-24 Plexxikon Inc Compuestos pirrolo [2,3-b] piridinas como moduladores de quinasa
CA2673736A1 (fr) 2006-12-21 2008-07-03 Plexxikon, Inc. Composes et procedes pour la modulation de kinases et indications pour celle-ci
WO2008079909A1 (fr) 2006-12-21 2008-07-03 Plexxikon, Inc. Composés et méthodes de modulation des kinases, et indications connexes
US20080199426A1 (en) 2007-01-11 2008-08-21 Sukhatme Vikas P Methods and compositions for the treatment and diagnosis of vascular inflammatory disorders or endothelial cell disorders
WO2008089388A2 (fr) 2007-01-19 2008-07-24 Bayer Healthcare Llc Traitement de cancers présentant une résistance à des agents chimiothérapeutiques
US20080234267A1 (en) 2007-03-20 2008-09-25 Karen Elizabeth Lackey Compounds and Methods of Treatment
US20110189167A1 (en) 2007-04-20 2011-08-04 Flynn Daniel L Methods and Compositions for the Treatment of Myeloproliferative Diseases and other Proliferative Diseases
CN101720322A (zh) 2007-05-04 2010-06-02 Irm责任有限公司 作为c-kit和pdgfr激酶抑制剂的化合物和组合物
WO2008138184A1 (fr) 2007-05-14 2008-11-20 Shanghai Hengrui Pharmaceutical Co.Ltd. Dérivés de pyrrolo-azacycles, leur procédé de fabrication et leur utilisation en tant qu'inhibiteurs de protéine kinases
US20090012045A1 (en) 2007-06-26 2009-01-08 Rigel Pharmaceuticals, Inc. Methods of Treating Cell Proliferative Disorders
AR067478A1 (es) 2007-07-09 2009-10-14 Astrazeneca Ab Compuestos derivados de morfolina pirimidina
US20100209488A1 (en) 2007-07-16 2010-08-19 The Regents Of The University Of California Protein kinase modulating compounds and methods for making and using them
AU2008276063B2 (en) 2007-07-17 2013-11-28 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
EP2178861B1 (fr) 2007-07-19 2014-08-20 Merck Sharp & Dohme Corp. Composés hétérocycliques d'amide en tant qu'inhibiteurs de protéine kinase
JP5506674B2 (ja) 2007-07-20 2014-05-28 ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ キナーゼ阻害剤として活性な置換インダゾール誘導体
WO2009017838A2 (fr) 2007-08-01 2009-02-05 Exelixis, Inc. Combinaisons d'inhibiteurs jak-2 et d'autres agents
DK2185698T3 (en) 2007-08-07 2015-07-27 Purdue Research Foundation Kinase Inhibitors and Uses thereof
EP2025678A1 (fr) 2007-08-17 2009-02-18 Oncalis AG Composés pyrazolo[3,4-d]pyrimidine et leur utilisation comme modulateur de protein kinase
WO2009042646A1 (fr) 2007-09-24 2009-04-02 Curis, Inc. Agents antiprolifératifs
MX2010004494A (es) 2007-10-23 2010-08-30 Novartis Ag Uso de anticuerpos de trkb para el tratamiento de trastornos respiratorios.
JP5400791B2 (ja) 2007-12-04 2014-01-29 ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ 置換ジヒドロプテリジン−6−オン誘導体、その製造方法及びキナーゼ阻害剤としてのその使用
CN101459004B (zh) 2007-12-14 2011-02-09 深圳富泰宏精密工业有限公司 电子装置的按键面板结构及制造该按键面板结构的方法
EP2235062A1 (fr) 2008-01-17 2010-10-06 Irm Llc Anticorps anti-trkb améliorés
US20090227556A1 (en) 2008-01-31 2009-09-10 Eisai R&D Management Co., Ltd. Receptor tyrosine kinase inhibitors comprising pyridine and pyrimidine derivatives
TW200938542A (en) 2008-02-01 2009-09-16 Irm Llc Compounds and compositions as kinase inhibitors
WO2009103076A1 (fr) 2008-02-15 2009-08-20 Oxigene, Inc. Méthodes et compositions pour améliorer l'efficacité des inhibiteurs des récepteurs tyrosine kinases (rtk)
US8822500B2 (en) 2008-03-19 2014-09-02 Chembridge Corporation Tyrosine kinase inhibitors
CN102036990B (zh) 2008-03-19 2015-09-30 凯姆桥公司 新型酪氨酸激酶抑制剂
US8207165B2 (en) 2008-03-28 2012-06-26 Nerviano Medical Sciences S.R.L. 3,4-dihydro-2H-pyrazino[1,2-A]indol-1-one derivatives active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them
WO2009143018A2 (fr) 2008-05-19 2009-11-26 Plexxikon, Inc. Composés et procédés de modulation des kinases, et indications associées
PE20091846A1 (es) 2008-05-19 2009-12-16 Plexxikon Inc DERIVADOS DE PIRROLO[2,3-d]-PIRIMIDINA COMO MODULADORES DE CINASAS
GEP20125502B (en) 2008-05-23 2012-04-25 Novartis Ag Derivatives of quinolines and quinoxalines as protein tyrosine kinase inhibitors
US20090298820A1 (en) * 2008-05-28 2009-12-03 Wyeth 3-substituted-1h-pyrrolo[2,3-b]pyridine and 3-substituted-1h-pyrrolo[3,2-b]pyridine compounds, their use as mtor kinase and pi3 kinase inhibitors, and their syntheses
CA2727389A1 (fr) 2008-06-10 2009-12-17 Prabha N. Ibrahim Derives 5h-pyrrolo-[2,3-b]-pyrazine destines a la modulation de kinases, et des indications pour ceux-ci
US20110212053A1 (en) 2008-06-19 2011-09-01 Dapeng Qian Phosphatidylinositol 3 kinase inhibitors
US8629135B2 (en) 2008-07-14 2014-01-14 Queen's University At Kingston Pharmaceutical compositions comprising RET inhibitors and methods for the treatment of cancer
US8946226B2 (en) 2008-07-29 2015-02-03 Nerviano Medical Sciences S.R.L. Use of CDK inhibitor for the treatment of glioma
US8410685B2 (en) 2008-09-01 2013-04-02 Sharp Kabushiki Kaisha Organic electroluminescent panel, organic electroluminescent display, organic electroluminescent lighting device, and production methods thereof
WO2010028254A2 (fr) 2008-09-05 2010-03-11 Auspek Pharmaceuticals, Inc. Inhibiteurs de tyrosine kinases de récepteur de facteur de croissance de type quinazoline substituée
EP2161271A1 (fr) 2008-09-08 2010-03-10 Università Degli Studi Di Milano - Bicocca Inhibiteurs d'alpha-carboline de NMP-ALK, RET, et Bcr-Abl
EP2376492B1 (fr) 2008-09-19 2015-04-08 Nerviano Medical Sciences S.r.l. Dérivés de 3,4-dihydro-2h-pyrrolo[1,2-a]pyrazine-1-one
PT2350075E (pt) 2008-09-22 2014-06-09 Array Biopharma Inc Compostos imidazo[1,2b]piridazina substituídos como inibidores da trk cinase
DK2331530T3 (da) 2008-09-26 2013-11-11 Nat Health Research Institutes Kondenserede multicycliske forbindelser som proteinkinaseinhibitorer
ME03010B (fr) 2008-10-22 2018-10-20 Array Biopharma Inc Pyrazolo [1,5-] pyrimidine en tant qu'inhibiteurs de kinases trk
US8551963B2 (en) 2008-11-06 2013-10-08 Ambit Biosciences Corporation Imidazolothiazole compounds and methods of use thereof
JP2012509859A (ja) 2008-11-24 2012-04-26 ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ 中皮腫の治療のためのcdk阻害物質
KR101061599B1 (ko) 2008-12-05 2011-09-02 한국과학기술연구원 비정상 세포 성장 질환의 치료를 위한 단백질 키나아제 저해제인 신규 인다졸 유도체, 이의 약학적으로 허용가능한염 및 이를 유효성분으로 함유하는 약학적 조성물
JO3265B1 (ar) 2008-12-09 2018-09-16 Novartis Ag مثبطات بيريديلوكسى اندولات vegf-r2 واستخدامها لعلاج المرض
WO2010111527A1 (fr) 2009-03-26 2010-09-30 Plexxikon, Inc. Pyrazolo [ 3, 4 -b] pyridines en tant qu'inhibiteurs de la kinase et leur utilisation médicale
TWI410418B (zh) 2009-04-29 2013-10-01 Ind Tech Res Inst 氮雜薁化合物、藥學組合物與抑制一細胞中蛋白質激酶之活性的方法
HUE026647T2 (en) 2009-05-08 2016-07-28 Astellas Pharma Inc Diamino heterocyclic carboxamide compound
CN102480966B (zh) 2009-06-12 2015-09-16 达娜-法勃肿瘤研究所公司 融合的杂环化合物及其用途
EP3045457B1 (fr) 2009-06-15 2018-05-09 Nerviano Medical Sciences S.r.l. Dérivés de pyrimidinylpyrrolopyridinone substitués, leur procédé de préparation et leur utilisation en tant qu'inhibiteurs de kinase
AR077468A1 (es) 2009-07-09 2011-08-31 Array Biopharma Inc Compuestos de pirazolo (1,5 -a) pirimidina sustituidos como inhibidores de trk- quinasa
JP5819831B2 (ja) 2009-08-17 2015-11-24 インテリカイン, エルエルシー 複素環式化合物およびそれらの使用
KR101256018B1 (ko) 2009-08-20 2013-04-18 한국과학기술연구원 단백질 키나아제 저해활성을 갖는 1,3,6-치환된 인돌 화합물
FR2951172B1 (fr) 2009-10-13 2014-09-26 Pf Medicament Derives pyrazolopyridines en tant qu'agent anticancereux
KR101147550B1 (ko) 2009-10-22 2012-05-17 한국과학기술연구원 단백질 키나아제 저해활성을 가지는 2,7-치환된 티에노[3,2-d]피리미딘 화합물
KR101116756B1 (ko) 2009-10-27 2012-03-13 한국과학기술연구원 단백질 키나아제 저해활성을 갖는 신규의 1,6-치환된 인돌 화합물
EA029273B1 (ru) 2009-10-29 2018-03-30 Джиноско Киназные ингибиторы
CA2780892C (fr) 2009-11-13 2017-02-14 Genosco Inhibiteurs de kinases
KR101094446B1 (ko) 2009-11-19 2011-12-15 한국과학기술연구원 단백질 키나아제 저해활성을 가지는 2,4,7-치환된 티에노[3,2-d]피리미딘 화합물
US9180127B2 (en) 2009-12-29 2015-11-10 Dana-Farber Cancer Institute, Inc. Type II Raf kinase inhibitors
SG182361A1 (en) 2010-01-29 2012-08-30 Hanmi Science Co Ltd THIENO[3,2-d]PYRIMIDINE DERIVATIVES HAVING INHIBITORY ACTIVITY ON PROTEIN KINASES
WO2011092120A1 (fr) 2010-01-29 2011-08-04 Nerviano Medical Sciences S.R.L. Dérivés de 6,7-dihydroimidazo[1,5-a]pyrazin-8(5h)-one comme modulateurs de protéines kinases
KR101483215B1 (ko) 2010-01-29 2015-01-16 한미약품 주식회사 단백질 키나아제 저해활성을 갖는 비시클릭 헤테로아릴 유도체
ES2594927T3 (es) 2010-02-18 2016-12-23 INSERM (Institut National de la Santé et de la Recherche Médicale) Métodos para prevenir las metástasis cancerosas
TWI619713B (zh) 2010-04-21 2018-04-01 普雷辛肯公司 用於激酶調節的化合物和方法及其適應症
PL2918588T3 (pl) 2010-05-20 2017-10-31 Array Biopharma Inc Związki makrocykliczne jako inhibitory kinazy TRK
WO2012034095A1 (fr) 2010-09-09 2012-03-15 Irm Llc Composés et compositions comme inhibiteurs de trk
US8637516B2 (en) 2010-09-09 2014-01-28 Irm Llc Compounds and compositions as TRK inhibitors
WO2012047017A2 (fr) 2010-10-05 2012-04-12 크리스탈지노믹스(주) Dérivé 2,3-dihydro-isoindol-1-one et composition le comprenant
JP2014005206A (ja) 2010-10-22 2014-01-16 Astellas Pharma Inc アリールアミノヘテロ環カルボキサミド化合物
ES2586588T3 (es) 2011-01-26 2016-10-17 Nerviano Medical Sciences S.R.L. Derivados tricíclicos, procedimiento para su preparación y su uso como inhibidores de quinasa
CN103339134B (zh) 2011-01-26 2015-12-23 内尔维阿诺医学科学有限公司 三环吡咯并衍生物、它们的制备方法和它们作为激酶抑制剂的应用
CN102093421B (zh) 2011-01-28 2014-07-02 北京康辰药业有限公司 一种含磷取代基的喹啉类化合物及其制备方法、以及含有该化合物的药物组合物及其应用
SI2672967T1 (sl) 2011-02-07 2018-12-31 Plexxikon Inc. Spojine in postopki za kinazno modulacijo in indikacije zanjo
EP2678336B1 (fr) 2011-02-24 2016-04-20 Nerviano Medical Sciences S.r.l. Dérivés de thiazolylphényl-benzènesulfonamido en tant qu'inhibiteurs de la kinase
MX2013009767A (es) 2011-02-25 2013-10-01 Irm Llc Compuestos y composiciones como inhibidores de trk.
US8791112B2 (en) 2011-03-30 2014-07-29 Arrien Pharmaceuticals Llc Substituted 5-(pyrazin-2-yl)-1H-pyrazolo [3, 4-B] pyridine and pyrazolo [3, 4-B] pyridine derivatives as protein kinase inhibitors
ES2759615T3 (es) 2011-04-01 2020-05-11 Univ Utah Res Found Análogos de N-fenilpirimidina-2-amina sustituidos como inhibidores de la quinasa AXL
US9284298B2 (en) 2011-04-11 2016-03-15 Nerviano Medical Sciences S.R.L. Pyrazolyl-pyrimidine derivatives as kinase inhibitors
EP2699564B1 (fr) 2011-04-19 2016-12-14 Nerviano Medical Sciences S.r.l. Pyrimidinylpyrroles substitués actifs en tant qu'inhibiteurs de kinases
AR086042A1 (es) * 2011-04-28 2013-11-13 Galapagos Nv Compuesto util para el tratamiento de enfermedades degenerativas e inflamatorias y composicion farmaceutica
EP2707359B1 (fr) 2011-05-12 2016-11-30 Nerviano Medical Sciences S.r.l. Dérivés d'indazole substitués actifs en tant qu'inhibiteurs de kinases
KR102001364B1 (ko) 2011-05-13 2019-07-22 어레이 바이오파마 인크. Trka 키나제 저해제로서의 피롤리디닐 유레아 및 피롤리디닐 티오유레아 화합물
RU2477723C2 (ru) 2011-06-16 2013-03-20 Общество С Ограниченной Ответственностью "Фьюжн Фарма" Ингибиторы протеинкиназ (варианты), их применение для лечения онкологических заболеваний и фармацевтическая композиция на их основе
CN102827073A (zh) 2011-06-17 2012-12-19 安吉奥斯医药品有限公司 治疗活性组合物和它们的使用方法
WO2013014039A1 (fr) 2011-07-28 2013-01-31 Nerviano Medical Sciences S.R.L. Pyrimidinyl-pyrroles substitués alcynyle agissant comme inhibiteurs de kinase
WO2013016720A2 (fr) 2011-07-28 2013-01-31 Gerinda Therapeutics, Inc. Nouveaux dérivés biaryl-hétérocycliques substitués en tant qu'inhibiteurs de protéine kinase pour le traitement du cancer et d'autres maladies
KR20140047138A (ko) 2011-08-04 2014-04-21 도쿠리츠교세이호진 고쿠리츠간켄큐센터 Kif5b 유전자와 ret 유전자와의 융합 유전자, 및 당해 융합 유전자를 표적으로 한 암 치료의 유효성을 판정하는 방법
WO2013028817A1 (fr) 2011-08-23 2013-02-28 Foundation Medicine , Inc. Molécules de fusion kif5b-ret inédites et leurs utilisations
AU2012341028C1 (en) 2011-09-02 2017-10-19 Mount Sinai School Of Medicine Substituted pyrazolo[3,4-D]pyrimidines and uses thereof
WO2013036232A2 (fr) 2011-09-08 2013-03-14 Deciphera Pharmaceuticals, Llc Méthodes et compositions pouvant être utilisées en vue du traitement de maladies myéloprolifératives et d'autres maladies prolifératives
US8846712B2 (en) * 2011-09-12 2014-09-30 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
WO2013042137A1 (fr) 2011-09-19 2013-03-28 Aurigene Discovery Technologies Limited Hétérocycles bicycliques convenant comme inhibiteurs de l'irak4
CN102408411B (zh) 2011-09-19 2014-10-22 北京康辰药业股份有限公司 一种含喹啉基的羟肟酸类化合物及其制备方法、以及含有该化合物的药物组合物及其应用
JP6063945B2 (ja) 2011-10-07 2017-01-18 ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ キナーゼ阻害剤としての4−アルキル置換3,4−ジヒドロピロロ[1,2−a]ピラジン−1(2H)−オン誘導体
EP2788351B1 (fr) 2011-10-07 2017-06-28 Nerviano Medical Sciences S.r.l. DÉRIVÉS DE LA 3,4-DIHYDROPYRROLO[1,2-a]PYRAZIN-1(2H)-ONE EN TANT QU'INHIBITEURS DE KINASES
BR112014011465A2 (pt) 2011-11-14 2017-05-09 Tesaro Inc modulação de determinadas quinases de tirosina
CN104080907A (zh) 2011-11-30 2014-10-01 日本国立癌症研究中心 诱导恶性干细胞
US8377946B1 (en) 2011-12-30 2013-02-19 Pharmacyclics, Inc. Pyrazolo[3,4-d]pyrimidine and pyrrolo[2,3-d]pyrimidine compounds as kinase inhibitors
ES2751608T3 (es) 2011-12-30 2020-04-01 Hanmi Pharm Ind Co Ltd Derivados de tieno[3,2-d]pirimidina que tienen actividad inhibitoria para las proteínas quinasas
JP2015109806A (ja) 2012-03-22 2015-06-18 アステラス製薬株式会社 新規ret融合体の検出法
US9242977B2 (en) 2012-04-26 2016-01-26 Ono Pharmaceutical Co., Ltd. Trk-inhibiting compound
US20150099721A1 (en) 2012-05-10 2015-04-09 Synta Pharmaceuticals Corp. Treating cancer with hsp90 inhibitory compounds
PL3333166T3 (pl) 2012-05-23 2020-09-07 Nerviano Medical Sciences S.R.L. Proces otrzymywania n-[5-(3,5-difluorobenzylo)-1h-indazol-3-ilo]- 4-(4-metylopiperazyn-1-ylo)-2-(tetrahydropiran- 4-yloamino)benzamidu
TWI585088B (zh) 2012-06-04 2017-06-01 第一三共股份有限公司 作爲激酶抑制劑之咪唑并[1,2-b]嗒衍生物
NZ703495A (en) 2012-07-11 2018-02-23 Blueprint Medicines Corp Inhibitors of the fibroblast growth factor receptor
JPWO2014017491A1 (ja) 2012-07-26 2016-07-11 国立研究開発法人国立がん研究センター Cep55遺伝子とret遺伝子との融合遺伝子
WO2014019908A2 (fr) 2012-08-02 2014-02-06 Nerviano Medical Sciences S.R.L. Pyrroles substitués actifs en tant qu'inhibiteurs de kinase
JP6513567B2 (ja) 2012-09-07 2019-05-15 エクセリクシス, インク. 肺腺癌の治療で使用するためのmet、vegfr、およびretの阻害剤
TWI603733B (zh) 2012-09-25 2017-11-01 中外製藥股份有限公司 Ret抑制劑
ES2755772T3 (es) 2012-11-07 2020-04-23 Nerviano Medical Sciences Srl Pirimidinil y piridinilpirrolopiridinonas sustituidas, proceso para su preparación y su uso como inhibidores de cinasas
EP2917183A1 (fr) 2012-11-12 2015-09-16 Ignyta, Inc. Dérivés de bendamustine et leurs procédés d'utilisation
US9809578B2 (en) 2012-11-13 2017-11-07 Array Biopharma Inc. Pyrazolyl urea, thiourea, guanidine and cyanoguanidine compounds as trkA kinase inhibitors
US9828360B2 (en) 2012-11-13 2017-11-28 Array Biopharma Inc. Pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
US9896435B2 (en) 2012-11-13 2018-02-20 Array Biopharma Inc. N-pyrrolidinyl,N′-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
WO2014078322A1 (fr) 2012-11-13 2014-05-22 Array Biopharma Inc. Composés de thiazolyl-urée, oxazolyl-urée, thio-urée, guanidine et cyanoguanidine en tant qu'inhibiteurs de la kinase trka
WO2014078325A1 (fr) 2012-11-13 2014-05-22 Array Biopharma Inc. Composés de n-aryle monocycliques, n'-pyrazolyl-urée, thiourée, guanidine et cyanoguanidine utiles comme inhibiteurs de trka kinase
US9969694B2 (en) 2012-11-13 2018-05-15 Array Biopharma Inc. N-(arylalkyl)-N′-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
ME02879B (fr) 2012-11-13 2018-04-20 Array Biopharma Inc Composes bicycliques a base d' uree, thiouree, guanidine ou cyanoguanidine utiles dans le traitement de la douleur
US9822118B2 (en) 2012-11-13 2017-11-21 Array Biopharma Inc. Bicyclic heteroaryl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
WO2014078328A1 (fr) 2012-11-13 2014-05-22 Array Biopharma Inc. Composés de n-pyrrolidinyle, n'-pyrazolyl-urée, thio-urée,guanidine et cyanoguanidine en tant qu'inhibiteurs de la kinase trka
WO2014078372A1 (fr) 2012-11-13 2014-05-22 Array Biopharma Inc. Composés de n-pyrrolidinyle urée, thio-urée,guanidine et cyanoguanidine en tant qu'inhibiteurs de la kinase trka
HK1213189A1 (zh) 2012-11-29 2016-06-30 耶达研究及发展有限公司 预防肿瘤转移、癌症治疗和预後及鉴定为推定转移抑制剂的试剂的方法
CN103848785B (zh) 2012-12-04 2016-07-13 上海医药集团股份有限公司 一类氘代3-氰基喹啉类化合物、其药用组合物、制备方法及其用途
FR3000493A1 (fr) 2012-12-28 2014-07-04 Oribase Pharma Nouveaux inhibiteurs de proteines kinases
MX386542B (es) 2012-12-28 2025-03-18 Crystalgenomics Inc Derivados de la 2,3-dihidro-isoindol-1-ona, como inhibidores de la btk quinasa y composiciones farmacéuticas que los incluyen.
FR3000492B1 (fr) 2012-12-28 2015-09-11 Oribase Pharma Nouveaux derives azaindole en tant qu'inhibiteurs multikinases
FR3000494B1 (fr) 2012-12-28 2015-08-21 Oribase Pharma Nouveaux derives d'azaindoles en tant qu'inhibiteurs de proteines kinases
TW201443037A (zh) * 2013-01-09 2014-11-16 Gilead Sciences Inc 治療用化合物
SG11201506514QA (en) 2013-02-19 2015-09-29 Ono Pharmaceutical Co Trk-INHIBITING COMPOUND
US20160151461A1 (en) 2013-03-14 2016-06-02 The Trustees Of The University Of Pennsylvania Cardio-Metabolic and Vascular Effects of GLP-1 Metabolites
EP3521284B1 (fr) * 2013-03-15 2020-12-02 The Trustees of Columbia University in the City of New York Composés de pyrazine comme modulateurs de map kinase et leurs utilisations
EP2970191B1 (fr) 2013-03-15 2016-12-21 GlaxoSmithKline Intellectual Property Development Limited Dérivés des pyridines comme inhibiteurs de la kinase arrangé pendant transfection (ret)
US8937071B2 (en) 2013-03-15 2015-01-20 Glaxosmithkline Intellectual Property Development Limited Compounds as rearranged during transfection (RET) inhibitors
EP2970231A1 (fr) 2013-03-15 2016-01-20 Blueprint Medicines Corporation Dérivés de pipérazine et leur utilisation comme modulateurs de kit
JP6397897B2 (ja) 2013-05-14 2018-09-26 ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ ピロロ[2,3−d]ピリミジン誘導体、その製造方法及びキナーゼ阻害剤としてのその使用
MX2015015966A (es) 2013-05-30 2016-04-13 Plexxikon Inc Compuestos para la modulacion de cinasas e indicaciones para los mismos.
WO2015017528A1 (fr) 2013-07-30 2015-02-05 Blueprint Medicines Corporation Fusions de pik3c2g
WO2015017533A1 (fr) 2013-07-30 2015-02-05 Blueprint Medicines Corporation Fusions de ntrk2
CN105658814A (zh) 2013-08-20 2016-06-08 日本国立癌症研究中心 在肺癌中检测出的新型融合基因
RU2016111675A (ru) 2013-08-30 2017-10-04 Эмбит Байосайенсиз Корпорейшн Соединения биарилацетамида и способы их применения
US9200002B2 (en) 2013-10-17 2015-12-01 Blueprint Medicines Corporation Compositions useful for treating disorders related to KIT
US9334263B2 (en) 2013-10-17 2016-05-10 Blueprint Medicines Corporation Compositions useful for treating disorders related to kit
HUE059037T2 (hu) 2013-10-25 2022-10-28 Blueprint Medicines Corp Fibroblaszt növekedési faktor receptor gátlók
GB201321146D0 (en) 2013-11-29 2014-01-15 Cancer Rec Tech Ltd Quinazoline compounds
WO2015082887A2 (fr) 2013-12-02 2015-06-11 Bergenbio As Utilisation d'inhibiteurs de kinases
WO2015108992A1 (fr) 2014-01-15 2015-07-23 Blueprint Medicines Corporation Composés hétérobicycliques et leur utilisation en tant qu'inhibiteurs du récepteur fgfr4
DK3636649T3 (da) 2014-01-24 2024-05-21 Turning Point Therapeutics Inc Diarylmakrocykler som modulatorer af proteinkinaser
WO2015123639A1 (fr) 2014-02-14 2015-08-20 Exelixis, Inc. Formes solides cristallines du n-{4-[(6,7-diméthoxyquinolin-4-yl)oxy]phényl}-n'-(4-fluorophényl)cyclopropane-1,1-dicarboxamide, procédés de préparation, et méthodes d'utilisation
TWI672141B (zh) 2014-02-20 2019-09-21 美商醫科泰生技 投予ros1突變癌細胞之分子
US20170044622A1 (en) 2014-04-18 2017-02-16 Blueprint Medicines Corporation Pik3ca fusions
WO2015161277A1 (fr) 2014-04-18 2015-10-22 Blueprint Medicines Corporation Fusions de met
HRP20191593T1 (hr) 2014-05-15 2019-11-29 Array Biopharma Inc 1-((3s,4r)-4-(3-fluorfenil)-1-(2-metoksietil)pirolidin-3-il)-3-(4-metil-3-(2-metilpirimidin-5-il)-1-fenil-1h-pirazol-5-il)urea kao inhibitor trka kinaze
EP3155118A1 (fr) 2014-06-10 2017-04-19 Blueprint Medicines Corporation Fusions de pkn1
EP3155131B1 (fr) 2014-06-10 2020-02-12 Blueprint Medicines Corporation Fusions de raf1
HUE046008T2 (hu) 2014-07-17 2020-02-28 Sunshine Lake Pharma Co Ltd I-(5-terc-butil)-izoxazol-3-il)-3-(4-((feniI)-etinil)-fenil)-kabamid származékok, valamint az ezekkel rokon vegyületek FLT-3 inhibitorokként rák kezelésére
EP3169809B1 (fr) 2014-07-17 2020-04-29 Blueprint Medicines Corporation Fusions de prkc
EP3169808B1 (fr) 2014-07-17 2019-05-22 Blueprint Medicines Corporation Fusion trio:tert dans le cancer
WO2016011141A1 (fr) 2014-07-17 2016-01-21 Blueprint Medicines Corporation Fusions de fgr
US9688680B2 (en) 2014-08-04 2017-06-27 Blueprint Medicines Corporation Compositions useful for treating disorders related to kit
AU2015304438B2 (en) 2014-08-18 2019-06-20 Ono Pharmaceutical Co., Ltd. Acid-addition salt of Trk-inhibiting compound
EP3191480A1 (fr) 2014-09-08 2017-07-19 GlaxoSmithKline Intellectual Property Development Limited Formes cristallines de 2-(4-(4-éthoxy-6-oxo-1,6-dihydropyridin-3-yl)-2-fluorophényl)-n-(5-(1,1,1-trifluoro-2-méthylpropan-2-yl)isoxazol-3-yl)acétamide
WO2016037578A1 (fr) 2014-09-10 2016-03-17 Glaxosmithkline Intellectual Property Development Limited Nouveaux composés utilisés comme inhibiteurs de la kinase réarrangée au cours de la transfection (ret)
CA2960768A1 (fr) 2014-09-10 2016-03-17 Glaxosmithkline Intellectual Property Development Limited Derives de pyridone a titre d'inhibiteurs de la kinase rearrangee au cours de la transfection (ret)
TWI538914B (zh) 2014-10-03 2016-06-21 國立交通大學 蛋白質激酶之選擇性抑制劑、其醫藥組成物及其用途
PL3218378T3 (pl) * 2014-11-14 2020-10-19 Nerviano Medical Sciences S.R.L. Pochodne 6-amino-7-bicyklo-7-deazapuryny jako inhibitory kinaz białkowych
TWI767858B (zh) 2014-11-16 2022-06-11 美商亞雷生物製藥股份有限公司 (S)-N-(5-((R)-2-(2,5-二氟苯基)-吡咯啶-1-基)-吡唑并[1,5-a]嘧啶-3-基)-3-羥基吡咯啶-1-甲醯胺硫酸氫鹽結晶型
US20170356052A1 (en) 2014-11-18 2017-12-14 Blueprint Medicines Corporation Prkacb fusions
US10336707B2 (en) 2014-12-16 2019-07-02 Eudendron S.R.L. Heterocyclic derivatives modulating activity of certain protein kinases
US10202365B2 (en) 2015-02-06 2019-02-12 Blueprint Medicines Corporation 2-(pyridin-3-yl)-pyrimidine derivatives as RET inhibitors
KR101675984B1 (ko) 2015-02-23 2016-11-14 한양대학교 에리카산학협력단 티에노디아제핀 유도체 또는 이의 약학적으로 허용가능한 염, 및 이를 유효성분으로 포함하는 약학적 조성물
EP3265079A4 (fr) 2015-03-03 2019-01-02 Caris MPI, Inc. Profilage moléculaire du cancer
CN108137593B (zh) 2015-04-21 2021-01-05 上海交通大学医学院附属瑞金医院 蛋白激酶抑制剂的制备和用途
GB201512365D0 (en) 2015-07-15 2015-08-19 King S College London Novel therapy
WO2017011776A1 (fr) 2015-07-16 2017-01-19 Array Biopharma, Inc. Composés substitués de pyrazolo[1,5-a]pyridines comme inhibiteurs de la kinase ret
EP3120851A1 (fr) 2015-07-21 2017-01-25 Pangaea Biotech S.L. 4-amino-6- (2,6-dichlorophényl) -8-methyl-2-(phénylamino) -pyrido[2,3-d]pyrimidin-7-(8h)-one pour le traitement de cancers solides
KR101766194B1 (ko) 2015-08-07 2017-08-10 한국과학기술연구원 RET 키나아제 저해제인 신규 3-(이속사졸-3-일)-피라졸로[3,4-d]피리미딘-4-아민 화합물
WO2017027883A1 (fr) 2015-08-13 2017-02-16 San Diego State University Research Foundation Atropisomérisme pour une sélectivité accrue des inhibiteurs de kinase
MA41559A (fr) 2015-09-08 2017-12-26 Taiho Pharmaceutical Co Ltd Composé de pyrimidine condensé ou un sel de celui-ci
WO2017049462A1 (fr) 2015-09-22 2017-03-30 合肥中科普瑞昇生物医药科技有限公司 Nouvel inhibiteur de la kinase flt3 et ses utilisations
CN105255927B (zh) 2015-09-30 2018-07-27 温州医科大学附属第一医院 一种kiaa1217-ret融合基因
MX384884B (es) 2015-11-02 2025-03-14 Blueprint Medicines Corp Inhibidores de ret.
US20190002988A1 (en) 2015-12-08 2019-01-03 Boehringer Ingelheim International Gmbh Method of using a ret fusion gene as a biomarker to select non small cell lung cancer (nsclc) and thyroid cancer patients for a cancer treatment
JP6871869B2 (ja) 2016-01-15 2021-05-19 公益財団法人がん研究会 新規融合体及びその検出法
TWI620748B (zh) 2016-02-05 2018-04-11 National Health Research Institutes 氨基噻唑化合物及其用途
ES2775751T3 (es) 2016-02-23 2020-07-28 Taiho Pharmaceutical Co Ltd Nuevo compuesto de pirimidina condensada o sal del mismo
WO2017145050A1 (fr) 2016-02-23 2017-08-31 Glaxosmithkline Intellectual Property Development Limited Dérivé de pyridylpyridone utile comme inhibiteur de la kinase ret dans le traitement du sci et du cancer
WO2017161269A1 (fr) 2016-03-17 2017-09-21 Blueprint Medicines Corporation Inhibiteurs des tyrosine kinases du récepteur ret
US10045991B2 (en) 2016-04-04 2018-08-14 Loxo Oncology, Inc. Methods of treating pediatric cancers
CA3020778A1 (fr) 2016-04-15 2017-10-19 Cancer Research Technology Limited Composes heterocycliques utilises en tant qu'inhibiteurs de kinase ret
SMT202200348T1 (it) * 2016-04-15 2022-11-18 Cancer Research Tech Ltd Composti eterociclici come inibitori della chinasi ret
TWI704148B (zh) 2016-10-10 2020-09-11 美商亞雷生物製藥股份有限公司 作為ret激酶抑制劑之經取代吡唑并[1,5-a]吡啶化合物
JOP20190077A1 (ar) 2016-10-10 2019-04-09 Array Biopharma Inc مركبات بيرازولو [1، 5-a]بيريدين بها استبدال كمثبطات كيناز ret

Also Published As

Publication number Publication date
SI3523301T1 (sl) 2020-08-31
IL277576B2 (en) 2023-05-01
TN2019000110A1 (en) 2020-10-05
US20180133200A1 (en) 2018-05-17
US20240066029A1 (en) 2024-02-29
JP7079303B2 (ja) 2022-06-01
JOP20190076B1 (ar) 2023-03-28
TW201825488A (zh) 2018-07-16
US10172851B2 (en) 2019-01-08
KR20190076976A (ko) 2019-07-02
MX2020011250A (es) 2022-09-08
JP2022062168A (ja) 2022-04-19
RS60536B1 (sr) 2020-08-31
PT3523301T (pt) 2020-08-26
MX395444B (es) 2025-03-25
BR112019007144B8 (pt) 2022-01-25
AU2017342022B2 (en) 2019-12-05
US20180134702A1 (en) 2018-05-17
ES2805087T3 (es) 2021-02-10
MD3523301T2 (ro) 2020-11-30
US10953005B1 (en) 2021-03-23
KR102143899B1 (ko) 2020-08-13
US11998545B2 (en) 2024-06-04
US10555944B2 (en) 2020-02-11
IL277576A (en) 2020-11-30
PH12019500775A1 (en) 2019-07-01
EP3523301B1 (fr) 2020-05-27
CN114163437A (zh) 2022-03-11
EP3523301A1 (fr) 2019-08-14
AU2017342022A1 (en) 2019-05-23
EP3753939A1 (fr) 2020-12-23
CA3039760C (fr) 2020-09-08
BR112019007144A2 (pt) 2018-04-19
US20210186959A1 (en) 2021-06-24
ECSP19032676A (es) 2019-07-31
JP2023134580A (ja) 2023-09-27
HUE051424T2 (hu) 2021-03-01
JOP20190076A1 (ar) 2019-04-09
MX2019004205A (es) 2019-08-21
UA125030C2 (uk) 2021-12-29
JP7502365B2 (ja) 2024-06-18
US20230090520A1 (en) 2023-03-23
DK3523301T3 (da) 2020-08-03
JP6776446B2 (ja) 2020-10-28
US10112942B2 (en) 2018-10-30
JP2020503247A (ja) 2020-01-30
CY1123201T1 (el) 2021-10-29
IL265916B (en) 2020-11-30
PE20190918A1 (es) 2019-06-26
CA3039760A1 (fr) 2018-04-19
SA519401541B1 (ar) 2022-08-04
IL277576B1 (en) 2023-01-01
CN114163437B (zh) 2025-03-04
JP7634606B2 (ja) 2025-02-21
US20190183886A1 (en) 2019-06-20
JP2021035944A (ja) 2021-03-04
SG11201903144PA (en) 2019-05-30
JP7311654B2 (ja) 2023-07-19
IL265916A (en) 2019-06-30
BR112019007144B1 (pt) 2020-07-14
CO2019004650A2 (es) 2019-05-21
WO2018071447A1 (fr) 2018-04-19
US20180133213A1 (en) 2018-05-17
US10137124B2 (en) 2018-11-27
HRP20201008T1 (hr) 2020-10-16
JP2025011247A (ja) 2025-01-23
MX376465B (es) 2025-03-07
JP2022116108A (ja) 2022-08-09
CN110382494B (zh) 2021-11-16
ZA202004040B (en) 2023-01-25
TWI704148B (zh) 2020-09-11
CN110382494A (zh) 2019-10-25
NZ752793A (en) 2023-01-27
MY195573A (en) 2023-02-02
CR20190218A (es) 2019-10-14
NZ792955A (en) 2025-02-28
DOP2019000090A (es) 2019-06-30
LT3523301T (lt) 2020-07-27
CL2019000941A1 (es) 2019-12-13
PL3523301T3 (pl) 2020-12-28
JP7761732B2 (ja) 2025-10-28

Similar Documents

Publication Publication Date Title
MA53675A (fr) Composés substitués de pyrazolo[1,5-a]pyridine en tant qu'inhibiteurs de la kinase ret
DK3523302T3 (da) Substituerede pyrazolo[1,5-A]pyridin-forbindelser som RET-kinase-inhibitorer
FR22C1006I2 (fr) Derives de pyrrolo-[2,3-d]pyrimidine en tant qu'inhibiteurs des janus kinases (jak)
ZA201800771B (en) Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors
LT3555097T (lt) Imidazo[4,5-d]pirolo[2,3-b]piridino junginiai kaip janus kinazės inhibitoriai
MA53487A (fr) Composés pyrazolo[3,4-b]pyridine utilisés en tant qu'inhibiteurs de kinases tam et met
MA52987A (fr) Dérivés de pyrazolo[1,5-a]pyrazin-4-yl en tant qu'inhibiteurs de jak
DK3478682T3 (da) [1,2,4]triazolo[1,5-a]pyridinylsubstituerede indolforbindelser
EP3345907A4 (fr) NOUVEAU COMPOSÉ PYRROLO[3,4-d]PYRIMIDINE OU SEL CORRESPONDANT
MA47013A (fr) Composés benzolactames utilisés en tant qu'inhibiteurs de protéine kinase
MA40774A (fr) Dérivés de diaryle-urée en tant qu'inhibiteurs de kinase p38
ME03672B (fr) 1h-pyrazolo [4,3-b]pyridines en tant qu'inhibiteurs de pde1
EP3452481A4 (fr) Imidazo[1,2-b]pyridazines substituées, imidazo[1,5-b]pyridazines substituées, composés apparentés et leur utilisation dans le traitement de troubles médicaux
EP3328840A4 (fr) Composés bicycliques triazolo substitués en tant qu'inhibiteurs de pde2
MA46690A (fr) Composés de [1,2,4]triazolo [1,5-a]pyrimidine en tant qu'inhibiteurs de pde2
EP3508487A4 (fr) COMPOSÉ DE PYRAZOLO [1,5-a]PYRIMIDINE
EP3666774A4 (fr) Composé 1h-pyrazolo[4,3-h]quinazoline servant en tant qu'inhibiteur de protéine kinase
EP3096762C0 (fr) Pyrazolo[1,5-a]pyrimidines comme composés antiviraux
EP3679042A4 (fr) Dérivés d'imidazo[1,5-a]pyrazine en tant qu'inhibiteurs de pi3kdelta
MA46463A (fr) Composés de pyrazolo[1,5-a]pyridine substitués en tant qu'inhibiteurs de la kinase ret
EP3330271A4 (fr) COMPOSÉ PYRROLO[2,3-d]PYRIMIDINE OU UN SEL DE CELUI-CI
TH1501006629A (th) อนุพันธ์พีร์โรโล[2,3-d]ไพริมิดีนในฐานะอะกอนิสต์ของ CB2 รีเซปเตอร์