IN2014CN00408A - - Google Patents

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Publication number
IN2014CN00408A
IN2014CN00408A IN408CHN2014A IN2014CN00408A IN 2014CN00408 A IN2014CN00408 A IN 2014CN00408A IN 408CHN2014 A IN408CHN2014 A IN 408CHN2014A IN 2014CN00408 A IN2014CN00408 A IN 2014CN00408A
Authority
IN
India
Prior art keywords
formula
relates
pyridine ring
present
membered fused
Prior art date
Application number
Other languages
English (en)
Inventor
Tjeerd A Barf
Christiaan Gerardus Johannes Maria Jans
De Adrianus Petrus Antonius Man
Arthur A Oubrie
Hans C A Raaijmakers
Johannes Bernardus Maria Rewinkel
Jan Gerard Sterrenburg
Jacobus C H M Wijkmans
Original Assignee
Merck Sharp & Dohme
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=47557677&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=IN2014CN00408(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Merck Sharp & Dohme filed Critical Merck Sharp & Dohme
Publication of IN2014CN00408A publication Critical patent/IN2014CN00408A/en

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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
    • A61K31/495Heterocyclic 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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/501Pyridazines; Hydrogenated pyridazines 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
    • A61K31/495Heterocyclic 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
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    • 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
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    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
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    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
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    • AHUMAN NECESSITIES
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    • AHUMAN NECESSITIES
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    • AHUMAN NECESSITIES
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    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • AHUMAN NECESSITIES
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    • AHUMAN NECESSITIES
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-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
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Immunology (AREA)
  • Diabetes (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Rheumatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Communicable Diseases (AREA)
  • Ophthalmology & Optometry (AREA)
  • Pulmonology (AREA)
  • Neurology (AREA)
  • Urology & Nephrology (AREA)
  • Dermatology (AREA)
  • Endocrinology (AREA)
  • Pain & Pain Management (AREA)
  • Biomedical Technology (AREA)
  • Transplantation (AREA)
  • Virology (AREA)
  • Neurosurgery (AREA)
  • Emergency Medicine (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Obesity (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
IN408CHN2014 2011-07-19 2012-07-11 IN2014CN00408A (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201161509397P 2011-07-19 2011-07-19
EP11174578 2011-07-19
PCT/EP2012/063552 WO2013010868A1 (fr) 2011-07-19 2012-07-11 4-imidazopyridazin-1-yl-benzamides et 4-imidazotriazin-1-yl-benzamides en tant qu'inhibiteurs de btk

Publications (1)

Publication Number Publication Date
IN2014CN00408A true IN2014CN00408A (fr) 2015-04-03

Family

ID=47557677

Family Applications (1)

Application Number Title Priority Date Filing Date
IN408CHN2014 IN2014CN00408A (fr) 2011-07-19 2012-07-11

Country Status (38)

Country Link
US (8) US9290504B2 (fr)
EP (4) EP3689878B1 (fr)
JP (6) JP5826931B2 (fr)
KR (2) KR101802689B1 (fr)
CN (2) CN106243113B (fr)
AU (4) AU2012285987C1 (fr)
BR (1) BR112014001255B1 (fr)
CA (1) CA2841886C (fr)
CL (1) CL2014000130A1 (fr)
CO (1) CO6940411A2 (fr)
CR (1) CR20140030A (fr)
CY (2) CY2021010I2 (fr)
DK (2) DK3689878T3 (fr)
DO (1) DOP2014000008A (fr)
EA (2) EA034558B1 (fr)
EC (1) ECSP14013217A (fr)
ES (3) ES2708224T3 (fr)
GT (1) GT201400009A (fr)
HR (2) HRP20190135T1 (fr)
HU (3) HUE056249T2 (fr)
IL (3) IL230511B (fr)
IN (1) IN2014CN00408A (fr)
LT (1) LT2734522T (fr)
MA (1) MA35348B1 (fr)
MX (1) MX342983B (fr)
MY (1) MY192354A (fr)
PE (1) PE20141681A1 (fr)
PH (2) PH12014500148A1 (fr)
PL (2) PL3689878T3 (fr)
PT (1) PT3689878T (fr)
RS (2) RS58177B1 (fr)
SG (1) SG10201605913VA (fr)
SI (2) SI2734522T1 (fr)
SM (2) SMT202100729T1 (fr)
TN (1) TN2014000027A1 (fr)
UA (1) UA115312C2 (fr)
WO (1) WO2013010868A1 (fr)
ZA (1) ZA202109164B (fr)

Families Citing this family (118)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120101113A1 (en) * 2007-03-28 2012-04-26 Pharmacyclics, Inc. Inhibitors of bruton's tyrosine kinase
NZ772688A (en) 2010-06-03 2022-09-30 Pharmacyclics Llc The use of inhibitors of bruton’s tyrosine kinase (btk)
EA025496B1 (ru) 2011-05-17 2016-12-30 Принсипиа Биофарма Инк. Ингибиторы тирозинкиназы
WO2012158795A1 (fr) 2011-05-17 2012-11-22 Principia Biopharma Inc. Dérivés de pyrazolopyrimidine utilisés comme inhibiteurs de tyrosine kinase
EA201490265A1 (ru) 2011-07-13 2014-12-30 Фармасайкликс, Инк. Ингибиторы тирозинкиназы брутона
AU2012285987C1 (en) * 2011-07-19 2016-09-08 Merck Sharp & Dohme B.V. 4 - imidazopyridazin- 1 -yl-benzamides and 4 - imidazotriazin- 1 - yl - benzamides as Btk- inhibitors
EP2548877A1 (fr) 2011-07-19 2013-01-23 MSD Oss B.V. Dérivés de 4-(pyridine condensée à 5 chaînons)benzamide comme inhibiteurs de BTK
AU2013293087B2 (en) 2012-07-24 2017-08-31 Pharmacyclics Llc Mutations associated with resistance to inhibitors of Bruton's tyrosine kinase (BTK)
US9266895B2 (en) 2012-09-10 2016-02-23 Principia Biopharma Inc. Substituted pyrazolo[3,4-d]pyrimidines as kinase inhibitors
MX2015003874A (es) * 2012-09-26 2015-12-16 Univ California Modulacion de ire1.
US9296703B2 (en) * 2012-10-04 2016-03-29 University Of Utah Research Foundation Substituted N-(3-(pyrimidin-4-yl)phenyl)acrylamide analogs as tyrosine receptor kinase BTK inhibitors
KR102229478B1 (ko) 2012-11-01 2021-03-18 인피니티 파마슈티칼스, 인코포레이티드 Pi3 키나아제 동형단백질 조절인자를 사용하는 암의 치료
WO2014113942A1 (fr) * 2013-01-23 2014-07-31 Merck Sharp & Dohme Corp. Inhibiteurs de btk
WO2014114185A1 (fr) 2013-01-23 2014-07-31 Merck Sharp & Dohme Corp. Inhibiteurs de btk
US8957080B2 (en) 2013-04-09 2015-02-17 Principia Biopharma Inc. Tyrosine kinase inhibitors
ES2834638T3 (es) * 2013-05-30 2021-06-18 Infinity Pharmaceuticals Inc Tratamiento de cánceres usando moduladores de isoforma de PI3 cinasa
MX367085B (es) * 2013-07-31 2019-08-05 Merck Patent Gmbh Piridinas, pirimidinas y pirazinas como inhibidores de tirosina cinasa de bruton e inhibidores y usos de las mismas.
WO2015057992A1 (fr) * 2013-10-16 2015-04-23 Izumi Raquel Inhibiteurs btk pour la mobilisation hématopoïétique
EA201691169A1 (ru) 2013-12-05 2016-09-30 Асерта Фарма Б.В. Терапевтическая комбинация ингибитора pi3k и ингибитора btk
EP3082809B1 (fr) 2013-12-20 2021-01-20 Merck Sharp & Dohme Corp. Inhibiteurs de btk
EP3082811B1 (fr) * 2013-12-20 2020-01-15 Merck Sharp & Dohme Corp. Inhibiteurs de btk
WO2015110923A2 (fr) 2014-01-21 2015-07-30 Acerta Pharma B.V. Méthodes de traitement de la leucémie lymphoïde chronique et du lymphome à petits lymphocytes en utilisant un inhibiteur de btk
US10272083B2 (en) 2014-01-21 2019-04-30 Acerta Pharma B.V. Methods of treating chronic lymphocytic leukemia and small lymphocytic leukemia using a BTK inhibitor
EP4681737A3 (fr) 2014-02-21 2026-03-11 Principia Biopharma Inc. Sels et forme solide d'un inhibiteur de btk
WO2015181633A2 (fr) 2014-04-11 2015-12-03 Acerta Pharma B.V. Procédés de blocage de la voie de signalisation cxcr4/sdf-1 à l'aide d'inhibiteurs de la tyrosine kinase de bruton
WO2015185998A2 (fr) 2014-04-11 2015-12-10 Acerta Pharma B.V. Procédés de blocage de la voie de signalisation des cxcr-4/sdf-1 à l'aide d'inhibiteurs de kinase x de moelle osseuse
TW201613644A (en) * 2014-06-17 2016-04-16 Acerta Pharma Bv Therapeutic combinations of a BTK inhibitor, a PI3K inhibitor, and/or a JAK-2 inhibitor
CA2959602A1 (fr) * 2014-08-01 2016-02-04 Pharmacyclics Llc Inhibiteurs de la tyrosine kinase de bruton
TW201618783A (zh) 2014-08-07 2016-06-01 艾森塔製藥公司 以布魯頓(Bruton)氏酪胺酸激酶(BTK)佔據和BTK再合成速率為基礎之治療癌症、免疫和自體免疫疾病及發炎性疾病之方法
RS62713B1 (sr) 2014-08-11 2022-01-31 Acerta Pharma Bv Terapeutske kombinacije btk inhibitora i bcl-2 inhibitora
US20170224819A1 (en) * 2014-08-11 2017-08-10 Acerta Pharma B.V. Therapeutic Combinations of a BTK Inhibitor, a PI3K Inhibitor, a JAK-2 Inhibitor, and/or a CDK 4/6 Inhibitor
HRP20220738T1 (hr) 2014-08-11 2022-08-19 Acerta Pharma B.V. Terapijske kombinacije inhibitora btk, inhibitora pd-1 i/ili inhibitora pd-l1
TW201609099A (zh) 2014-08-11 2016-03-16 艾森塔製藥公司 使用布魯頓(Bruton)氏酪胺酸激酶(BTK)抑制劑以治療慢性淋巴球性白血病和小淋巴球性白血病之方法
TW201618774A (zh) * 2014-08-11 2016-06-01 艾森塔製藥公司 使用btk抑制劑透過調變腫瘤微環境來治療實體腫瘤及其他疾病之方法
MX369646B (es) 2014-08-18 2019-11-15 Eisai R&D Man Co Ltd Sal de derivado de piridina monociclico y su cristal.
WO2016040858A1 (fr) * 2014-09-12 2016-03-17 G1 Therapeutics, Inc. Combinaisons et régimes posologiques pour traiter des tumeurs rb-positives
WO2016055982A1 (fr) * 2014-10-10 2016-04-14 Acerta Pharma B.V. Composés quinoléine et quinazoline
WO2016087994A1 (fr) 2014-12-05 2016-06-09 Acerta Pharma B.V. Inhibiteurs de btk pour le traitement de tumeurs solides par modulation du micro-environnement tumoral
US10485797B2 (en) * 2014-12-18 2019-11-26 Principia Biopharma Inc. Treatment of pemphigus
WO2016106626A1 (fr) * 2014-12-31 2016-07-07 Merck Sharp & Dohme Corp. Analogues de l'imidazopyrazine avec substitutions sur carbone tertiaire 3 en tant qu'inhibiteurs de btk
WO2016106625A1 (fr) * 2014-12-31 2016-07-07 Merck Sharp & Dohme Corp. Inhibiteurs de btk
WO2016106627A1 (fr) * 2014-12-31 2016-07-07 Merck Sharp & Dohme Corp. Inhibiteurs de btk
WO2016106624A1 (fr) 2014-12-31 2016-07-07 Merck Sharp & Dohme Corp. Inhibiteurs de la btk comprenant une imidazopyrazine d'alcool tertiaire
WO2016106623A1 (fr) 2014-12-31 2016-07-07 Merck Sharp & Dohme Corp. Composés benzamides et imidazopyrazines utilisés comme inhibiteurs de la btk
WO2016106629A1 (fr) * 2014-12-31 2016-07-07 Merck Sharp & Dohme Corp. Inhibiteurs de btk
WO2016128912A1 (fr) * 2015-02-12 2016-08-18 Acerta Pharma B.V. Combinaisons thérapeutiques d'un inhibiteur de btk, d'un inhibiteur de pi3k, d'un inhibiteur de jak-2, d'un inhibiteur de pd-1, et/ou d'un inhibiteur de pd-l1
AU2016237222B2 (en) 2015-03-25 2021-04-29 Eisai R&D Management Co., Ltd. Therapeutic agent for bile duct cancer
WO2016161571A1 (fr) 2015-04-08 2016-10-13 Merck Sharp & Dohme Corp. Inhibiteurs de la btk de type indazole et azaindazole
WO2016192074A1 (fr) * 2015-06-04 2016-12-08 Merck Sharp & Dohme Corp. Inhibiteurs de la btk
TW201718572A (zh) 2015-06-24 2017-06-01 普林斯匹亞生物製藥公司 酪胺酸激酶抑制劑
RU2018103913A (ru) * 2015-07-02 2019-08-02 Асерта Фарма Б.В. Твердые формы и композиции (s)-4-(8-амино-3-(1-(бут-2- иноил)пирролидин-2-ил)имидазо[1,5-a]пиразин-1-ил)-n-(пиридин-2-ил)бензамида
US20190008859A1 (en) * 2015-08-21 2019-01-10 Acerta Pharma B.V. Therapeutic Combinations of a MEK Inhibitor and a BTK Inhibitor
US20190022092A1 (en) 2015-09-15 2019-01-24 Acerta Pharma B.V. Therapeutic Combinations of a BTK Inhibitor and a GITR Binding Molecule, a 4-1BB Agonist, or an OX40 Agonist
ES2980794T3 (es) * 2015-09-15 2024-10-03 Acerta Pharma Bv Combinaciones terapéuticas de un inhibidor de CD19 y un inhibidor de BTK
WO2017077507A1 (fr) 2015-11-06 2017-05-11 Acerta Pharma B.V. Inhibiteurs de type imidazopyrazine de tyrosine kinase de bruton
CA3001969C (fr) 2015-12-17 2023-10-03 Eisai R&D Management Co., Ltd. Agent therapeutique destine au cancer du sein
DK3402503T3 (da) 2016-01-13 2020-12-21 Acerta Pharma Bv Terapeutiske kombinationer af et antifolat og en btk-hæmmer
IL293621B2 (en) 2016-06-29 2023-09-01 Principia Biopharma Inc Modified release formulations of 2-[3-[4-amino-3-(2-fluoro-4-phenoxy-phenyl)pyrazolo[4,3-d]pyrimidin-1-yl]piperidine-1-carbonyl]-4 -Methyl-4-[4-(oxane-3-yl)piperazine-1-yl)penta-2-ananitrile
WO2018002958A1 (fr) 2016-06-30 2018-01-04 Sun Pharma Advanced Research Company Limited Nouveaux composés contenant de l'hydrazide utilisés comme inhibiteurs de btk
ES2878973T3 (es) * 2016-06-30 2021-11-19 Hangzhou Bangshun Pharmaceutical Co Ltd Derivado de fenilo de imidazopiridinamina y uso del mismo
EP3492471B1 (fr) 2016-08-17 2020-12-02 Shenzhen TargetRx, Inc. Composé bicyclique fusionné pour inhiber l'activité de la tyrosine kinase
WO2018064797A1 (fr) * 2016-10-05 2018-04-12 杭州领业医药科技有限公司 Forme cristalline d'acp-196, procédé de préparation et composition pharmaceutique associés
CN107056786B (zh) * 2016-10-14 2019-05-07 苏州明锐医药科技有限公司 阿卡替尼的制备方法
CN108101905A (zh) * 2016-11-24 2018-06-01 中国科学院上海药物研究所 嘧啶并[5,4-b]吲嗪或嘧啶并[5,4-b]吡呤化合物、其制备方法及用途
MY203083A (en) * 2016-12-21 2024-06-07 Acerta Pharma Bv Imidazopyrazine inhibitors of bruton's tyrosine kinase
WO2018115965A1 (fr) 2016-12-23 2018-06-28 Acerta Pharma Bv Formes solides de composés d'imidazopyrazine
CN106588937B (zh) 2017-01-16 2018-09-21 东莞市真兴贝特医药技术有限公司 咪唑并吡嗪类化合物及其制备方法和应用
US20190376971A1 (en) 2017-01-19 2019-12-12 Acerta Pharma B.V. Compositions and Methods for the Assessment of Drug Target Occupancy for Bruton's Tyrosine Kinase
CN106831787B (zh) * 2017-01-20 2018-10-23 成都倍特药业有限公司 用作布鲁顿酪氨酸激酶抑制剂的化合物及其制备方法和应用
CN110312723B (zh) * 2017-02-20 2022-02-11 杭州领业医药科技有限公司 Acp-196盐的晶型、其制备方法、药物组合物和用途
WO2018156901A1 (fr) 2017-02-24 2018-08-30 Gilead Sciences, Inc. Inhibiteurs de tyrosine kinase de bruton
AR110998A1 (es) 2017-02-24 2019-05-22 Gilead Sciences Inc Inhibidores de la tirosina cinasa de bruton
US11554118B2 (en) * 2017-03-22 2023-01-17 Xibin Liao Bruton's tyrosine kinase inhibitors
SI3609886T1 (sl) 2017-04-14 2024-05-31 Biogen Ma Inc. Analogi benzoazepina kot inhibicijska sredstva za brutonovo tirozin kinazo
US10800787B2 (en) 2017-04-20 2020-10-13 Apotex Inc. Process for the preparation of acalabrutinib
WO2018229613A1 (fr) * 2017-06-13 2018-12-20 Dr. Reddy's Laboratories Limited Formes solides d'acalabrutinib et procédé de préparation correspondant
CN107522701B (zh) * 2017-09-01 2019-11-08 苏州富士莱医药股份有限公司 一种治疗慢性淋巴细胞白血病的BTK抑制剂Acalabrutinib的合成方法
CN107602564B (zh) * 2017-09-20 2019-08-30 南京亘泰医药技术有限公司 布鲁顿酪氨酸激酶抑制剂
WO2019058348A1 (fr) 2017-09-25 2019-03-28 Astrazeneca Ab Combinaison d'un inhibiteur de btk et d'un inhibiteur de cdk9 pour traiter le cancer
CN109836416B (zh) * 2017-11-27 2023-02-03 苏州鹏旭医药科技有限公司 一种化合物的制备方法
WO2019090269A1 (fr) 2017-11-06 2019-05-09 Peng Wang Processus de production de l'acalabrutinib
EP3736273A4 (fr) 2018-01-05 2021-02-24 Crystal Pharmaceutical (Suzhou) Co., Ltd. Nouvelle forme cristalline d'acalabrutinib, son procédé de préparation et son utilisation
CN108250186B (zh) * 2018-02-07 2020-01-14 杭州科巢生物科技有限公司 Acalabrutinib及其中间体的合成方法
CN110256438B (zh) * 2018-03-12 2020-07-17 新发药业有限公司 一种阿可替尼的制备方法
JPWO2019189241A1 (ja) 2018-03-28 2021-03-18 エーザイ・アール・アンド・ディー・マネジメント株式会社 肝細胞癌治療剤
EP3789040A4 (fr) 2018-04-27 2022-03-09 ONO Pharmaceutical Co., Ltd. Agent préventif et/ou thérapeutique pour maladie auto-immune comprenant un composé ayant une activité inhibitrice de btk en tant que principe actif
TW202014184A (zh) 2018-04-30 2020-04-16 瑞典商阿斯特捷利康公司 用於治療癌症之組合
WO2019239374A1 (fr) 2018-06-13 2019-12-19 Acerta Pharma B.V. Inhibiteurs imidazopyrazines de kinase de lymphocytes t inductible par l'interleukine-2
MA52966A (fr) 2018-06-19 2021-04-28 Regeneron Pharma Anticorps anti-facteur xii/xiia et leurs utilisations
EP3587421A1 (fr) 2018-06-29 2020-01-01 Sandoz AG Formes cristallines de (s)-4-(8-amino-3-(1-(but-2-ynoyl)pyrrolidin-2-yl)imidazo [1,5-alpha]pyrazin-1-yl-n-(pyridin-2-yl)benzamide
CN120904205A (zh) * 2018-08-29 2025-11-07 安塞塔制药公司 制备阿卡拉布替尼的方法
WO2020053795A2 (fr) 2018-09-13 2020-03-19 Fresenius Kabi Oncology Ltd. Procédé de préparation d'acalabrutinib et de ses intermédiaires
WO2020065667A1 (fr) 2018-09-25 2020-04-02 Cipla Limited Nouveaux polymorphes d'acalabrutinib, un inhibiteur de la tyrosine kinase de bruton
CN109020977B (zh) * 2018-10-26 2020-11-13 安庆奇创药业有限公司 一种Acalabrutinib的制备方法
CN120698983A (zh) 2018-12-20 2025-09-26 C4医药公司 靶向蛋白降解
CA3124330A1 (fr) 2018-12-21 2020-06-25 Daiichi Sankyo Company, Limited Combinaison d'un conjugue anticorps-medicament et d'un inhibiteur de kinase
CN111377928A (zh) * 2018-12-28 2020-07-07 南京艾德凯腾生物医药有限责任公司 一种制备Acalabrutinib的方法
CN111377929A (zh) * 2018-12-28 2020-07-07 南京艾德凯腾生物医药有限责任公司 一种可用于治疗白血病阿卡替尼(Acalabrutinib)制备的方法
CN118955506A (zh) 2019-01-18 2024-11-15 杭州邦顺制药有限公司 布鲁顿酪氨酸激酶抑制剂
CA3131386A1 (fr) * 2019-02-27 2020-09-03 Richard Keenan Composes d'imidazolopyrazine pour inhibition d'ire1
EP3942045A1 (fr) 2019-03-21 2022-01-26 Onxeo Molécule dbait associée à un inhibiteur de kinase pour le traitement du cancer
WO2020198429A1 (fr) * 2019-03-27 2020-10-01 Assia Chemical Industries Ltd Formes à l'état solide d'acalabrutinib
WO2020225831A1 (fr) * 2019-05-09 2020-11-12 Msn Laboratories Private Limited, R&D Center Procédé amélioré pour la préparation de 4-{8-amino-3-[(2s)-1-(but-2-ynoyl)pyrrolidin-2-yl] imidazo[1,5-a]pyrazin-1-yl)}-n-(pyridine-2-yl)benzamide
WO2021038540A1 (fr) 2019-08-31 2021-03-04 Sun Pharma Advanced Research Company Limited Acides cycloalkylidènecarboxyliques et dérivés en tant qu'inhibiteurs de la btk
CN110563733A (zh) * 2019-09-12 2019-12-13 安帝康(无锡)生物科技有限公司 作为选择性btk抑制剂的咪唑并吡嗪类化合物
JP7795454B2 (ja) 2019-10-14 2026-01-07 プリンシピア バイオファーマ インコーポレイテッド (r)-2-[3-[4-アミノ-3-(2-フルオロ-4-フェノキシ-フェニル)ピラゾロ[3,4-d]ピリミジン-1-イル]ピペリジン-1-カルボニル]-4-メチル-4-[4-(オキセタン-3-イル)ピペラジン-1-イル]ペンタ-2-エンニトリルを投与することにより免疫性血小板減少症を治療する方法
JP7575454B2 (ja) 2019-11-04 2024-10-29 アストラゼネカ・アクチエボラーグ B細胞悪性腫瘍を処置するためのアカラブルチニブとカピバセルチブとの治療的組み合わせ
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
US12534467B2 (en) 2019-12-02 2026-01-27 Natco Pharma Limited Process for the preparation of Acalabrutinib
AU2021209884A1 (en) 2020-01-22 2022-09-15 Principia Biopharma Inc. Crystalline forms of 2-[3-[4-amino-3-(2-fluoro-4-phenoxy-phenyl)-1h-pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carbonyl]-4-methyl-4-[4-(oxetan-3-yl)piperazin-1-yl]pent-2-enenitrile
WO2021148581A1 (fr) 2020-01-22 2021-07-29 Onxeo Nouvelle molécule dbait et son utilisation
JP7824232B2 (ja) * 2020-06-01 2026-03-04 エフ. ホフマン-ラ ロシュ アーゲー 新規イミダゾピラジン誘導体
CA3186141A1 (fr) 2020-06-19 2021-12-23 Acerta Pharma B.V. Formes posologiques de maleate d'acalabrutinib
CN112386597B (zh) * 2020-10-15 2022-03-15 天津济坤医药科技有限公司 泽布替尼在制备治疗肺纤维化疾病药物中的应用
CN113264938B (zh) * 2021-07-21 2021-11-02 北京鑫开元医药科技有限公司 一种咪唑并[1,5-a]吡嗪-8-胺类化合物、制备方法、药物组合物和应用
WO2023014817A1 (fr) 2021-08-03 2023-02-09 Syros Pharmaceuticals, Inc. Compositions et méthodes pour traiter des lymphomes avec un inhibiteur de cdk7 en combinaison avec un inhibiteur de btk
WO2025125383A1 (fr) 2023-12-11 2025-06-19 Synthon B.V. Formes cristallines d'hydrogénomaléate d'acalabrutinib
US12414950B1 (en) 2024-05-21 2025-09-16 Telios Pharma Inc. Methods of treating indolent systemic mastocytosis

Family Cites Families (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HK1039326A1 (zh) 1998-09-18 2002-04-19 Abbott Gmbh & Co. Kg 4氨基吡咯并嘧啶作为激酶抑制剂
US6921763B2 (en) 1999-09-17 2005-07-26 Abbott Laboratories Pyrazolopyrimidines as therapeutic agents
WO2001019828A2 (fr) 1999-09-17 2001-03-22 Basf Aktiengesellschaft Inhibiteurs de kinase utilises comme agents therapeutiques
US6998391B2 (en) 2002-02-07 2006-02-14 Supergen.Inc. Method for treating diseases associated with abnormal kinase activity
WO2005014599A1 (fr) 2003-06-04 2005-02-17 Cellular Genomics, Inc. Imidazo[1,2-a]pyrazin-8-ylamines et methodes d'inhibition de la tyrosine kinase de bruton par de tels composes
ES2372694T3 (es) 2003-10-15 2012-01-25 OSI Pharmaceuticals, LLC Inhibidores de tirosina cinasa de imidazo[1,5-a]pirazina.
HRP20090495T1 (hr) 2004-04-02 2009-10-31 Osi Pharmaceuticals Heterobiciklički inhibitori protein kinaze supstituirani 6,6-bicikličkim prstenom
ES2436877T3 (es) 2005-11-17 2014-01-07 OSI Pharmaceuticals, LLC Intermedios para la preparación de inhibidores de mTOR bicíclicos condensados
PE20070855A1 (es) 2005-12-02 2007-10-14 Bayer Pharmaceuticals Corp Derivados de 4-amino-pirrolotriazina sustituida como inhibidores de quinasas
AR057960A1 (es) 2005-12-02 2007-12-26 Osi Pharm Inc Inhibidores de proteina quinasa biciclicos
WO2007106503A2 (fr) 2006-03-13 2007-09-20 Osi Pharmaceuticals, Inc. Traitement combiné avec un inhibiteur de kinase egfr et un agent sensibilisant les cellules tumorales aux effets des inhibiteurs de kinase egfr
PL2526933T3 (pl) 2006-09-22 2015-08-31 Pharmacyclics Llc Inhibitory kinazy tyrozynowej Brutona
SG10201508035TA (en) * 2007-03-28 2015-10-29 Pharmacyclics Inc Inhibitors of bruton's tyrosine kinase
US20120101113A1 (en) 2007-03-28 2012-04-26 Pharmacyclics, Inc. Inhibitors of bruton's tyrosine kinase
CN101896177A (zh) 2007-12-13 2010-11-24 诺瓦提斯公司 用于治疗癌症的治疗剂的组合
AU2009233711B2 (en) * 2008-04-09 2015-02-12 Infinity Pharmaceuticals, Inc Inhibitors of fatty acid amide hydrolase
US9095592B2 (en) 2008-11-07 2015-08-04 The Research Foundation For The State University Of New York Bruton's tyrosine kinase as anti-cancer drug target
WO2010126960A1 (fr) * 2009-04-29 2010-11-04 Locus Pharmaceuticals, Inc. Composés de pyrrolotriazine
KR101661383B1 (ko) * 2010-02-08 2016-09-29 머크 샤프 앤 도메 비.브이. 8-메틸-1-페닐-이미다졸[1,5-a]피라진 화합물
UY33288A (es) 2010-03-25 2011-10-31 Glaxosmithkline Llc Derivados de indolina inhibidores de la proteina quinasa r del reticulo endoplasmatico
MX2012013622A (es) 2010-05-31 2013-02-01 Ono Pharmaceutical Co Derivado de purinona.
NZ772688A (en) 2010-06-03 2022-09-30 Pharmacyclics Llc The use of inhibitors of bruton’s tyrosine kinase (btk)
US20120053189A1 (en) 2010-06-28 2012-03-01 Pharmacyclics, Inc. Btk inhibitors for the treatment of immune mediated conditions
HUE048834T2 (hu) 2011-05-17 2020-08-28 Univ California Kináz inhibitorok
BR112013033534A2 (pt) 2011-06-28 2017-02-07 Pharmacyclics Inc métodos e composições para inibição de reabsorção de osso
EA201490265A1 (ru) 2011-07-13 2014-12-30 Фармасайкликс, Инк. Ингибиторы тирозинкиназы брутона
EP2548877A1 (fr) 2011-07-19 2013-01-23 MSD Oss B.V. Dérivés de 4-(pyridine condensée à 5 chaînons)benzamide comme inhibiteurs de BTK
AU2012285987C1 (en) * 2011-07-19 2016-09-08 Merck Sharp & Dohme B.V. 4 - imidazopyridazin- 1 -yl-benzamides and 4 - imidazotriazin- 1 - yl - benzamides as Btk- inhibitors
JP2014522860A (ja) 2011-07-19 2014-09-08 メルク・シャープ・アンド・ドーム・ベー・フェー Btk阻害剤としての4−イミダゾピリダジン−1−イル−ベンズアミドおよび4−イミダゾトリアジン−1−イル−ベンズアミド
CN110801454A (zh) 2011-10-19 2020-02-18 药品循环有限责任公司 布鲁顿酪氨酸激酶(btk)抑制剂的用途
US20140212425A1 (en) 2011-12-05 2014-07-31 Immunomedics, Inc. Therapeutic use of anti-cd22 antibodies for inducing trogocytosis
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
WO2014114185A1 (fr) 2013-01-23 2014-07-31 Merck Sharp & Dohme Corp. Inhibiteurs de btk
EP2968341A4 (fr) 2013-03-14 2016-11-23 Pharmacyclics Llc Combinaisons d'inhibiteurs de tyrosine kinase de burton et d'inhibiteurs de cyp3a4
WO2014143807A2 (fr) 2013-03-15 2014-09-18 Stromatt Scott Anticorps anti-cd37 et polythérapie par antagoniste de la voie bcr pour le traitement de malignités b et de troubles des lymphocytes b
AU2014251028A1 (en) 2013-04-08 2015-11-05 Janssen Pharmaceutica Nv Ibrutinib combination therapy
WO2015018522A1 (fr) 2013-08-06 2015-02-12 Oncoethix Sa Inhibiteur de bromodomaine bet présentant une synergie avec plusieurs agents anti-cancéreux dans des modèles cliniques de lymphome diffus de cellule b de grande taille (dlbcl)

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JP5826931B2 (ja) 2015-12-02
EP3689878A1 (fr) 2020-08-05
MX2014000746A (es) 2014-05-07
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JP6251220B2 (ja) 2017-12-20
EA201992270A3 (ru) 2020-03-31
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EP3495368A1 (fr) 2019-06-12
CY1125613T1 (el) 2024-02-16
HUE041987T2 (hu) 2019-06-28
EP4249076A2 (fr) 2023-09-27
EA201490300A1 (ru) 2014-05-30
KR20140036324A (ko) 2014-03-25
PL2734522T3 (pl) 2019-04-30
AU2017279778A1 (en) 2018-01-25
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US20190276456A1 (en) 2019-09-12
BR112014001255A2 (pt) 2017-02-21
US10239883B2 (en) 2019-03-26
MA35348B1 (fr) 2014-08-01
PT3689878T (pt) 2022-01-05
US20160151364A1 (en) 2016-06-02
US20230331729A1 (en) 2023-10-19
KR101802689B1 (ko) 2017-11-28
IL230511A0 (en) 2014-03-31
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US20180179212A1 (en) 2018-06-28
US10934296B2 (en) 2021-03-02
PL3689878T3 (pl) 2022-02-14
ZA202109164B (en) 2025-04-30
WO2013010868A1 (fr) 2013-01-24
EP2734522A1 (fr) 2014-05-28
US20160159810A1 (en) 2016-06-09
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CN103889987A (zh) 2014-06-25
JP2016034968A (ja) 2016-03-17
EP3689878B1 (fr) 2021-10-06
US9290504B2 (en) 2016-03-22
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DK2734522T3 (en) 2019-02-18
RS58177B1 (sr) 2019-03-29
HRP20212021T1 (hr) 2022-04-01
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AU2017279778B2 (en) 2019-09-19
EA037644B1 (ru) 2021-04-26
CL2014000130A1 (es) 2014-08-22
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CN106243113A (zh) 2016-12-21
JP2022088618A (ja) 2022-06-14
PH12017500166A1 (en) 2017-09-04
AU2016203837B2 (en) 2018-01-25
CN106243113B (zh) 2018-12-18
CY2021010I2 (el) 2021-06-25
CN103889987B (zh) 2016-09-14
EA201992270A2 (ru) 2020-01-16
US9790226B2 (en) 2017-10-17
EP2734522B1 (fr) 2018-10-31
CA2841886C (fr) 2016-08-16
AU2012285987A1 (en) 2014-02-06
CA2841886A1 (fr) 2013-01-24
UA115312C2 (uk) 2017-10-25
IL266894A (en) 2019-07-31
GT201400009A (es) 2017-09-28
ES2950569T3 (es) 2023-10-11
HUS2100012I1 (hu) 2021-05-28
IL266894B (en) 2022-04-01
JP2018035184A (ja) 2018-03-08
SI3689878T1 (sl) 2021-12-31
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PH12017500166B1 (en) 2018-10-26

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