HRP20171835T1 - Inhibitorni spojevi - Google Patents

Inhibitorni spojevi Download PDF

Info

Publication number
HRP20171835T1
HRP20171835T1 HRP20171835TT HRP20171835T HRP20171835T1 HR P20171835 T1 HRP20171835 T1 HR P20171835T1 HR P20171835T T HRP20171835T T HR P20171835TT HR P20171835 T HRP20171835 T HR P20171835T HR P20171835 T1 HRP20171835 T1 HR P20171835T1
Authority
HR
Croatia
Prior art keywords
methyl
methoxy
pyrazol
phenyl
pyrido
Prior art date
Application number
HRP20171835TT
Other languages
English (en)
Croatian (hr)
Inventor
Swen Hoelder
Julian Blagg
Savade SOLANKI
Hannah Woodward
Sebastien Naud
Vassilios Bavetsias
Peter SHELDRAKE
Paolo INNOCENTI
Kwai-Ming J. Cheung
Butrus Atrash
Original Assignee
Cancer Research Technology Limited
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 Cancer Research Technology Limited filed Critical Cancer Research Technology Limited
Publication of HRP20171835T1 publication Critical patent/HRP20171835T1/hr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/4353—Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4375—Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/472—Non-condensed isoquinolines, e.g. papaverine
    • A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D519/00—Heterocyclic 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)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (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)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
HRP20171835TT 2012-09-07 2013-09-09 Inhibitorni spojevi HRP20171835T1 (hr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB1216017.2A GB201216017D0 (en) 2012-09-07 2012-09-07 Inhibitor compounds
PCT/GB2013/052360 WO2014037750A1 (en) 2012-09-07 2013-09-09 Inhibitor compounds
EP13760106.8A EP2892889B1 (en) 2012-09-07 2013-09-09 Inhibitor compounds

Publications (1)

Publication Number Publication Date
HRP20171835T1 true HRP20171835T1 (hr) 2017-12-29

Family

ID=47137117

Family Applications (1)

Application Number Title Priority Date Filing Date
HRP20171835TT HRP20171835T1 (hr) 2012-09-07 2013-09-09 Inhibitorni spojevi

Country Status (22)

Country Link
US (6) US9409907B2 (enExample)
EP (2) EP3293183B1 (enExample)
JP (2) JP6216791B2 (enExample)
CN (1) CN104837829B (enExample)
AU (2) AU2013311434B2 (enExample)
BR (1) BR112015004489B1 (enExample)
CA (1) CA2884006C (enExample)
CY (1) CY1119714T1 (enExample)
DK (2) DK2892889T3 (enExample)
ES (2) ES2742442T3 (enExample)
GB (1) GB201216017D0 (enExample)
HR (1) HRP20171835T1 (enExample)
HU (1) HUE036259T2 (enExample)
LT (1) LT2892889T (enExample)
NO (1) NO2892889T3 (enExample)
PL (1) PL2892889T3 (enExample)
PT (1) PT2892889T (enExample)
RS (1) RS56750B1 (enExample)
RU (1) RU2673079C2 (enExample)
SI (1) SI2892889T1 (enExample)
SM (1) SMT201700596T1 (enExample)
WO (1) WO2014037750A1 (enExample)

Families Citing this family (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9017724B2 (en) 2004-02-24 2015-04-28 The General Hospital Corporation Catalytic radiofluorination
EP3231804B1 (en) 2008-03-21 2021-03-03 The General Hospital Corporation Compounds and compositions for the detection and treatment of alzheimer's disease and related disorders
GB201104267D0 (en) 2011-03-14 2011-04-27 Cancer Rec Tech Ltd Pyrrolopyridineamino derivatives
GB201216017D0 (en) 2012-09-07 2012-10-24 Cancer Rec Tech Ltd Inhibitor compounds
GB201216018D0 (en) 2012-09-07 2012-10-24 Cancer Rec Tech Ltd Pharmacologically active compounds
ES3069593T3 (en) * 2013-08-23 2026-06-09 Neupharma Inc Quinazolin-8-yl derivatives for use in methods of treating melanoma, non-small cell lung cancer, thyroid cancer, ovarian cancer, or colon cancer
GB201403536D0 (en) 2014-02-28 2014-04-16 Cancer Rec Tech Ltd Inhibitor compounds
JP6616934B2 (ja) * 2014-05-22 2019-12-04 株式会社 資生堂 レナリドミドの光学分割方法
EP3270694A4 (en) * 2015-02-17 2018-09-05 Neupharma, Inc. Certain chemical entities, compositions, and methods
EP3283642B1 (en) 2015-04-17 2023-10-11 Netherlands Translational Research Center Holding B.V. Prognostic biomarkers for ttk inhibitor chemotherapy
US10124004B2 (en) * 2015-05-29 2018-11-13 Teijin Pharma Limited Pyrido[3,4-d]pyrimidine derivative and pharmaceutically acceptable salt thereof
US10494378B2 (en) 2015-07-21 2019-12-03 Guangzhou Maxinovel Pharmaceuticals Co., Ltd. Fused ring pyrimidine compound, intermediate, and preparation method, composition and use thereof
GB201522532D0 (en) * 2015-12-21 2016-02-03 Cancer Rec Tech Ltd Novel pyrrolo[3,2-c]pyridine-6-amino derivatives
CN109843858B (zh) 2016-08-15 2023-05-05 润新生物公司 某些化学实体、组合物及方法
TWI755452B (zh) 2016-11-28 2022-02-21 日商帝人製藥股份有限公司 吡啶并〔3﹐4-d〕嘧啶衍生物或其溶劑合物之結晶
HUE053220T2 (hu) * 2016-11-28 2021-06-28 Teijin Pharma Ltd ((Piridin-2-il)-amino)pirido[3,4-d]pirimidin és ((piridazin-3-il)-amino)pirido[3,4-d]pirimidin származékok mint CDK4/6 inhibitorok pl. reumatoid artritisz, érelmeszesedés, tüdõfibrózis, agyi infartus vagy rák kezelésére
GB201709840D0 (en) * 2017-06-20 2017-08-02 Inst Of Cancer Research: Royal Cancer Hospital Methods and medical uses
WO2018234778A1 (en) * 2017-06-20 2018-12-27 The Institute Of Cancer Research: Royal Cancer Hospital METHODS AND MEDICAL USES
EP3701304B1 (en) 2017-10-26 2022-05-04 CommScope Connectivity Belgium BVBA Telecommunications system
GB201809460D0 (en) * 2018-06-08 2018-07-25 Crt Pioneer Fund Lp Salt form
GB201809458D0 (en) * 2018-06-08 2018-07-25 Crt Pioneer Fund Lp Salt form
BR112022008375A2 (pt) 2019-10-30 2022-07-12 Genfleet Therapeutics Shanghai Inc Composto cíclico heterocíclico fundido substituído, método de preparação e uso farmacêutico deste
KR102396930B1 (ko) * 2020-01-15 2022-05-12 한국과학기술연구원 피리도[3,4-d]피리미딘 유도체 및 이를 포함하는 치료용 약학 조성물
EP4090663A1 (en) * 2020-01-15 2022-11-23 Blueprint Medicines Corporation Map4k1 inhibitors
CN115916747A (zh) * 2020-07-01 2023-04-04 四川海思科制药有限公司 一种并环杂环衍生物及其在医药上的应用
US11267788B2 (en) * 2020-07-16 2022-03-08 Dermavant Sciences GmbH Isoquinoline compounds and their use in treating AhR imbalance
CN115942937B (zh) * 2020-08-17 2025-07-25 浙江扬厉医药技术有限公司 嘧啶并环类化合物
PE20231311A1 (es) 2020-11-18 2023-08-24 Deciphera Pharmaceuticals Llc Inhibidores de gcn2 y perk quinasas y metodos de uso de los mismos
CN115583946B (zh) * 2021-07-06 2026-01-16 赛诺哈勃药业(成都)有限公司 杂环化合物及其作为cdk抑制剂的用途
AR128015A1 (es) * 2021-12-16 2024-03-20 Transthera Sciences Nanjing Inc Inhibidor de cdk9 y uso del mismo
CN121548580A (zh) * 2023-05-15 2026-02-17 亚历克西亚治疗公司 Cdk抑制剂化合物
WO2025038785A1 (en) * 2023-08-16 2025-02-20 Biotheryx, Inc. Sos1 protein degraders, pharmaceutical compositions, and therapeutic applications
CN117800875B (zh) * 2023-12-21 2024-10-22 泰州精英化成医药科技有限公司 一种反式-(N-Boc-4-氨基环己基)乙酸的制备方法
TW202545531A (zh) * 2024-01-17 2025-12-01 美商依安彼克醫療有限公司 氮—喹唑啉化合物之使用方法

Family Cites Families (55)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2697710A (en) 1953-01-02 1954-12-21 Burroughs Wellcome Co Pyrido (2,3-d) pyrimidines and method of preparing same
US3021332A (en) 1954-01-04 1962-02-13 Burroughs Wellcome Co Pyrido (2, 3-d) pyrimidine compounds and method of making
FI971953A7 (fi) 1994-11-14 1997-05-12 Warner Lambert Co Proteiinityrosiinikinaasin välittämää soluproliferaatiota inhiboivat 6 -aryyli-pyrido(2,3-d)pyrimidiinit ja naftyridiinit
US7053070B2 (en) 2000-01-25 2006-05-30 Warner-Lambert Company Pyrido[2,3-d]pyrimidine-2,7-diamine kinase inhibitors
WO2001055147A1 (en) 2000-01-25 2001-08-02 Warner-Lambert Company PYRIDO[2,3-d]PYRIMIDINE-2,7-DIAMINE KINASE INHIBITORS
US6653332B2 (en) 2000-05-03 2003-11-25 Tularik Inc. Combination therapeutic compositions and method of use
WO2002090360A1 (en) 2001-05-10 2002-11-14 Smithkline Beecham Corporation Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases
AU2002324450A1 (en) 2001-06-21 2003-01-08 Ariad Pharmaceuticals, Inc. Novel pyridopyrimidines and uses thereof
EP1463505A2 (en) 2001-12-13 2004-10-06 Abbott Laboratories 3-(phenyl-alkoxy)-5-(phenyl)-pyridine derivatives and related compounds as kinase inhibitors for the treatment of cancer
US20030187026A1 (en) 2001-12-13 2003-10-02 Qun Li Kinase inhibitors
KR100714519B1 (ko) 2002-03-07 2007-05-07 에프. 호프만-라 로슈 아게 이환 피리딘 및 피리미딘 p38 키나아제 억제제
RU2324695C2 (ru) * 2002-08-06 2008-05-20 Ф.Хоффманн-Ля Рош Аг 6-АЛКОКСИПИРИДОПИРИМИДИНЫ И ФАРМАЦЕВТИЧЕСКАЯ КОМПОЗИЦИЯ, ОБЛАДАЮЩАЯ АКТИВНОСТЬЮ ИНГИБИТОРОВ КИНАЗЫ МАР р38
CA2765093A1 (en) 2002-11-12 2004-05-27 Abbott Laboratories Bicyclic-substituted amines as histamine-3 receptor ligands
US20040092521A1 (en) 2002-11-12 2004-05-13 Altenbach Robert J. Bicyclic-substituted amines as histamine-3 receptor ligands
EP1590341B1 (en) 2003-01-17 2009-06-17 Warner-Lambert Company LLC 2-aminopyridine substituted heterocycles as inhibitors of cellular proliferation
US20050256118A1 (en) 2004-05-12 2005-11-17 Altenbach Robert J Bicyclic-substituted amines having cyclic-substituted monocyclic substituents
US7098222B2 (en) 2004-05-12 2006-08-29 Abbott Laboratories Bicyclic-substituted amines having cyclic-substituted monocyclic substituents
EP1899322B1 (en) 2005-06-28 2009-09-02 Sanofi-Aventis Isoquinoline derivatives as inhibitors of rho-kinase
ATE541844T1 (de) * 2005-12-21 2012-02-15 Abbott Lab Antivirale verbindungen
TW200808739A (en) * 2006-04-06 2008-02-16 Novartis Vaccines & Diagnostic Quinazolines for PDK1 inhibition
WO2007125405A2 (en) 2006-05-01 2007-11-08 Pfizer Products Inc. Substituted 2-amino-fused heterocyclic compounds
TWI398252B (zh) 2006-05-26 2013-06-11 諾華公司 吡咯并嘧啶化合物及其用途
CA2673003A1 (en) * 2006-12-22 2008-07-03 Novartis Ag Quinazolines for pdk1 inhibition
WO2008135232A1 (en) 2007-05-02 2008-11-13 Riccardo Cortese Use and compositions of purine derivatives for the treatment of proliferative disorders
WO2009032703A1 (en) 2007-08-28 2009-03-12 Irm Llc 2- (het) arylamino-6-aminopyridine derivatives and fused forms thereof as anaplastic lymphoma kinase inhibitors
WO2009084695A1 (ja) * 2007-12-28 2009-07-09 Carna Biosciences Inc. 2-アミノキナゾリン誘導体
GB0803018D0 (en) 2008-02-19 2008-03-26 Cancer Rec Tech Ltd Therapeutic compounds and their use
GB0812969D0 (en) 2008-07-15 2008-08-20 Sentinel Oncology Ltd Pharmaceutical compounds
JP5789252B2 (ja) 2009-05-07 2015-10-07 インテリカイン, エルエルシー 複素環式化合物およびその使用
EP2937345B1 (en) 2009-12-29 2018-03-21 Dana-Farber Cancer Institute, Inc. Type ii raf kinase inhibitors
CA2791738C (en) 2010-03-01 2020-06-09 Gtx, Inc. Aryl imidazolyl compounds for the treatment of cancer
GB201011182D0 (en) 2010-07-02 2010-08-18 Wireless Fibre Systems Ltd Riser wireless communications system
US9333205B2 (en) * 2010-07-30 2016-05-10 Nerviano Medical Sciences S.R.L. Isoxazolo-quinazolines as modulators of protein kinase activity
ES2377610B1 (es) 2010-09-01 2013-02-05 Institut Químic de Sarriá CETS Fundació Privada Preparación de compuestos pirido[2,3-d]pirimidin-7(8h)-ona sustituidos.
JP2013540145A (ja) 2010-10-21 2013-10-31 ウニベルシテート デス ザールランデス コルチゾール依存性疾患の治療用の選択的cyp11b1阻害剤
WO2012064973A2 (en) 2010-11-10 2012-05-18 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
CA2817460A1 (en) 2010-12-17 2012-06-21 F. Hoffmann-La Roche Ag Substituted 6,6-fused nitrogenous heterocyclic compounds and uses thereof
EP2655334B1 (en) 2010-12-22 2018-10-03 Eutropics Pharmaceuticals, Inc. Compositions and methods useful for treating diseases
TWI450891B (zh) 2010-12-29 2014-09-01 Dev Center Biotechnology 新穎微管蛋白抑制劑
US8975267B2 (en) * 2011-01-26 2015-03-10 Nerviano Medical Sciences S.R.L. Tricyclic pyrrolo derivatives, process for their preparation and their use as kinase inhibitors
GB201104267D0 (en) 2011-03-14 2011-04-27 Cancer Rec Tech Ltd Pyrrolopyridineamino derivatives
US9745191B2 (en) 2011-04-11 2017-08-29 Saudi Arabian Oil Company Auto thermal reforming (ATR) catalytic structures
US9517229B2 (en) 2011-07-29 2016-12-13 Medivation Prostate Therapeutics, Inc. Treatment of breast cancer
EP2766352B1 (en) 2011-10-12 2018-06-06 University Health Network (UHN) Indazole compounds as kinase inhibitors and method of treating cancer with same
GB201216017D0 (en) * 2012-09-07 2012-10-24 Cancer Rec Tech Ltd Inhibitor compounds
GB201216018D0 (en) 2012-09-07 2012-10-24 Cancer Rec Tech Ltd Pharmacologically active compounds
EP2961409A1 (en) 2013-02-26 2016-01-06 Senex Biotechnology, Inc. Inhibitors of cdk8/19 for use in treating estrogen receptor positive breast cancer
MX2016007282A (es) 2013-12-06 2016-09-07 Hoffmann La Roche Modulador del receptor de estrogenos para el tratamiento de cancer de mama positivo al receptor de estrogenos localmente avanzado o metastasico.
GB201403536D0 (en) 2014-02-28 2014-04-16 Cancer Rec Tech Ltd Inhibitor compounds
SG10201807838SA (en) 2014-03-11 2018-10-30 Council Queensland Inst Medical Res Determining cancer aggressiveness, prognosis and responsiveness to treatment
WO2016010886A1 (en) 2014-07-14 2016-01-21 Signal Pharmaceuticals, Llc Methods of treating a cancer using substituted pyrrolopyrimidine compounds, compositions thereof
US10611765B2 (en) 2014-11-06 2020-04-07 Ohio State Innovation Foundation Pyrrolopyrimidine derivatives as Mps1/TTK kinase inhibitors
GB201522532D0 (en) 2015-12-21 2016-02-03 Cancer Rec Tech Ltd Novel pyrrolo[3,2-c]pyridine-6-amino derivatives
WO2018234778A1 (en) 2017-06-20 2018-12-27 The Institute Of Cancer Research: Royal Cancer Hospital METHODS AND MEDICAL USES
GB201709840D0 (en) 2017-06-20 2017-08-02 Inst Of Cancer Research: Royal Cancer Hospital Methods and medical uses

Also Published As

Publication number Publication date
LT2892889T (lt) 2017-12-11
US20150239884A1 (en) 2015-08-27
EP3293183A1 (en) 2018-03-14
US20220402912A1 (en) 2022-12-22
JP6496376B2 (ja) 2019-04-03
EP2892889B1 (en) 2017-10-18
EP3293183B1 (en) 2019-07-24
US11897877B2 (en) 2024-02-13
CN104837829B (zh) 2019-07-05
BR112015004489A2 (pt) 2017-07-04
CA2884006C (en) 2021-01-19
AU2013311434A1 (en) 2015-04-02
SMT201700596T1 (it) 2018-01-11
CY1119714T1 (el) 2018-06-27
PT2892889T (pt) 2018-01-09
DK3293183T3 (da) 2019-08-12
HUE036259T2 (hu) 2018-06-28
AU2013311434B2 (en) 2017-10-19
EP2892889A1 (en) 2015-07-15
US9890157B2 (en) 2018-02-13
DK2892889T3 (en) 2017-12-11
AU2017268488A1 (en) 2017-12-14
SI2892889T1 (sl) 2017-12-29
US20160222009A1 (en) 2016-08-04
US9834552B2 (en) 2017-12-05
HK1211921A1 (en) 2016-06-03
NO2892889T3 (enExample) 2018-03-17
RS56750B1 (sr) 2018-03-30
JP2015527387A (ja) 2015-09-17
RU2015112580A (ru) 2016-10-27
US9409907B2 (en) 2016-08-09
US20160220570A1 (en) 2016-08-04
ES2742442T3 (es) 2020-02-14
JP2018027967A (ja) 2018-02-22
CA2884006A1 (en) 2014-03-13
US11046688B2 (en) 2021-06-29
US20180141944A1 (en) 2018-05-24
AU2017268488B2 (en) 2019-06-13
GB201216017D0 (en) 2012-10-24
CN104837829A (zh) 2015-08-12
BR112015004489B1 (pt) 2020-09-29
JP6216791B2 (ja) 2017-10-18
WO2014037750A1 (en) 2014-03-13
US20200165241A1 (en) 2020-05-28
PL2892889T3 (pl) 2018-03-30
ES2655194T3 (es) 2018-02-19
US10479788B2 (en) 2019-11-19
RU2673079C2 (ru) 2018-11-22

Similar Documents

Publication Publication Date Title
RU2015112580A (ru) Ингибиторные соединения
RU2473549C2 (ru) Пиримидиновые соединения, композиции и способы применения
JP7576552B2 (ja) イミダゾ[1,2-a]ピリジニル誘導体及び疾患の処置におけるその使用
ES2960411T3 (es) Compuestos de 4-azaindol
RU2431635C2 (ru) Соединения и композиции в качестве ингибиторов активности каннабиноидного рецептора 1
JP7644029B2 (ja) P2x3阻害剤としてのアミノキナゾリン誘導体
CA3007412C (en) The use of 1,4-disubstituted pyridazine compounds to treat huntington's disease
CN104093426B (zh) 用于lrrk2的正电子发射体层摄影(pet)成像的氟-18和碳-11标记的放射性配体
ES2616679T3 (es) Nuevos derivados de indolizina, procedimiento para su preparación y composiciones farmacéuticas que los contienen para el tratamiento del cáncer
AU2015357585B2 (en) 4,6-substituted-pyrazolo[1,5-a]pyrazines as Janus kinase inhibitors
CA2926908C (en) Amino pyrimidine derivatives
JP2020524170A5 (ja) 医薬組成物
AU2010279019B2 (en) Compounds for the reduction of beta-amyloid production
ME02595B (me) Heterociklilamini kao inhibitori pi3k
JP2019535664A5 (enExample)
RS62913B1 (sr) Jedinjenja i sastavi kao inhibitori endozomskih toličnih receptora
RU2009140469A (ru) Производные пирролопиримидин-7-она и их применение в качестве фармацевтических средств
RU2014152257A (ru) Гетероциклильные пиримидиновые аналоги в качестве ингибиторов tyk2
MX2014008647A (es) Compuesto de pirazin-carboxamida.
CA2623982A1 (en) Pyrazolo[1,5-a]pyrimidine compounds as cannabinoid receptor antagonists
JP2013515688A (ja) Jak阻害剤としてのイミダゾピリジン誘導体
GB2609879A (en) Antagonists of the adenosine A2a receptor
RU2011116447A (ru) Модуляторы амилоида бета
JP2022539373A (ja) イミダゾ[1,2-a]ピリジニル誘導体及び疾患の処置におけるそれらの使用
WO2025230862A1 (en) Macrocyclic amino compounds as modulators of kras and uses therof