PL3102577T3 - Pochodne chinolonowe jako inhibitory receptora czynnika wzrostu fibroblastów - Google Patents

Pochodne chinolonowe jako inhibitory receptora czynnika wzrostu fibroblastów

Info

Publication number
PL3102577T3
PL3102577T3 PL15706577T PL15706577T PL3102577T3 PL 3102577 T3 PL3102577 T3 PL 3102577T3 PL 15706577 T PL15706577 T PL 15706577T PL 15706577 T PL15706577 T PL 15706577T PL 3102577 T3 PL3102577 T3 PL 3102577T3
Authority
PL
Poland
Prior art keywords
growth factor
factor receptor
fibroblast growth
receptor inhibitors
quinolone derivatives
Prior art date
Application number
PL15706577T
Other languages
English (en)
Polish (pl)
Inventor
Erik Verner
Kenneth Albert Brameld
Original Assignee
Principia 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 Principia Biopharma Inc. filed Critical Principia Biopharma Inc.
Publication of PL3102577T3 publication Critical patent/PL3102577T3/pl

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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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
    • A61K31/4375Heterocyclic 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
    • 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
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with 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
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (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)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Plural Heterocyclic Compounds (AREA)
PL15706577T 2014-02-07 2015-02-04 Pochodne chinolonowe jako inhibitory receptora czynnika wzrostu fibroblastów PL3102577T3 (pl)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201461937211P 2014-02-07 2014-02-07
US201462007562P 2014-06-04 2014-06-04
US201462069932P 2014-10-29 2014-10-29
PCT/US2015/014460 WO2015120049A1 (en) 2014-02-07 2015-02-04 Quinolone derivatives as fibroblast growth factor receptor inhibitors
EP15706577.2A EP3102577B1 (en) 2014-02-07 2015-02-04 Quinolone derivatives as fibroblast growth factor receptor inhibitors

Publications (1)

Publication Number Publication Date
PL3102577T3 true PL3102577T3 (pl) 2019-03-29

Family

ID=52589764

Family Applications (1)

Application Number Title Priority Date Filing Date
PL15706577T PL3102577T3 (pl) 2014-02-07 2015-02-04 Pochodne chinolonowe jako inhibitory receptora czynnika wzrostu fibroblastów

Country Status (19)

Country Link
US (6) US9815834B2 (enExample)
EP (1) EP3102577B1 (enExample)
JP (1) JP6553629B2 (enExample)
KR (1) KR102046448B1 (enExample)
CN (1) CN106459034B (enExample)
AU (1) AU2015214328B2 (enExample)
BR (1) BR112016017137B1 (enExample)
CA (1) CA2937746C (enExample)
CY (1) CY1121444T1 (enExample)
DK (1) DK3102577T3 (enExample)
ES (1) ES2689421T3 (enExample)
HU (1) HUE041594T2 (enExample)
IL (1) IL246933B (enExample)
MX (1) MX369369B (enExample)
PL (1) PL3102577T3 (enExample)
PT (1) PT3102577T (enExample)
RU (1) RU2721723C2 (enExample)
SI (1) SI3102577T1 (enExample)
WO (1) WO2015120049A1 (enExample)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9815834B2 (en) 2014-02-07 2017-11-14 Principia Biopharma, Inc. Quinolone derivatives as fibroblast growth factor receptor inhibitors
WO2016015598A1 (en) 2014-07-26 2016-02-04 Sunshine Lake Pharma Co., Ltd. 2-amino-pyrido[2,3-d]pyrimidin-7(8h)-one derivatives as cdk inhibitors and uses thereof
TWI695831B (zh) 2014-09-13 2020-06-11 香港商南北兄弟藥業投資有限公司 Crth2拮抗劑化合物及其用途
KR102183356B1 (ko) 2015-08-11 2020-11-27 프린시피아 바이오파마, 인코퍼레이티드 Fgfr 억제제를 제조하기 위한 방법
CN108264510A (zh) * 2017-01-02 2018-07-10 上海喆邺生物科技有限公司 一种选择性抑制激酶化合物及其用途
RU2745035C1 (ru) * 2017-02-27 2021-03-18 Бетта Фармасьютикалз Ко., Лтд. Ингибитор fgfr и его применение
AU2018229148B2 (en) * 2017-03-03 2022-08-04 Auckland Uniservices Limited FGFR kinase inhibitors and pharmaceutical uses
WO2019015593A1 (zh) * 2017-07-19 2019-01-24 江苏奥赛康药业股份有限公司 嘧啶并吡啶酮或者吡啶并吡啶酮类化合物及其应用
CN109384790B (zh) * 2017-08-08 2022-05-10 药捷安康(南京)科技股份有限公司 成纤维细胞生长因子受体抑制剂及其用途
CN110016026B (zh) * 2018-01-08 2022-11-25 上海凌济生物科技有限公司 一类具有抗肿瘤活性的嘧啶并吡啶酮类化合物、制备方法和用途
AU2019338992B2 (en) 2018-09-14 2022-01-20 Abbisko Therapeutics Co., Ltd. FGFR inhibitor, preparation method therefor and application thereof
JP2022515198A (ja) 2018-12-19 2022-02-17 アレイ バイオファーマ インコーポレイテッド FGFRチロシンキナーゼの阻害剤としての置換ピラゾロ[1,5-a]ピリジン化合物
CN113474337A (zh) 2018-12-19 2021-10-01 奥瑞生物药品公司 作为fgfr抑制剂用于治疗癌症的7-((3,5-二甲氧基苯基)氨基)喹喔啉衍生物
MX2021012491A (es) * 2019-04-19 2022-01-24 Pfizer Agentes antiproliferativos para el tratamiento de la hipertensión arterial pulmonar.
US11535609B2 (en) 2019-08-08 2022-12-27 Zhangzhou Pien Tze Huang Pharmaceutical Co., Ltd. Pyrazine-2(1H)-ketone compound preparation method
US11697648B2 (en) 2019-11-26 2023-07-11 Theravance Biopharma R&D Ip, Llc Fused pyrimidine pyridinone compounds as JAK inhibitors
CN119013260A (zh) * 2022-03-31 2024-11-22 优领医药科技(香港)有限公司 螺双环化合物
CN115368219B (zh) * 2022-10-25 2022-12-27 苏州康纯医药科技有限公司 一种fgfr抑制剂关键中间体的制备方法

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5620981A (en) 1995-05-03 1997-04-15 Warner-Lambert Company Pyrido [2,3-D]pyrimidines for inhibiting protein tyrosine kinase mediated cellular proliferation
WO2004063195A1 (en) * 2003-01-03 2004-07-29 Sloan-Kettering Institute For Cancer Research Pyridopyrimidine kinase inhibitors
WO2005047284A1 (en) 2003-11-13 2005-05-26 F. Hoffmann-La Roche Ag Hydroxyalkyl substituted pyrido-7-pyrimidin-7-ones
WO2005105097A2 (en) 2004-04-28 2005-11-10 Gpc Biotech Ag Pyridopyrimidines for treating inflammatory and other diseases
EP1846403A1 (en) 2005-02-02 2007-10-24 Ranbaxy Laboratories Limited Azabicyclo derivatives as anti-inflammatory agents
WO2008150260A1 (en) 2007-06-06 2008-12-11 Gpc Biotech, Inc. 8-oxy-2-aminopyrido (2, 3-d) pyrimidin-7-one derivatives as kinase inhibitors and anticancer agents
IT1395724B1 (it) 2009-02-25 2012-10-19 Neuroscienze Pharmaness S C A R L Composti farmaceutici
PL2710007T3 (pl) 2011-05-17 2020-06-01 The Regents Of The University Of California Inhibitory kinazy
CN102219860B (zh) * 2011-05-20 2012-09-12 烟台荣昌生物工程有限公司 FGFR-Fc融合蛋白及其用途
KR20140105451A (ko) * 2011-11-04 2014-09-01 아프락시스 홀딩즈 인코포레이티드 유약 x 증후군의 치료를 위한 pak 억제제
DK2872491T3 (da) * 2012-07-11 2021-08-09 Blueprint Medicines Corp Inhibitorer af fibroblastvækstfaktorreceptoren
US9630963B2 (en) 2013-05-09 2017-04-25 Principia Biopharma, Inc. Quinolone derivatives as fibroblast growth factor inhibitors
US9851834B2 (en) 2013-09-10 2017-12-26 Alsentis, Llc Time domain differential techniques to characterize various stimuli
US9815834B2 (en) 2014-02-07 2017-11-14 Principia Biopharma, Inc. Quinolone derivatives as fibroblast growth factor receptor inhibitors
US10538517B2 (en) 2015-05-22 2020-01-21 Principia Biopharma, Inc. Quinolone derivatives as FGFR inhibitors
KR102183356B1 (ko) 2015-08-11 2020-11-27 프린시피아 바이오파마, 인코퍼레이티드 Fgfr 억제제를 제조하기 위한 방법

Also Published As

Publication number Publication date
RU2016130932A3 (enExample) 2018-06-19
SI3102577T1 (sl) 2019-03-29
CA2937746C (en) 2020-09-01
IL246933A0 (en) 2016-09-29
IL246933B (en) 2021-05-31
MX2016010106A (es) 2016-11-15
US20190233418A1 (en) 2019-08-01
EP3102577A1 (en) 2016-12-14
CN106459034A (zh) 2017-02-22
US9567334B2 (en) 2017-02-14
CA2937746A1 (en) 2015-08-13
AU2015214328B2 (en) 2019-04-18
CN106459034B (zh) 2018-01-12
US20160200725A1 (en) 2016-07-14
RU2721723C2 (ru) 2020-05-21
US20240092777A1 (en) 2024-03-21
US20180065960A1 (en) 2018-03-08
WO2015120049A1 (en) 2015-08-13
HUE041594T2 (hu) 2019-05-28
AU2015214328A1 (en) 2016-08-04
JP6553629B2 (ja) 2019-07-31
RU2016130932A (ru) 2018-03-13
DK3102577T3 (en) 2018-11-12
US10294223B2 (en) 2019-05-21
CY1121444T1 (el) 2020-05-29
US11078199B2 (en) 2021-08-03
KR102046448B1 (ko) 2019-11-19
JP2017505782A (ja) 2017-02-23
PT3102577T (pt) 2018-10-23
BR112016017137A2 (enExample) 2017-08-08
US20160229849A1 (en) 2016-08-11
US9815834B2 (en) 2017-11-14
US12162882B2 (en) 2024-12-10
EP3102577B1 (en) 2018-07-18
MX369369B (es) 2019-11-06
ES2689421T3 (es) 2018-11-14
US20210292323A1 (en) 2021-09-23
BR112016017137B1 (pt) 2022-10-11
KR20160121520A (ko) 2016-10-19

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