PL2325181T3 - Inhibitor STAT3 zawierający jako składnik aktywny pochodną chinolinokarboksyamidu - Google Patents

Inhibitor STAT3 zawierający jako składnik aktywny pochodną chinolinokarboksyamidu

Info

Publication number
PL2325181T3
PL2325181T3 PL09794208T PL09794208T PL2325181T3 PL 2325181 T3 PL2325181 T3 PL 2325181T3 PL 09794208 T PL09794208 T PL 09794208T PL 09794208 T PL09794208 T PL 09794208T PL 2325181 T3 PL2325181 T3 PL 2325181T3
Authority
PL
Poland
Prior art keywords
active ingredient
inhibitor containing
stat3 inhibitor
quinolinecarboxamide derivative
quinolinecarboxamide
Prior art date
Application number
PL09794208T
Other languages
English (en)
Inventor
Akira Asai
Kenji Matsuno
Naohisa Ogo
Takane Yokotagawa
Osamu Takahashi
Yasuto Akiyama
Tadashi Ashizawa
Tadashi Okawara
Original Assignee
General Incorporated Association Pharma Valley Project Supporting Organization
Shizuoka Prefecture
Kumamoto Health Science University
Kabushiki Kaisha Yakult Honsha
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 General Incorporated Association Pharma Valley Project Supporting Organization, Shizuoka Prefecture, Kumamoto Health Science University, Kabushiki Kaisha Yakult Honsha filed Critical General Incorporated Association Pharma Valley Project Supporting Organization
Publication of PL2325181T3 publication Critical patent/PL2325181T3/pl

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
    • C07D401/02—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
    • C07D401/12—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 linked by a chain containing hetero atoms as chain links
    • 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
    • A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • 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
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

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)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Rheumatology (AREA)
  • Epidemiology (AREA)
  • Pain & Pain Management (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
PL09794208T 2008-07-10 2009-07-10 Inhibitor STAT3 zawierający jako składnik aktywny pochodną chinolinokarboksyamidu PL2325181T3 (pl)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2008180433 2008-07-10

Publications (1)

Publication Number Publication Date
PL2325181T3 true PL2325181T3 (pl) 2017-09-29

Family

ID=41506885

Family Applications (1)

Application Number Title Priority Date Filing Date
PL09794208T PL2325181T3 (pl) 2008-07-10 2009-07-10 Inhibitor STAT3 zawierający jako składnik aktywny pochodną chinolinokarboksyamidu

Country Status (12)

Country Link
US (1) US8466290B2 (pl)
EP (1) EP2325181B1 (pl)
JP (1) JP5650529B2 (pl)
KR (1) KR101696936B1 (pl)
CN (1) CN102099352B (pl)
AU (1) AU2009269410B2 (pl)
CA (1) CA2729988C (pl)
EA (1) EA021306B1 (pl)
ES (1) ES2622575T3 (pl)
NZ (2) NZ590355A (pl)
PL (1) PL2325181T3 (pl)
WO (1) WO2010004761A1 (pl)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5794922B2 (ja) * 2009-12-28 2015-10-14 一般社団法人ファルマバレープロジェクト支援機構 1,3,4−オキサジアゾール−2−カルボキサミド化合物
ES2553771T3 (es) * 2010-10-08 2015-12-11 Nivalis Therapeutics, Inc. Nuevos compuestos de quinolina sustituidos como inhibidores de la S-nitrosoglutatión reductasa
WO2013074059A2 (en) 2010-11-05 2013-05-23 Regents Of The University Of Minnesota Cytosine deaminase modulators for enhancement of dna transfection
JPWO2012121168A1 (ja) * 2011-03-04 2014-07-17 国立大学法人京都大学 キナーゼ阻害剤
CN102827142B (zh) * 2011-06-17 2014-11-12 中国科学院上海药物研究所 一类喹啉-8-甲酰胺类化合物、其制备方法及其医药用途
CN102417479B (zh) * 2011-08-29 2014-02-26 南京大学 Stat3小分子选择性抑制剂及其制备方法和应用
HK1218709A1 (zh) * 2012-05-25 2017-03-10 多伦多大学管理委员会 新水楊酸衍生物、其藥學上可接受的鹽、其組合物以及其使用方法
US8791067B2 (en) 2012-07-24 2014-07-29 Morehouse School Of Medicine Method for treating malaria
CN103910727B (zh) * 2012-12-31 2016-06-15 北京大学 STAT3-Hif1α信号通路抑制剂及其在抗肿瘤中的应用
US10562912B2 (en) * 2013-06-05 2020-02-18 C&C Research Laboratories Heterocyclic derivatives and use thereof
WO2015106272A1 (en) * 2014-01-13 2015-07-16 Harki Daniel A Small molecule inhibitors of apobec3g and apobec3b
WO2015120436A2 (en) 2014-02-10 2015-08-13 H. Lee Moffitt Cancer Center And Research Institute, Inc. Stat3 phosphorylation during graft-versus-host disease
KR20160066490A (ko) * 2014-12-02 2016-06-10 주식회사 씨앤드씨신약연구소 헤테로사이클 유도체 및 그의 용도
WO2016202935A1 (en) * 2015-06-19 2016-12-22 Bayer Pharma Aktiengesellschaft Glucose transport inhibitors
WO2017013270A1 (en) 2015-07-23 2017-01-26 Universite De Strasbourg Use of leptin signaling inhibitor for protecting kidneys from patients having ciliopathy
AU2017330443B2 (en) * 2016-09-26 2023-08-24 Dana-Farber Cancer Institute, Inc. Chromobox protein inhibitors and uses thereof
TWI853814B (zh) 2018-05-31 2024-09-01 南韓商C&C新藥研究所 雜環衍生物及其用途
US20220008409A1 (en) * 2018-09-18 2022-01-13 Kabushiki Kaisha Yakult Honsha Cancer combination therapy using quinoline carboxamide derivative
CN113613730A (zh) * 2019-03-22 2021-11-05 株式会社益力多本社 喹啉甲酰胺衍生物和其制造中间物的制造方法
CN113891749A (zh) * 2019-03-28 2022-01-04 埃皮齐梅股份有限公司 喹啉衍生物及其用于治疗癌症的用途
WO2020219792A1 (en) * 2019-04-26 2020-10-29 Purdue Research Foundation Cf3-, ocf3-, scf3- and sf5-containing antibacterial agents
WO2020218432A1 (ja) * 2019-04-26 2020-10-29 株式会社ヤクルト本社 キノリンカルボキサミド誘導体を用いる免疫チェックポイント阻害剤併用療法
CN117186086B (zh) * 2023-09-06 2026-03-27 中山大学 一种苯并吡啶类化合物及其制备方法与应用

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9823871D0 (en) * 1998-10-30 1998-12-23 Pharmacia & Upjohn Spa 2-Amino-thiazole derivatives, process for their preparation, and their use as antitumour agents
MXPA02001498A (es) 1999-08-12 2003-07-21 Pharmacia & Italia S P A Derivados de 3(5)-amino-pirazol, procedimiento para la preparacion de los mismos y usos como agentes antitumorales.
JP4883862B2 (ja) * 1999-11-15 2012-02-22 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ ファルネシルトランスフェラーゼ阻害剤としてのトリアゾール類
US7049324B1 (en) 1999-11-15 2006-05-23 Ashis Kumar Saha Triazoles as farnesyl transferase inhibitors
GB0109122D0 (en) 2001-04-11 2001-05-30 Smithkline Beecham Spa Novel compounds
CN1665808A (zh) 2002-05-06 2005-09-07 沃泰克斯药物股份有限公司 噻二唑或噁二唑及其作为jak蛋白激酶抑制剂的用途
AR042052A1 (es) 2002-11-15 2005-06-08 Vertex Pharma Diaminotriazoles utiles como inhibidores de proteinquinasas
WO2004078731A1 (en) 2003-03-06 2004-09-16 'chemical Diversity Research Institute', Ltd. Quinoline-carboxylic acids and the derivatives thereof, a focused library
EP1820504A1 (en) * 2004-11-15 2007-08-22 Taisho Pharmaceutical Co., Ltd Imine compound
CA2599992A1 (en) 2005-03-03 2006-09-08 Sirtris Pharmaceuticals, Inc. Acridine and quinoline dervatives as sirtuin modulators
US20090054445A1 (en) 2006-01-27 2009-02-26 Astrazeneca Ab Amide Substituted Quinolines
US20080033000A1 (en) * 2006-05-15 2008-02-07 Senex Biotechnology, Inc. Identification of CDKI pathway inhibitors
UA95978C2 (ru) 2006-10-02 2011-09-26 Оцука Фармас'Ютікел Ко., Лтд. Ингибитор активации stat3/5

Also Published As

Publication number Publication date
EP2325181A1 (en) 2011-05-25
US8466290B2 (en) 2013-06-18
JPWO2010004761A1 (ja) 2011-12-22
KR20110039221A (ko) 2011-04-15
NZ590355A (en) 2013-01-25
ES2622575T3 (es) 2017-07-06
CN102099352B (zh) 2014-02-26
AU2009269410B2 (en) 2013-12-05
WO2010004761A1 (ja) 2010-01-14
US20110172429A1 (en) 2011-07-14
EA021306B1 (ru) 2015-05-29
CA2729988A1 (en) 2010-01-14
EA201170176A1 (ru) 2011-08-30
JP5650529B2 (ja) 2015-01-07
CA2729988C (en) 2016-09-13
EP2325181A4 (en) 2012-03-07
EP2325181B1 (en) 2017-03-29
AU2009269410A1 (en) 2010-01-14
NZ602099A (en) 2014-06-27
KR101696936B1 (ko) 2017-01-16
CN102099352A (zh) 2011-06-15

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