NO20074311L - Kinazolinderivat med tyrosinkinase-inhiberendeaktivitet - Google Patents

Kinazolinderivat med tyrosinkinase-inhiberendeaktivitet

Info

Publication number
NO20074311L
NO20074311L NO20074311A NO20074311A NO20074311L NO 20074311 L NO20074311 L NO 20074311L NO 20074311 A NO20074311 A NO 20074311A NO 20074311 A NO20074311 A NO 20074311A NO 20074311 L NO20074311 L NO 20074311L
Authority
NO
Norway
Prior art keywords
substituted
alkyl group
hydrogen atom
tyrosine kinase
inhibitory activity
Prior art date
Application number
NO20074311A
Other languages
English (en)
Other versions
NO343403B1 (no
Inventor
Masaharu Kume
Kenji Matsuo
Naoki Omori
Masami Takayama
Aiko Omori
Takeshi Endo
Original Assignee
Shionogi & Co
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 Shionogi & Co filed Critical Shionogi & Co
Publication of NO20074311L publication Critical patent/NO20074311L/no
Publication of NO343403B1 publication Critical patent/NO343403B1/no

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72—Quinazolines; Hydrogenated quinazolines
    • C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
    • C07D239/94—Nitrogen atoms
    • 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
    • A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
    • 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
    • A61K31/535—Heterocyclic 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
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • 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
    • C07D401/12—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
    • 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
    • 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
    • C07D405/06—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 linked by a carbon chain containing only aliphatic carbon atoms
    • 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
    • C07D405/12—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 linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
    • C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 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
    • C07D417/02—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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

En forbindelse representert ved den generelle formel (I) eller et farmasøytisk aksepterbart salt derav eller et solvat av forbindelsen eller saltet: (I) hvor Rx representerer en gruppe representert ved formel (II): hvor representerer et hydrogenatom, en alkylgmppe som kan være substituert eller lignende,. Z representerer -O-, -N(R)- eller lignende, Rrepresenterer et hydrogenatom, en alkylgruppe eller lignende, Rrepresenterer et hydrogenatom, en alkylgruppe som kan være substituert eller lignende, R representerer et hydrogenatom, en alkylgruppe som kan være substituert eller lignende, Rrepresenterer en alkylgruppe som kan være substituert eller lignende, Wrepresenterer en ikke-aromatisk nitrogenert heterocyklisk gruppe som kan være substituert, og Rrepresenterer et hydrogenatom, en alkylgruppe som kan være substituert eller lignende; Rog Rrepresenterer uavhengig et hydrogenatom, en alkylgruppe som kan være substituert eller lignende; X representerer -O-, -S-, -N(R)- eller lignende; R representerer et hydrogenatom, en alkylgruppe eller lignende; og A representerer en fenylgruppe som kan være substituert eller lignende. Forbindelsen kan inhibere både EGF reseptor-tyrosinkinase og HER2 tyrosinkinase.
NO20074311A 2005-02-23 2007-08-23 Kinazolinderivat med tyrosinkinase-inhiberende aktivitet og farmasøytisk sammensetning NO343403B1 (no)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2005047383 2005-02-23
JP2005156828 2005-05-30
PCT/JP2006/303125 WO2006090717A1 (ja) 2005-02-23 2006-02-22 チロシンキナーゼ阻害作用を有するキナゾリン誘導体

Publications (2)

Publication Number Publication Date
NO20074311L true NO20074311L (no) 2007-11-23
NO343403B1 NO343403B1 (no) 2019-02-25

Family

ID=36927355

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20074311A NO343403B1 (no) 2005-02-23 2007-08-23 Kinazolinderivat med tyrosinkinase-inhiberende aktivitet og farmasøytisk sammensetning

Country Status (16)

Country Link
US (2) US8202879B2 (no)
EP (1) EP1854789B1 (no)
JP (1) JP4137174B2 (no)
KR (1) KR100910333B1 (no)
CN (1) CN101163684B (no)
AU (1) AU2006216266C1 (no)
BR (1) BRPI0606905B1 (no)
CA (1) CA2599328C (no)
DK (1) DK1854789T3 (no)
ES (1) ES2431843T3 (no)
NO (1) NO343403B1 (no)
PL (1) PL1854789T3 (no)
PT (1) PT1854789E (no)
RU (1) RU2414457C2 (no)
TW (1) TWI372147B (no)
WO (1) WO2006090717A1 (no)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2006216266C1 (en) * 2005-02-23 2010-08-26 Shionogi & Co., Ltd. Quinazoline derivative having tyrosine kinase inhibitory activity
CN101003514A (zh) * 2006-01-20 2007-07-25 上海艾力斯医药科技有限公司 喹唑啉衍生物、其制备方法及用途
US7547781B2 (en) 2006-09-11 2009-06-16 Curis, Inc. Quinazoline based EGFR inhibitors containing a zinc binding moiety
CA2662617C (en) * 2006-09-11 2014-11-18 Changgeng Qian Quinazoline based egfr inhibitors containing a zinc binding moiety
WO2010053572A2 (en) 2008-11-07 2010-05-14 Massachusetts Institute Of Technology Aminoalcohol lipidoids and uses thereof
TWI466872B (zh) * 2008-12-25 2015-01-01 Shionogi & Co 喹唑啉衍生物之製造方法
CA2831392C (en) 2011-03-28 2020-04-28 Massachusetts Institute Of Technology Conjugated lipomers and uses thereof
US9512073B2 (en) 2011-10-27 2016-12-06 Massachusetts Institute Of Technology Amino acid-, peptide-and polypeptide-lipids, isomers, compositions, and uses thereof
CN103288756B (zh) * 2012-02-29 2016-04-20 江苏先声药物研究有限公司 一种喹唑啉中间体的甲醇溶剂合物及其制备方法
EA201591746A1 (ru) 2013-03-14 2016-08-31 КОНВЕРДЖЕН ЭлЭлСи Способы и композиции для ингибирования бромодомен-содержащих белков
JP6099182B2 (ja) * 2014-05-29 2017-03-22 塩野義製薬株式会社 アルキニルケトン誘導体の製造方法
JP6334065B2 (ja) * 2015-07-29 2018-05-30 塩野義製薬株式会社 キナゾリン誘導体の塩またはその結晶およびそれらの製造方法
US20190112317A1 (en) 2015-10-05 2019-04-18 The Trustees Of Columbia University In The City Of New York Activators of autophagic flux and phospholipase d and clearance of protein aggregates including tau and treatment of proteinopathies
EP3380469B1 (en) 2015-11-25 2022-03-16 Convergene Llc Bicyclic bet bromodomain inhibitors and uses thereof
US20180030403A1 (en) 2016-07-28 2018-02-01 Bobban Subhadra Devices, systems and methods for the production of humanized gut commensal microbiota
WO2018139626A1 (ja) 2017-01-30 2018-08-02 塩野義製薬株式会社 キナゾリン誘導体を含有する固形製剤
WO2020219168A1 (en) 2019-04-24 2020-10-29 Convergene, Llc Small molecule bromodomain inhibitors and uses thereof

Family Cites Families (18)

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DE69222637T2 (de) 1991-05-10 1998-02-26 Rhone Poulenc Rorer Int Bis mono- und bicyclische aryl- und heteroarylderivate mit inhibierender wirkung auf die egf und/oder pdgf-rezeptor tyrosinkinase
NZ243082A (en) 1991-06-28 1995-02-24 Ici Plc 4-anilino-quinazoline derivatives; pharmaceutical compositions, preparatory processes, and use thereof
AU661533B2 (en) 1992-01-20 1995-07-27 Astrazeneca Ab Quinazoline derivatives
GB9323290D0 (en) * 1992-12-10 1994-01-05 Zeneca Ltd Quinazoline derivatives
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GB9624482D0 (en) * 1995-12-18 1997-01-15 Zeneca Phaema S A Chemical compounds
GB9603095D0 (en) * 1996-02-14 1996-04-10 Zeneca Ltd Quinazoline derivatives
US6391874B1 (en) * 1996-07-13 2002-05-21 Smithkline Beecham Corporation Fused heterocyclic compounds as protein tyrosine kinase inhibitors
HK1046688A1 (zh) 1999-09-21 2003-01-24 Astrazeneca Ab 喹唑啉化合物和含有喹唑啉化合物的藥物組合物
RU2276151C2 (ru) * 2000-06-06 2006-05-10 Астразенека Аб Хиназолиновые производные для лечения опухолей
JP4285996B2 (ja) * 2001-02-21 2009-06-24 田辺三菱製薬株式会社 キナゾリン誘導体
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Also Published As

Publication number Publication date
US8202879B2 (en) 2012-06-19
JP4137174B2 (ja) 2008-08-20
BRPI0606905A2 (pt) 2009-07-28
JPWO2006090717A1 (ja) 2008-07-24
KR100910333B1 (ko) 2009-07-31
RU2414457C2 (ru) 2011-03-20
AU2006216266A1 (en) 2006-08-31
CN101163684A (zh) 2008-04-16
DK1854789T3 (da) 2013-10-21
AU2006216266A8 (en) 2009-04-02
EP1854789A1 (en) 2007-11-14
BRPI0606905B1 (pt) 2021-06-01
AU2006216266C1 (en) 2010-08-26
AU2006216266B2 (en) 2010-02-18
ES2431843T3 (es) 2013-11-28
KR20070098941A (ko) 2007-10-05
NO343403B1 (no) 2019-02-25
TWI372147B (en) 2012-09-11
CN101163684B (zh) 2012-08-29
EP1854789A4 (en) 2009-06-17
US8349857B2 (en) 2013-01-08
TW200640880A (en) 2006-12-01
RU2007135023A (ru) 2009-03-27
US20120123114A1 (en) 2012-05-17
US20090143414A1 (en) 2009-06-04
PL1854789T3 (pl) 2014-03-31
EP1854789B1 (en) 2013-10-09
CA2599328C (en) 2012-04-17
WO2006090717A1 (ja) 2006-08-31
AU2006216266A2 (en) 2006-08-31
CA2599328A1 (en) 2006-08-31
PT1854789E (pt) 2013-10-23

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