ATE510840T1 - Kondensierte thiazol-derivate als kinasehemmer - Google Patents

Kondensierte thiazol-derivate als kinasehemmer

Info

Publication number
ATE510840T1
ATE510840T1 AT07733382T AT07733382T ATE510840T1 AT E510840 T1 ATE510840 T1 AT E510840T1 AT 07733382 T AT07733382 T AT 07733382T AT 07733382 T AT07733382 T AT 07733382T AT E510840 T1 ATE510840 T1 AT E510840T1
Authority
AT
Austria
Prior art keywords
kinase inhibitors
thiazole derivatives
condensed thiazole
condensed
substituted
Prior art date
Application number
AT07733382T
Other languages
English (en)
Inventor
Rikki Alexander
Pavandeep Aujla
Karen Crepy
Anne Foley
Richard Franklin
Alan Haughan
Helen Horsley
William Jones
Benedicte Lallemand
Stephen Mack
Trevor Morgan
Patrick Pasau
David Phillips
Verity Sabin
George Buckley
Kerry Jenkins
Benjamin Perry
Original Assignee
Ucb Pharma Sa
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
Priority claimed from GB0612644A external-priority patent/GB0612644D0/en
Priority claimed from GB0620062A external-priority patent/GB0620062D0/en
Application filed by Ucb Pharma Sa filed Critical Ucb Pharma Sa
Application granted granted Critical
Publication of ATE510840T1 publication Critical patent/ATE510840T1/de

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • 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
    • A61P35/00—Antineoplastic agents
    • A61P35/04—Antineoplastic agents specific for metastasis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains three hetero rings
    • 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
AT07733382T 2006-06-26 2007-06-26 Kondensierte thiazol-derivate als kinasehemmer ATE510840T1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB0612644A GB0612644D0 (en) 2006-06-26 2006-06-26 Therapeutic agents
GB0620062A GB0620062D0 (en) 2006-10-10 2006-10-10 Therapeutic agents
PCT/GB2007/002390 WO2008001076A1 (en) 2006-06-26 2007-06-26 Fused thiazole derivatives as kinase inhibitors

Publications (1)

Publication Number Publication Date
ATE510840T1 true ATE510840T1 (de) 2011-06-15

Family

ID=38671000

Family Applications (1)

Application Number Title Priority Date Filing Date
AT07733382T ATE510840T1 (de) 2006-06-26 2007-06-26 Kondensierte thiazol-derivate als kinasehemmer

Country Status (20)

Country Link
US (3) US8242116B2 (de)
EP (2) EP2035436B1 (de)
CN (1) CN101687885B (de)
AT (1) ATE510840T1 (de)
AU (1) AU2008269577B2 (de)
CA (1) CA2692085C (de)
CO (1) CO6270229A2 (de)
CY (1) CY1114419T1 (de)
DK (1) DK2170906T3 (de)
EA (1) EA017187B1 (de)
ES (2) ES2365258T3 (de)
HR (1) HRP20130523T1 (de)
IL (1) IL202659A0 (de)
ME (1) ME01592B (de)
MX (1) MX2009013740A (de)
MY (1) MY148852A (de)
PL (1) PL2170906T3 (de)
PT (1) PT2170906E (de)
RS (1) RS52824B (de)
WO (1) WO2008001076A1 (de)

Families Citing this family (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009071890A1 (en) * 2007-12-04 2009-06-11 Ucb Pharma S.A. Tricyclic kinase inhibitors
WO2009071895A1 (en) * 2007-12-04 2009-06-11 Ucb Pharma S.A. Fused thiazole and thiophene derivatives as kinase inhibitors
MX2010006457A (es) 2007-12-19 2010-07-05 Amgen Inc Compuestos fusionados de piridina, pirimidina y triazina como inhibidores de ciclo celular.
EP2278973B1 (de) 2008-04-07 2011-11-02 Amgen Inc. Gem-disubstituierte und spirocyclische aminopyridine/pyrimidine als zellcyclus-inhibitoren
JPWO2009130900A1 (ja) * 2008-04-24 2011-08-11 日本曹達株式会社 オキシム誘導体、中間体化合物および植物病害防除剤
WO2010011871A2 (en) * 2008-07-23 2010-01-28 The Regents Of The University Of California Methods and compositions for providing salicylic acid-independent pathogen resistance in plants
JPWO2010027002A1 (ja) * 2008-09-05 2012-02-02 塩野義製薬株式会社 Ｐｉ３ｋ阻害活性を有する縮環モルホリン誘導体
AU2010216219A1 (en) 2009-02-17 2011-09-01 Vertex Pharmaceuticals Incorporated Tetrahydrothiazolopyridine inhibitors of phosphatidylinositol 3-kinase
AU2010226829A1 (en) * 2009-03-18 2011-09-15 Schering Corporation Bicyclic compounds as inhibitors of diacylglycerol acyltransferase
UY32582A (es) * 2009-04-28 2010-11-30 Amgen Inc Inhibidores de fosfoinositida 3 cinasa y/u objetivo mamífero
JP5554833B2 (ja) 2009-05-20 2014-07-23 グラクソスミスクライン エルエルシー Ｐｉ３キナーゼ阻害剤としてのチアゾロピリミジノン誘導体
GB0912946D0 (en) 2009-07-24 2009-09-02 Addex Pharmaceuticals Sa New compounds 5
US9200007B2 (en) 2009-08-20 2015-12-01 Karus Therapeutics Limited Tricyclic heterocyclic compounds as phosphoinositide 3-kinase inhibitors
CA2782950A1 (en) 2009-12-18 2011-06-23 Janssen Pharmaceutica Nv Bicyclic thiazoles as allosteric modulators of mglur5 receptors
JP5763673B2 (ja) 2009-12-18 2015-08-12 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Ｊａｎｓｓｅｎ Ｐｈａｒｍａｃｅｕｔｉｃａ Ｎａａｍｌｏｚｅ Ｖｅｎｎｏｏｔｓｃｈａｐ ｍＧｌｕＲ５受容体のアロステリック調節因子としての二環式チアゾール
WO2011157663A1 (de) 2010-06-15 2011-12-22 Bayer Cropscience Ag Neue ortho-substituierte arylamid-derivate
US20130184320A1 (en) 2010-10-01 2013-07-18 Basf Se Imine Compounds
WO2012051410A2 (en) * 2010-10-13 2012-04-19 Millennium Pharmaceuticals, Inc. Heteroaryls and uses thereof
CA2818885A1 (en) * 2010-11-24 2012-05-31 Exelixis, Inc. Benzoxazepines as inhibitors of mtor and methods of their use and manufacture
CN102649777B (zh) * 2011-02-25 2014-03-12 中国中化股份有限公司 一种制备1-芳基-3-羧基-5-吡唑啉酮类化合物的方法
ES2543569T3 (es) 2011-03-23 2015-08-20 Amgen Inc. Inhibidores duales tricíclicos condensados de CDK 4/6 y FLT3
LT2794600T (lt) 2011-12-22 2018-02-26 Novartis Ag 2,3-dihidro-benzo[1,4]oksazino dariniai ir giminingi junginiai kaip fosfoinozitido-3 kinazės (pi3k) inhibitoriai, skirti gydymui, pavyzdžiui, reumatoidinio artrito
WO2014153214A1 (en) 2013-03-14 2014-09-25 Epizyme, Inc. Arginine methyl transferase inhibtors and uses thereof
US9120757B2 (en) 2013-03-14 2015-09-01 Epizyme, Inc. Arginine methyltransferase inhibitors and uses thereof
WO2014153172A1 (en) 2013-03-14 2014-09-25 Epizyme, Inc. Pyrazole derivatives as prmt1 inhibitors and uses thereof
EP2970181B1 (de) 2013-03-14 2017-06-07 Epizyme, Inc. Argininmethyltransferaseinhibitoren und verwendungen davon
US9346761B2 (en) 2013-03-14 2016-05-24 Epizyme, Inc. Arginine methyltransferase inhibitors and uses thereof
US20160031839A1 (en) 2013-03-14 2016-02-04 Epizyme, Inc. Arginine methyltransferase inhibitors and uses thereof
US9023883B2 (en) 2013-03-14 2015-05-05 Epizyme, Inc. PRMT1 inhibitors and uses thereof
US9765035B2 (en) 2013-03-14 2017-09-19 Epizyme, Inc. Arginine methyltransferase inhibitors and uses thereof
EP2970134B1 (de) 2013-03-14 2018-02-28 Epizyme, Inc. Pyrazolderivate als prmt1 inhbitoren und ihre verwendung
BR112015022785A2 (pt) 2013-03-14 2017-07-18 Epizyme Inc composto; composição farmacêutica; kit ou artigo farmacêutico embalado; método de inibição de uma arginina metil transferase (rmt); método de modulação da expressão genética; método de modulação da transcrição; e método de tratamento de um distúrbio mediado por rmt
JP6461942B2 (ja) * 2013-10-21 2019-01-30 ユミコア・アクチエンゲゼルシャフト・ウント・コムパニー・コマンディットゲゼルシャフトＵｍｉｃｏｒｅ ＡＧ ＆ Ｃｏ．ＫＧ 芳香族アミンのモノアリール化
GB201402431D0 (en) 2014-02-12 2014-03-26 Karus Therapeutics Ltd Compounds
GB201514754D0 (en) * 2015-08-19 2015-09-30 Karus Therapeutics Ltd Compounds
GB201514758D0 (en) 2015-08-19 2015-09-30 Karus Therapeutics Ltd Formulation
WO2017156350A1 (en) 2016-03-09 2017-09-14 K-Gen, Inc. Methods of cancer treatment
CN108570043A (zh) * 2018-06-20 2018-09-25 王延娇 一种化合物及其作为选择性pi3k抑制剂在***中的应用
US20220202824A1 (en) 2018-09-13 2022-06-30 Stemline Therapeutics, Inc. Methods for Treating Centronuclear Myopathy
WO2020127685A1 (en) 2018-12-19 2020-06-25 Leo Pharma A/S Amino-acid anilides as small molecule modulators of il-17
WO2020145250A1 (ja) * 2019-01-08 2020-07-16 杏林製薬株式会社 １５－ｐｇｄｈ阻害薬

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0508471D0 (en) * 2005-04-26 2005-06-01 Celltech R&D Ltd Therapeutic agents

Also Published As

Publication number Publication date
CN101687885B (zh) 2012-08-22
US8710054B2 (en) 2014-04-29
US20130079330A1 (en) 2013-03-28
HRP20130523T1 (en) 2013-07-31
US20110003785A1 (en) 2011-01-06
DK2170906T3 (da) 2013-06-24
CO6270229A2 (es) 2011-04-20
EA201000038A1 (ru) 2010-06-30
ME01592B (me) 2014-09-20
AU2008269577A1 (en) 2008-12-31
CA2692085A1 (en) 2008-12-31
PT2170906E (pt) 2013-06-25
EP2035436A1 (de) 2009-03-18
AU2008269577B2 (en) 2012-12-20
WO2008001076A1 (en) 2008-01-03
RS52824B (de) 2013-10-31
CA2692085C (en) 2015-10-13
US8338592B2 (en) 2012-12-25
EP2035436B1 (de) 2011-05-25
CY1114419T1 (el) 2016-08-31
MY148852A (en) 2013-06-14
EP2170906A1 (de) 2010-04-07
US8242116B2 (en) 2012-08-14
IL202659A0 (en) 2010-06-30
ES2365258T3 (es) 2011-09-27
EA017187B1 (ru) 2012-10-30
MX2009013740A (es) 2010-02-01
EP2170906B1 (de) 2013-04-03
PL2170906T3 (pl) 2013-08-30
ES2416364T3 (es) 2013-07-31
US20100137302A1 (en) 2010-06-03
CN101687885A (zh) 2010-03-31

Similar Documents

Publication Publication Date Title
ATE510840T1 (de) Kondensierte thiazol-derivate als kinasehemmer
ATE526021T1 (de) Kondensierte thiazol-derivate als kinase-hemmer
NO20083739L (no) Tieno-pyridinderivater som MEK-inhibitorer
SMT201600089B (it) Composti di 3,4-diidropirazino[2,3-b]pirazin-2(1 h)-one come inibitori di chinasi mtor per indicazioni oncologiche e malattie associate al percorso mtor/p13k/akt
WO2009081105A3 (en) Quinoxaline and quinoline derivatives as kinase inhibitors
NO20081133L (no) Tieno[2,3-B]-pyridin-5-karbonitriler som protein kinase inhibitorer
MX2010001218A (es) Metodos y composiciones para tratamiento contra esquizofrenia mediante uso de terapia combinada de agentes antipsicoticos.
WO2010052448A3 (en) Fused pyrazine derivatives as kinase inhibitors
CL2008003280A1 (es) Compuestos derivados de 1h-pirazolo[3,4-b]piridina)-4-aril sustituidas; la composicion farmaceutica que los contiene; y sus procesos de preparacion.
NO20060279L (no) Thienopyridonderivater som kinaseinhibitorer
MX2009012595A (es) Derivados de espiroindolinona.
EA202192170A1 (ru) ТИЕНО[3,2-b]ПИРИДИН-7-АМИНОВЫЕ СОЕДИНЕНИЯ ДЛЯ ЛЕЧЕНИЯ СЕМЕЙНОЙ ВЕГЕТО-СОСУДИСТОЙ ДИСТОНИИ
NO20092657L (no) Bicyclic heterocyclic compounds as FGFR inhibitors
CO6220934A2 (es) Derivados de imidazolidinacaboxamida como inhibidores de lipasas y foffolipasas
HUE036953T2 (hu) 2,3-dihidro-benzo[1,4]oxazin-származékok és rokon vegyületek, mint foszfoinozitid-3-kináz (PI3K) inhibitorok például reumatoid arthritis kezelésére
WO2006098961A3 (en) Fused thieno [2, 3-b] pyridine and thiazolo [5, 4-b] pyridine compounds for inhibiting ksp kinesin activity
DK2285811T3 (da) 3-(3-pyrimidin-2-yl-benzyl)-[1,2,4]-triazolo[4,3-b]pyridazinderivater som met-kinaseinhibitorer
DK2124944T3 (da) Pyrazolo[3,4-b]pyridinderivater som phosphodiesteraseinhibitorer
CL2012001027A1 (es) Compuestos derivados de 7-(fenilamina)-5-oxo-1,2,3,5-tetrahidro-imidazo[1,2-a]piridina, 7-(fenilamina)5-oxo-2,3-dihidro-5h-tiazolo[3,2-a]piridina, 7-(fenulaminas)-5-oxo-2,3-dihidro-2hoxazolo[3,2-a]piridina: composicion farmaceutica; utiles en el tratamiento de enfermedades, trastornos o sindrome asociado con la inhibicion mek.
NO20091817L (no) Kinase inhibitorer
DK3840832T3 (da) Imidazo[1,2-b]pyridaziner som trk-inhibitorer
UA99469C2 (ru) Конденсированные производные тиазола как ингибиторы киназы
ATE485298T1 (de) Pteridinonderivate als inhibitoren von pi3- kinasen
UY32280A (es) DERIVADOS DE 6-CICLOAMINO-3-(1H-PIRROLO[2,3-b]PIRIDIN-4-IL)IMIDAZO[1,2-b]-PIRIDAZINA, SU PREPARACIÓN Y SU APLICACIÓN EN TERAPÉUTICA
DOP2009000289A (es) Derivados de tiazol fusionados como inhibidores de quinasa

Legal Events

Date Code Title Description
RER Ceased as to paragraph 5 lit. 3 law introducing patent treaties