JP2010538001A5 - - Google Patents

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JP2010538001A5
JP2010538001A5 JP2010523095A JP2010523095A JP2010538001A5 JP 2010538001 A5 JP2010538001 A5 JP 2010538001A5 JP 2010523095 A JP2010523095 A JP 2010523095A JP 2010523095 A JP2010523095 A JP 2010523095A JP 2010538001 A5 JP2010538001 A5 JP 2010538001A5
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JP
Japan
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alkyl
aryl
independently
heterocycle
optionally substituted
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JP2010523095A
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Japanese (ja)
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JP5718053B2 (ja
JP2010538001A (ja
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Priority claimed from PCT/US2008/074353 external-priority patent/WO2009029632A1/en
Publication of JP2010538001A publication Critical patent/JP2010538001A/ja
Publication of JP2010538001A5 publication Critical patent/JP2010538001A5/ja
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Publication of JP5718053B2 publication Critical patent/JP5718053B2/ja
Expired - Fee Related legal-status Critical Current
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JP2010523095A 2007-08-27 2008-08-26 治療用イソオキサゾール化合物 Expired - Fee Related JP5718053B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US96820507P 2007-08-27 2007-08-27
US60/968,205 2007-08-27
PCT/US2008/074353 WO2009029632A1 (en) 2007-08-27 2008-08-26 Therapeutic isoxazole compounds

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2015050436A Division JP2015110666A (ja) 2007-08-27 2015-03-13 治療用イソオキサゾール化合物

Publications (3)

Publication Number Publication Date
JP2010538001A JP2010538001A (ja) 2010-12-09
JP2010538001A5 true JP2010538001A5 (OSRAM) 2011-09-22
JP5718053B2 JP5718053B2 (ja) 2015-05-13

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ID=40387754

Family Applications (3)

Application Number Title Priority Date Filing Date
JP2010523095A Expired - Fee Related JP5718053B2 (ja) 2007-08-27 2008-08-26 治療用イソオキサゾール化合物
JP2015050436A Withdrawn JP2015110666A (ja) 2007-08-27 2015-03-13 治療用イソオキサゾール化合物
JP2016138293A Expired - Fee Related JP6250746B2 (ja) 2007-08-27 2016-07-13 治療用イソオキサゾール化合物

Family Applications After (2)

Application Number Title Priority Date Filing Date
JP2015050436A Withdrawn JP2015110666A (ja) 2007-08-27 2015-03-13 治療用イソオキサゾール化合物
JP2016138293A Expired - Fee Related JP6250746B2 (ja) 2007-08-27 2016-07-13 治療用イソオキサゾール化合物

Country Status (11)

Country Link
US (5) US8222243B2 (OSRAM)
EP (2) EP2182809B1 (OSRAM)
JP (3) JP5718053B2 (OSRAM)
KR (2) KR101567454B1 (OSRAM)
CN (2) CN101820764B (OSRAM)
AU (2) AU2008293542B9 (OSRAM)
CA (2) CA2696609C (OSRAM)
ES (2) ES2748599T3 (OSRAM)
IL (3) IL203910A (OSRAM)
MX (1) MX2010002258A (OSRAM)
WO (1) WO2009029632A1 (OSRAM)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SI1907382T1 (sl) 2005-07-26 2015-10-30 Bial-Portela & Ca S.A., Nitrokateholni derivati kot inhibitorji COMT
EP1845097A1 (en) 2006-04-10 2007-10-17 Portela & Ca., S.A. Oxadiazole derivatives as COMT inhibitors
ES2597705T3 (es) 2007-01-31 2017-01-20 Bial - Portela & Ca., S.A. Derivados de nitrocatecol como inhibidores de COMT administrados con un régimen de dosificación específico
JP5718053B2 (ja) * 2007-08-27 2015-05-13 ヘリコン・セラピューティクス・インコーポレーテッド 治療用イソオキサゾール化合物
EP2276758B1 (en) 2008-03-17 2016-01-06 Bial-Portela & CA, S.A. Crystal forms of 5- [3- (2, 5-dichloro-4, 6-dimethyl-1-oxy-pyridine-3-yl) [1,2,4] oxadiazol-5-yl]-3-nit robenzene-1, 2-diol
DE102009041241A1 (de) 2009-09-11 2011-08-04 Bayer Schering Pharma Aktiengesellschaft, 13353 Substituierte Aryl-Verbindungen und ihre Verwendung
DE102009041242A1 (de) 2009-09-11 2011-12-15 Bayer Schering Pharma Aktiengesellschaft Heterocyclisch substituierte Aryl-Verbindungen und ihre Verwendung
KR102329271B1 (ko) 2009-04-01 2021-11-22 바이알 - 포르텔라 앤드 씨에이 에스에이 니트로카테콜 유도체를 포함하는 제약 제제 및 그의 제조 방법
AR079545A1 (es) * 2009-12-21 2012-02-01 Bayer Cropscience Ag Tienilpiri(mi)dinilazol
US20140045900A1 (en) 2011-02-11 2014-02-13 Bial-Portela & Ca, S.A. Administration regime for nitrocatechols
CN102229606B (zh) * 2011-06-03 2014-07-02 浙江工业大学 含异噁唑杂环的2-甲基苯并呋喃类衍生物及制备与应用
CN102229603B (zh) * 2011-06-03 2014-07-02 浙江工业大学 含三唑杂环的2-甲基苯并呋喃类化合物及其制备与应用
WO2013008162A1 (en) 2011-07-08 2013-01-17 Novartis Ag Novel trifluoromethyl-oxadiazole derivatives and their use in the treatment of disease
WO2013066839A2 (en) * 2011-10-31 2013-05-10 Glaxosmithkline Llc Compounds and methods
JP5966014B2 (ja) * 2011-11-28 2016-08-10 ノバルティス アーゲー 新規トリフルオロメチル−オキサジアゾール誘導体および疾患の処置におけるその使用
PL2791134T3 (pl) 2011-12-13 2020-03-31 BIAL - PORTELA & Cª S.A. Związek chemiczny użyteczny jako związek pośredni do wytwarzania inhibitora katechol-o-metylotransferazy
EP3345902B1 (en) 2013-03-14 2019-10-30 Dart Neuroscience (Cayman) Ltd. Substituted pyridine and pyrazine compounds as pde4 inhibitors
RU2661156C2 (ru) 2013-03-14 2018-07-12 Дарт Нейросайенс (Кайман) Лтд. Замещенные нафтиридиновые и хинолиновые соединения как ингибиторы мао
CN104016938B (zh) * 2014-05-28 2016-08-17 浙江工业大学 一种含苯硒基的噁二唑类化合物及其制备与应用
CN104016939B (zh) * 2014-05-28 2016-06-15 浙江工业大学 一种2-亚乙基-3-乙酰基-1,3,4-噁二唑类化合物及其制备与应用
MA39415A (fr) * 2014-09-17 2016-03-24 Dart Neuroscience Cayman Ltd Inhibiteurs de mao-b et rééducation
RU2017120184A (ru) 2014-11-28 2018-12-28 БИАЛ - ПОРТЕЛА ЭНД Ка, С.А. Лекарства для замедления течения болезни паркинсона
WO2016179428A2 (en) 2015-05-05 2016-11-10 Dart Neuroscience, Llc Cognitive test execution and control
UY37623A (es) * 2017-03-03 2018-09-28 Syngenta Participations Ag Derivados de oxadiazol tiofeno fungicidas
WO2018177993A1 (de) 2017-03-31 2018-10-04 Bayer Cropscience Aktiengesellschaft Pyrazole zur bekämpfung von arthropoden
US20210084900A1 (en) 2017-05-04 2021-03-25 Basf Se Substituted 5-(haloalkyl)-5-hydroxy-isoxazoles for Combating Phytopathogenic Fungi
AR114169A1 (es) * 2017-12-22 2020-07-29 Bayer Cropscience Ag Hidroxiisoxazolinas y derivados de estos
US10902558B2 (en) * 2018-05-18 2021-01-26 Gopro, Inc. Multiscale denoising of raw images with noise estimation
US10853215B2 (en) * 2018-09-10 2020-12-01 Microsoft Technology Licensing, Llc Intelligent configuration management of user devices
WO2024187126A1 (en) * 2023-03-09 2024-09-12 Aquinnah Pharmaceuticals, Inc. Inhibitors of tdp-43 and tau aggregation

Family Cites Families (89)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB935523A (en) * 1961-06-17 1963-08-28 Acraf New sulphamido-oxadiazoles
GB1051322A (OSRAM) * 1967-08-09
US3995048A (en) * 1975-10-20 1976-11-30 Sandoz, Inc. Isoxazolyl benzamides useful as tranquilizers and sleep-inducers
JPS6183181A (ja) * 1984-06-11 1986-04-26 イ−・アイ・デユポン・デ・ニモアス・アンド・カンパニ− 除草剤性チオフエンスルホンアミド類およびピリジンスルホンアミド類
AU576868B2 (en) 1984-06-11 1988-09-08 E.I. Du Pont De Nemours And Company Thiophene and pyridine sulfonamides
DD265317A5 (de) * 1985-12-05 1989-03-01 Bayer Ag,De Herbizide und pflanzenwuchsregulierende mittel
DE3602016A1 (de) 1985-12-05 1987-06-11 Bayer Ag Pyri(mi)dyl-oxy- und thio-benzoesaeure-derivate
US5204482A (en) 1988-07-28 1993-04-20 Hoffman-Laroche Inc. Compounds for treating and preventing cognitive diseases and depression and methods of making same
US4938949A (en) 1988-09-12 1990-07-03 University Of New York Treatment of damaged bone marrow and dosage units therefor
US5047554A (en) * 1989-04-18 1991-09-10 Pfizer Inc. 3-substituted-2-oxindole derivatives
DE3929233A1 (de) * 1989-09-02 1991-03-07 Bayer Ag 5-heterocyclyl-pyridin-3-carbon-benzylamide und -anilide
DE4126937A1 (de) 1991-08-10 1993-02-11 Basf Ag Salicyl(thio)etherderivate, verfahren und zwischenprodukte zu ihrer herstellung
GB2265371A (en) * 1992-03-06 1993-09-29 Shell Int Research Isoxazole compounds
US5246914A (en) * 1992-08-07 1993-09-21 Basf Aktiengesellschaft Salicyloyl (thio)ether derivatives, their preparation and intermediates for their preparation
PL185544B1 (pl) * 1995-02-13 2003-05-30 Nowa pochodna podstawionego izoksazolu i środek farmaceutyczny
US5935966A (en) * 1995-09-01 1999-08-10 Signal Pharmaceuticals, Inc. Pyrimidine carboxylates and related compounds and methods for treating inflammatory conditions
CA2257196A1 (en) * 1996-06-06 1997-12-11 Morris Padgett Rorer Herbicidal pyridinyl and pyrazolylphenyl ketones
WO1998037068A1 (en) * 1997-02-21 1998-08-27 Bristol-Myers Squibb Company Benzoic acid derivatives and related compounds as antiarrhythmic agents
SK141799A3 (en) * 1997-04-16 2000-08-14 Abbott Lab 5,7-disubstituted 4-aminopyrido[2,3-d]pyrimidine compounds and their use as adenosine kinase inhibitors
JPH11139975A (ja) * 1997-08-26 1999-05-25 Sankyo Co Ltd A型モノアミンオキシダーゼ阻害薬
DE19743435A1 (de) 1997-10-01 1999-04-08 Merck Patent Gmbh Benzamidinderivate
DE19744026A1 (de) 1997-10-06 1999-04-08 Hoechst Marion Roussel De Gmbh Pyrazol-Derivate, ihre Herstellung und ihre Verwendung in Arzneimitteln
AU751139B2 (en) 1997-10-13 2002-08-08 Astellas Pharma Inc. Amide derivative
JP4385414B2 (ja) 1997-10-13 2009-12-16 アステラス製薬株式会社 アミド若しくはアミン誘導体
DE19904389A1 (de) * 1999-02-04 2000-08-10 Bayer Ag Verwendung von substituierten Isoxazolcarbonsäuren und Derivate und neue Stoffe
PL351374A1 (en) * 1999-04-19 2003-04-07 Shionogi & Co Sulfonamide derivatives having oxadiazole rings
AR025884A1 (es) 1999-10-01 2002-12-18 Takeda Pharmaceutical Compuestos de amina ciclica, su produccion y su uso
US7291641B2 (en) 1999-10-11 2007-11-06 Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R.A.S.) Derivatives of heterocycles with 5 members, their preparation and their use as medicaments
AU4398801A (en) * 2000-03-22 2001-10-03 Banyu Pharmaceutical Co., Ltd. Sulfur substituted aryldifluoromethylphosphonic acids as ptp-1b inhibitors
CN1199956C (zh) 2000-04-21 2005-05-04 盐野义制药株式会社 具有抗癌作用的噁二唑衍生物
JP2001316378A (ja) * 2000-04-28 2001-11-13 Takeda Chem Ind Ltd ベンズアミド誘導体およびその用途
US6579880B2 (en) * 2000-06-06 2003-06-17 Ortho-Mcneil Pharmaceutical, Inc. Isoxazoles and oxadiazoles as anti-inflammatory inhibitors of IL-8
JP2004506734A (ja) 2000-08-21 2004-03-04 ファルマシア・アンド・アップジョン・カンパニー 疾患治療用のキヌクリド置換ヘテロアリール部分
WO2002015662A2 (en) 2000-08-21 2002-02-28 Pharmacia & Upjohn Company Quinuclidine-substituted heteroaryl moieties for treatment of disease (nicotinic acetylcholine receptor antagonists
US6500840B2 (en) 2000-08-21 2002-12-31 Pharmacia & Upjohn Company Quinuclidine-substituted heteroaryl moieties for treatment of disease
DE60122176T2 (de) * 2000-09-15 2007-07-05 Vertex Pharmaceuticals Inc., Cambridge Isoxazole und ihre verwendung als erk-inhibitoren
PL369598A1 (en) 2001-02-21 2005-05-02 Nps Pharmaceuticals, Inc. Heteropolycyclic compounds and their use as metabotropic glutamate receptor antagonists
WO2003000249A1 (en) * 2001-06-26 2003-01-03 Takeda Chemical Industries, Ltd. Function regulator for retinoid relative receptor
EA005934B1 (ru) 2001-07-05 2005-08-25 Х. Лундбекк А/С Замещённые анилиновые пиперидины в качестве селективных антагонистов мсн
US6727264B1 (en) 2001-07-05 2004-04-27 Synaptic Pharmaceutical Corporation Substituted anilinic piperidines as MCH selective antagonists
US6562816B2 (en) 2001-08-24 2003-05-13 Pharmacia & Upjohn Company Substituted-heteroaryl-7-aza[2.2.1]bicycloheptanes for the treatment of disease
US6660736B2 (en) * 2002-03-27 2003-12-09 Hoffmann-La Roche Inc. Phthalimido derivatives and a process for their preparation
TW200400035A (en) * 2002-03-28 2004-01-01 Glaxo Group Ltd Novel compounds
US7329401B2 (en) * 2002-04-15 2008-02-12 The Regents Of The University Of California Cyclooxygenase-2 selective agents useful as imaging probes and related methods
CA2484233A1 (en) 2002-05-13 2003-11-27 Eli Lilly And Company Multicyclic compounds for use as melanin concentrating hormone antagonists in the treatment of obesity and diabetes
RU2005105696A (ru) * 2002-08-02 2005-11-10 Арджента Дискавери Лимитед (Gb) Замещенные тиенилгидроксамовые кислоты в качестве ингибиторов гистондеацетилазы
AU2003258287A1 (en) 2002-08-19 2004-03-03 Helicon Therapeutics, Inc. Screening methods for cognitive enhancers
TW200406152A (en) * 2002-08-30 2004-05-01 Syngenta Participations Ag 4-(3,3-Dihalo-allyloxy) phenol derivatives having pesticidal properties
SE0300010D0 (sv) 2003-01-07 2003-01-07 Astrazeneca Ab Novel Compounds
EA009919B1 (ru) 2003-02-11 2008-04-28 Вернэлис (Кембридж) Лимитед Соединения изоксазола
GB0303503D0 (en) 2003-02-14 2003-03-19 Novartis Ag Organic compounds
CA2512886A1 (en) 2003-02-28 2004-09-10 Galderma Research & Development, S.N.C. Ligands that modulate lxr-type receptors
WO2004085401A1 (en) 2003-03-28 2004-10-07 Pfizer Products Inc. 1,2,4-substituted 1,2,3,4-tetrahydro-and 1,2 dihydro-quinoline and 1,2,3,4-tetrahydro-quinoxaline derivatives as cetp inhibitors for the treatment of atherosclerosis and obesity
DE10315571A1 (de) 2003-04-05 2004-10-14 Merck Patent Gmbh Pyrazolverbindungen
EP1615637A1 (en) * 2003-04-11 2006-01-18 Novo Nordisk A/S Pharmaceutical use of substituted 1,2,4-triazoles
JPWO2005004021A1 (ja) 2003-07-07 2006-08-17 富士通株式会社 サービス提供装置、方法及びプログラム
US7199149B2 (en) 2003-10-01 2007-04-03 Bristol Myers Squibb Company Monocyclic and bicyclic lactams as factor Xa inhibitors
GB0324159D0 (en) * 2003-10-15 2003-11-19 Glaxo Group Ltd Novel compounds
US7037927B2 (en) * 2003-10-16 2006-05-02 Abbott Laboratories Amides that inhibit vanilloid receptor subtype 1 (VR1) receptor
RU2006125446A (ru) * 2003-12-15 2008-01-27 Джапан Тобакко Инк. (Jp) Производные n-замещенного n-сульфониламиноциклопропана и их фармацевтическое применение
DE602004031777D1 (en) 2004-01-05 2011-04-21 Astrazeneca Ab Thiophenderivate als chk-1-inhibitoren
CN1930136B (zh) * 2004-03-05 2012-02-08 日产化学工业株式会社 异*唑啉取代苯甲酰胺化合物及有害生物防除剂
TW200538098A (en) 2004-03-22 2005-12-01 Astrazeneca Ab Therapeutic agents
EP1742627A4 (en) * 2004-05-06 2009-08-26 Plexxikon Inc PDE4B HEMMER AND ITS USE
US20050256118A1 (en) * 2004-05-12 2005-11-17 Altenbach Robert J Bicyclic-substituted amines having cyclic-substituted monocyclic substituents
WO2005120584A2 (en) * 2004-06-03 2005-12-22 The Trustees Of Columbia University In The City Of New York Radiolabeled arylsulfonyl compounds and uses thereof
CN101018774A (zh) * 2004-07-20 2007-08-15 锡耶纳生物技术股份公司 α7烟碱性乙酰胆碱受体的调节剂和其治疗用途
GB0418267D0 (en) * 2004-08-16 2004-09-15 Glaxo Group Ltd Novel compounds
US7338967B2 (en) 2004-09-10 2008-03-04 Syngenta Limited Substituted isoxazoles as fungicides
MX2007004862A (es) 2004-10-29 2007-05-09 Astrazeneca Ab Nuevos derivados de sulfonamida como moduladores del receptor de glucocorticoides para el tratamiento de enfermedades inflamatorias.
JP2008522978A (ja) * 2004-12-07 2008-07-03 エナンタ ファーマシューティカルズ インコーポレイテッド 3,6−ビシクロライド
AU2006206654A1 (en) * 2005-01-19 2006-07-27 Merck & Co., Inc. Tertiary carbinamines having substituted heterocycles, which are active as inhibitors of beta-secretase, for the treatment of Alzheimer's disease
GB0504103D0 (en) * 2005-02-28 2005-04-06 Syngenta Ltd Novel method
JP2006316054A (ja) * 2005-04-15 2006-11-24 Tanabe Seiyaku Co Ltd 高コンダクタンス型カルシウム感受性kチャネル開口薬
WO2006134481A1 (en) * 2005-06-16 2006-12-21 Pfizer Inc. Inhibitors of 11-beta hydroxysteroid dehydrogenase type 1
US7452892B2 (en) * 2005-06-17 2008-11-18 Bristol-Myers Squibb Company Triazolopyrimidine cannabinoid receptor 1 antagonists
MX2008000141A (es) 2005-06-27 2008-04-07 Exelixis Inc Moduladores de lxr basados en imidazol.
JP5114395B2 (ja) * 2005-06-30 2013-01-09 プロシディオン・リミテッド Gpcrアゴニスト
JP2009509932A (ja) 2005-09-07 2009-03-12 プレキシコン,インコーポレーテッド Ppar活性化合物
DOP2006000210A (es) * 2005-10-04 2007-06-15 Aventis Pharma Inc Compuestos de pirimidina amida como inhibidores de pgds
EP1932833B1 (en) * 2005-10-07 2012-08-01 Kissei Pharmaceutical Co., Ltd. Nitrogenated heterocyclic compound and pharmaceutical composition comprising the same
GB0603041D0 (en) * 2006-02-15 2006-03-29 Angeletti P Ist Richerche Bio Therapeutic compounds
WO2007100851A1 (en) * 2006-02-28 2007-09-07 Helicon Therapeutics, Inc. Therapeutic compounds
WO2007103456A2 (en) * 2006-03-06 2007-09-13 Trimeris, Inc. Piperazine and piperidine biaryl derivatives
KR20090042971A (ko) * 2006-08-24 2009-05-04 욱크하르트 리서치 센터 항미생물 활성을 갖는 신규한 마크로라이드 및 케토라이드
US20080167286A1 (en) 2006-12-12 2008-07-10 Abbott Laboratories Pharmaceutical compositions and their methods of use
NZ579892A (en) 2007-03-30 2012-03-30 Sanofi Aventis Pyrimidine hydrazide compounds as prostaglandin D synthase inhibitors
JP5718053B2 (ja) 2007-08-27 2015-05-13 ヘリコン・セラピューティクス・インコーポレーテッド 治療用イソオキサゾール化合物
US8389550B2 (en) 2009-02-25 2013-03-05 Hoffmann-La Roche Inc. Isoxazoles / O-pyridines with ethyl and ethenyl linker

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