JP2006522813A5 - - Google Patents

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Publication number
JP2006522813A5
JP2006522813A5 JP2006509755A JP2006509755A JP2006522813A5 JP 2006522813 A5 JP2006522813 A5 JP 2006522813A5 JP 2006509755 A JP2006509755 A JP 2006509755A JP 2006509755 A JP2006509755 A JP 2006509755A JP 2006522813 A5 JP2006522813 A5 JP 2006522813A5
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JP
Japan
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optionally substituted
alkyl
heterocyclyl
compound
compound according
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JP2006509755A
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English (en)
Japanese (ja)
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JP4881725B2 (ja
JP2006522813A (ja
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Priority claimed from PCT/US2004/010626 external-priority patent/WO2004091480A2/en
Publication of JP2006522813A publication Critical patent/JP2006522813A/ja
Publication of JP2006522813A5 publication Critical patent/JP2006522813A5/ja
Application granted granted Critical
Publication of JP4881725B2 publication Critical patent/JP4881725B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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JP2006509755A 2003-04-09 2004-04-08 Tie−2モジュレータと使用方法 Expired - Fee Related JP4881725B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US46147103P 2003-04-09 2003-04-09
US60/461,471 2003-04-09
PCT/US2004/010626 WO2004091480A2 (en) 2003-04-09 2004-04-08 Tie-2 modulators and methods of use

Publications (3)

Publication Number Publication Date
JP2006522813A JP2006522813A (ja) 2006-10-05
JP2006522813A5 true JP2006522813A5 (https=) 2007-06-14
JP4881725B2 JP4881725B2 (ja) 2012-02-22

Family

ID=33299820

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006509755A Expired - Fee Related JP4881725B2 (ja) 2003-04-09 2004-04-08 Tie−2モジュレータと使用方法

Country Status (6)

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US (1) US8178570B2 (https=)
EP (1) EP1611123B8 (https=)
JP (1) JP4881725B2 (https=)
AU (1) AU2004229392A1 (https=)
CA (1) CA2520255C (https=)
WO (1) WO2004091480A2 (https=)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW200533357A (en) * 2004-01-08 2005-10-16 Millennium Pharm Inc 2-(amino-substituted)-4-aryl pyrimidines and related compounds useful for treating inflammatory diseases
WO2006039356A2 (en) * 2004-09-29 2006-04-13 Cytovia, Inc. Substituted n-aryl-9-oxo-9h-fluorene-1-carboxamides and analogs as activators of caspases and inducers of apoptosis
ZA200703912B (en) 2004-10-20 2008-09-25 Serono Lab 3-arylamino pyridine derivatives
ATE525073T1 (de) * 2005-01-28 2011-10-15 Novartis Ag Verwendung von pyrimidylaminobenzamiden zur behandlung von durch modulation einer tie-2 kinase-aktivität verursachten krankheiten
EA200802050A1 (ru) * 2006-04-19 2009-04-28 Лаборатуар Сероно Са Новые гетероарилзамещенные ариламинопиридиновые производные в качестве мек ингибиторов
CL2008000986A1 (es) 2007-04-06 2008-10-17 Neurocrine Biosciences Inc COMPUESTO DERIVADO DE HETEROCICLOS DE NITROGENO, AGONISTAS DEL RECEPTOR GnRH; COMPOSICION FARMACEUTICA QUE COMPRENDE A DICHO COMPUESTO; Y USO PARA TRATAR UNA AFECCION RELACIONADA CON LAS HORMONAS SEXUALES, ENDOMETRIOSIS, DISMENORREA, ENFERMEDAD DE OV
EP2155194B1 (en) 2007-04-06 2015-01-21 Neurocrine Biosciences, Inc. Gonadotropin-releasing hormone receptor antagonists and methods relating thereto
UA103319C2 (en) 2008-05-06 2013-10-10 Глаксосмитклайн Ллк Thiazole- and oxazole-benzene sulfonamide compounds
EP2307456B1 (en) 2008-06-27 2014-10-15 Amgen Inc. Ang-2 inhibition to treat multiple sclerosis
JO3078B1 (ar) 2009-11-27 2017-03-15 Janssen Pharmaceutica Nv مورفولينوثيازولات بصفتها منظمات الوستيرية نوع الفا 7 موجبة
JP2013147428A (ja) * 2010-04-27 2013-08-01 Dainippon Sumitomo Pharma Co Ltd 新規2−ヘテロアリール単環ピリミジン誘導体
WO2012153729A1 (ja) * 2011-05-10 2012-11-15 大正製薬株式会社 ヘテロ芳香環誘導体
AU2014233363B2 (en) * 2013-03-15 2017-06-29 EyePoint, Inc. Compositions, formulations and methods for treating ocular diseases
US20150050277A1 (en) 2013-03-15 2015-02-19 Aerpio Therapeutics Inc. Compositions and methods for treating ocular diseases
JP2015131783A (ja) * 2014-01-14 2015-07-23 株式会社日本ファインケム アリール−1,2,4−トリアゾール誘導体の製造方法
US9598381B2 (en) * 2014-07-31 2017-03-21 Abbvie Inc. SMYD2 inhibitors
CN110177581B (zh) * 2016-11-16 2023-01-03 通用医疗公司 髓过氧化物酶显像剂
US11066404B2 (en) 2018-10-11 2021-07-20 Incyte Corporation Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors
US11384083B2 (en) 2019-02-15 2022-07-12 Incyte Corporation Substituted spiro[cyclopropane-1,5′-pyrrolo[2,3-d]pyrimidin]-6′(7′h)-ones as CDK2 inhibitors
TW202100520A (zh) 2019-03-05 2021-01-01 美商英塞特公司 作為cdk2 抑制劑之吡唑基嘧啶基胺化合物
WO2020205560A1 (en) 2019-03-29 2020-10-08 Incyte Corporation Sulfonylamide compounds as cdk2 inhibitors
CA3137138A1 (en) * 2019-04-18 2020-10-22 EyePoint Pharmaceuticals, Inc. Methods of treating hypertension with activators of tie-2
US11447494B2 (en) 2019-05-01 2022-09-20 Incyte Corporation Tricyclic amine compounds as CDK2 inhibitors
WO2020223469A1 (en) 2019-05-01 2020-11-05 Incyte Corporation N-(1-(methylsulfonyl)piperidin-4-yl)-4,5-di hydro-1h-imidazo[4,5-h]quinazolin-8-amine derivatives and related compounds as cyclin-dependent kinase 2 (cdk2) inhibitors for treating cancer
CA3150681A1 (en) 2019-08-14 2021-02-18 Incyte Corporation Imidazolyl pyrimidinylamine compounds as cdk2 inhibitors
US11851426B2 (en) 2019-10-11 2023-12-26 Incyte Corporation Bicyclic amines as CDK2 inhibitors
US11981671B2 (en) 2021-06-21 2024-05-14 Incyte Corporation Bicyclic pyrazolyl amines as CDK2 inhibitors
US11976073B2 (en) 2021-12-10 2024-05-07 Incyte Corporation Bicyclic amines as CDK2 inhibitors

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MC598A1 (fr) 1966-02-16 1967-03-21 Mauvernay Roland Yves Nouveaux composés chimiques et procédé pour leur préparation
US3647809A (en) * 1968-04-26 1972-03-07 Chinoin Gyogyszer Es Vegyeszet Certain pyridyl-1 2 4-oxadiazole derivatives
US3978054A (en) 1974-11-29 1976-08-31 Merck & Co., Inc. 1,3,5-Trisubstituted-1,2,4-triazole compounds
AR230994A1 (es) 1981-08-31 1984-08-31 Pfizer Procedimiento para preparar compuesto de 3'-substituido-5'-(2-amino-4-piridil)-1',2',4'-triazol
GB8829296D0 (en) 1988-12-15 1989-01-25 Ici Plc Anti-tumour compounds
JPH0813446B2 (ja) * 1990-05-30 1996-02-14 株式会社日立製作所 スリツプキヤステイング法
JP3217846B2 (ja) 1992-03-04 2001-10-15 クミアイ化学工業株式会社 トリアゾール誘導体及び殺虫剤
WO2002032896A1 (en) * 2000-10-16 2002-04-25 Novo Nordisk A/S Furazanyl-triazole derivates for the treatment of diseases
CA2445568A1 (en) * 2001-04-27 2002-11-07 Vertex Pharmaceuticals Incorporated Triazole-derived kinase inhibitors and uses thereof
JP2005504014A (ja) * 2001-06-08 2005-02-10 サイトビア インコーポレイテッド カスパーゼの活性化因子およびアポトーシスの誘導因子としての置換された3−アリール−5−アリール−[1,2,4]−オキサジアゾール類および類似体、並びにその使用法
US20050004186A1 (en) * 2002-12-20 2005-01-06 Pfizer Inc MEK inhibiting compounds
JP2007223901A (ja) 2004-03-24 2007-09-06 Takeda Chem Ind Ltd 複素環化合物およびその用途

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