JP2012513990A5 - - Google Patents

Download PDF

Info

Publication number
JP2012513990A5
JP2012513990A5 JP2011543458A JP2011543458A JP2012513990A5 JP 2012513990 A5 JP2012513990 A5 JP 2012513990A5 JP 2011543458 A JP2011543458 A JP 2011543458A JP 2011543458 A JP2011543458 A JP 2011543458A JP 2012513990 A5 JP2012513990 A5 JP 2012513990A5
Authority
JP
Japan
Prior art keywords
alkyl
heterocyclyl
heteroaryl
aryl
alkoxy
Prior art date
Legal status (The legal status 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 status listed.)
Granted
Application number
JP2011543458A
Other languages
English (en)
Japanese (ja)
Other versions
JP2012513990A (ja
JP5657566B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/PT2009/000080 external-priority patent/WO2010074588A2/en
Publication of JP2012513990A publication Critical patent/JP2012513990A/ja
Publication of JP2012513990A5 publication Critical patent/JP2012513990A5/ja
Application granted granted Critical
Publication of JP5657566B2 publication Critical patent/JP5657566B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2011543458A 2008-12-24 2009-12-23 医薬品 Expired - Fee Related JP5657566B2 (ja)

Applications Claiming Priority (11)

Application Number Priority Date Filing Date Title
US14064008P 2008-12-24 2008-12-24
US61/140,640 2008-12-24
US15928109P 2009-03-11 2009-03-11
US61/159,281 2009-03-11
US17471209P 2009-05-01 2009-05-01
US61/174,712 2009-05-01
US22116609P 2009-06-29 2009-06-29
US61/221,166 2009-06-29
US24247209P 2009-09-15 2009-09-15
US61/242,472 2009-09-15
PCT/PT2009/000080 WO2010074588A2 (en) 2008-12-24 2009-12-23 Pharmaceutical compounds

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2014237957A Division JP2015071622A (ja) 2008-12-24 2014-11-25 医薬品

Publications (3)

Publication Number Publication Date
JP2012513990A JP2012513990A (ja) 2012-06-21
JP2012513990A5 true JP2012513990A5 (enExample) 2013-02-14
JP5657566B2 JP5657566B2 (ja) 2015-01-21

Family

ID=42288334

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2011543458A Expired - Fee Related JP5657566B2 (ja) 2008-12-24 2009-12-23 医薬品
JP2014237957A Pending JP2015071622A (ja) 2008-12-24 2014-11-25 医薬品

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2014237957A Pending JP2015071622A (ja) 2008-12-24 2014-11-25 医薬品

Country Status (17)

Country Link
US (1) US9353082B2 (enExample)
EP (1) EP2382012A2 (enExample)
JP (2) JP5657566B2 (enExample)
KR (1) KR101715190B1 (enExample)
CN (2) CN102333568B (enExample)
AR (1) AR075111A1 (enExample)
AU (1) AU2009330821B2 (enExample)
BR (2) BRPI0923819B1 (enExample)
CA (1) CA2747784C (enExample)
IL (1) IL213747A (enExample)
MX (1) MX342128B (enExample)
NZ (1) NZ593418A (enExample)
RU (1) RU2553451C2 (enExample)
SG (1) SG172301A1 (enExample)
TW (1) TWI469979B (enExample)
WO (1) WO2010074588A2 (enExample)
ZA (1) ZA201104336B (enExample)

Families Citing this family (59)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2009314629B2 (en) 2008-11-14 2014-09-25 The Scripps Research Institute Methods and compositions related to targeting monoacylglycerol lipase
PE20120493A1 (es) 2009-06-29 2012-05-20 Incyte Corp Pirimidinonas como inhibidores de pi3k
US9051296B2 (en) 2009-11-16 2015-06-09 Raqualia Pharma Inc. Aryl carboxamide derivatives as TTX-S blockers
US8759359B2 (en) 2009-12-18 2014-06-24 Incyte Corporation Substituted heteroaryl fused derivatives as PI3K inhibitors
WO2011085216A2 (en) 2010-01-08 2011-07-14 Ironwood Pharmaceuticals, Inc. Use of faah inhibitors for treating parkinson's disease and restless legs syndrome
US20130224151A1 (en) 2010-03-31 2013-08-29 United States Of America Use of FAAH Inhibitors for Treating Abdominal, Visceral and Pelvic Pain
AR081823A1 (es) 2010-04-14 2012-10-24 Incyte Corp DERIVADOS FUSIONADOS COMO INHIBIDORES DE PI3Kd
WO2011163195A1 (en) 2010-06-21 2011-12-29 Incyte Corporation Fused pyrrole derivatives as pi3k inhibitors
ES2603032T3 (es) * 2010-07-15 2017-02-23 Bayer Intellectual Property Gmbh Compuestos de 3-piridil-heteroarilcarboxamida como pesticidas
EP2606035B1 (en) * 2010-07-29 2017-09-06 BIAL - Portela & CA., S.A. Proces for the synthesis of substituted urea compounds
ES2764848T3 (es) 2010-12-20 2020-06-04 Incyte Holdings Corp N-(1-(fenilo sustituido)etilo)-9H-purina-6-aminas como inhibidores de PI3K
WO2012125629A1 (en) 2011-03-14 2012-09-20 Incyte Corporation Substituted diamino-pyrimidine and diamino-pyridine derivatives as pi3k inhibitors
WO2012135009A1 (en) 2011-03-25 2012-10-04 Incyte Corporation Pyrimidine-4,6-diamine derivatives as pi3k inhibitors
US9108930B2 (en) * 2011-04-06 2015-08-18 The Scripps Research Institute N1- and N2-carbamoyl-1,2,3-triazole serine hydrolase inhibitors and methods
WO2012168315A1 (en) * 2011-06-09 2012-12-13 Boehringer Ingelheim International Gmbh Substituted piperidines as gpr119 modulators for the treatment of metabolic disorders
KR20230038593A (ko) 2011-09-02 2023-03-20 인사이트 홀딩스 코포레이션 Pi3k 억제제로서 헤테로시클릴아민
AR090548A1 (es) 2012-04-02 2014-11-19 Incyte Corp Azaheterociclobencilaminas biciclicas como inhibidores de pi3k
SG11201500498SA (en) * 2012-07-24 2015-03-30 Bial Portela & Ca Sa Urea compounds and their use as enzyme inhibitors
BR112015001769A2 (pt) 2012-07-27 2017-08-22 Bial Portela & Ca Sa Processo para a síntese de compostos de ureia substituída
CN105793247B (zh) * 2013-07-24 2018-03-16 比亚尔-珀特拉和Ca股份公司 咪唑甲酰胺类及其作为faah抑制剂的用途
CA2919844A1 (en) 2013-08-01 2015-02-05 Bial - Portela & Ca, S.A. Urea compounds and their use as faah enzyme inhibitors
GB201313903D0 (en) 2013-08-02 2013-09-18 Bial Portela & Ca Sa Urea compounds and their use as enzyme inhibitors
GB201401198D0 (en) * 2014-01-24 2014-03-12 Bial Portela & Ca Sa Process for the syntheis of substituted urea compounds
US10093630B2 (en) 2014-05-21 2018-10-09 Abide Therapeutics, Inc. Pyrazole compounds and methods of making and using same
WO2015191677A1 (en) 2014-06-11 2015-12-17 Incyte Corporation Bicyclic heteroarylaminoalkyl phenyl derivatives as pi3k inhibitors
BR112017003918B1 (pt) 2014-08-29 2022-05-03 Fmc Corporation Composto, composições e mistura herbicida e método para o controle do crescimento da vegetação
CN104292172B (zh) * 2014-09-12 2016-08-17 浙江理工大学 一种苯并三氮唑类衍生物及其制备方法
PH12017501538B1 (en) 2015-02-27 2024-02-14 Incyte Holdings Corp Salts of p13k inhibitor and processes for their preparation
US9988401B2 (en) 2015-05-11 2018-06-05 Incyte Corporation Crystalline forms of a PI3K inhibitor
US9732097B2 (en) 2015-05-11 2017-08-15 Incyte Corporation Process for the synthesis of a phosphoinositide 3-kinase inhibitor
WO2017087863A1 (en) * 2015-11-20 2017-05-26 Abide Therapeutics, Inc. Pyrazole compounds and methods of making and using same
CN108601769B (zh) * 2015-11-20 2021-09-03 H.隆德贝克有限公司 吡唑化合物及其制备和使用方法
US10385057B2 (en) 2015-11-20 2019-08-20 Lundbeck La Jolla Research Center, Inc. Pyrazole compounds and methods of making and using same
US10583137B2 (en) 2015-12-02 2020-03-10 The Scripps Research Institute Triazole DAGLα inhibitors
US11629146B2 (en) 2016-11-28 2023-04-18 Praxis Precision Medicines, Inc. Substituted [1,2,4]triazolo[4,3-a]pyrazines as modulators of sodium channel activity
US11261188B2 (en) 2016-11-28 2022-03-01 Praxis Precision Medicines, Inc. Fused heteroaryl compounds, and methods thereof for treating diseases, disorders, and conditions relating to aberrant function of a sodium channel
MX2019008626A (es) * 2017-01-20 2019-09-19 Pfizer Derivados de 1,1,1-trifluoro-3-hidroxipropan-2-ilcarbamato como inhibidores de monoacilglicerol lipasa (magl).
EP3571202B1 (en) 2017-01-23 2021-06-30 Pfizer Inc. Heterocyclic spiro compounds as magl inhibitors
WO2018148745A1 (en) 2017-02-13 2018-08-16 Praxis Precision Medicines , Inc. Compounds and their methods of use
WO2018187480A1 (en) * 2017-04-04 2018-10-11 Praxis Precision Medicines, Inc. Compounds and their methods of use
JOP20190267A1 (ar) 2017-05-23 2019-11-18 Lundbeck La Jolla Research Center Inc مثبطات بيرازول magl
US10927105B1 (en) 2017-05-23 2021-02-23 Lundbeck La Jolla Research Center, Inc. Pyrazole MAGL inhibitors
LT3630744T (lt) * 2017-05-23 2023-03-10 H. Lundbeck A/S Pirazolo magl inhibitoriai
US11278535B2 (en) 2017-08-15 2022-03-22 Praxis Precision Medicines, Inc. Compounds and their methods of use
AU2018358663B2 (en) * 2017-11-06 2022-09-29 Acelot, Inc. Small molecule drugs and related methods for treatment of diseases related to AB42 oligomer formation
CN111801325A (zh) * 2018-03-02 2020-10-20 洛桑大学 作为Wnt信号转导通路的抑制剂的吡唑衍生物
CN112423760A (zh) 2018-05-30 2021-02-26 普拉克西斯精密药物股份有限公司 离子通道调节剂
CN112469418A (zh) 2018-06-01 2021-03-09 因赛特公司 治疗pi3k相关病症的给药方案
CN108912112A (zh) * 2018-08-14 2018-11-30 李敬敬 一种化合物、制备方法以及其在治疗疼痛中的应用
EA202092908A1 (ru) 2018-09-28 2021-05-14 Праксис Пресижн Медсинз, Инк. Модуляторы ионных каналов
US12268672B2 (en) 2018-10-23 2025-04-08 Japan Science And Technology Agency PPARδ activator
AU2019382504B2 (en) * 2018-11-20 2024-11-14 Sironax Ltd Cyclic ureas
US11773099B2 (en) 2019-05-28 2023-10-03 Praxis Precision Medicines, Inc. Compounds and their methods of use
US11505554B2 (en) 2019-05-31 2022-11-22 Praxis Precision Medicines, Inc. Substituted pyridines as ion channel modulators
US11279700B2 (en) 2019-05-31 2022-03-22 Praxis Precision Medicines, Inc. Ion channel modulators
US11767325B2 (en) 2019-11-26 2023-09-26 Praxis Precision Medicines, Inc. Substituted [1,2,4]triazolo[4,3-a]pyrazines as ion channel modulators
EP4387617A4 (en) * 2021-08-18 2025-10-29 Univ California ACID CERAMIDASE INHIBITORS AND THEIR USES
CN115707699B (zh) * 2021-08-18 2025-08-19 中国医学科学院医药生物技术研究所 一组抗骨质疏松的化合物及其应用
US12234205B1 (en) 2024-05-22 2025-02-25 King Saud University Sulfonylhydrazide derivatives as anticancer agents

Family Cites Families (63)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3248398A (en) * 1961-01-05 1966-04-26 Bayer Ag Substituted ureas
GB1408877A (en) * 1971-12-07 1975-10-08 Boots Co Ltd Substituted imidazoles and their use as pesticides
US3940484A (en) * 1971-12-07 1976-02-24 The Boots Company Limited Insecticidal compositions and methods of combatting insects using substituted imidazoles
US3932444A (en) * 1972-04-28 1976-01-13 E. I. Du Pont De Nemours & Co. 4-Imidazolylsulfonylimidazoles
CA1035188A (en) * 1974-08-15 1978-07-25 Eastman Kodak Company Blocked development restrainers
DE2834879A1 (de) * 1978-08-07 1980-02-21 Schering Ag 1,2,3-triazolcarbonsaeureamide, verfahren zur herstellung dieser verbindungen sowie diese enthaltende biozide mittel
CA1126999A (en) * 1978-10-20 1982-07-06 Michael J. Simons Use of azole compounds with a n,n disubstituted carbamoyl group on a ring nitrogen as development restrainer precursors in photographic elements
GB8426367D0 (en) * 1984-10-18 1984-11-21 Shell Int Research Heteroaromatic ether herbicides
FR2579596B1 (fr) 1985-03-26 1987-11-20 Inst Nat Sante Rech Med (imidazolyl-4) piperidines, leur preparation et leur application en therapeutique
JPH0753716B2 (ja) 1986-07-02 1995-06-07 吉富製薬株式会社 イミダゾ−ルカルボキサミド誘導体
DD295852A5 (de) * 1988-07-18 1991-11-14 Arzneimittelwerk Dresden Gmbh,De Verfahren zur herstellung von acylureido-benzylpenicillinen und deren salzen
JPH02124559A (ja) * 1988-11-02 1990-05-11 Fuji Photo Film Co Ltd ネガ型ハロゲン化銀写真感光材料
US4942248A (en) * 1988-12-01 1990-07-17 Ppg Industries, Inc. Tertiary-alkyl esters of 1H-benzotriazole-1-carboxylic acids
JPH03246206A (ja) * 1990-02-21 1991-11-01 Sumitomo Chem Co Ltd トリハロイミダゾール誘導体を有効成分とするゴキブリ用殺虫剤
JPH0559017A (ja) * 1990-10-26 1993-03-09 Ube Ind Ltd 1,2,3−トリアゾール誘導体、その製法及び有害生物防除剤
US5656762A (en) 1990-12-28 1997-08-12 Neurogen Corporation 4-piperidino-and piperazinomethyl-2-phenylimidazole derivatives, dopamine receptor subtype specific ligands
FR2671083B1 (fr) * 1990-12-31 1994-12-23 Inst Nat Sante Rech Med Nouvelles 4-(4-imidazolyl) piperidines substituees en 1, leur preparation ainsi que leurs applications therapeutiques.
JPH0649041A (ja) * 1992-07-28 1994-02-22 Mitsubishi Petrochem Co Ltd カルバモイルトリアゾール誘導体、それを有効成分とする除草剤およびその製造方法
US6262093B1 (en) * 1995-04-12 2001-07-17 The Proctor & Gamble Company Methods of treating cancer with benzimidazoles
US5798374A (en) * 1995-06-07 1998-08-25 Sugen Inc. Methods of inhibiting phosphatase activity and treatment of disorders associated therewith
JPH11338100A (ja) * 1998-05-22 1999-12-10 Fuji Photo Film Co Ltd 記録材料
MY138097A (en) * 2000-03-22 2009-04-30 Du Pont Insecticidal anthranilamides
JP2001302640A (ja) * 2000-04-19 2001-10-31 Tokuyama Corp カルボニルジアゾール誘導体の製造方法
US6472133B1 (en) * 2000-06-13 2002-10-29 Eastman Kodak Company Silver halide element with improved high temperature storage
US6372421B1 (en) * 2000-06-13 2002-04-16 Eastman Kodak Company Photothermographic imaging element having improved contrast and methods of image formation
JP2004509949A (ja) * 2000-09-26 2004-04-02 ザ ユニバーシティ オブ アリゾナ ファウンデーション 化合物および癌またはウイルス性感染症治療におけるその使用方法
US20020128232A1 (en) * 2000-10-12 2002-09-12 Henderson Scott A. Heterocyclic angiogenesis inhibitors
GB0100624D0 (en) * 2001-01-10 2001-02-21 Vernalis Res Ltd Chemical compounds VII
WO2002072576A1 (en) * 2001-03-09 2002-09-19 Pfizer Products Inc. Benzimidazole anti-inflammatory compounds
US6727364B2 (en) * 2001-04-30 2004-04-27 The Procter & Gamble Company Triazole compounds useful in treating diseases associated with unwanted cytokine activity
US6787555B2 (en) * 2001-04-30 2004-09-07 The Procter & Gamble Company Triazole compounds useful in treating diseases associated with unwanted cytokine activity
JP2003005323A (ja) * 2001-06-20 2003-01-08 Konica Corp 熱現像写真感光材料及び画像形成方法
US6589997B2 (en) * 2001-06-29 2003-07-08 North Shore-Long Island Jewish Health System Small-molecule modulators of hepatocyte growth factor/scatter factor activities
PL373156A1 (en) * 2001-12-14 2005-08-22 Novo Nordisk A/S Compounds and uses thereof for decreasing activity of hormone-sensitive lipase
JP2003327532A (ja) * 2002-05-10 2003-11-19 Takeda Chem Ind Ltd ペプチダーゼ阻害剤
MXPA05003715A (es) * 2002-10-07 2005-09-30 Univ California Modulacion de ansiedad a traves de bloqueo de hidrolisis de anandamida.
AU2003275493A1 (en) * 2002-10-08 2004-05-04 The Scripps Research Institute Inhibitors of fatty acid amide hydrolase
DE10247680B4 (de) * 2002-10-12 2005-09-01 Aventis Pharma Deutschland Gmbh Neue bicyclische Inhibitoren der Hormon Sensitiven Lipase
US7208504B2 (en) 2002-10-12 2007-04-24 Sanofi-Aventis Deutschland Gmbh Bicyclic inhibitors of hormone sensitive lipase
AR042052A1 (es) * 2002-11-15 2005-06-08 Vertex Pharma Diaminotriazoles utiles como inhibidores de proteinquinasas
PE20050226A1 (es) 2003-06-04 2005-05-18 Aventis Pharma Sa Productos aril-heteroaromaticos y composiciones que los contienen
WO2005014576A1 (ja) * 2003-08-12 2005-02-17 Takeda Pharmaceutical Company Limited イソキノリノン誘導体、その製造法および用途
EP1794130A1 (en) * 2004-09-20 2007-06-13 Biolipox AB Pyrazole compounds useful in the treatment of inflammation
TW200633990A (en) * 2004-11-18 2006-10-01 Takeda Pharmaceuticals Co Amide compound
EP2937341B1 (en) * 2004-12-30 2017-07-05 Janssen Pharmaceutica N.V. 4-(benzyl)-piperazine-1-carboxylic acid phenylamide derivatives and related compounds as modulators of fatty acid amide hydrolase (faah) for the treatment of anxiety, pain and other conditions
US7541359B2 (en) * 2005-06-30 2009-06-02 Janssen Pharmaceutica N.V. N-heteroarylpiperazinyl ureas as modulators of fatty acid amide hydrolase
TW200738701A (en) * 2005-07-26 2007-10-16 Du Pont Fungicidal carboxamides
US7884119B2 (en) * 2005-09-07 2011-02-08 Rigel Pharmaceuticals, Inc. Triazole derivatives useful as Axl inhibitors
DE102005049954A1 (de) * 2005-10-19 2007-05-31 Sanofi-Aventis Deutschland Gmbh Triazolopyridin-derivate als Inhibitoren von Lipasen und Phospholipasen
DE102005049953A1 (de) * 2005-10-19 2007-04-26 Sanofi-Aventis Deutschland Gmbh Carbamoylbenzotriazol-derivate als Inhibitoren von Lipasen und Phospholipasen
TW200732320A (en) * 2005-10-31 2007-09-01 Biolipox Ab Pyrazoles useful in the treatment of inflammation
CA2665804A1 (en) * 2006-08-23 2008-02-28 Astellas Pharma Inc. Urea compound or salt thereof
JO3598B1 (ar) * 2006-10-10 2020-07-05 Infinity Discovery Inc الاحماض والاسترات البورونية كمثبطات اميد هيدروليز الحامض الدهني
WO2008063888A2 (en) * 2006-11-22 2008-05-29 Plexxikon, Inc. Compounds modulating c-fms and/or c-kit activity and uses therefor
FR2915199B1 (fr) * 2007-04-18 2010-01-22 Sanofi Aventis Derives de triazolopyridine-carboxamides et triazolopyrimidine-carboxamides, leur preparation et leur application en therapeutique.
FR2915197B1 (fr) * 2007-04-18 2009-06-12 Sanofi Aventis Sa Derives de triazolopyridine-carboxamides, leur preparation et leur application therapeutique.
FR2915198B1 (fr) 2007-04-18 2009-12-18 Sanofi Aventis Derives de triazolopyridine-carboxamides et triazolopyridine -carboxamides, leur preparation et leur application en therapeutique.
FI20075264A0 (fi) * 2007-04-18 2007-04-18 Kuopion Yliopisto Heterosykliset fenyylikarbamaatit uusina FAAH-inhibiittoreina
CA2932121A1 (en) * 2007-11-30 2009-06-11 Newlink Genetics Corporation Ido inhibitors
AU2008345225A1 (en) * 2007-12-21 2009-07-09 University Of Rochester Method for altering the lifespan of eukaryotic organisms
WO2009117444A1 (en) 2008-03-17 2009-09-24 Northeastern University Inhibitors of fatty acid amide hydrolase and monoacylglycerol lipase for modulation of cannabinoid receptors
JP5620365B2 (ja) * 2008-03-21 2014-11-05 エンソン インコーポレイテッド 多官能分子システムを用いた積層体への金属の接着促進
ES2937247T3 (es) * 2019-05-02 2023-03-27 Teepack Spezialmaschinen Gmbh & Co Kg Dispositivo y procedimiento para fabricar una bolsa provista de un envoltorio que contiene un material apto para infusión

Similar Documents

Publication Publication Date Title
JP2012513990A5 (enExample)
CA2493225A1 (en) Quinoline derivatives and their use as mycobacterial inhibitors
JP2006504658A5 (enExample)
JP2017533968A5 (enExample)
JP2018515555A5 (enExample)
JP2011505347A5 (enExample)
JP2019513770A5 (enExample)
JP2013513613A5 (enExample)
JP2014511892A5 (enExample)
JP2018509418A5 (enExample)
JP2013537203A5 (enExample)
NZ593030A (en) Pyridyloxyindoles inhibitors of vegf-r2 and use thereof for treatment of disease
EP2620432A3 (en) Diarylhydantoin compounds
CA2476983A1 (en) Methods and compositions using 3-(4-amino-1-oxo-1,3-dihydroisoindol-2-yl)-piperidine-2,6-dione for treatment and management of multiple myeloma
TW200716648A (en) Heterocycles as nicotinic acid receptor agonists for the treatment of dyslipidemia
JP2015508103A5 (enExample)
CA2566544A1 (en) Use of substituted quinoline derivatives for the treatment of drug resistant mycobacterial diseases
JP2013544860A5 (enExample)
MX2008009413A (es) Heterociclos como agonistas del receptor de acido nicotinico para el tratamiento de la dislipidemia.
JP2010515750A5 (enExample)
JP2012513416A5 (enExample)
JP2014505723A5 (enExample)
JP2017502063A5 (enExample)
GB0417910D0 (en) Organic compounds
JP2007500222A5 (enExample)