JP2010506950A5 - - Google Patents

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Publication number
JP2010506950A5
JP2010506950A5 JP2009533499A JP2009533499A JP2010506950A5 JP 2010506950 A5 JP2010506950 A5 JP 2010506950A5 JP 2009533499 A JP2009533499 A JP 2009533499A JP 2009533499 A JP2009533499 A JP 2009533499A JP 2010506950 A5 JP2010506950 A5 JP 2010506950A5
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JP
Japan
Prior art keywords
hydrogen
lower alkyl
independently
formula
alkoxy
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JP2009533499A
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English (en)
Japanese (ja)
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JP5298022B2 (ja
JP2010506950A (ja
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Priority claimed from PCT/US2007/081607 external-priority patent/WO2008048991A2/en
Publication of JP2010506950A publication Critical patent/JP2010506950A/ja
Publication of JP2010506950A5 publication Critical patent/JP2010506950A5/ja
Application granted granted Critical
Publication of JP5298022B2 publication Critical patent/JP5298022B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2009533499A 2006-10-18 2007-10-17 有機化合物 Expired - Fee Related JP5298022B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US82998006P 2006-10-18 2006-10-18
US60/829,980 2006-10-18
US95234107P 2007-07-27 2007-07-27
US60/952,341 2007-07-27
PCT/US2007/081607 WO2008048991A2 (en) 2006-10-18 2007-10-17 Organic compounds

Publications (3)

Publication Number Publication Date
JP2010506950A JP2010506950A (ja) 2010-03-04
JP2010506950A5 true JP2010506950A5 (enExample) 2010-11-25
JP5298022B2 JP5298022B2 (ja) 2013-09-25

Family

ID=39276877

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2009533499A Expired - Fee Related JP5298022B2 (ja) 2006-10-18 2007-10-17 有機化合物

Country Status (15)

Country Link
US (1) US8222248B2 (enExample)
EP (1) EP2074089B1 (enExample)
JP (1) JP5298022B2 (enExample)
KR (1) KR20090071642A (enExample)
AR (1) AR063311A1 (enExample)
AU (1) AU2007311087B2 (enExample)
BR (1) BRPI0718478A2 (enExample)
CA (1) CA2666880A1 (enExample)
CL (1) CL2007002974A1 (enExample)
ES (1) ES2440253T3 (enExample)
MX (1) MX2009004047A (enExample)
PE (1) PE20080888A1 (enExample)
RU (1) RU2009118489A (enExample)
TW (1) TW200829563A (enExample)
WO (1) WO2008048991A2 (enExample)

Families Citing this family (50)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX2007007101A (es) 2004-12-14 2007-08-21 Astrazeneca Ab Derivados de oxadiazol como inhibidores de acil coa:diacilglicerol aciltransferasa.
AR058562A1 (es) 2005-12-22 2008-02-13 Astrazeneca Ab Derivados de pirimido [4,5 b] (1,4) oxazinas , procedimientos de obtencion y su uso como inhibidores de acetil coa y dgat 1
CA2651663A1 (en) 2006-05-30 2007-12-06 Astrazeneca Ab Chemical compounds
BRPI0712802A2 (pt) 2006-05-30 2012-10-23 Astrazeneca Ab composto, métodos para produzir uma inibição da atividade de dgat1, e para tratar diabete melito e/ou obesidade em um animal de sangue quente, uso de um composto, composição farmacêutica, e, processo para preparar um composto
CN101932562B (zh) 2007-12-20 2013-06-12 阿斯利康(瑞典)有限公司 作为dgat1抑制剂190的氨基甲酰基化合物
WO2009112445A1 (en) * 2008-03-10 2009-09-17 Novartis Ag Method of increasing cellular phosphatidyl choline by dgat1 inhibition
WO2010039668A2 (en) * 2008-10-01 2010-04-08 The Regents Of The University Of California Inhibitors of cyclin kinase inhibitor p21
GB0821913D0 (en) 2008-12-02 2009-01-07 Price & Co Antibacterial compounds
EP2408744A1 (en) * 2009-03-18 2012-01-25 Schering Corporation Bicyclic compounds as inhibitors of diacylglycerol acyltransferase
WO2010146395A1 (en) 2009-06-19 2010-12-23 Astrazeneca Ab Pyrazine carboxamides as inhibitors of dgat1
WO2011011722A1 (en) * 2009-07-23 2011-01-27 Vanderbilt University Substituted benzoimidazolesulfonamides and substituted indolesulfonamides as mglur4 potentiators
KR101194995B1 (ko) * 2009-10-14 2012-10-29 주식회사 이큐스앤자루 신규한 2-페닐-벤즈이미다졸 또는 2-페닐-벤즈옥사졸 유도체 또는 이의 약학적으로 허용가능한 염, 이의 제조방법 및 이를 유효성분으로 함유하는 항바이러스용 약학적 조성물
WO2011099832A2 (en) * 2010-02-12 2011-08-18 Crystalgenomics, Inc. Novel benzimidazole compound, preparation method thereof and pharmaceutical composition comprising the same
SI2575968T1 (sl) 2010-06-01 2016-06-30 Summit Therapeutics Plc Spojine za zdravljenje bolezni, ki je povezana s clostridium difficile
EP2800568A4 (en) * 2012-01-06 2015-06-10 Univ South Florida COMPOSITIONS, USE METHOD AND TREATMENT METHOD THEREFOR
KR102212923B1 (ko) 2012-12-21 2021-02-04 플렉시콘 인코퍼레이티드 키나제 조절을 위한 화합물 및 방법, 및 그에 대한 적응증
US9233961B2 (en) 2013-03-15 2016-01-12 Novartis Ag Compounds and compositions for the treatment of parasitic diseases
WO2014151729A1 (en) 2013-03-15 2014-09-25 Irm Llc Compounds and compositions for the treatment of parasitic diseases
US9296754B2 (en) 2013-03-15 2016-03-29 Novartis Ag Compounds and compositions for the treatment of parasitic diseases
RS58053B1 (sr) 2013-12-19 2019-02-28 Novartis Ag [1,2,4] triazolo [1,5-a] pirimidin derivati kao proteazomski inhibitori protozoa za tretman parazitskih bolesti kao što je lišmanijaza
SI3102576T1 (sl) 2014-02-03 2019-08-30 Vitae Pharmaceuticals, Llc Inhibitorji dihidropirolopiridina ROR-gama
WO2015166398A1 (en) * 2014-04-30 2015-11-05 Aurigene Discovery Technologies Limited 3h-imidazo[4,5-b]pyridine derivatives as dihydroorotate dehydrogenase inhibitors
BR112017007460A2 (pt) 2014-10-14 2017-12-19 Vitae Pharmaceuticals Inc inibidores de di-hidropirrolopiridina de ror-gama
US9845308B2 (en) 2014-11-05 2017-12-19 Vitae Pharmaceuticals, Inc. Isoindoline inhibitors of ROR-gamma
US9663515B2 (en) 2014-11-05 2017-05-30 Vitae Pharmaceuticals, Inc. Dihydropyrrolopyridine inhibitors of ROR-gamma
CA2986930C (en) * 2015-06-24 2023-09-26 Duke University Chemical modulators of signaling pathways and therapeutic use
ES2856931T3 (es) 2015-08-05 2021-09-28 Vitae Pharmaceuticals Llc Moduladores de ROR-gamma
WO2017087608A1 (en) 2015-11-20 2017-05-26 Vitae Pharmaceuticals, Inc. Modulators of ror-gamma
TWI757266B (zh) 2016-01-29 2022-03-11 美商維它藥物有限責任公司 ROR-γ調節劑
US9481674B1 (en) 2016-06-10 2016-11-01 Vitae Pharmaceuticals, Inc. Dihydropyrrolopyridine inhibitors of ROR-gamma
CN110234640B (zh) 2016-09-20 2023-04-07 利昂贝拉尔中心 作为抗癌剂的苯并咪唑衍生物
KR20200053481A (ko) 2017-07-24 2020-05-18 비타이 파마슈티컬즈, 엘엘씨 RORγ의 억제제
WO2019018975A1 (en) 2017-07-24 2019-01-31 Vitae Pharmaceuticals, Inc. INHIBITORS OF ROR GAMMA
US10513515B2 (en) 2017-08-25 2019-12-24 Biotheryx, Inc. Ether compounds and uses thereof
CA3106239A1 (en) 2018-07-27 2020-01-30 Biotheryx, Inc. Bifunctional compounds as cdk modulators
PE20211644A1 (es) 2018-09-18 2021-08-24 Terns Inc Compuestos para tratar ciertas leucemias
WO2020120576A1 (en) * 2018-12-11 2020-06-18 Fundació Institut De Recerca Biomèdica (Irb Barcelona) p38α AUTOPHOSPHORYLATION INHIBITORS
EP3997081A1 (en) 2019-07-11 2022-05-18 Escape Bio, Inc. Indazoles and azaindazoles as lrrk2 inhibitors
CA3166429A1 (en) * 2020-01-28 2021-08-05 Bradley Dean Tait Compounds, compositions and methods for stabilizing transthyretin and inhibiting transthyretin misfolding
EP4143329A4 (en) 2020-04-28 2024-10-16 Anwita Biosciences, Inc. Interleukin-2 polypeptides and fusion proteins thereof, and their pharmaceutical compositions and therapeutic applications
BR112022021920A2 (pt) 2020-04-29 2023-01-17 Plexxikon Inc Síntese de compostos heterocíclicos
JP2023552638A (ja) * 2020-12-11 2023-12-18 ティーエムイーエム16エー リミテッド 呼吸器疾患を治療するためのベンゾイミダゾール誘導体
JP7728367B2 (ja) 2021-06-14 2025-08-22 スコーピオン・セラピューティクス・インコーポレイテッド がんを処置するために使用され得る尿素誘導体
AU2022306297A1 (en) 2021-07-09 2024-02-08 Plexium, Inc. Aryl compounds and pharmaceutical compositions that modulate ikzf2
WO2023134708A1 (en) * 2022-01-12 2023-07-20 Beigene , Ltd. Thiazolopyridyl amide derivatives as dna polymerase theta inhibitors
EP4265247A1 (en) * 2022-04-22 2023-10-25 Université Paris Cité Compounds inducing production of proteins by immune cells
CN116253755A (zh) * 2023-02-28 2023-06-13 湖南大学 一种二芳基硼酸酯类化合物的合成方法
CN117327020A (zh) * 2023-10-07 2024-01-02 中国科学院过程工程研究所 一种含苯并氮杂环结构的氨基芳香化合物及其制备方法和应用
US11970468B1 (en) 2023-10-23 2024-04-30 King Faisal University 2-(benzo[d]oxazol-2-yl)-N′-(3,5-dichlorobenzoyloxy)acetimidamide as an antimicrobial compound
CN120118037B (zh) * 2023-12-07 2025-11-28 南华大学 一类含苯甲酸酯结构的苯并咪唑类化合物、制造方法及其用途

Family Cites Families (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3551443A (en) * 1968-10-30 1970-12-29 Ciba Ltd 2-phenylbenzoxazole derivatives
JPH0678308B2 (ja) * 1985-04-24 1994-10-05 三共株式会社 フタルイミド誘導体およびそれを含有する農園芸用殺菌剤
HUP9900625A3 (en) * 1995-12-28 2003-04-28 Fujisawa Pharmaceutical Co Benzimidazole derivatives, pharmaceutical compositions containing them and process for preparing the compounds
CA2281927C (en) 1997-02-25 2004-01-27 Christopher J. Michejda Substituted benzimidazoles as non-nucleoside inhibitors of reverse transcriptase
US6251689B1 (en) * 1998-05-14 2001-06-26 Telik, Inc. Methods for the solid phase synthesis of combinatorial libraries of benzimidazoles benzoxazoles benzothiazoles and derivatives thereof
JP2000095767A (ja) * 1998-09-28 2000-04-04 Takeda Chem Ind Ltd 性腺刺激ホルモン放出ホルモン拮抗剤
PT1194425E (pt) * 1999-06-23 2005-10-31 Aventis Pharma Gmbh Benzimidazoles substituidos
WO2001014343A1 (en) 1999-08-26 2001-03-01 The Government Of The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Substituted benzimidazoles as non-nucleoside inhibitors of reverse transcriptase
CN1315805C (zh) * 2000-09-19 2007-05-16 斯皮罗根公司 Cc-1065和多卡米新的非手性类似物的组合物及其使用方法
AU2002221239A1 (en) 2000-12-07 2002-06-18 Astrazeneca Ab Therapeutic benzimidazole compounds
FR2821721B1 (fr) * 2001-03-08 2004-07-09 Laurent Locatelli Composition pour alimentation animale, utilisation de cette composition, et produit pour alimentation animale comprenant cette composition
DE60221804T2 (de) 2001-03-12 2008-05-15 Avanir Pharmaceuticals, San Diego Benzimidazolderivate zur ige-modulierung und zellproliferationshemmung
EP1435947B1 (en) * 2001-10-19 2007-08-15 Ortho-McNeil Pharmaceutical, Inc. 2-phenyl benzimidazoles and imidazo-¬4,5|-pyridines as cds1/chk2-inhibitors and adjuvants to chemotherapy or radiation therapy in the treatment of cancer
TW200303742A (en) 2001-11-21 2003-09-16 Novartis Ag Organic compounds
AU2002366803A1 (en) 2001-12-19 2003-07-09 Millennium Pharmaceuticals, Inc. Human diacylglycerol acyltransferase 2 (dgat2) family members and uses therefor
TW200304820A (en) * 2002-03-25 2003-10-16 Avanir Pharmaceuticals Use of benzimidazole analogs in the treatment of cell proliferation
AU2003242233A1 (en) * 2002-06-12 2003-12-31 Bf Research Institute, Inc. Probe compound for image diagnosis of disease with amyloid accumulation, compound for staining age spots/diffuse age spots, and remedy for disease with amyloid accumulation
EP1550462B1 (en) * 2002-08-06 2012-01-25 Toray Industries, Inc. Remedy or preventive for kidney disease and method of diagnosing kidney disease
WO2004063155A1 (en) 2003-01-06 2004-07-29 Eli Lilly And Company Fused heterocyclic derivatives as ppar modulators
DE10306250A1 (de) * 2003-02-14 2004-09-09 Aventis Pharma Deutschland Gmbh Substituierte N-Arylheterozyklen, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
WO2004098494A2 (en) 2003-04-30 2004-11-18 Cytokinetics, Inc. Compounds, compositions, and methods
KR100909918B1 (ko) 2003-05-20 2009-07-29 노파르티스 아게 과산화소체 증식체-활성화 수용체의 리간드로서의 n-아실질소 헤테로환
WO2005108370A1 (ja) * 2004-04-16 2005-11-17 Ajinomoto Co., Inc. ベンゼン化合物
MX2007004217A (es) 2004-10-15 2007-06-11 Bayer Pharmaceuticals Corp Preparacion y uso de derivados de acido bifenil-4-il-carbonilamino para el tratamiento de obesidad.
CA2600570C (en) * 2005-03-14 2011-12-06 Transtech Pharma, Inc. Benzazole derivatives, compositions, and methods of use as .beta.-secretase inhibitors
GT200600429A (es) 2005-09-30 2007-04-30 Compuestos organicos
JP2009001495A (ja) * 2005-10-13 2009-01-08 Taisho Pharmaceutical Co Ltd 2−アリール−ベンゾイミダゾール−5−カルボキサミド誘導体
EP2298770A1 (en) * 2005-11-03 2011-03-23 ChemBridge Corporation Heterocyclic compounds as TrkA modulators
KR101472248B1 (ko) * 2006-02-10 2014-12-16 서미트 코포레이션 피엘씨 뒤시엔느 근이영양증의 치료

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