JP2008534486A5 - - Google Patents

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Publication number
JP2008534486A5
JP2008534486A5 JP2008502490A JP2008502490A JP2008534486A5 JP 2008534486 A5 JP2008534486 A5 JP 2008534486A5 JP 2008502490 A JP2008502490 A JP 2008502490A JP 2008502490 A JP2008502490 A JP 2008502490A JP 2008534486 A5 JP2008534486 A5 JP 2008534486A5
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JP
Japan
Prior art keywords
alkyl
pain
ring
alkoxy
halo
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JP2008502490A
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English (en)
Japanese (ja)
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JP5097696B2 (ja
JP2008534486A (ja
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Priority claimed from GBGB0506147.8A external-priority patent/GB0506147D0/en
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Publication of JP2008534486A publication Critical patent/JP2008534486A/ja
Publication of JP2008534486A5 publication Critical patent/JP2008534486A5/ja
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Publication of JP5097696B2 publication Critical patent/JP5097696B2/ja
Expired - Fee Related legal-status Critical Current
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JP2008502490A 2005-03-24 2006-03-21 Vr1拮抗剤としての2,3−置換縮合ピリミジン−4(3h)−オン Expired - Fee Related JP5097696B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB0506147.8 2005-03-24
GBGB0506147.8A GB0506147D0 (en) 2005-03-24 2005-03-24 Therapeutic agents
PCT/GB2006/050060 WO2006100520A1 (en) 2005-03-24 2006-03-21 2,3-substituted fused pyrimidin-4(3h)-ones as vr1 antagonists

Publications (3)

Publication Number Publication Date
JP2008534486A JP2008534486A (ja) 2008-08-28
JP2008534486A5 true JP2008534486A5 (cg-RX-API-DMAC7.html) 2012-06-07
JP5097696B2 JP5097696B2 (ja) 2012-12-12

Family

ID=34566491

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008502490A Expired - Fee Related JP5097696B2 (ja) 2005-03-24 2006-03-21 Vr1拮抗剤としての2,3−置換縮合ピリミジン−4(3h)−オン

Country Status (7)

Country Link
US (1) US20110152242A1 (cg-RX-API-DMAC7.html)
EP (1) EP1866310B1 (cg-RX-API-DMAC7.html)
JP (1) JP5097696B2 (cg-RX-API-DMAC7.html)
AU (1) AU2006226084B2 (cg-RX-API-DMAC7.html)
CA (1) CA2602395A1 (cg-RX-API-DMAC7.html)
GB (1) GB0506147D0 (cg-RX-API-DMAC7.html)
WO (1) WO2006100520A1 (cg-RX-API-DMAC7.html)

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CL2007002752A1 (es) 2006-09-26 2008-07-11 Celgene Corp Soc Organizada Ba Compuestos derivados de 3-(4-oxo-4h-quinazolin-3-il)-piperidina-2,6-diona; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar o prevenir enfermedades tales como cancer, dolor, degeneracion macular, trastorno pulmonar, tr
CN101558069A (zh) * 2006-11-06 2009-10-14 神经能质公司 顺式环己基取代的嘧啶酮衍生物
NZ576997A (en) * 2006-11-13 2012-02-24 Icos Corp Thienopyrimidinones for treatment of inflammatory disorders and cancers
US7803940B2 (en) 2006-11-24 2010-09-28 Takeda Pharmaceutical Company Limited Heteromonocyclic compound or a salt thereof having strong antihypertensive action, insulin sensitizing activity and the like production thereof and use thereof for prophylaxis or treatment of cardiovascular diseases, metabolic diseases and/or central nervous system diseases
JP5643112B2 (ja) 2008-01-28 2014-12-17 アモーレパシフィック コーポレイションAmorepacific Corporation バニロイド受容体としての新規化合物、その異性体または薬剤学的に許容し得る塩、及びこれを含有する医薬組成物
KR101621444B1 (ko) 2008-07-02 2016-05-19 (주)아모레퍼시픽 바닐로이드 수용체 길항제로 작용하는 신규 화합물, 이의 이성질체 또는 이의 약제학적으로 허용 가능한 염, 및 이를 포함하는 약학 조성물
US8349852B2 (en) 2009-01-13 2013-01-08 Novartis Ag Quinazolinone derivatives useful as vanilloid antagonists
US9206173B2 (en) 2009-05-28 2015-12-08 Otsuka Pharmaceutical Co., Ltd. Heterocyclic compounds for the treatment of stress-related conditions
CN102762572A (zh) 2010-02-01 2012-10-31 诺瓦提斯公司 作为CRF-1受体拮抗剂的吡唑并[5,1b]*唑衍生物
AR080056A1 (es) 2010-02-01 2012-03-07 Novartis Ag Derivados de ciclohexil-amida como antagonistas de los receptores de crf
US8835444B2 (en) 2010-02-02 2014-09-16 Novartis Ag Cyclohexyl amide derivatives as CRF receptor antagonists
US10280171B2 (en) 2016-05-31 2019-05-07 Board Of Regents, The University Of Texas System Heterocyclic inhibitors of PTPN11
US11466017B2 (en) 2011-03-10 2022-10-11 Board Of Regents, The University Of Texas System Heterocyclic inhibitors of PTPN11
PE20140983A1 (es) 2011-03-11 2014-08-25 Celgene Corp Formas solidas de 3-(5-amino-2-metil-4-oxo-4h-quinazolin-3-il)-piperidin-2,6-diona, y sus composiciones farmaceuticas y sus usos
US8940742B2 (en) 2012-04-10 2015-01-27 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
JP2015531776A (ja) 2012-09-04 2015-11-05 セルジーン コーポレイション 3−(5−アミノ−2−メチル−4−オキソキナゾリン−3(4h)−イル)ピペリジン−2,6−ジオンのアイソトポログ及びその製造方法
WO2015051241A1 (en) 2013-10-04 2015-04-09 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
SG10201902074UA (en) 2013-10-04 2019-04-29 Infinity Pharmaceuticals Inc Heterocyclic compounds and uses thereof
PT3119397T (pt) 2014-03-19 2022-04-11 Infinity Pharmaceuticals Inc Compostos heterocíclicos para utilização no tratamento de distúrbios mediados por pi3k-gama
WO2016054491A1 (en) 2014-10-03 2016-04-07 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
US9957267B2 (en) 2015-07-01 2018-05-01 Crinetics Pharmaceuticals, Inc. Somatostatin modulators and uses thereof
KR102787845B1 (ko) 2015-09-14 2025-03-31 트웰브 테라퓨틱스, 아이엔씨. 이소퀴놀리논의 고체형, 그의 제조 방법, 이를 포함하는 조성물 및 이를 사용하는 방법
DE102015012049A1 (de) * 2015-09-15 2017-03-16 Merck Patent Gmbh Verbindungen als ASIC-Inhibitoren und deren Verwendungen
WO2017156397A1 (en) * 2016-03-11 2017-09-14 Board Of Regents, The University Of Texas Sysytem Heterocyclic inhibitors of ptpn11
US10759806B2 (en) 2016-03-17 2020-09-01 Infinity Pharmaceuticals, Inc. Isotopologues of isoquinolinone and quinazolinone compounds and uses thereof as PI3K kinase inhibitors
US10919914B2 (en) 2016-06-08 2021-02-16 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
US11028068B2 (en) 2017-07-25 2021-06-08 Crinetics Pharmaceuticals, Inc. Somatostatin modulators and uses thereof
IL278297B2 (en) 2018-05-02 2023-12-01 Navire Pharma Inc Substituted heterocyclic inhibitors of ptpn11
SG11202100199UA (en) 2018-08-10 2021-02-25 Navire Pharma Inc 6-(4-amino-3-methyl-2-oxa-8-azaspiro[4.5]decan-8-yl)-3-(2,3-dichlorophenyl)-2-methylpyrimidin-4(3h)-one derivatives and related compounds as ptpn11 (shp2) inhibitors for treating cancer

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1950990A1 (de) * 1968-10-17 1970-05-14 Ciba Geigy Verfahren zur Herstellung von neuen triazacyclischen Verbindungen
WO2002076946A2 (en) * 2001-03-26 2002-10-03 Novartis Ag Fused pyridine derivatives for use as vanilloid receptor antagonists for treating pain.
WO2003014064A1 (en) * 2001-07-31 2003-02-20 Bayer Healthcare Ag Naphthylurea and naphthylacetamide derivatives as vanilloid receptor 1 (vr1) antagonists
EP1687306A1 (en) * 2003-11-14 2006-08-09 MERCK SHARP & DOHME LTD. Bicyclic pyrimidin-4-(3h)-ones and analogues and derivatives thereof which modulate the function of the vanilloid-1 receptor (vr1)
AR051596A1 (es) * 2004-10-26 2007-01-24 Irm Llc Compuestos heterociclicos condensados nitrogenados como inhibidores de la actividad del receptor canabinoide 1; composiciones farmaceuticas que los contienen y su empleo en la preparacion de medicamentos para el tratamiento de trastornos alimentarios

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