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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JP2008534486A (ja
JP5097696B2 (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
Application granted granted Critical
Publication of JP5097696B2 publication Critical patent/JP5097696B2/ja
Anticipated expiration legal-status Critical
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
GBGB0506147.8A GB0506147D0 (en) 2005-03-24 2005-03-24 Therapeutic agents
GB0506147.8 2005-03-24
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-DMAC10.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-DMAC10.html)
EP (1) EP1866310B1 (cg-RX-API-DMAC10.html)
JP (1) JP5097696B2 (cg-RX-API-DMAC10.html)
AU (1) AU2006226084B2 (cg-RX-API-DMAC10.html)
CA (1) CA2602395A1 (cg-RX-API-DMAC10.html)
GB (1) GB0506147D0 (cg-RX-API-DMAC10.html)
WO (1) WO2006100520A1 (cg-RX-API-DMAC10.html)

Families Citing this family (29)

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Publication number Priority date Publication date Assignee Title
HUE035389T2 (en) 2006-09-26 2018-05-02 Celgene Corp 5-substituted quinazolinone derivatives as anticancer agents
CA2668579A1 (en) * 2006-11-06 2008-06-05 Neurogen Corporation Cis-cyclohexyl substituted pyrimidinone derivatives
EP2441768A1 (en) * 2006-11-13 2012-04-18 Eli Lilly & Co. 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
WO2009096701A2 (en) 2008-01-28 2009-08-06 Amorepacific Corporation Novel compounds, isomer thereof, or pharmaceutically acceptable salts thereof as vanilloid receptor antagonist; and pharmaceutical compositions containing the same
JP5438103B2 (ja) 2008-07-02 2014-03-12 アモーレパシフィック コーポレイション バニロイド受容体アンタゴニストとしての新規化合物、その異性体またはその薬学的に許容される塩、並びにそれを含む医薬組成物
US8349852B2 (en) 2009-01-13 2013-01-08 Novartis Ag Quinazolinone derivatives useful as vanilloid antagonists
TW201109327A (en) * 2009-05-28 2011-03-16 Otsuka Pharma Co Ltd Heterocyclic compound
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
EP2531490B1 (en) 2010-02-02 2014-10-15 Novartis AG Cyclohexyl amide derivatives as crf receptor antagonists
US11466017B2 (en) 2011-03-10 2022-10-11 Board Of Regents, The University Of Texas System Heterocyclic inhibitors of PTPN11
RU2611007C2 (ru) 2011-03-11 2017-02-17 Селджин Корпорейшн Твердые формы 3-(5-амино-2-метил-4-оксо-4н-хиназолин-3-ил)пиперидин-2, 6-диона и их фармацевтические композиции и применение
US8940742B2 (en) 2012-04-10 2015-01-27 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
WO2014039421A1 (en) 2012-09-04 2014-03-13 Celgene Corporation Isotopologues of 3-(5-amino-2-methyl-4-oxoquinazolin-3(4h)-yl) piperidine-2-6-dione and methods of preparation thereof
WO2015051241A1 (en) 2013-10-04 2015-04-09 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
EP3964507A1 (en) 2013-10-04 2022-03-09 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
CN106456628A (zh) 2014-03-19 2017-02-22 无限药品股份有限公司 用于治疗PI3K‑γ介导的障碍的杂环化合物
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
CN114230571B (zh) 2015-09-14 2025-07-08 无限药品股份有限公司 异喹啉酮的固体形式、其制备方法、包含其的组合物及其使用方法
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
WO2017161116A1 (en) 2016-03-17 2017-09-21 Infinity Pharmaceuticals, Inc. Isotopologues of isoquinolinone and quinazolinone compounds and uses thereof as pi3k kinase inhibitors
WO2017210134A1 (en) 2016-05-31 2017-12-07 Board Of Regents, University Of Texas System Heterocyclic inhibitors of ptpn11
US10919914B2 (en) 2016-06-08 2021-02-16 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
WO2019023278A1 (en) 2017-07-25 2019-01-31 Crinetics Pharmaceuticals, Inc. MODULATORS OF SOMATOSTATIN AND USES THEREOF
KR102611661B1 (ko) 2018-05-02 2023-12-08 나비레 파르마, 인코퍼레이티드 Ptpn11의 치환된 헤테로사이클릭 억제제
PL3833670T3 (pl) 2018-08-10 2024-08-19 Navire Pharma, Inc. Pochodne 6-(4-amino-3-metylo-2-oksa-8-azaspiro[4.5]dekan-8-ylo)-3-(2,3-dichlorofenylo)-2-metylopirymidyn-4(3h)-onu oraz powiązane związki jako inhibitory ptpn11 (shp2) do leczenia raka

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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
CZ20032561A3 (cs) * 2001-03-26 2003-12-17 Novartis Ag Deriváty pyridinu, způsob jejich přípravy a farmaceutický prostředek, který je obsahuje
JP2005501873A (ja) * 2001-07-31 2005-01-20 バイエル・ヘルスケア・アクチェンゲゼルシャフト アミン誘導体
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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