JP2008504304A5 - - Google Patents

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Publication number
JP2008504304A5
JP2008504304A5 JP2007518382A JP2007518382A JP2008504304A5 JP 2008504304 A5 JP2008504304 A5 JP 2008504304A5 JP 2007518382 A JP2007518382 A JP 2007518382A JP 2007518382 A JP2007518382 A JP 2007518382A JP 2008504304 A5 JP2008504304 A5 JP 2008504304A5
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JP
Japan
Prior art keywords
alkyl
group
compound
heteroalkyl
membered
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.)
Pending
Application number
JP2007518382A
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English (en)
Japanese (ja)
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JP2008504304A (ja
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Publication date
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Priority claimed from PCT/US2005/023275 external-priority patent/WO2006004925A1/en
Publication of JP2008504304A publication Critical patent/JP2008504304A/ja
Publication of JP2008504304A5 publication Critical patent/JP2008504304A5/ja
Pending legal-status Critical Current

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JP2007518382A 2004-06-28 2005-06-28 テトラヒドロキナゾリン−4(3h)−オン関連、及びテトラヒドロピリド[2,3−d]ピリミジン−4(3h)−オン関連化合物、組成物、及びそれらの使用方法 Pending JP2008504304A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US58382304P 2004-06-28 2004-06-28
PCT/US2005/023275 WO2006004925A1 (en) 2004-06-28 2005-06-28 Tetrahydroquinazolin-4(3h)-one-related and tetrahydropyrido[2,3-d]pyrimidin-4(3h)-one-related compounds, compositions and methods for their use

Publications (2)

Publication Number Publication Date
JP2008504304A JP2008504304A (ja) 2008-02-14
JP2008504304A5 true JP2008504304A5 (cg-RX-API-DMAC7.html) 2008-08-14

Family

ID=34982539

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007518382A Pending JP2008504304A (ja) 2004-06-28 2005-06-28 テトラヒドロキナゾリン−4(3h)−オン関連、及びテトラヒドロピリド[2,3−d]ピリミジン−4(3h)−オン関連化合物、組成物、及びそれらの使用方法

Country Status (7)

Country Link
US (1) US7375102B2 (cg-RX-API-DMAC7.html)
EP (1) EP1765818A1 (cg-RX-API-DMAC7.html)
JP (1) JP2008504304A (cg-RX-API-DMAC7.html)
AU (1) AU2005260630A1 (cg-RX-API-DMAC7.html)
CA (1) CA2572084A1 (cg-RX-API-DMAC7.html)
MX (1) MX2007000044A (cg-RX-API-DMAC7.html)
WO (1) WO2006004925A1 (cg-RX-API-DMAC7.html)

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US6858615B2 (en) 2002-02-19 2005-02-22 Parion Sciences, Inc. Phenyl guanidine sodium channel blockers
US7939538B2 (en) * 2004-06-28 2011-05-10 Amgen Inc. Compounds, compositions and methods for prevention and treatment of inflammatory and immunoregulatory disorders and diseases
TW200714610A (en) * 2005-02-16 2007-04-16 Univ Maryland CXCR3 is a gliadin receptor
WO2006129679A1 (ja) * 2005-05-31 2006-12-07 Ono Pharmaceutical Co., Ltd. スピロピペリジン化合物およびその医薬用途
CA2612585A1 (en) * 2005-06-27 2007-01-04 Amgen Inc. Anti-inflammatory aryl nitrile compounds
US20110034487A1 (en) * 2008-01-22 2011-02-10 Amgen Inc. Cxcr3 antagonists
AU2008363295B2 (en) 2008-10-20 2015-05-07 Forschungsverbund Berlin E.V. Low molecular weight thyroid stimulating hormone receptor (TSHR) agonists
AU2011237421B2 (en) 2010-04-08 2016-10-13 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Inverse agonists and neutral antagonists for the TSH receptor
BR112013032771B1 (pt) 2011-06-27 2021-01-12 Parion Sciences, Inc. dipeptídio quimicamente e metabolicamente estável possuindo potente atividade bloqueadora de canais de sódio
AR086745A1 (es) 2011-06-27 2014-01-22 Parion Sciences Inc 3,5-diamino-6-cloro-n-(n-(4-(4-(2-(hexil(2,3,4,5,6-pentahidroxihexil)amino)etoxi)fenil)butil)carbamimidoil)pirazina-2-carboxamida
PH12014500126A1 (en) 2011-07-13 2014-02-24 Novartis Ag 4-piperidinyl compounds for use as tankyrase inhibitors
EP2731942B1 (en) 2011-07-13 2015-09-23 Novartis AG Novel 2-piperidin-1-yl-acetamide compounds for use as tankyrase inhibitors
EP2731951B1 (en) 2011-07-13 2015-08-19 Novartis AG 4-oxo-3,5,7,8-tetrahydro-4h-pyrano {4,3-d} pyrminidinyl compounds for use as tankyrase inhibitors
US8940742B2 (en) 2012-04-10 2015-01-27 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
AU2013267504B2 (en) 2012-05-29 2017-11-02 Parion Sciences, Inc. Dendrimer like amino amides possessing sodium channel blocker activity for the treatment of dry eye and other mucosal diseases
ES2674665T3 (es) 2012-12-17 2018-07-03 Parion Sciences, Inc. Compuestos de 3,5-diamino-6-cloro-N-(N-(4-fenilbutilo)carbamimidoilo)-pirazina-2-carboxamida
CN108658876A (zh) 2012-12-17 2018-10-16 帕里昂科学公司 3,5-二氨基-6-氯-n-(n-(4-苯基丁基)甲脒基)吡嗪-2-甲酰胺化合物
HUE032891T2 (hu) 2012-12-17 2017-11-28 Parion Sciences Inc Klórpirazin-karboxamid-származékok nem kielégítõ nyálkahártya-hidratáció által elõsegített megbetegedések kezelésére
MX389256B (es) 2013-10-04 2025-03-20 Infinity Pharmaceuticals Inc Compuestos heterociclicos y usos de los mismos.
US9751888B2 (en) 2013-10-04 2017-09-05 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
US9102633B2 (en) 2013-12-13 2015-08-11 Parion Sciences, Inc. Arylalkyl- and aryloxyalkyl-substituted epithelial sodium channel blocking compounds
CN113616656B (zh) 2014-03-19 2023-02-17 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
US9708348B2 (en) 2014-10-03 2017-07-18 Infinity Pharmaceuticals, Inc. Trisubstituted bicyclic heterocyclic compounds with kinase activities 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
US10759806B2 (en) 2016-03-17 2020-09-01 Infinity Pharmaceuticals, Inc. Isotopologues of isoquinolinone and quinazolinone compounds and uses thereof as PI3K kinase inhibitors
WO2017214269A1 (en) 2016-06-08 2017-12-14 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
JP7226321B2 (ja) * 2017-09-14 2023-02-21 住友金属鉱山株式会社 近赤外線吸収繊維およびこれを用いた繊維製品、並びにそれらの製造方法

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