JP2008545686A5 - - Google Patents

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Publication number
JP2008545686A5
JP2008545686A5 JP2008513411A JP2008513411A JP2008545686A5 JP 2008545686 A5 JP2008545686 A5 JP 2008545686A5 JP 2008513411 A JP2008513411 A JP 2008513411A JP 2008513411 A JP2008513411 A JP 2008513411A JP 2008545686 A5 JP2008545686 A5 JP 2008545686A5
Authority
JP
Japan
Prior art keywords
methoxy
dimethylamino
dihydro
chromen
tetrahydronaphthalen
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
JP2008513411A
Other languages
English (en)
Japanese (ja)
Other versions
JP2008545686A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/SE2006/000593 external-priority patent/WO2006126939A1/en
Publication of JP2008545686A publication Critical patent/JP2008545686A/ja
Publication of JP2008545686A5 publication Critical patent/JP2008545686A5/ja
Pending legal-status Critical Current

Links

JP2008513411A 2005-05-23 2006-05-22 5ht6受容体を調節する新規な8−スルホニルアミノ−3アミノ置換クロマンまたはテトラヒドロナフタレン誘導体 Pending JP2008545686A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
SE0501166 2005-05-23
SE0501168 2005-05-23
PCT/SE2006/000593 WO2006126939A1 (en) 2005-05-23 2006-05-22 Novel 8-sulfonylamino-3 aminosubstituted chroman or tetrahydronaphtalene derivatives modulating the 5ht6 receptor

Publications (2)

Publication Number Publication Date
JP2008545686A JP2008545686A (ja) 2008-12-18
JP2008545686A5 true JP2008545686A5 (enExample) 2009-07-09

Family

ID=37452274

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008513411A Pending JP2008545686A (ja) 2005-05-23 2006-05-22 5ht6受容体を調節する新規な8−スルホニルアミノ−3アミノ置換クロマンまたはテトラヒドロナフタレン誘導体

Country Status (13)

Country Link
US (1) US20090030038A1 (enExample)
EP (1) EP1888517A1 (enExample)
JP (1) JP2008545686A (enExample)
KR (1) KR20080016810A (enExample)
AR (1) AR054363A1 (enExample)
AU (1) AU2006250117A1 (enExample)
BR (1) BRPI0610119A2 (enExample)
CA (1) CA2609747A1 (enExample)
IL (1) IL187099A0 (enExample)
MX (1) MX2007014263A (enExample)
NO (1) NO20076638L (enExample)
TW (1) TW200716529A (enExample)
WO (1) WO2006126939A1 (enExample)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7754148B2 (en) 2006-12-27 2010-07-13 Progentech Limited Instrument for cassette for sample preparation
US7727473B2 (en) 2005-10-19 2010-06-01 Progentech Limited Cassette for sample preparation
EP2205596A1 (en) 2007-09-24 2010-07-14 Comentis, Inc. (3-hydroxy-4-amino-butan-2-yl) -3- (2-thiazol-2-yl-pyrrolidine-1-carbonyl) benzamide derivatives and related compounds as beta-secretase inhibitors for treating
WO2009073118A1 (en) 2007-12-04 2009-06-11 Merck & Co., Inc. Tryptamine sulfonamides as 5-ht6 antagonists
EP2116547A1 (en) 2008-05-09 2009-11-11 Laboratorios Del. Dr. Esteve, S.A. Substituted N-imidazo(2, 1-b) thiazole-5-sulfonamide derivatives as 5-TH6 ligands
EP2116546A1 (en) 2008-05-09 2009-11-11 Laboratorios Del. Dr. Esteve, S.A. Substituted N-phenyl-2,3-dihydroimidazo[2,1-b]thiazole-5-sulfonamide derivatives as 5-HT6 ligands
EP4043546A1 (en) 2010-02-23 2022-08-17 Luminex Corporation Apparatus and methods for integrated sample preparation, reaction and detection
US20130109672A1 (en) 2010-04-29 2013-05-02 The United States Of America,As Represented By The Secretary, Department Of Health And Human Service Activators of human pyruvate kinase
JP5641436B2 (ja) * 2011-03-28 2014-12-17 国立大学法人 鹿児島大学 抗hiv薬
WO2012151473A2 (en) 2011-05-04 2012-11-08 Luminex Corporation Apparatus and methods for integrated sample preparation, reaction and detection
CN105085436B (zh) * 2014-04-19 2019-08-16 广东东阳光药业有限公司 磺酰胺类衍生物及其在药物上的应用
CA2957566C (en) 2014-08-12 2023-08-01 Daniel Paul Becker Indoline sulfonamide inhibitors of dape and ndm-1 and use of the same
IL273428B2 (en) 2017-09-22 2023-09-01 Jubilant Epipad LLC Heterocyclic compounds as pad inhibitors
CN111225915B (zh) 2017-10-18 2023-03-07 朱比兰特埃皮帕德有限公司 作为pad抑制剂的咪唑并吡啶化合物
BR112020008851A2 (pt) 2017-11-06 2020-10-20 Jubilant Prodel LLC composto da fórmula i, processo de preparação de compostos da fórmula i, composição farmacêutica, método para o tratamento e/ou prevenção de várias doenças, uso, método para o tratamento de câncer, método de tratamento de câncer e método para o tratamento e/ou prevenção de câncer e doenças infecciosas
JP7368369B2 (ja) 2017-11-24 2023-10-24 ジュビラント・エピスクライブ・エルエルシー Prmt5阻害剤としてのヘテロ環式化合物
JP7279063B6 (ja) 2018-03-13 2024-02-15 ジュビラント プローデル エルエルシー Pd1/pd-l1相互作用/活性化の阻害剤としての二環式化合物

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2752659A1 (de) * 1976-12-07 1978-06-08 Sandoz Ag Neue tetralinderivate, ihre herstellung und verwendung
CH637363A5 (en) * 1977-11-24 1983-07-29 Sandoz Ag Process for preparing novel 2-aminotetralins
WO1999002502A2 (en) * 1997-07-11 1999-01-21 Smithkline Beecham Plc Sulphonamide derivatives being 5-ht6 receptor antagonists and process for their preparation
CN1561338A (zh) * 2001-10-04 2005-01-05 惠氏公司 作为5-羟基色胺-6配体的苯并二氢吡喃衍生物
RU2442781C2 (ru) * 2004-10-14 2012-02-20 Абботт ГмбХ унд Ко. КГ Арилсульфонилметильные или арилсульфонамидные производные ароматических соединений, фармацевтическая композиция на их основе и способ лечения расстройств, восприимчивых к лечению лигандами дофаминовых d3 рецепторов, с их помощью

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