JP2010529986A5 - - Google Patents

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Publication number
JP2010529986A5
JP2010529986A5 JP2010512211A JP2010512211A JP2010529986A5 JP 2010529986 A5 JP2010529986 A5 JP 2010529986A5 JP 2010512211 A JP2010512211 A JP 2010512211A JP 2010512211 A JP2010512211 A JP 2010512211A JP 2010529986 A5 JP2010529986 A5 JP 2010529986A5
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JP
Japan
Prior art keywords
independently
compound
alkyl
halo
pharmaceutical composition
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JP2010512211A
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English (en)
Japanese (ja)
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JP2010529986A (ja
JP5513378B2 (ja
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Priority claimed from PCT/US2008/007458 external-priority patent/WO2008156707A1/en
Publication of JP2010529986A publication Critical patent/JP2010529986A/ja
Publication of JP2010529986A5 publication Critical patent/JP2010529986A5/ja
Application granted granted Critical
Publication of JP5513378B2 publication Critical patent/JP5513378B2/ja
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JP2010512211A 2007-06-15 2008-06-13 治療化合物 Active JP5513378B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US93474307P 2007-06-15 2007-06-15
US60/934,743 2007-06-15
US7038608P 2008-03-21 2008-03-21
US61/070,386 2008-03-21
PCT/US2008/007458 WO2008156707A1 (en) 2007-06-15 2008-06-13 Therapeutic compounds

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2014066482A Division JP6063410B2 (ja) 2007-06-15 2014-03-27 治療化合物

Publications (3)

Publication Number Publication Date
JP2010529986A JP2010529986A (ja) 2010-09-02
JP2010529986A5 true JP2010529986A5 (enExample) 2011-08-04
JP5513378B2 JP5513378B2 (ja) 2014-06-04

Family

ID=40156534

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2010512211A Active JP5513378B2 (ja) 2007-06-15 2008-06-13 治療化合物
JP2014066482A Expired - Fee Related JP6063410B2 (ja) 2007-06-15 2014-03-27 治療化合物

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2014066482A Expired - Fee Related JP6063410B2 (ja) 2007-06-15 2014-03-27 治療化合物

Country Status (4)

Country Link
US (2) US8586634B2 (enExample)
EP (1) EP2164324B1 (enExample)
JP (2) JP5513378B2 (enExample)
WO (1) WO2008156707A1 (enExample)

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* Cited by examiner, † Cited by third party
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GB0905515D0 (en) * 2009-03-31 2009-05-13 Ge Healthcare Ltd Radiolabelling methods
US9024071B2 (en) * 2009-05-05 2015-05-05 University Of Florida Research Foundation, Inc. Therapeutic compounds
WO2012030957A2 (en) 2010-09-01 2012-03-08 Arena Pharmaceuticals, Inc. Non-hygroscopic salts of 5-ht2c agonists
US20130267500A1 (en) 2010-09-01 2013-10-10 Arena Pharmaceuticals, Inc. 5-ht2c receptor agonists in the treatment of disorders ameliorated by reduction of norepinephrine level
MX2013002422A (es) 2010-09-01 2013-05-17 Arena Pharm Inc Sales de lorcaserina con acidos opticamente activos.
CN103347523A (zh) 2010-09-01 2013-10-09 艾尼纳制药公司 向具有肾损伤的个体给药氯卡色林
KR20180118801A (ko) 2010-09-01 2018-10-31 에자이 알앤드디 매니지먼트 가부시키가이샤 체중 관리에 유용한 5-ht2c 작동제의 변형-방출 투여 형태
WO2014058441A1 (en) 2012-10-09 2014-04-17 Arena Pharmaceuticals, Inc. Method of weight management
WO2015066344A1 (en) 2013-11-01 2015-05-07 Arena Pharmaceuticals, Inc. 5-ht2c receptor agonists and compositions and methods of use
ES2967976T3 (es) 2014-05-19 2024-05-06 Univ Northeastern Compuestos dirigidos a receptor de serotonina
BR112017024745A2 (pt) 2015-05-19 2018-11-13 Univ Northeastern compostos e métodos para modulação de receptores de serotonina na periferia.
WO2023288027A1 (en) * 2021-07-14 2023-01-19 Northeastern University Serotonin 5-ht2a, 5-ht2b, and 5-ht2c receptor inverse agonists
EP4486448A1 (en) 2022-03-04 2025-01-08 Reset Pharmaceuticals, Inc. Co-crystals or salts comprising psilocin

Family Cites Families (17)

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Publication number Priority date Publication date Assignee Title
CH427780A (de) 1962-08-30 1967-01-15 Sandoz Ag Verfahren zur Herstellung von neuen Aryl-tetralyl-Verbindungen
FR1480455A (fr) 1965-05-05 1967-05-12 Geigy Ag J R Méthano-benzazocines et leur préparation
FR2319332A1 (fr) * 1975-07-28 1977-02-25 Roussel Uclaf Nouveaux derives de l'aminobenzocycloheptene et leurs sels, procede de preparation et application a titre de medicaments desdits produits
FR2353519A1 (fr) 1975-12-08 1977-12-30 Roussel Uclaf Nouveaux derives de l'aminobenzocycloheptene et leurs sels, procede de preparation et application a titre de medicaments desdits produits
HU199805B (en) 1986-01-16 1990-03-28 Schering Corp Process for producing condensed benzazepine derivatives and pharmaceutical compositions comprising such compounds
KR950000699B1 (ko) 1988-07-29 1995-01-27 쉐링 코포레이션 헥사하이드로-벤조[d]나프토[2,1-b]아제핀에 대한 중간물질의 에난티오특이 합성방법
JPH05217455A (ja) 1992-01-31 1993-08-27 Tanaka Kikinzoku Kogyo Kk 電気接点の製造方法
US5461147A (en) 1993-09-27 1995-10-24 Schering Corporation Process for preparing benzazepine intermediates for the synthesis of D1 antagonists
WO2000055205A1 (en) 1999-03-15 2000-09-21 Merck & Co., Inc. ISOFORMS OF MOUSE SEROTONIN 5-HT2c RECEPTOR
US6875866B2 (en) * 2002-02-21 2005-04-05 Schering Corporation Process for synthesis of D1 receptor antagonists
WO2003072093A1 (en) * 2002-02-22 2003-09-04 The Regent Of The University Of California METHOD OF TREATMENT OF HYPERTENSION USING SELECTIVE SEROTONIN RE-UPTAKE INHIBITORS (SSRIs)
EP1449538A1 (en) 2003-02-21 2004-08-25 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. Inhibition of TACE or amphiregulin for the modulation of EGF receptor signal transactivation
US7504391B2 (en) 2003-05-22 2009-03-17 Schering Corporation Selective D1/D5 receptor antagonists for the treatment of obesity and CNS disorders
US7115767B2 (en) 2003-07-18 2006-10-03 Abbott Laboratories Tetraline derivatives as ghrelin receptor modulators
WO2005101979A2 (en) * 2004-04-22 2005-11-03 Mor Research Applications Ltd. Method of food intake management
CA2604887A1 (en) * 2005-04-07 2006-10-19 Hythiam, Inc. Improved methods of and compositions for the prevention of anxiety, substance abuse, and dependence
US8053603B2 (en) * 2006-01-06 2011-11-08 Sunovion Pharmaceuticals Inc. Tetralone-based monoamine reuptake inhibitors

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