JP2001518468A5 - - Google Patents

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Publication number
JP2001518468A5
JP2001518468A5 JP2000513838A JP2000513838A JP2001518468A5 JP 2001518468 A5 JP2001518468 A5 JP 2001518468A5 JP 2000513838 A JP2000513838 A JP 2000513838A JP 2000513838 A JP2000513838 A JP 2000513838A JP 2001518468 A5 JP2001518468 A5 JP 2001518468A5
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JP
Japan
Prior art keywords
halogen
hydrogen
och
compound
group
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
JP2000513838A
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English (en)
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JP2001518468A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US1998/020427 external-priority patent/WO1999016752A1/en
Publication of JP2001518468A publication Critical patent/JP2001518468A/ja
Publication of JP2001518468A5 publication Critical patent/JP2001518468A5/ja
Pending legal-status Critical Current

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Description

【特許請求の範囲】
【請求項1】
以下の構造式を有する化合物または薬学的に受容可能なその塩。
【化1】
Figure 2001518468
{式中、
1およびR3は、水素、ハロゲン、アルキル、アリールアルキル、CF3およびOCH3からなる群から相互に独立に選択され、
2は、水素、ハロゲン、OH、OCH3、OCH2COOH、C(O)−アリール、NCS、NH2、N3、NHR8、NHCH2COOH、NHCOR13、NHCONHR13およびNHCOSR13からなる群から選択され、
4およびR5は、水素、OHおよびハロゲンからなる群から相互に独立に選択され、
6およびR7は、水素およびハロゲンからなる群から相互に独立に選択され、
8は、水素、炭素数1〜約8の低級アルキル、ハロゲン、OCH3およびCF3からなる群から選択され、
13は、水素、炭素数1〜約8の低級アルキル、フェニル、ハロゲン、OCH3、CF3および−CH2R’(式中、R’はハロゲンである。)からなる群から選択され、
1、R2およびR3の1つのみが、OCH3または水素であり、R4およびR5の一方のみが、OHである。}
【請求項2】
4がOHであり、R5が水素またはハロゲンである、請求項1に記載の化合物。
【請求項3】
5がOHであり、R4が水素またはハロゲンである、請求項1に記載の化合物。
【請求項4】
6およびR7が、それぞれハロゲンである、請求項1に記載の化合物。
【請求項5】
6およびR7が、それぞれ水素である、請求項1に記載の化合物。
【請求項6】
2がOCH3、NH2またはNHCOR13である、請求項1に記載の化合物。
【請求項7】
1およびR3がハロゲンである、請求項1に記載の化合物。
【請求項8】
1がハロゲンであり、R2がOCR3またはNH2であり、R3が水素である、請求項1に記載の化合物。
【請求項9】
5がOHであり、R4が水素またはハロゲンであり、R2がOCH3、NH2またはNHCOR13であり、R1およびR3がハロゲンである、請求項1に記載の化合物。
【請求項10】
薬学的に受容可能なキャリアと、請求項1〜9のいずれかに記載の化合物の少なくとも1つとを含む医薬組成物。
JP2000513838A 1997-09-30 1998-09-30 β3アドレナリン受容体拮抗薬、拮抗薬合成物およびこれらの応用方法 Pending JP2001518468A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US6115297P 1997-09-30 1997-09-30
US60/061,152 1997-09-30
PCT/US1998/020427 WO1999016752A1 (en) 1997-09-30 1998-09-30 β3-ADRENORECEPTOR AGONISTS, AGONIST COMPOSITIONS AND METHODS OF USING

Publications (2)

Publication Number Publication Date
JP2001518468A JP2001518468A (ja) 2001-10-16
JP2001518468A5 true JP2001518468A5 (ja) 2006-01-05

Family

ID=22033968

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2000513838A Pending JP2001518468A (ja) 1997-09-30 1998-09-30 β3アドレナリン受容体拮抗薬、拮抗薬合成物およびこれらの応用方法

Country Status (5)

Country Link
US (2) US6825213B2 (ja)
EP (1) EP1023269A4 (ja)
JP (1) JP2001518468A (ja)
AU (1) AU9512298A (ja)
WO (1) WO1999016752A1 (ja)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6043253A (en) * 1998-03-03 2000-03-28 Merck & Co., Inc. Fused piperidine substituted arylsulfonamides as β3-agonists
US6593341B2 (en) * 2001-03-29 2003-07-15 Molecular Design International, Inc. β3-adrenoreceptor agonists, agonist compositions and methods of making and using the same
AU782148B2 (en) * 2001-03-29 2005-07-07 Molecular Design International, Inc. Beta3-adrenoreceptor agonists, agonist compositions and methods of making and using the same
AU2003230665B2 (en) * 2002-03-13 2010-02-18 University Of Tennessee Research Foundation Substituted tetrahydroisoquinoline compounds, methods of making, and their use
US6596734B1 (en) 2002-10-11 2003-07-22 Molecular Design International, Inc. Tetrahydroisoquinoline compounds for use as β3-adrenoreceptor agonists
EP2225250A2 (en) * 2007-11-30 2010-09-08 Biota Scientific Management Pty Ltd Bicyclic ppat inhibitors as antibacterial agents
TW201038569A (en) * 2009-02-16 2010-11-01 Abbott Gmbh & Co Kg Heterocyclic compounds, pharmaceutical compositions containing them, and their use in therapy
KR101036882B1 (ko) * 2009-04-24 2011-05-25 주식회사 코스핀 공작기계의 스핀들용 부스터
TWI621438B (zh) * 2014-05-23 2018-04-21 資元堂生物科技股份有限公司 異喹啉生物鹼衍生物用於製備促進ampk活性的藥物之用途
CN105078992B (zh) * 2014-05-23 2017-11-21 资元堂生物科技股份有限公司 异喹啉生物碱衍生物用于制备促进ampk活性的药物的用途
WO2021034548A1 (en) * 2019-08-19 2021-02-25 The Board Of Trustees Of The Leland Stanford Junior University Mitochondrial modulation to improve metabolic syndrome during aging

Family Cites Families (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1250828B (de) * 1962-10-10 1967-09-28 Chinoin Gyogyszer es Vegyeszeti Termekek Gyära R.T., Budapest Verfahren zur Herstellung des spasmolytisch wirksamen 6,7,3',4' - Tetraäthoxy -l-benzyliden-1,2,3,4tetrahydroisochinolins und seiner Salze
US3497516A (en) * 1965-12-08 1970-02-24 Tanabe Seiyaku Co Tetrahydroisoquinoline compounds and preparation thereof
US3438989A (en) * 1967-03-10 1969-04-15 Warner Lambert Pharmaceutical Process for the production of ( ) dihydrothebainone
IL33480A (en) * 1968-12-10 1973-03-30 Tanabe Seiyaku Co 6,7-diacyloxy-tetrahydro-isoquinolines and their preparation
US3818015A (en) * 1970-12-17 1974-06-18 Tanabe Seiyaku Co 1(polymethoxybenzyl) 6 hydroxyl 1,2,3,4 tetrahydro isoquinolines
US3873704A (en) * 1970-12-17 1975-03-25 Tanabe Seiyaku Co Novel tetrahydroisoquinoline compounds in a pharmaceutical composition
US3910927A (en) * 1971-09-27 1975-10-07 Mead Johnson & Co 3-Hydroxyisoquinoline ethers
US3872130A (en) * 1971-09-27 1975-03-18 Mead Johnson & Co 1-hydroxyisoquinolones
US3910915A (en) * 1973-07-23 1975-10-07 Searle & Co 1-Aryl-2-{8 (substituted amino)alkanoyl{9 -1,2,3,4-tetrahydroisoquinolines
US3988339A (en) * 1974-02-08 1976-10-26 Smithkline Corporation Pharmaceutical compositions and methods of inhibiting phenylethanolamine N-methyltransferase
JPS5247474B2 (ja) * 1974-11-20 1977-12-02
JPS5295676A (en) 1976-02-05 1977-08-11 Dainippon Pharmaceut Co Ltd Tetrahydropapaverine derivatives
FR2368277A1 (fr) * 1976-10-21 1978-05-19 Sobio Lab Nouveaux derives hydrogenes de l'isoquinoleine, ayant une activite vasoactive et spasmolytique
US4321254A (en) * 1980-09-26 1982-03-23 Smithkline Corporation Antiallergic imidodisulfamides
US4456757A (en) * 1981-03-20 1984-06-26 Asahi Kasei Kogyo Kabushiki Kaisha Isoquinolinesulfonyl derivatives and process for the preparation thereof
BG38182A1 (en) * 1983-06-21 1985-11-15 Ivanova Tocolytic means
US4536510A (en) * 1983-07-22 1985-08-20 Smith Kline Beckman Corporation Method of antagonizing the effects of thromboxane
GB8518634D0 (en) * 1985-07-23 1985-08-29 Smithkline Beckman Corp Chemical compounds
JPH0667926B2 (ja) * 1985-11-12 1994-08-31 旭化成工業株式会社 環状のイソキノリンスルホンアミド誘導体
US4737504A (en) * 1986-07-25 1988-04-12 Ohio State University Research Foundation 5-fluoro-and 8-fluoro-trimetoquinol compounds and the processes for their preparation
DE3766472D1 (de) * 1986-10-28 1991-01-10 Smith Kline French Lab Tetrahydroisochinolin-2-yl-derivate von carbonsaeuren als thromboxan a2-antagonisten.
US4857301A (en) * 1987-09-25 1989-08-15 Schering Corporation Sulfonamide compounds, compositions and method of use
GB8807922D0 (en) * 1988-04-05 1988-05-05 Fujisawa Pharmaceutical Co Isoquinoline compound & process for preparation thereof
US5210088A (en) * 1989-09-20 1993-05-11 John Wyeth & Brother, Limited Method of treatment and heterocyclic compounds used therein
US5340811A (en) * 1990-03-08 1994-08-23 Asahi Kasei Kogyo Kabushiki Kaisha Isoquinoline-or quinoline-sulfonamide derivative and a pharmaceutical composition comprising the same
DE4026115A1 (de) * 1990-08-17 1992-02-20 Consortium Elektrochem Ind Verfahren zur herstellung von 1-alkylisochinolinderivaten
GB9027055D0 (en) * 1990-12-13 1991-02-06 Sandoz Ltd Organic compounds
US5362736A (en) * 1991-02-27 1994-11-08 Banyu Pharmaceutical Co., Ltd. Isoquinoline derivatives
US5238935A (en) * 1991-05-20 1993-08-24 Schering Corporation N-acyl-tetrahydroisoquinolines as inhibitors of acyl-coenzyme A: cholesterol acyl transferase
GB9127306D0 (en) * 1991-12-23 1992-02-19 Boots Co Plc Therapeutic agents
US5246943A (en) * 1992-05-19 1993-09-21 Warner-Lambert Company Substituted 1,2,3,4-tetahydroisoquinolines with angiotensin II receptor antagonist properties
JPH06247935A (ja) * 1993-02-25 1994-09-06 Banyu Pharmaceut Co Ltd 6,7−ジアルコキシ−3,4−ジヒドロイソキノリン−8−オール類、その製造法及び該化合物を用いた6,7−ジアルコキシ−1,2,3,4−テトラヒドロイソキノリン−8−オール類の製造法
SK280108B6 (sk) * 1993-06-22 1999-08-06 Knoll Aktiengesellschaft Tetraizochinolínové deriváty, farmaceutické prostr
GB9322976D0 (en) * 1993-11-08 1994-01-05 Pfizer Ltd Therapeutic agents
GB9508622D0 (en) * 1995-04-28 1995-06-14 Pfizer Ltd Therapeutic agants
US5707985A (en) * 1995-06-07 1998-01-13 Tanabe Seiyaku Co. Ltd. Naphthyl-, quinolyl- and isoquinolyl- sulfonamide derivatives as cell adhesion modulators
KR19990082174A (ko) * 1996-02-02 1999-11-25 니뽄 신야쿠 가부시키가이샤 이소퀴놀린 유도체 및 의약
TW436484B (en) * 1996-04-24 2001-05-28 Dev Center Biotechnology 1,2,3,4-tetrahydroisoquinoline derivatives having a nitrogen-containing heterocyclic methyl substituent, the preparation process and pharmaceutical composition thereof
US5929085A (en) * 1996-11-06 1999-07-27 Astra Aktiebolag Amidine and isothiourea derivatives, compositions containing them and their use as inhibitors of nitric oxide synthase
US5880285A (en) * 1996-12-23 1999-03-09 Roche Vitamins Inc. Process for manufacture of optically active isochinole compounds
GB9726695D0 (en) * 1997-12-17 1998-02-18 Smithkline Beecham Plc Novel compounds
DZ2446A1 (fr) * 1997-03-18 2003-01-11 Smithkline Beecham Plc Nouveaux composés
ES2241133T3 (es) * 1997-04-28 2005-10-16 Encysive Pharmaceuticals Inc. Sulfamidas para el tratamiento de los trastornos inducidos por la endotelina.
US6063925A (en) * 1997-09-17 2000-05-16 B.I. Chemicals, Inc. Separation of enantiomers of octahydroisoquinoline
GB9724372D0 (en) * 1997-11-18 1998-01-14 Smithkline Beecham Plc Novel compounds
AU2790999A (en) 1998-03-03 1999-09-20 Merck & Co., Inc. Fused piperidine substituted arylsulfonamides as beta3-agonists
US6043253A (en) * 1998-03-03 2000-03-28 Merck & Co., Inc. Fused piperidine substituted arylsulfonamides as β3-agonists
AU3768799A (en) * 1998-04-28 1999-11-16 Trega Biosciences, Inc. Isoquinoline compound melanocortin receptor ligands and methods of using same

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