RU2470016C2 - Производное бипиразола - Google Patents

Производное бипиразола Download PDF

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RU2470016C2
RU2470016C2 RU2010119648/04A RU2010119648A RU2470016C2 RU 2470016 C2 RU2470016 C2 RU 2470016C2 RU 2010119648/04 A RU2010119648/04 A RU 2010119648/04A RU 2010119648 A RU2010119648 A RU 2010119648A RU 2470016 C2 RU2470016 C2 RU 2470016C2
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pharmaceutically acceptable
bipyrazolyl
hydroxyadamantan
obesity
butyl
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RU2010119648A (ru
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Кевин Уилльям АНДЕРСОН
Надер ФОТУИ
Пол ДЖИЛЛЕСПАЙ
Роберт Алан Джр. ГУДНАУ
Кевин Ричард ГУИРТИН
Нанси-Эллен ХЕЙНЕС
Майкл Пол МАЙЕРС
Шерри Линн ПИТРАНИКОКОУЛ
Лида ЦИ
Памела Лорин РОССМАН
Натан Роберт СКОТТ
Кшитий Чхабилбхай ТАККАР
Джефферсон Райт ТИЛЛИ
Цян Чжан
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Ф.Хоффманн-Ля Рош Аг
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    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond

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  • Obesity (AREA)
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Abstract

Изобретение относится к фармацевтической композиции для лечения диабета, ожирения или метаболического синдрома, которая включает терапевтически эффективное количество (5-гидроксиадамантан-2-ил)амида транс-2'-трет-бутил-2'H-[1,3']бипиразолил-4'-карбоновой кислоты или его фармацевтически приемлемых солей, и фармацевтически приемлемый носитель. Изобретение также относится и к применению вышеназванного соединения для приготовления лекарственного средства, предназначенного для лечения указанных выше заболеваний. 2 н.п. ф-лы, 1 табл., 99 пр.

Description

Текст описания приведен в факсимильном виде.
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Claims (2)

1. Фармацевтическая композиция для лечения диабета, ожирения или метаболического синдрома, включающая терапевтически эффективное количество (5-гидроксиадамантан-2-ил)амида транс-2'-трет-бутил-2'H-[1,3']бипиразолил-4'-карбоновой кислоты или его фармацевтически приемлемых солей, и фармацевтически приемлемый носитель.
2. Применение (5-гидроксиадамантан-2-ил)амида транс-2'-трет-бутил-2'H-[1,3']бипиразолил-4'-карбоновой кислоты для приготовления лекарственных средств, предназначенных для лечения диабета, ожирения или метаболического синдрома.
RU2010119648/04A 2006-03-22 2007-03-12 Производное бипиразола RU2470016C2 (ru)

Applications Claiming Priority (4)

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US78483106P 2006-03-22 2006-03-22
US60/784,831 2006-03-22
US87527406P 2006-12-15 2006-12-15
US60/875,274 2006-12-15

Related Parent Applications (1)

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RU2008141434/04A Division RU2402517C2 (ru) 2006-03-22 2007-03-12 Пиразолы в качестве ингибиторов 11-бета-hsd-1

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RU2010119648A RU2010119648A (ru) 2011-11-27
RU2470016C2 true RU2470016C2 (ru) 2012-12-20

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RU2010119648/04A RU2470016C2 (ru) 2006-03-22 2007-03-12 Производное бипиразола
RU2008141434/04A RU2402517C2 (ru) 2006-03-22 2007-03-12 Пиразолы в качестве ингибиторов 11-бета-hsd-1

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US (1) US7728029B2 (ru)
EP (2) EP1999114B1 (ru)
JP (1) JP5031817B2 (ru)
KR (2) KR20110007258A (ru)
CN (1) CN101405270B (ru)
AR (1) AR059983A1 (ru)
AU (1) AU2007228887B2 (ru)
BR (1) BRPI0708974A2 (ru)
CA (1) CA2645856C (ru)
CR (1) CR10288A (ru)
DK (1) DK1999114T3 (ru)
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HK (1) HK1130780A1 (ru)
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MX (1) MX2008012017A (ru)
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NZ (1) NZ570973A (ru)
PL (1) PL1999114T3 (ru)
PT (1) PT1999114E (ru)
RS (1) RS54216B1 (ru)
RU (2) RU2470016C2 (ru)
SG (1) SG155961A1 (ru)
SI (1) SI1999114T1 (ru)
TW (2) TW201103916A (ru)
WO (1) WO2007107470A2 (ru)

Families Citing this family (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2630665C (en) 2005-11-21 2011-03-15 Shionogi & Co., Ltd. Heterocyclic compound having inhibitory activity on 11-.beta.-hydroxysteroid dehydrogenase type i
EP2610241A1 (en) * 2006-11-02 2013-07-03 Shionogi & Co., Ltd. Process for production of hydroxyadamantaneamine
TW200827346A (en) 2006-11-03 2008-07-01 Astrazeneca Ab Chemical compounds
US20100144717A1 (en) * 2006-12-15 2010-06-10 Janelle Comita-Prevoir 2-quinolinone and 2-quinoxalinone-derivatives and their use as antibacterial agents
TW200836719A (en) 2007-02-12 2008-09-16 Astrazeneca Ab Chemical compounds
CN103288738B (zh) * 2007-05-18 2016-03-16 盐野义制药株式会社 具有11β-羟基类固醇脱氢酶I型抑制活性的含氮杂环衍生物
RU2440989C2 (ru) * 2007-07-17 2012-01-27 Ф.Хоффманн-Ля Рош Аг ИНГИБИТОРЫ 11β-ГИДРОКСИСТЕРОИДНОЙ ДЕГИДРОГЕНАЗЫ
EP2025674A1 (de) 2007-08-15 2009-02-18 sanofi-aventis Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
EP2072497A1 (de) * 2007-12-21 2009-06-24 Bayer CropScience AG Verfahren zum Herstellen von 2-Fluoracyl-3-amino-acrylsäure-Derivaten
US7951833B2 (en) * 2008-02-04 2011-05-31 Astrazeneca Ab Crystalline forms of 4-[4-(2-adamantylcarbamoyl)-5-tert-butyl-pyrazol-1-yl]Benzoic acid 471
CN102300851A (zh) * 2009-01-30 2011-12-28 阿斯利康(瑞典)有限公司 制备含羧基的吡唑酰氨基化合物597的新方法
EP2243479A3 (en) 2009-04-20 2011-01-19 Abbott Laboratories Novel amide and amidine derivates and uses thereof
US8871208B2 (en) * 2009-12-04 2014-10-28 Abbvie Inc. 11-β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitors and uses thereof
EP2518051A4 (en) * 2009-12-22 2013-10-16 Shionogi & Co ADAMANTANAMINE DERIVATIVE
CN102127583A (zh) * 2010-01-19 2011-07-20 上海博康精细化工有限公司 一种反式对氨基金刚烷醇的制备方法
WO2011107494A1 (de) 2010-03-03 2011-09-09 Sanofi Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung
US8680098B2 (en) 2010-03-05 2014-03-25 Janssen Pharmaceutica, Nv Substituted aza-bicyclic imidazole derivatives useful as TRPM8 receptor modulators
EP2582709B1 (de) 2010-06-18 2018-01-24 Sanofi Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen
US8530413B2 (en) 2010-06-21 2013-09-10 Sanofi Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments
TW201215388A (en) 2010-07-05 2012-04-16 Sanofi Sa (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments
TW201221505A (en) 2010-07-05 2012-06-01 Sanofi Sa Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament
TW201215387A (en) 2010-07-05 2012-04-16 Sanofi Aventis Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament
CN103209957A (zh) 2010-08-09 2013-07-17 盐野义制药株式会社 氨基金刚烷氨基甲酸酯衍生物的制备方法
JP5605104B2 (ja) * 2010-09-10 2014-10-15 セントラル硝子株式会社 ピラゾール化合物の製造方法
EP2683704B1 (de) 2011-03-08 2014-12-17 Sanofi Verzweigte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung
US8871758B2 (en) 2011-03-08 2014-10-28 Sanofi Tetrasubstituted oxathiazine derivatives, method for producing them, their use as medicine and drug containing said derivatives and the use thereof
WO2012120054A1 (de) 2011-03-08 2012-09-13 Sanofi Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung
EP2683699B1 (de) 2011-03-08 2015-06-24 Sanofi Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung
US8901114B2 (en) 2011-03-08 2014-12-02 Sanofi Oxathiazine derivatives substituted with carbocycles or heterocycles, method for producing same, drugs containing said compounds, and use thereof
US8471027B2 (en) 2011-04-06 2013-06-25 Hoffmann-La Roche Inc. Adamantyl compounds
CH706864B1 (de) 2011-06-22 2016-03-31 Central Glass Co Ltd Verfahren zur Herstellung einer Pyrazol-Verbindung.
JP5915004B2 (ja) * 2011-06-22 2016-05-11 セントラル硝子株式会社 ピラゾール化合物の製造方法
JP2013023476A (ja) * 2011-07-22 2013-02-04 Sagami Chemical Research Institute 5−フルオロ−1h−ピラゾール−4−カルボン酸類の製造方法
WO2013037390A1 (en) 2011-09-12 2013-03-21 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
WO2013045413A1 (en) 2011-09-27 2013-04-04 Sanofi 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
JP5992054B2 (ja) 2011-11-29 2016-09-14 ノバルティス アーゲー ピラゾロピロリジン化合物
AR089656A1 (es) 2011-11-30 2014-09-10 Bayer Ip Gmbh Derivados de n-bicicloalquil- y n-tricicloalquil-(tio)-carboxamida fungicidas
CN102633659B (zh) * 2012-02-23 2013-12-04 浙江普洛康裕制药有限公司 一种反式4-氨基-1-羟基金刚烷盐酸盐的合成方法
NO2953942T3 (ru) 2013-02-06 2018-03-24
KR101763284B1 (ko) 2013-07-24 2017-07-31 볼보 컨스트럭션 이큅먼트 에이비 건설기계용 유압회로
EP3083566B1 (en) * 2013-11-27 2022-12-21 Bayer Animal Health GmbH Process for the preparation of 5-fluoro-1h-pyrazoles
MX2016006977A (es) 2013-11-27 2016-09-07 Bayer Cropscience Ag Proceso para la preparacion de 5-fluoro-1h-pirazoles.
MX2016008653A (es) 2014-01-03 2016-09-26 Bayer Animal Health Gmbh Nuevas pirazolil-heteroarilamidas como agentes plaguicidas.
CN105315284A (zh) * 2014-07-23 2016-02-10 上海医药工业研究院 阿拉格列汀中间体的制备方法
CN104961698A (zh) * 2015-07-13 2015-10-07 佛山市赛维斯医药科技有限公司 末端硝基取代的三氮唑亚砜类化合物、其制备方法及其用途
KR101759874B1 (ko) * 2015-08-07 2017-07-21 코스맥스 주식회사 11β-hydroxysteroid dehydrogenase type 1의 활성을 저해하는 화합물을 포함하는 화장료 조성물 또는 피부 외용제 조성물
EP3976599A1 (en) * 2019-05-24 2022-04-06 Fmc Corporation Pyrazole-substituted pyrrolidinones as herbicides

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004089896A1 (en) * 2003-04-11 2004-10-21 Novo Nordisk A/S 11β-HYDROXYSTEROID DEHYDROGENASE TYPE 1 ACTIVE COMPOUNDS
RU2005122936A (ru) * 2002-12-20 2006-01-20 Мерк энд Ко., Инк. (US) Производные триазола как ингибиторы 11-бета-гидроксистероиддегидрогеназы-1
RU2381217C2 (ru) * 2005-04-05 2010-02-10 Ф.Хоффман-Ля Рош Аг Пиразолы

Family Cites Families (54)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH307629A (de) 1952-05-23 1955-06-15 Ag J R Geigy Verfahren zur Herstellung eines monosubstituierten Hydrazins.
DE2635841C2 (de) 1976-08-10 1983-02-24 Dynamit Nobel Ag, 5210 Troisdorf Verfahren zur Herstellung von Alkoxymethylenmalonsäurenitrilen
US4620865A (en) 1983-11-07 1986-11-04 Eli Lilly And Company Herbicidal and algicidal 1,5-disubstituted-1H-pyrazole-4-carboxamides
US4742074A (en) 1984-10-29 1988-05-03 Sumitomo Chemical Company, Limited Pyrazolecarboxamide derivative and fungicide containing it as active ingredient
US4792565A (en) 1986-04-24 1988-12-20 Mitsui Toatsu Chemicals, Inc. Pyrazolecarbonylamine derivatives and agricultural and horticultural fungicides containing said compounds
DE4010797A1 (de) 1990-04-04 1991-10-10 Hoechst Ag Substituierte azole, verfahren zu deren herstellung, diese enthaltende mittel und deren verwendung
US6020121A (en) 1995-09-29 2000-02-01 Microcide Pharmaceuticals, Inc. Inhibitors of regulatory pathways
DE19615976A1 (de) 1996-04-22 1997-10-23 Basf Ag Mittel und Verfahren zur Bekämpfung von Schadpilzen
WO1998041519A1 (en) 1997-03-18 1998-09-24 Smithkline Beecham Corporation Novel cannabinoid receptor agonists
JP4398088B2 (ja) 1997-12-18 2010-01-13 ビーエーエスエフ ソシエタス・ヨーロピア アミド化合物及びモルホリン又はピペリジン誘導体を基礎とする殺菌剤混合物
WO1999067235A1 (fr) 1998-06-25 1999-12-29 Sumitomo Pharmaceuticals Co., Ltd. Composes cycliques a cinq elements
GB9824310D0 (en) 1998-11-05 1998-12-30 Univ London Activators of soluble guanylate cyclase
DE19853827A1 (de) 1998-11-21 2000-05-25 Aventis Cropscience Gmbh Kombinationen aus Herbiziden und Safenern
US20010044445A1 (en) 1999-04-08 2001-11-22 Bamaung Nwe Y. Azole inhibitors of cytokine production
US6331539B1 (en) 1999-06-10 2001-12-18 3M Innovative Properties Company Sulfonamide and sulfamide substituted imidazoquinolines
IL136360A (en) 1999-06-18 2004-08-31 Mitsui Chemicals Inc History 5 - Aminopyrazole-4 - Carboxylate and processes for their preparation
KR100743262B1 (ko) 1999-07-20 2007-07-27 다우 아그로사이언시즈 엘엘씨 살균성 헤테로고리 방향족 아미드 및 그 조성물, 사용 및제조방법
WO2001014339A2 (en) 1999-08-20 2001-03-01 Dow Agrosciences Llc Fungicidal heterocyclic aromatic amides and their compositions, methods of use and preparation
AU780572B2 (en) 1999-10-18 2005-04-07 University Of Connecticut, The Pyrazole derivatives as cannabinoid receptor antagonists
US6096898A (en) 1999-10-22 2000-08-01 Dow Agrosciences Llc One pot synthesis of 1,2,4-triazoles
US6569885B1 (en) 1999-12-23 2003-05-27 Icos Corporation Cyclic AMP-specific phosphodiesterase inhibitors
JP2002003410A (ja) 2000-06-27 2002-01-09 Fuji Photo Film Co Ltd 芳香族ハロゲン化物の製造方法。
WO2002044133A1 (en) 2000-11-28 2002-06-06 Pfizer Products Inc. Preparation of sodium-hydrogen exchanger type-1 inhibitors
PE20020870A1 (es) 2001-02-13 2002-11-18 Aventis Pharma Gmbh 6,7,8,9-tetrahidro-5h-benzocicloheptenil aminas aciladas
TWI243164B (en) 2001-02-13 2005-11-11 Aventis Pharma Gmbh Acylated indanyl amines and their use as pharmaceuticals
PE20020856A1 (es) 2001-02-13 2002-11-11 Aventis Pharma Gmbh 1,2,3,4-tetrahidronaftil aminas aciladas
WO2003028641A2 (en) 2001-10-01 2003-04-10 Taisho Pharmaceutical Co., Ltd. Mch receptor antagonists
CA2465207C (en) 2001-11-01 2011-01-04 Icagen, Inc. Pyrazole-amides and -sulfonamides
DE10161978A1 (de) 2001-12-17 2003-06-26 Bayer Ag Verfahren zur Herstellung von 2-Halogenacyl-3-amino-acrylsäure-derivate
MXPA04004685A (es) 2001-12-19 2004-08-12 Pfizer Prod Inc Procedimientos para preparar inhibidores de tipo-1 de intercambiador sodio-hidrogeno.
US6818772B2 (en) 2002-02-22 2004-11-16 Abbott Laboratories Antagonists of melanin concentrating hormone effects on the melanin concentrating hormone receptor
WO2003070244A1 (en) 2002-02-22 2003-08-28 Abbott Laboratories Antagonist of melanin concentrating hormone and their uses
US20030236287A1 (en) 2002-05-03 2003-12-25 Piotrowski David W. Positive allosteric modulators of the nicotinic acetylcholine receptor
EP1388535A1 (en) 2002-08-07 2004-02-11 Aventis Pharma Deutschland GmbH Acylated arylcycloalkylamines and their use as pharmaceuticals
CN1703395A (zh) 2002-08-09 2005-11-30 特兰斯泰克制药公司 芳基和杂芳基化合物以及调节凝血的方法
KR100729878B1 (ko) 2003-02-17 2007-06-18 에프. 호프만-라 로슈 아게 피페리딘-벤젠설폰아마이드 유도체
WO2004089416A2 (en) 2003-04-11 2004-10-21 Novo Nordisk A/S Combination of an 11beta-hydroxysteroid dehydrogenase type 1 inhibitor and an antihypertensive agent
EP1615667A2 (en) 2003-04-11 2006-01-18 Novo Nordisk A/S Combinations of an 11-beta-hydroxysteroid dehydrogenase type 1 inhibitor and a glucocorticoid receptor agonist
PL1618092T3 (pl) 2003-05-01 2011-02-28 Bristol Myers Squibb Co Związki amidopirazolowe z podstawnikami arylowymi jako inhibitory kinazy
US20040220170A1 (en) 2003-05-01 2004-11-04 Atkinson Robert N. Pyrazole-amides and sulfonamides as sodium channel modulators
WO2005000793A1 (ja) 2003-06-26 2005-01-06 Taisho Pharmaceutical Co., Ltd. 2位置換シクロアルキルカルボン酸誘導体
CA2526455C (en) 2003-06-26 2012-10-09 Novartis Ag 5-membered heterocycle-based p38 kinase inhibitors
CA2534221A1 (en) 2003-08-07 2005-02-24 Merck & Co., Inc. Pyrazole carboxamides as inhibitors of 11-beta-hydroxysteroid dehydrogenase-1
CA2535265C (en) 2003-08-22 2014-01-28 Dendreon Corporation Compositions and methods for the treatment of disease associated with trp-p8 expression
US7750160B2 (en) 2003-11-13 2010-07-06 Ambit Biosciences Corporation Isoxazolyl urea derivatives as kinase modulators
CN101367748B (zh) 2004-01-28 2014-03-12 三井化学株式会社 酰胺衍生物及其制备方法和作为杀虫剂的使用方法
CN1976905A (zh) 2004-03-30 2007-06-06 大正制药株式会社 嘧啶衍生物以及与其应用有关的治疗方法
DE102004023635A1 (de) 2004-05-10 2006-04-13 Grünenthal GmbH Heteroarylsubstituierte Cyclohexyl-1,4-diamin-Derivate
WO2006007864A1 (en) 2004-07-17 2006-01-26 Max Planck Geselllschaft Zur Förderung Der Wissenschaft Treating neurodegenerative conditions
GB0417910D0 (en) 2004-08-11 2004-09-15 Novartis Ag Organic compounds
WO2006031806A2 (en) 2004-09-10 2006-03-23 Atherogenics, Inc. 2-thiopyrimidinones as therapeutic agents
US20080090863A1 (en) 2004-09-30 2008-04-17 Taisho Pharmaceutical Co., Ltd. Pyridine Derivatives and Their Use as Medicaments for Treating Diseases Related to Mch Receptor
GB0506133D0 (en) 2005-03-24 2005-05-04 Sterix Ltd Compound
CA2630665C (en) * 2005-11-21 2011-03-15 Shionogi & Co., Ltd. Heterocyclic compound having inhibitory activity on 11-.beta.-hydroxysteroid dehydrogenase type i

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2005122936A (ru) * 2002-12-20 2006-01-20 Мерк энд Ко., Инк. (US) Производные триазола как ингибиторы 11-бета-гидроксистероиддегидрогеназы-1
WO2004089896A1 (en) * 2003-04-11 2004-10-21 Novo Nordisk A/S 11β-HYDROXYSTEROID DEHYDROGENASE TYPE 1 ACTIVE COMPOUNDS
RU2381217C2 (ru) * 2005-04-05 2010-02-10 Ф.Хоффман-Ля Рош Аг Пиразолы

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