NO20081772L - Ikke-basiske antagonister av melaninkonsentrerende hormon-reseptor-1 - Google Patents
Ikke-basiske antagonister av melaninkonsentrerende hormon-reseptor-1Info
- Publication number
- NO20081772L NO20081772L NO20081772A NO20081772A NO20081772L NO 20081772 L NO20081772 L NO 20081772L NO 20081772 A NO20081772 A NO 20081772A NO 20081772 A NO20081772 A NO 20081772A NO 20081772 L NO20081772 L NO 20081772L
- Authority
- NO
- Norway
- Prior art keywords
- formula
- present application
- melanin
- antagonists
- basic
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A61K31/52—Purines, e.g. adenine
- A61K31/522—Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Child & Adolescent Psychology (AREA)
- Emergency Medicine (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Saccharide Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US73045305P | 2005-10-26 | 2005-10-26 | |
| US11/586,255 US8618115B2 (en) | 2005-10-26 | 2006-10-25 | Substituted thieno[3,2-d]pyrimidinones as MCHR1 antagonists and methods for using them |
| PCT/US2006/041725 WO2007050726A2 (fr) | 2005-10-26 | 2006-10-26 | Antagonistes du recepteur 1 de l'hormone de concentration de la melanine non basiques |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO20081772L true NO20081772L (no) | 2008-05-19 |
Family
ID=37888159
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20081772A NO20081772L (no) | 2005-10-26 | 2008-04-11 | Ikke-basiske antagonister av melaninkonsentrerende hormon-reseptor-1 |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US8618115B2 (fr) |
| EP (2) | EP1948665B1 (fr) |
| JP (1) | JP2009513658A (fr) |
| KR (1) | KR20080067681A (fr) |
| AR (1) | AR056155A1 (fr) |
| AU (1) | AU2006306140A1 (fr) |
| BR (1) | BRPI0617945A2 (fr) |
| CA (1) | CA2627653A1 (fr) |
| EA (1) | EA016126B1 (fr) |
| GE (1) | GEP20115213B (fr) |
| IL (1) | IL190898A0 (fr) |
| NO (1) | NO20081772L (fr) |
| NZ (1) | NZ567659A (fr) |
| PE (1) | PE20070532A1 (fr) |
| TW (1) | TW200728289A (fr) |
| WO (1) | WO2007050726A2 (fr) |
Families Citing this family (34)
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|---|---|---|---|---|
| US7285557B2 (en) * | 2001-10-15 | 2007-10-23 | Smithkline Beecham P.L.C. | Pyrimidinones as melanin concentrating hormone receptor 1 |
| US7553836B2 (en) * | 2006-02-06 | 2009-06-30 | Bristol-Myers Squibb Company | Melanin concentrating hormone receptor-1 antagonists |
| AU2007283113A1 (en) | 2006-08-08 | 2008-02-14 | Sanofi-Aventis | Arylaminoaryl-alkyl-substituted imidazolidine-2,4-diones, processes for preparing them, medicaments comprising these compounds, and their use |
| WO2008061109A2 (fr) * | 2006-11-15 | 2008-05-22 | Forest Laboratories Holdings Limited | Dérivés d'indazole utiles en tant que ligands des récepteurs de l'hormone concentrant la mélanine |
| JP2010525077A (ja) | 2007-04-25 | 2010-07-22 | ブリストル−マイヤーズ スクイブ カンパニー | 非塩基性メラニン凝集ホルモン受容体−1アンタゴニスト |
| EP2242745A1 (fr) * | 2008-02-07 | 2010-10-27 | Sanofi-Aventis | Nouvelles imidazolidines substituées par un phényle, procédé de production, médicaments contenant ces composés et leur utilisation |
| PE20091928A1 (es) * | 2008-05-29 | 2009-12-31 | Bristol Myers Squibb Co | Tienopirimidinas hidroxisustituidas como antagonistas de receptor-1 de hormona concentradora de melanina no basicos |
| US8470841B2 (en) | 2008-07-09 | 2013-06-25 | Sanofi | Heterocyclic compounds, processes for their preparation, medicaments comprising these compounds, and the use thereof |
| CN102272135A (zh) * | 2008-10-08 | 2011-12-07 | 百时美施贵宝公司 | 唑并吡咯酮黑色素浓集激素受体-1拮抗剂 |
| US8580959B2 (en) | 2008-10-08 | 2013-11-12 | Bristol-Myers Squibb Company | Azolotriazinone melanin concentrating hormone receptor-1 antagonists |
| WO2010068601A1 (fr) | 2008-12-08 | 2010-06-17 | Sanofi-Aventis | Hydrate de fluoroglycoside hétéroaromatique cristallin, ses procédés de fabrication, ses procédés d'utilisation et compositions pharmaceutiques le contenant |
| US8278316B2 (en) | 2009-03-09 | 2012-10-02 | Bristol-Myers Squibb Company | Aza pyridone analogs useful as melanin concentrating hormone receptor-1 antagonists |
| EP2405913A1 (fr) | 2009-03-09 | 2012-01-18 | Bristol-Myers Squibb Company | Analogues de pyridone utiles comme antagonistes du récepteur 1 de l'hormone concentrant la mélanine |
| JP2013503135A (ja) | 2009-08-26 | 2013-01-31 | サノフイ | 新規な結晶性複素芳香族フルオログリコシド水和物、その化合物を含んでなる医薬及びその使用 |
| EP2683699B1 (fr) | 2011-03-08 | 2015-06-24 | Sanofi | Dérivés oxathiazine di- et tri-substitués, procédé pour leur préparation, utilisation en tant que médicament, agent pharmaceutique contenant ces dérivés et utilisation |
| EP2683704B1 (fr) | 2011-03-08 | 2014-12-17 | Sanofi | Dérivés oxathiazine ramifiés, procédé pour leur préparation, utilisation en tant que médicament, agents pharmaceutiques contenant ces dérivés et leur utilisation |
| EP2766349B1 (fr) | 2011-03-08 | 2016-06-01 | Sanofi | Dérivés d'oxathiazine substitués par des carbocycles ou des hétérocycles, leur procédé de préparation, médicaments contenant ces composés et leur utilisation |
| WO2012120056A1 (fr) | 2011-03-08 | 2012-09-13 | Sanofi | Dérivés oxathiazine tétra-substitués, procédé pour leur préparation, utilisation en tant que médicament, agent pharmaceutique contenant ces dérivés et utilisation |
| WO2012120054A1 (fr) | 2011-03-08 | 2012-09-13 | Sanofi | Dérivés oxathiazine di- et tri-substitués, procédé pour leur préparation, utilisation en tant que médicament, agent pharmaceutique contenant ces dérivés et utilisation |
| HUP1100241A3 (en) | 2011-05-06 | 2013-12-30 | Richter Gedeon Nyrt | Oxetane substituted pyrimidones |
| CN103130819B (zh) * | 2011-12-01 | 2016-01-20 | 中国科学院上海药物研究所 | 噻吩[3,2-d]并嘧啶-4-酮类化合物、其制备方法、药物组合物及用途 |
| WO2014078568A1 (fr) | 2012-11-14 | 2014-05-22 | The Johns Hopkins University | Méthodes et compositions pour le traitement de la schizophrénie |
| WO2015114663A1 (fr) | 2014-01-30 | 2015-08-06 | Council Of Scientific & Industrial Research | Nouveaux composés thiéno [2,3-d] pyrimidin-4 (3h)-one à propriétés antimycobactériennes |
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| MA41291A (fr) | 2014-12-30 | 2017-11-07 | Forma Therapeutics Inc | Dérivés de la pyrrolotriazinone et de l'imidazotriazinone en tant qu'inhibiteurs de la protéase spécifique de l'ubiquitine n° 7 (usp7) pour le traitement d'un cancer |
| JP2018504430A (ja) | 2015-02-05 | 2018-02-15 | フォーマ セラピューティクス,インコーポレイテッド | ユビキチン特異的プロテアーゼ7阻害物質としてのキナゾリノン及びアザキナゾリノン |
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| JP2018504431A (ja) | 2015-02-05 | 2018-02-15 | フォーマ セラピューティクス,インコーポレイテッド | ユビキチン特異的プロテアーゼ7阻害物質としてのチエノピリミジノン |
| DK3386591T3 (da) | 2015-12-09 | 2020-09-28 | Cadent Therapeutics Inc | Heteroaromatic nmda receptor modulators and uses thereof |
| WO2017100593A1 (fr) | 2015-12-09 | 2017-06-15 | Luc Therapeutics | Modulateurs de récepteurs nmda de type thiénopyrimidinone et utilisations associées |
| CN107216339B (zh) * | 2016-03-22 | 2021-05-04 | 中国科学院上海药物研究所 | 一种dppiv抑制剂马来酸盐的多晶型及其制备方法 |
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| CA3175193A1 (fr) * | 2020-04-08 | 2021-10-14 | Dominic Reynolds | Composes et procedes de modulation de l'epissage |
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| US6147089A (en) | 1998-09-17 | 2000-11-14 | Pfizer Inc. | Annulated 4-carboxyamino-2-methyl-1,2,3,4,-tetrahydroquinolines |
| WO2000030665A1 (fr) | 1998-11-25 | 2000-06-02 | Nutri Pharma Asa | Composition contenant des proteines de soja, des fibres alimentaires et un compose de phytoestrogene et son utilisation pour la prevention et/ou le traitement de maladies cardiovasculaires |
| WO2000038722A1 (fr) | 1998-12-23 | 2000-07-06 | G.D. Searle & Co. | COMBINAISONS D'INHIBITEURS DE LA PROTEINE DE TRANSFERT DE L'ESTER DE CHOLESTERYLE ET D'INHIBITEURS DE LA HMG CoA-REDUCTASE UTILISEES DANS LE CADRE DE TROUBLES CARDIO-VASCULAIRES |
| GB9828442D0 (en) | 1998-12-24 | 1999-02-17 | Karobio Ab | Novel thyroid receptor ligands and method II |
| DE60027551T2 (de) | 1999-02-24 | 2007-05-10 | The Johns Hopkins University | Zusammensetzungen und verfahren zur regulierung des serumcholesterins |
| WO2000073288A1 (fr) | 1999-05-28 | 2000-12-07 | Vertex Pharmaceuticals Incorporated | Procede de preparation d'oxazoles substitues en position 5 |
| US6414002B1 (en) * | 1999-09-22 | 2002-07-02 | Bristol-Myers Squibb Company | Substituted acid derivatives useful as antidiabetic and antiobesity agents and method |
| CN1444573A (zh) | 2000-07-31 | 2003-09-24 | 史密丝克莱恩比彻姆有限公司 | 甲酰胺化合物及其作为人11cby受体拮抗剂的用途 |
| JPWO2002101146A1 (ja) | 2001-05-11 | 2004-10-14 | 阿里奈 中山 | 蓄光紙及びその製造方法並びにその利用方法 |
| GB0124627D0 (en) | 2001-10-15 | 2001-12-05 | Smithkline Beecham Plc | Novel compounds |
| KR20040048995A (ko) | 2001-10-25 | 2004-06-10 | 다케다 야쿠힌 고교 가부시키가이샤 | 퀴놀린 화합물 |
| CN1747949A (zh) | 2002-12-20 | 2006-03-15 | 法马西亚公司 | 无环吡唑化合物 |
| CA2521832A1 (fr) | 2003-04-11 | 2004-10-28 | Smithkline Beecham Corporation | Antagonistes heterocycliques de mchr1 |
| JP2006193426A (ja) | 2003-09-05 | 2006-07-27 | Sankyo Co Ltd | 置換された縮環ピリミジン−4(3h)−オン化合物 |
| JP2007509158A (ja) | 2003-10-23 | 2007-04-12 | グラクソ グループ リミテッド | 肥満、糖尿病、うつ病及び不安を治療するためのmchr1アンタゴニストとしての3−(4−アミノフェニル)チエノピリミド−4−オン誘導体 |
| US20050176738A1 (en) | 2003-11-07 | 2005-08-11 | Neurocrine Biosciences, Inc. | Melanin-concentrating hormone receptor antagonists and compositions and methods related thereto |
| WO2005103039A1 (fr) | 2004-04-15 | 2005-11-03 | Neurocrine Biosciences, Inc. | 2- (3-aminopyrrolidin-1-yl) pyridines utilisees comme antagonistes du recepteur de l'hormone concentrant la melanine, et compositions et procedes associes |
| RU2266906C1 (ru) | 2004-04-29 | 2005-12-27 | Общество с ограниченной ответственностью "Исследовательский Институт Химического Разнообразия" (ООО "Исследовательский Институт Химического Разнообразия") | Анелированные карбамоилазагетероциклы, способы их получения (варианты), фармацевтическая композиция, фокусированная библиотека |
| US7745447B2 (en) * | 2005-10-26 | 2010-06-29 | Bristol-Myers Squibb Company | Substituted thieno[3,2-D]pyrimidines as non-basic melanin concentrating hormone receptor-1 antagonists |
| US7553836B2 (en) | 2006-02-06 | 2009-06-30 | Bristol-Myers Squibb Company | Melanin concentrating hormone receptor-1 antagonists |
-
2006
- 2006-10-25 AR ARP060104665A patent/AR056155A1/es not_active Application Discontinuation
- 2006-10-25 US US11/586,255 patent/US8618115B2/en active Active
- 2006-10-26 PE PE2006001304A patent/PE20070532A1/es not_active Application Discontinuation
- 2006-10-26 AU AU2006306140A patent/AU2006306140A1/en not_active Abandoned
- 2006-10-26 CA CA002627653A patent/CA2627653A1/fr not_active Abandoned
- 2006-10-26 JP JP2008537932A patent/JP2009513658A/ja not_active Withdrawn
- 2006-10-26 WO PCT/US2006/041725 patent/WO2007050726A2/fr not_active Ceased
- 2006-10-26 EP EP06817387A patent/EP1948665B1/fr active Active
- 2006-10-26 NZ NZ567659A patent/NZ567659A/en not_active IP Right Cessation
- 2006-10-26 GE GEAP200610710A patent/GEP20115213B/en unknown
- 2006-10-26 KR KR1020087012373A patent/KR20080067681A/ko not_active Ceased
- 2006-10-26 EP EP10013754A patent/EP2298776A1/fr not_active Withdrawn
- 2006-10-26 BR BRPI0617945-2A patent/BRPI0617945A2/pt not_active IP Right Cessation
- 2006-10-26 EA EA200801165A patent/EA016126B1/ru not_active IP Right Cessation
- 2006-10-26 TW TW095139575A patent/TW200728289A/zh unknown
-
2008
- 2008-04-11 NO NO20081772A patent/NO20081772L/no not_active Application Discontinuation
- 2008-04-15 IL IL190898A patent/IL190898A0/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US20070093509A1 (en) | 2007-04-26 |
| JP2009513658A (ja) | 2009-04-02 |
| AU2006306140A1 (en) | 2007-05-03 |
| AR056155A1 (es) | 2007-09-19 |
| NZ567659A (en) | 2011-06-30 |
| PE20070532A1 (es) | 2007-06-14 |
| GEP20115213B (en) | 2011-05-10 |
| WO2007050726A3 (fr) | 2007-08-30 |
| IL190898A0 (en) | 2008-11-03 |
| EP2298776A1 (fr) | 2011-03-23 |
| KR20080067681A (ko) | 2008-07-21 |
| EA200801165A1 (ru) | 2008-10-30 |
| BRPI0617945A2 (pt) | 2011-08-09 |
| TW200728289A (en) | 2007-08-01 |
| CA2627653A1 (fr) | 2007-05-03 |
| EA016126B1 (ru) | 2012-02-28 |
| EP1948665B1 (fr) | 2013-02-27 |
| US8618115B2 (en) | 2013-12-31 |
| EP1948665A2 (fr) | 2008-07-30 |
| WO2007050726A2 (fr) | 2007-05-03 |
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