MA28935B1 - Preparation et utilisation de derives de biphenyl-4-yl-carbonylamino-acide dans le traitement de l'obesite - Google Patents
Preparation et utilisation de derives de biphenyl-4-yl-carbonylamino-acide dans le traitement de l'obesiteInfo
- Publication number
- MA28935B1 MA28935B1 MA29831A MA29831A MA28935B1 MA 28935 B1 MA28935 B1 MA 28935B1 MA 29831 A MA29831 A MA 29831A MA 29831 A MA29831 A MA 29831A MA 28935 B1 MA28935 B1 MA 28935B1
- Authority
- MA
- Morocco
- Prior art keywords
- biphenyl
- obesity
- preparation
- treatment
- acid derivatives
- Prior art date
Links
- -1 BIPHENYL-4-YL CARBONYLAMINO Chemical class 0.000 title abstract 2
- 208000008589 Obesity Diseases 0.000 title abstract 2
- 239000002253 acid Substances 0.000 title abstract 2
- 235000020824 obesity Nutrition 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles 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 in position 2
- C07D235/30—Nitrogen atoms not forming part of a nitro radical
-
- 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
-
- 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
- A61P3/06—Antihyperlipidemics
-
- 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
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
- A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
- A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/12—Antidiuretics, e.g. drugs for diabetes insipidus
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
- C07D263/58—Benzoxazoles; Hydrogenated benzoxazoles 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 in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles 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 in position 2
- C07D277/82—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Emergency Medicine (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US61897504P | 2004-10-15 | 2004-10-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA28935B1 true MA28935B1 (fr) | 2007-10-01 |
Family
ID=36203612
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA29831A MA28935B1 (fr) | 2004-10-15 | 2007-04-17 | Preparation et utilisation de derives de biphenyl-4-yl-carbonylamino-acide dans le traitement de l'obesite |
Country Status (21)
| Country | Link |
|---|---|
| US (2) | US7759376B2 (fr) |
| EP (1) | EP1805156B1 (fr) |
| JP (1) | JP2008516978A (fr) |
| KR (1) | KR20070063546A (fr) |
| CN (1) | CN101087769A (fr) |
| AT (1) | ATE492542T1 (fr) |
| AU (1) | AU2005295453A1 (fr) |
| BR (1) | BRPI0516483A (fr) |
| CA (1) | CA2583784A1 (fr) |
| CR (1) | CR9034A (fr) |
| DE (1) | DE602005025517D1 (fr) |
| EA (1) | EA200700851A1 (fr) |
| EC (1) | ECSP077397A (fr) |
| ES (1) | ES2357015T3 (fr) |
| IL (1) | IL182218A0 (fr) |
| MA (1) | MA28935B1 (fr) |
| MX (1) | MX2007004217A (fr) |
| NO (1) | NO20072461L (fr) |
| TN (1) | TNSN07111A1 (fr) |
| WO (1) | WO2006044775A2 (fr) |
| ZA (1) | ZA200703002B (fr) |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ555683A (en) | 2004-12-14 | 2010-09-30 | Astrazeneca Ab | Oxadiazole derivatives as dgat inhibitors |
| AU2006318260B2 (en) | 2005-11-21 | 2012-05-17 | Anadys Pharmaceuticals, Inc. | Process for the preparation of 5-amino-3H- thiazolo [4 , 5 -d] pyrimidin- 2 -one |
| EP1966221A1 (fr) | 2005-12-22 | 2008-09-10 | AstraZeneca AB | Pyrimido-[4,5-]-oxazines pour utilisation en tant qu'inhibiteurs de dgat |
| SG10201408806UA (en) | 2006-03-31 | 2015-02-27 | Novartis Ag | New compounds |
| DE602007011446D1 (en) | 2006-05-30 | 2011-02-03 | Astrazeneca Ab | Substituierte 5-phenylamino-1,3,4-oxadiazol-2-ylcarbonylamino-4-phenoxycyclohexancarbonsäuren als inhibitoren von acetylcoenzym-a-diacylglycerolacyltransferase |
| WO2007138304A1 (fr) | 2006-05-30 | 2007-12-06 | Astrazeneca Ab | Dérivés du 1,3,4-oxadiazole en tant qu'inhibiteurs de dgat1 |
| KR100811100B1 (ko) | 2006-09-27 | 2008-03-06 | 한국생명공학연구원 | 벤즈아졸 유도체를 유효성분으로 함유하는 대사성 질환예방 및 치료용 약학적 조성물 |
| KR100795462B1 (ko) | 2006-09-27 | 2008-01-16 | 한국생명공학연구원 | 인돌 유도체, 이의 제조방법 및 이를 유효성분으로함유하는 대사성 질환 예방 및 치료용 약학적 조성물 |
| PE20080888A1 (es) | 2006-10-18 | 2008-08-26 | Novartis Ag | COMPUESTOS HETEROCICLICOS COMO INHIBIDORES DE LA ACIL-TRANSFERASA DE ACIL-CoA-DIACIL-GLICEROL 1 (DGAT1) |
| CN101600437A (zh) * | 2006-12-11 | 2009-12-09 | 诺瓦提斯公司 | 预防或治疗心肌缺血的方法 |
| CN101678019B (zh) | 2007-06-08 | 2016-03-30 | 詹森药业有限公司 | 哌啶/哌嗪衍生物 |
| ES2483898T3 (es) * | 2007-06-08 | 2014-08-08 | Janssen Pharmaceutica, N.V. | Derivados de piperidina/piperazina |
| JO2972B1 (en) | 2007-06-08 | 2016-03-15 | جانسين فارماسوتيكا ان. في | Piperidine / piperazine derivatives |
| JP5443342B2 (ja) | 2007-06-08 | 2014-03-19 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | ピペリジン/ピペラジン誘導体 |
| AR066169A1 (es) | 2007-09-28 | 2009-07-29 | Novartis Ag | Derivados de benzo-imidazoles, utiles para trastornos asociados con la actividad de dgat |
| ES2535083T3 (es) | 2007-12-20 | 2015-05-05 | Astrazeneca Ab | Compuestos de carbamoilo como inhibidores 190 de DGAT1 |
| SG190620A1 (en) | 2008-05-05 | 2013-06-28 | Sanofi Aventis | Acylamino-substituted fused cyclopentanecarboxylic acid derivatives and their use as pharmaceuticals |
| WO2009147170A2 (fr) | 2008-06-05 | 2009-12-10 | Janssen Pharmaceutica Nv | Combinaisons de médicaments comprenant un inhibiteur de dgat et un agoniste de ppar |
| US20100168079A1 (en) * | 2008-12-23 | 2010-07-01 | Daniela Angst | Biaryl Benzylamine Derivatives |
| EP2389366A1 (fr) * | 2009-01-23 | 2011-11-30 | Msd K.K. | Dérivés de benzodiazépin-2-one |
| WO2010108051A2 (fr) | 2009-03-20 | 2010-09-23 | Ligand Pharmaceuticals | Inhibiteurs de diacylglycérol o-acétyltransférase 1 (dgat-1) et leurs utilisations |
| US8268820B2 (en) | 2009-03-26 | 2012-09-18 | Hoffmann-La Roche Inc. | 2,3-diaryl- or heteroaryl-substituted 1,1,1-trifluoro-2-hydroxypropyl compounds |
| EP2411005A1 (fr) | 2009-03-27 | 2012-02-01 | Bristol-Myers Squibb Company | Procédés destinés à prévenir des événements cardiovasculaires indésirables majeurs par des inhibiteurs de la dpp-iv |
| WO2010146395A1 (fr) | 2009-06-19 | 2010-12-23 | Astrazeneca Ab | Carboxamides de pyrazine utiles comme inhibiteurs de la dgat1 |
| AR079022A1 (es) * | 2009-11-02 | 2011-12-21 | Sanofi Aventis | Derivados de acido carboxilico ciclico sustituidos con acilamino, su uso como productos farmaceuticos, composicion farmaceutica y metodo de preparacion |
| AU2010316669B2 (en) | 2009-11-05 | 2014-10-23 | Piramal Enterprises Limited | Carboxy oxazole or thiazole compounds as DGAT - 1 inhibitors useful for the treatment of obesity |
| SG181702A1 (en) | 2009-12-16 | 2012-07-30 | Pola Chem Ind Inc | Preventing or ameliorating agent for pigmentation |
| EP2552441B1 (fr) | 2010-03-30 | 2016-05-04 | Novartis AG | Utilisations d'inhibiteurs de dgat1 |
| WO2012150784A2 (fr) | 2011-05-03 | 2012-11-08 | 한국생명공학연구원 | Nouveau dérivé d'indole ou sel pharmaceutiquement acceptable de celui-ci, procédé de préparation de celui-ci, et composition pharmaceutique pour prévenir ou traiter des maladies métaboliques contenant celui-ci en tant que substance active |
| WO2013055910A1 (fr) | 2011-10-12 | 2013-04-18 | Arena Pharmaceuticals, Inc. | Modulateurs du récepteur gpr119 et traitement de troubles associés |
| WO2014039412A1 (fr) | 2012-09-05 | 2014-03-13 | Bristol-Myers Squibb Company | Antagonistes du récepteur 1 d'hormone concentrant la mélanine de type pyrrolone ou pyrrolidinone |
| EP2892896B1 (fr) | 2012-09-05 | 2016-06-29 | Bristol-Myers Squibb Company | Antagonistes du récepteur 1 de l'hormone de concentration de pyrrolone ou pyrrolidinone mélanine |
| WO2014074668A1 (fr) | 2012-11-08 | 2014-05-15 | Arena Pharmaceuticals, Inc. | Modulateurs de gpr119 et traitement de troubles associés à ceux-ci |
| EP3174875B1 (fr) * | 2014-08-01 | 2020-08-19 | Bayer Pharma Aktiengesellschaft | Procédé pour fabriquer du (4s)-4-(4-cyano-2-méthoxyphényl)-5-éthoxy-2,8-diméthyl-1,4-dihydro-1,6-naphthyridin-3-carboxamide et le purifier en vue de l'utiliser en tant que principe actif pharmaceutique |
| CN105646510A (zh) * | 2014-12-02 | 2016-06-08 | 重庆宁牧生态农业有限公司 | 一种用作抗肥胖剂的化合物 |
| MX2020009604A (es) | 2018-03-16 | 2023-01-25 | Anji Pharmaceuticals Inc | Composiciones y metodos para tratar el estre?imiento grave. |
| US20220304984A1 (en) * | 2019-06-12 | 2022-09-29 | Vanderbilt University | Amino acid transport inhibitors and the uses thereof |
| CN112336718A (zh) * | 2020-10-19 | 2021-02-09 | 济南大学 | 一种苯并咪唑衍生物作为α-葡萄糖苷酶抑制剂及其应用 |
| WO2023085931A1 (fr) | 2021-11-11 | 2023-05-19 | Koninklijke Nederlandse Akademie Van Wetenschappen | Organoïdes hépatiques |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4164645B2 (ja) * | 2002-08-09 | 2008-10-15 | 株式会社大塚製薬工場 | Dgat阻害剤 |
| CN1753897A (zh) * | 2002-11-22 | 2006-03-29 | 日本烟草产业株式会社 | 稠合双环含氮杂环 |
| AR044152A1 (es) * | 2003-05-09 | 2005-08-24 | Bayer Corp | Derivados de alquilarilo, metodo de preparacion y uso para el tratamiento de la obesidad |
-
2005
- 2005-10-14 CA CA002583784A patent/CA2583784A1/fr not_active Abandoned
- 2005-10-14 KR KR1020077008522A patent/KR20070063546A/ko not_active Withdrawn
- 2005-10-14 JP JP2007536988A patent/JP2008516978A/ja active Pending
- 2005-10-14 BR BRPI0516483-4A patent/BRPI0516483A/pt not_active IP Right Cessation
- 2005-10-14 EP EP05812611A patent/EP1805156B1/fr not_active Expired - Lifetime
- 2005-10-14 WO PCT/US2005/037215 patent/WO2006044775A2/fr not_active Ceased
- 2005-10-14 US US11/665,317 patent/US7759376B2/en not_active Expired - Fee Related
- 2005-10-14 CN CNA2005800433280A patent/CN101087769A/zh active Pending
- 2005-10-14 DE DE602005025517T patent/DE602005025517D1/de not_active Expired - Lifetime
- 2005-10-14 ES ES05812611T patent/ES2357015T3/es not_active Expired - Lifetime
- 2005-10-14 MX MX2007004217A patent/MX2007004217A/es not_active Application Discontinuation
- 2005-10-14 AU AU2005295453A patent/AU2005295453A1/en not_active Abandoned
- 2005-10-14 EA EA200700851A patent/EA200700851A1/ru unknown
- 2005-10-14 AT AT05812611T patent/ATE492542T1/de not_active IP Right Cessation
-
2007
- 2007-03-27 IL IL182218A patent/IL182218A0/en unknown
- 2007-03-28 TN TNP2007000111A patent/TNSN07111A1/en unknown
- 2007-03-30 CR CR9034A patent/CR9034A/es not_active Application Discontinuation
- 2007-04-12 ZA ZA200703002A patent/ZA200703002B/xx unknown
- 2007-04-13 EC EC2007007397A patent/ECSP077397A/es unknown
- 2007-04-17 MA MA29831A patent/MA28935B1/fr unknown
- 2007-05-14 NO NO20072461A patent/NO20072461L/no not_active Application Discontinuation
-
2010
- 2010-07-14 US US12/836,035 patent/US20110118302A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| ECSP077397A (es) | 2007-05-30 |
| US7759376B2 (en) | 2010-07-20 |
| CR9034A (es) | 2008-11-18 |
| EP1805156A4 (fr) | 2009-06-10 |
| CN101087769A (zh) | 2007-12-12 |
| WO2006044775A2 (fr) | 2006-04-27 |
| ATE492542T1 (de) | 2011-01-15 |
| AU2005295453A1 (en) | 2006-04-27 |
| TNSN07111A1 (en) | 2008-06-02 |
| KR20070063546A (ko) | 2007-06-19 |
| US20110118302A1 (en) | 2011-05-19 |
| CA2583784A1 (fr) | 2006-04-27 |
| NO20072461L (no) | 2007-07-03 |
| EP1805156B1 (fr) | 2010-12-22 |
| BRPI0516483A (pt) | 2008-09-02 |
| EP1805156A2 (fr) | 2007-07-11 |
| US20070265298A1 (en) | 2007-11-15 |
| EA200700851A1 (ru) | 2007-12-28 |
| DE602005025517D1 (de) | 2011-02-03 |
| JP2008516978A (ja) | 2008-05-22 |
| IL182218A0 (en) | 2007-09-20 |
| ES2357015T3 (es) | 2011-04-15 |
| WO2006044775A3 (fr) | 2006-06-15 |
| MX2007004217A (es) | 2007-06-11 |
| ZA200703002B (en) | 2008-08-27 |
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