MA31949B1 - Dérivés d'aminotriazole comme agonistes d'alx - Google Patents
Dérivés d'aminotriazole comme agonistes d'alxInfo
- Publication number
- MA31949B1 MA31949B1 MA32968A MA32968A MA31949B1 MA 31949 B1 MA31949 B1 MA 31949B1 MA 32968 A MA32968 A MA 32968A MA 32968 A MA32968 A MA 32968A MA 31949 B1 MA31949 B1 MA 31949B1
- Authority
- MA
- Morocco
- Prior art keywords
- alx
- antagonist
- aminotriazole derivatives
- derivatives act
- aminotriazole
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- 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
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/04—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic 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
- C07D417/02—Heterocyclic 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
- C07D417/06—Heterocyclic 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 linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic 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
- C07D417/14—Heterocyclic 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 three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Virology (AREA)
- Pain & Pain Management (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
La présente invention concerne des dérivés d'aminotriazole de la formule (i), dans laquelle a, e, r1 et r2 sont tels que définis dans la description, ainsi que leur préparation et leur utilisation comme composés pharmaceutiquement actifs. Les composés sont utiles pour la prévention ou le traitement de maladies qui répondent à la modulation du récepteur alx telles que des maladies inflammatoires.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IB2007055199 | 2007-12-18 | ||
| IB2008054369 | 2008-10-23 | ||
| PCT/IB2008/055375 WO2009077990A1 (fr) | 2007-12-18 | 2008-12-17 | Dérivés d'aminotriazole comme agonistes d'alx |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA31949B1 true MA31949B1 (fr) | 2010-12-01 |
Family
ID=40404773
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA32968A MA31949B1 (fr) | 2007-12-18 | 2010-06-29 | Dérivés d'aminotriazole comme agonistes d'alx |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US8536209B2 (fr) |
| EP (1) | EP2225231B1 (fr) |
| JP (1) | JP4656674B2 (fr) |
| KR (1) | KR101213007B1 (fr) |
| CN (1) | CN101903378B (fr) |
| AR (1) | AR069801A1 (fr) |
| AT (1) | ATE520689T1 (fr) |
| AU (1) | AU2008337097B2 (fr) |
| BR (1) | BRPI0821115A8 (fr) |
| CA (1) | CA2706839C (fr) |
| CY (1) | CY1112465T1 (fr) |
| DK (1) | DK2225231T3 (fr) |
| HR (1) | HRP20110825T1 (fr) |
| IL (1) | IL206399A (fr) |
| MA (1) | MA31949B1 (fr) |
| MX (1) | MX2010006241A (fr) |
| MY (1) | MY153985A (fr) |
| NZ (1) | NZ586735A (fr) |
| PL (1) | PL2225231T3 (fr) |
| PT (1) | PT2225231E (fr) |
| RU (1) | RU2492167C2 (fr) |
| SI (1) | SI2225231T1 (fr) |
| TW (1) | TWI434685B (fr) |
| WO (1) | WO2009077990A1 (fr) |
| ZA (1) | ZA201005080B (fr) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR069650A1 (es) | 2007-12-14 | 2010-02-10 | Actelion Pharmaceuticals Ltd | Derivados de aminopirazol como agonistas no peptidicos del receptor alx humano |
| SI2432760T1 (sl) * | 2009-05-18 | 2013-10-30 | Actelion Pharmaceuticals Ltd. | Premoĺ äśeni derivati spiro (2.4) heptana kot alx-receptorji in/ali fprl2-agonisti |
| BRPI1010738A8 (pt) | 2009-06-09 | 2017-12-26 | Actelion Pharmaceuticals Ltd | Derivados de aminotriazol fluorado |
| JP5624130B2 (ja) * | 2009-06-12 | 2014-11-12 | アクテリオンファーマシューティカルズ リミテッドActelion Pharmaceuticals Ltd | Alx受容体アゴニストとしてのオキサゾール及びチアゾール誘導体 |
| WO2012066488A2 (fr) | 2010-11-17 | 2012-05-24 | Actelion Pharmaceuticals Ltd | Dérivés à ponts ester de spiro [2.4] heptane |
| MX2013006420A (es) | 2010-12-07 | 2013-07-29 | Actelion Pharmaceuticals Ltd | Derivados de aminotriazol hidrolixado como agonistas del receptor de alx. |
| ES2526132T3 (es) * | 2010-12-07 | 2015-01-07 | Actelion Pharmaceuticals Ltd. | Derivados de oxazolil-metiléter como agonistas del receptor de ALX |
| EP2707373A1 (fr) | 2011-05-10 | 2014-03-19 | Bayer Intellectual Property GmbH | (thio)carbonylamidines bicycliques |
| EP2739143B1 (fr) * | 2011-08-05 | 2018-07-11 | Gary A. Flynn | Préparation et procédés d'utilisation d'ortho-aryle hétéroaryle à 5 chaînons -carboxamide contenant des inhibiteurs de kinases multicibles |
| CN102558117B (zh) * | 2011-12-15 | 2014-10-08 | 北京金骄生物质化工有限公司 | 一种利用废弃生物质制备5-硝基-2-糠酸酯的方法 |
| EP2850058B1 (fr) | 2012-05-16 | 2016-07-13 | Actelion Pharmaceuticals Ltd. | Dérivés de 1- (p-tolyl) cyclopropyl substituted bridged spiro [2,4] heptane en tant qu' agonistes du récepteur alx. |
| MA37618B1 (fr) | 2012-05-16 | 2017-08-31 | Actelion Pharmaceuticals Ltd | Dérivés pontés fluorés de spiro[2.4]heptane en tant qu'agonistes de récepteur alx |
| KR101689093B1 (ko) | 2012-06-04 | 2016-12-22 | 액테리온 파마슈티칼 리미티드 | 벤즈이미다졸-프롤린 유도체 |
| JP6244365B2 (ja) | 2012-10-10 | 2017-12-06 | アクテリオン ファーマシューティカルズ リミテッドActelion Pharmaceuticals Ltd | [オルトビ−(ヘテロ−)アリール]−[2−(メタビ−(ヘテロ−)アリール)−ピロリジン−1−イル]−メタノン誘導体であるオレキシン受容体アンタゴニスト |
| JP2016505550A (ja) * | 2012-12-03 | 2016-02-25 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | 置換トリアゾール及びイミダゾール化合物 |
| CN105051040A (zh) | 2013-03-12 | 2015-11-11 | 埃科特莱茵药品有限公司 | 作为食欲素受体拮抗剂的氮杂环丁烷酰胺衍生物 |
| AR096686A1 (es) | 2013-06-25 | 2016-01-27 | Actelion Pharmaceuticals Ltd | Derivados de espiro[2.4]heptano puenteados sustituidos con difluoroetil-oxazol como agonistas del receptor de alx |
| AU2014292064B2 (en) | 2013-07-18 | 2018-07-05 | Idorsia Pharmaceuticals Ltd | Piperazine substituted bridged spiro[2.4]heptane derivatives as alx receptor agonists |
| AR097279A1 (es) | 2013-08-09 | 2016-03-02 | Actelion Pharmaceuticals Ltd | Derivados de benzimidazolil-metil urea como agonistas del receptor de alx |
| EP3075726B1 (fr) | 2013-11-28 | 2017-11-08 | Kyorin Pharmaceutical Co., Ltd. | Dérivés d'urée ou leurs sels pharmacologiquement acceptables en tant qu'agonistes du récepteur fprl-1 |
| MX366642B (es) | 2013-12-04 | 2019-07-17 | Idorsia Pharmaceuticals Ltd | Uso de derivados de bencimidazol-prolina. |
| CA2987235A1 (fr) | 2015-05-27 | 2016-12-01 | Kyorin Pharmaceutical Co., Ltd. | Derive de l'uree ou sel pharmacologiquement acceptable de ce dernier |
| WO2016189877A1 (fr) | 2015-05-27 | 2016-12-01 | Kyorin Pharmaceutical Co., Ltd. | Dérivé d'urée ou sel pharmacologiquement acceptable de ce dernier |
| CA3006291A1 (fr) * | 2015-11-24 | 2017-06-01 | Bristol-Myers Squibb Company | Ciblage du recepteur 2 de peptide formyle / du recepteur de la lipoxine a4 (fpr2/alx) pour le traitement de maladies cardiaques |
| KR102803660B1 (ko) | 2018-03-05 | 2025-05-02 | 브리스톨-마이어스 스큅 컴퍼니 | 페닐피롤리디논 포르밀 펩티드 2 수용체 효능제 |
| US11629143B2 (en) | 2020-10-01 | 2023-04-18 | Vibliome Therapeutics, Llc | HipK4 inhibitors and uses thereof |
| JP7743010B2 (ja) * | 2021-03-12 | 2025-09-24 | 国立大学法人 長崎大学 | ハロカルボニル化合物の製造方法 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62234018A (ja) | 1986-04-02 | 1987-10-14 | Rooto Seiyaku Kk | 糖尿病併発症治療剤 |
| WO2003035006A2 (fr) | 2001-10-26 | 2003-05-01 | Government Of The United States Of America, As Represented By The Secretary, Department Of Health And Human Services, The | Amyloide $g(b), ligand des recepteurs de la classe fpr |
| WO2003082314A2 (fr) | 2002-04-03 | 2003-10-09 | Bayer Healthcare Ag | Diagnostics et therapies pour maladies liees a un recepteur de type 1 de peptides n-formyl (fprl1) |
| JP2007516434A (ja) * | 2003-11-07 | 2007-06-21 | アカディア ファーマシューティカルズ インコーポレイティド | リポキシン受容体fprl1の、疼痛および炎症の治療に有効な化合物を識別する手段としての使用 |
| EP1751120A4 (fr) * | 2004-05-25 | 2010-05-05 | Metabolex Inc | Triazoles substitués comme modulateurs de ppar et méthodes de préparation |
| ZA200704809B (en) * | 2004-12-13 | 2008-08-27 | Leo Pharma A S | Triazole substituted aminobenzophenone compounds |
| AU2006312083A1 (en) * | 2005-11-03 | 2007-05-18 | Merck Sharp & Dohme Corp. | Histone deacetylase inhibitors with aryl-pyrazolyl motifs |
| JP2009535393A (ja) * | 2006-05-01 | 2009-10-01 | ファイザー・プロダクツ・インク | 置換2−アミノ縮合複素環式化合物 |
| CN101828111B (zh) | 2007-08-21 | 2014-07-23 | 塞诺米克斯公司 | 人t2r苦味受体及其用途 |
| AR069650A1 (es) | 2007-12-14 | 2010-02-10 | Actelion Pharmaceuticals Ltd | Derivados de aminopirazol como agonistas no peptidicos del receptor alx humano |
| SI2432760T1 (sl) | 2009-05-18 | 2013-10-30 | Actelion Pharmaceuticals Ltd. | Premoĺ äśeni derivati spiro (2.4) heptana kot alx-receptorji in/ali fprl2-agonisti |
| BRPI1010738A8 (pt) | 2009-06-09 | 2017-12-26 | Actelion Pharmaceuticals Ltd | Derivados de aminotriazol fluorado |
| JP5624130B2 (ja) | 2009-06-12 | 2014-11-12 | アクテリオンファーマシューティカルズ リミテッドActelion Pharmaceuticals Ltd | Alx受容体アゴニストとしてのオキサゾール及びチアゾール誘導体 |
-
2008
- 2008-12-17 CA CA2706839A patent/CA2706839C/fr not_active Expired - Fee Related
- 2008-12-17 US US12/809,545 patent/US8536209B2/en not_active Expired - Fee Related
- 2008-12-17 RU RU2010129272/04A patent/RU2492167C2/ru not_active IP Right Cessation
- 2008-12-17 HR HR20110825T patent/HRP20110825T1/hr unknown
- 2008-12-17 NZ NZ586735A patent/NZ586735A/en not_active IP Right Cessation
- 2008-12-17 EP EP08862134A patent/EP2225231B1/fr not_active Not-in-force
- 2008-12-17 SI SI200830412T patent/SI2225231T1/sl unknown
- 2008-12-17 KR KR1020107015871A patent/KR101213007B1/ko not_active Expired - Fee Related
- 2008-12-17 PL PL08862134T patent/PL2225231T3/pl unknown
- 2008-12-17 AT AT08862134T patent/ATE520689T1/de active
- 2008-12-17 JP JP2010539015A patent/JP4656674B2/ja not_active Expired - Fee Related
- 2008-12-17 PT PT08862134T patent/PT2225231E/pt unknown
- 2008-12-17 AU AU2008337097A patent/AU2008337097B2/en not_active Ceased
- 2008-12-17 WO PCT/IB2008/055375 patent/WO2009077990A1/fr not_active Ceased
- 2008-12-17 TW TW097149199A patent/TWI434685B/zh not_active IP Right Cessation
- 2008-12-17 MY MYPI2010002834A patent/MY153985A/en unknown
- 2008-12-17 DK DK08862134.7T patent/DK2225231T3/da active
- 2008-12-17 BR BRPI0821115A patent/BRPI0821115A8/pt not_active IP Right Cessation
- 2008-12-17 MX MX2010006241A patent/MX2010006241A/es active IP Right Grant
- 2008-12-17 CN CN200880122188.XA patent/CN101903378B/zh not_active Expired - Fee Related
- 2008-12-18 AR ARP080105522A patent/AR069801A1/es not_active Application Discontinuation
-
2010
- 2010-06-16 IL IL206399A patent/IL206399A/en not_active IP Right Cessation
- 2010-06-29 MA MA32968A patent/MA31949B1/fr unknown
- 2010-07-16 ZA ZA2010/05080A patent/ZA201005080B/en unknown
-
2011
- 2011-11-17 CY CY20111101111T patent/CY1112465T1/el unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA31949B1 (fr) | Dérivés d'aminotriazole comme agonistes d'alx | |
| MA33365B1 (fr) | Dérivés de spiro[2.4]heptane pontés utiles en tant qu'agonistes du récepteur de alx et/ou du récepteur fprl2 | |
| MA30232B1 (fr) | Inhibiteurs de kinase bases sur l'hydantoine | |
| MA29170B1 (fr) | Derives puriniques agissant comme des agonistes du recepteur a2a | |
| MA30207B1 (fr) | Modulateurs des recepteurs de la progesterone a base d'indole sulfonamide | |
| MA27427A1 (fr) | Composes de benzimidazole-1-yl-thiophene utilises en cancerotherapie | |
| TN2010000230A1 (fr) | Agonistes nouveaux des recepteurs de glucocorticoides | |
| MA32070B1 (fr) | Dérivés hétérocycliques réunis par fusion et procédés d'utilisation associés | |
| MA34655B1 (fr) | Dérivés de 2,3- dihydroimidazo[1,2-c]quinazoléine substitués par un aminoalcool utiles pour traiter des troubles hyperprolifératifs et des maladies associées à l'angiogenèse | |
| MA31683B1 (fr) | Composes et procedes pour moduler fxr | |
| MA34650B1 (fr) | Antagonistes du récepteur cgrp de pipéridinone carboxamide azaindane | |
| MA27647A1 (fr) | Antagonistes de ccr5 utiles comme agents therapeutiques | |
| MA31906B1 (fr) | Inhibiteurs de la replication du virus de limmunodeficience humaine | |
| MA30539B1 (fr) | Derives de piperazinyle utiles dans le traitement de maladies induites par le recepteur gpr38. | |
| MA31766B1 (fr) | Composés organiques | |
| MA32655B1 (fr) | Composés modulant sélectivement le récepteur cb2 | |
| MA30911B1 (fr) | Nouveaux derives de sulfonamide en tant qu'antagonistes de bradykinine | |
| MA29378B1 (fr) | Composition pharmaceutique comprenant une diphenyluree substituee par un omega-carboxyaryle pour le traitement du cancer | |
| MA29377B1 (fr) | Derives de la pyrimidine pour traitement de troubles a caractere hyperproliferatif | |
| MA30696B1 (fr) | Derives de l'acide (3-amino-1,2,3,4-tetrahydro-9h-carbazol-9-yl)-acetique | |
| MA27728A1 (fr) | Antagonistes des recepteurs de cgrp | |
| MA29213B1 (fr) | Quinolones a substitution macrolones - amino | |
| MA29685B1 (fr) | Composes spiroheterocycliques et leurs utilisations en tant qu'agents therapeutiques | |
| TN2009000324A1 (fr) | Composes tricycliques et leur utilisation comme modulateurs du recepteur de glucocorticoides | |
| MA45598B1 (fr) | Stéroles 24-hydroxylés substitués en position 11 pour le traitement des maladies liées au récepteur nmda |