MA35128B1 - Nouveaux dérivés d'imidazole utiles pour le traitement de l'arthrite - Google Patents
Nouveaux dérivés d'imidazole utiles pour le traitement de l'arthriteInfo
- Publication number
- MA35128B1 MA35128B1 MA36452A MA36452A MA35128B1 MA 35128 B1 MA35128 B1 MA 35128B1 MA 36452 A MA36452 A MA 36452A MA 36452 A MA36452 A MA 36452A MA 35128 B1 MA35128 B1 MA 35128B1
- Authority
- MA
- Morocco
- Prior art keywords
- arthritis
- treatment
- imidazole derivatives
- derivatives useful
- novel imidazole
- Prior art date
Links
- 206010003246 arthritis Diseases 0.000 title 1
- 150000002460 imidazoles Chemical class 0.000 title 1
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 4
- 150000003839 salts Chemical class 0.000 abstract 2
- 201000008482 osteoarthritis Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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
- C07D233/88—Nitrogen atoms, e.g. allantoin
-
- 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
- C07D401/12—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 chain containing hetero atoms as chain links
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- 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]
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Physical Education & Sports Medicine (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Rheumatology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pain & Pain Management (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
La présente invention concerne des composés de la formule ci-dessous : dans laquelle a, x et r1-r6 sont tels que présentement décrits, un sel pharmaceutique de celui-ci, et une composition pharmaceutique contenant ce composé ; des procédés de traitement de la douleur associés à l'arthrose en utilisant un des composés ou un sel pharmaceutiquement acceptable de celui-ci, et des procédés pour préparer les composés.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161490222P | 2011-05-26 | 2011-05-26 | |
| PCT/US2012/037200 WO2012161965A1 (fr) | 2011-05-26 | 2012-05-10 | Nouveaux dérivés d'imidazole utiles pour le traitement de l'arthrite |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA35128B1 true MA35128B1 (fr) | 2014-05-02 |
Family
ID=46148987
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA36452A MA35128B1 (fr) | 2011-05-26 | 2013-11-15 | Nouveaux dérivés d'imidazole utiles pour le traitement de l'arthrite |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US8648200B2 (fr) |
| EP (1) | EP2714679A1 (fr) |
| JP (1) | JP2014518886A (fr) |
| KR (1) | KR20130143138A (fr) |
| CN (1) | CN103562200A (fr) |
| AR (1) | AR086254A1 (fr) |
| AU (1) | AU2012259234A1 (fr) |
| BR (1) | BR112013029692A2 (fr) |
| CA (1) | CA2836240A1 (fr) |
| CO (1) | CO6811858A2 (fr) |
| CR (1) | CR20130534A (fr) |
| DO (1) | DOP2013000276A (fr) |
| EA (1) | EA201391568A1 (fr) |
| EC (1) | ECSP13013047A (fr) |
| IL (1) | IL229318A0 (fr) |
| MA (1) | MA35128B1 (fr) |
| MX (1) | MX2013013859A (fr) |
| PH (1) | PH12013502435A1 (fr) |
| SG (1) | SG195020A1 (fr) |
| TN (1) | TN2013000434A1 (fr) |
| TW (1) | TW201311658A (fr) |
| WO (1) | WO2012161965A1 (fr) |
| ZA (1) | ZA201308609B (fr) |
Families Citing this family (51)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8871947B2 (en) | 2013-02-04 | 2014-10-28 | KingChem LLC | Preparation of alkyl 3-difluoromethyl-1-methyl-1H-pyrazole-4-carboxylic acid ester |
| CN103467379A (zh) * | 2013-08-23 | 2013-12-25 | 江苏恒安化工有限公司 | 3-三氟甲基-1-甲基吡唑-4-甲酸的制备方法 |
| CN103483250B (zh) * | 2013-10-08 | 2015-07-22 | 南京复兴生物科技有限公司 | 一种5-氨甲基烟酸的制备方法 |
| CN103601675B (zh) * | 2013-10-08 | 2015-10-28 | 南京复兴生物科技有限公司 | 一种5-氨甲基烟酸的制备方法 |
| WO2015085464A1 (fr) | 2013-12-09 | 2015-06-18 | King Chem, Llc | Procédé de préparation de 3-difluorométhyl-1-méthyl-1h-pyrazole-4-carboxylate d'alkyle et de ses analogues |
| TWI651310B (zh) | 2014-02-20 | 2019-02-21 | 日商日本煙草產業股份有限公司 | 三化合物及其醫藥用途 |
| EP3119394B1 (fr) * | 2014-03-19 | 2021-05-12 | Curza Global LLC | Compositions et procédés comprenant des 2- (acylamino) imidazoles |
| CN105636951B (zh) | 2014-04-14 | 2018-05-15 | 上海恒瑞医药有限公司 | 酰胺类衍生物及其可药用盐、其制备方法及其在医药上的应用 |
| AR105711A1 (es) * | 2015-08-17 | 2017-11-01 | Japan Tobacco Inc | Compuestos de hidroxitriazina y sus usos farmacéuticos |
| US11447503B2 (en) | 2019-06-14 | 2022-09-20 | Janssen Pharmaceutica Nv | Pyridine carbamates and their use as GLUN2B receptor modulators |
| WO2018184019A1 (fr) | 2017-03-31 | 2018-10-04 | Curza Global, Llc | Compositions et procédés comprenant des 2-aminoimidazoles substitués |
| CN109293567A (zh) * | 2018-11-23 | 2019-02-01 | 上海睿腾医药科技有限公司 | 一种5-溴-2-甲基烟酸乙酯的合成方法 |
| MX2021015452A (es) | 2019-06-25 | 2022-02-11 | Gilead Sciences Inc | Proteinas de fusion flt3l-fc y metodos de uso. |
| MX2022004370A (es) | 2019-10-18 | 2022-05-06 | Forty Seven Inc | Terapias de combinacion para tratar sindromes mielodisplasicos y leucemia mieloide aguda. |
| WO2021087064A1 (fr) | 2019-10-31 | 2021-05-06 | Forty Seven, Inc. | Traitement d'un cancer du sang basé sur une thérapie anti-cd47 et anti-cd20 |
| TWI778443B (zh) | 2019-11-12 | 2022-09-21 | 美商基利科學股份有限公司 | Mcl1抑制劑 |
| CN110845426A (zh) * | 2019-11-29 | 2020-02-28 | 都创(上海)医药科技有限公司 | 一种2-氯-5-氰基嘧啶化合物制备方法 |
| JP7711068B2 (ja) | 2019-12-24 | 2025-07-22 | カルナバイオサイエンス株式会社 | ジアシルグリセロールキナーゼ調節化合物 |
| IL295023A (en) | 2020-02-14 | 2022-09-01 | Jounce Therapeutics Inc | Antibodies and fusion proteins that bind to ccr8 and their uses |
| CR20220547A (es) | 2020-05-01 | 2022-12-15 | Gilead Sciences Inc | Compuestos de 2,4-dioxopirimidina inhibidores de cd73 |
| TW202302145A (zh) | 2021-04-14 | 2023-01-16 | 美商基利科學股份有限公司 | CD47/SIRPα結合及NEDD8活化酶E1調節次單元之共抑制以用於治療癌症 |
| TW202313094A (zh) | 2021-05-18 | 2023-04-01 | 美商基利科學股份有限公司 | 使用FLT3L—Fc融合蛋白之方法 |
| AU2022298639C1 (en) | 2021-06-23 | 2025-07-17 | Gilead Sciences, Inc. | Diacylglyercol kinase modulating compounds |
| KR20240005901A (ko) | 2021-06-23 | 2024-01-12 | 길리애드 사이언시즈, 인코포레이티드 | 디아실글리세롤 키나제 조절 화합물 |
| AU2022299051B2 (en) | 2021-06-23 | 2025-03-13 | Gilead Sciences, Inc. | Diacylglyercol kinase modulating compounds |
| KR20240025616A (ko) | 2021-06-23 | 2024-02-27 | 길리애드 사이언시즈, 인코포레이티드 | 다이아실글리세롤 키나제 조절 화합물 |
| JP2024539252A (ja) | 2021-10-28 | 2024-10-28 | ギリアード サイエンシーズ, インコーポレイテッド | ピリジジン-3(2h)-オン誘導体 |
| CA3235986A1 (fr) | 2021-10-29 | 2023-05-04 | Gilead Science, Inc. | Composes cd73 |
| EP4667056A1 (fr) | 2021-12-22 | 2025-12-24 | Gilead Sciences, Inc. | Agents de dégradation de la famille des doigts de zinc de l'ikaros et leurs utilisations |
| EP4452414A2 (fr) | 2021-12-22 | 2024-10-30 | Gilead Sciences, Inc. | Agents de dégradation de doigt de zinc de la famille ikaros et utilisations associées |
| CA3244639A1 (fr) | 2021-12-28 | 2025-06-13 | Nippon Shinyaku Co., Ltd. | Composé d'indazole et son utilisation pharmaceutique |
| TW202340168A (zh) | 2022-01-28 | 2023-10-16 | 美商基利科學股份有限公司 | Parp7抑制劑 |
| LT4245756T (lt) | 2022-03-17 | 2024-11-25 | Gilead Sciences, Inc. | Ikaros cinko pirštų šeimos skaidymo medžiagos ir jų panaudojimas |
| AU2023240346A1 (en) | 2022-03-24 | 2024-09-19 | Gilead Sciences, Inc. | Combination therapy for treating trop-2 expressing cancers |
| TWI876305B (zh) | 2022-04-05 | 2025-03-11 | 美商基利科學股份有限公司 | 用於治療結腸直腸癌之組合療法 |
| US20230374036A1 (en) | 2022-04-21 | 2023-11-23 | Gilead Sciences, Inc. | Kras g12d modulating compounds |
| IL317958A (en) | 2022-07-01 | 2025-02-01 | Gilead Sciences Inc | CD73 compounds |
| WO2024064668A1 (fr) | 2022-09-21 | 2024-03-28 | Gilead Sciences, Inc. | POLYTHÉRAPIE ANTICANCÉREUSE PAR RAYONNEMENT IONISANT FOCAL ET PERTURBATION CD47/SIRPα |
| EP4638436A1 (fr) | 2022-12-22 | 2025-10-29 | Gilead Sciences, Inc. | Inhibiteurs de prmt5 et leurs utilisations |
| EP4695260A1 (fr) | 2023-04-11 | 2026-02-18 | Gilead Sciences, Inc. | Composés modulateurs de kras |
| KR20250175331A (ko) | 2023-04-21 | 2025-12-16 | 길리애드 사이언시즈, 인코포레이티드 | Prmt5 억제제 및 이의 용도 |
| AU2024306338A1 (en) | 2023-06-30 | 2026-01-08 | Gilead Sciences, Inc. | Kras modulating compounds |
| AU2024297978A1 (en) | 2023-07-26 | 2026-02-05 | Gilead Sciences, Inc. | Parp7 inhibitors |
| AU2024300557A1 (en) | 2023-07-26 | 2026-02-05 | Gilead Sciences, Inc. | Parp7 inhibitors |
| US20250101042A1 (en) | 2023-09-08 | 2025-03-27 | Gilead Sciences, Inc. | Kras g12d modulating compounds |
| WO2025054530A1 (fr) | 2023-09-08 | 2025-03-13 | Gilead Sciences, Inc. | Dérivés polycycliques contenant une pyrimidine utilisés comme composés de modulation de kras g12d |
| US20250154172A1 (en) | 2023-11-03 | 2025-05-15 | Gilead Sciences, Inc. | Prmt5 inhibitors and uses thereof |
| WO2025137640A1 (fr) | 2023-12-22 | 2025-06-26 | Gilead Sciences, Inc. | Inhibiteurs azaspiro de wrn |
| WO2025245003A1 (fr) | 2024-05-21 | 2025-11-27 | Gilead Sciences, Inc. | Inhibiteurs de prmt5 et leurs utilisations |
| CN119161260A (zh) * | 2024-06-26 | 2024-12-20 | 安徽大学 | 一种1-(2-氨基-4-氟-5-甲氧基苯基)-1-丙酮的合成方法 |
| WO2026039365A1 (fr) | 2024-08-12 | 2026-02-19 | Gilead Sciences, Inc. | Composés de modulation de kras |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7439360B2 (en) * | 2004-10-15 | 2008-10-21 | Amgen Inc. | Vanilloid receptor ligands and their use in treatments |
| WO2009079001A1 (fr) * | 2007-12-18 | 2009-06-25 | Janssen Pharmaceutica N.V. | Imidazoles bicycliques substitué par hétéroaryle constituant des modulateurs du récepteur de l'histamine h4 |
| US20100324086A1 (en) | 2008-02-19 | 2010-12-23 | Novasaid Ab | Compounds and methods |
| UY32470A (es) | 2009-03-05 | 2010-10-29 | Boehringer Ingelheim Int | Derivados de 2-{2-cloro-5-[(sustituido) metil]fenilamino} -1-metil]fenilamino}-1-metilbencimidazol-5-carboxamidas-n-(sustituidas) y sus sales fisiológicamente aceptables, composiciones conteniéndolos y aplicaciones |
| WO2010127152A2 (fr) * | 2009-04-29 | 2010-11-04 | Irm Llc | Composés et compositions comme inhibiteurs de la prostaglandine e synthase-1 microsomale |
| JP5579862B2 (ja) * | 2009-10-23 | 2014-08-27 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | ミクロソームプロスタグランジンe2シンターゼ−1のインヒビター |
| AR084174A1 (es) * | 2010-12-21 | 2013-04-24 | Lilly Co Eli | Compuestos de imidazol-2-benzamida utiles para el tratamiento de osteoartritis y una composicion farmaceutica |
-
2012
- 2012-05-03 AR ARP120101556A patent/AR086254A1/es not_active Application Discontinuation
- 2012-05-04 TW TW101116086A patent/TW201311658A/zh unknown
- 2012-05-10 MX MX2013013859A patent/MX2013013859A/es unknown
- 2012-05-10 AU AU2012259234A patent/AU2012259234A1/en not_active Abandoned
- 2012-05-10 PH PH1/2013/502435A patent/PH12013502435A1/en unknown
- 2012-05-10 BR BR112013029692A patent/BR112013029692A2/pt not_active IP Right Cessation
- 2012-05-10 EP EP12723323.7A patent/EP2714679A1/fr not_active Withdrawn
- 2012-05-10 CA CA2836240A patent/CA2836240A1/fr not_active Abandoned
- 2012-05-10 US US13/468,122 patent/US8648200B2/en not_active Expired - Fee Related
- 2012-05-10 WO PCT/US2012/037200 patent/WO2012161965A1/fr not_active Ceased
- 2012-05-10 SG SG2013085154A patent/SG195020A1/en unknown
- 2012-05-10 CN CN201280025230.2A patent/CN103562200A/zh active Pending
- 2012-05-10 KR KR1020137030893A patent/KR20130143138A/ko not_active Ceased
- 2012-05-10 JP JP2014512861A patent/JP2014518886A/ja active Pending
- 2012-05-10 EA EA201391568A patent/EA201391568A1/ru unknown
-
2013
- 2013-10-18 CR CR20130534A patent/CR20130534A/es unknown
- 2013-10-24 TN TNP2013000434A patent/TN2013000434A1/fr unknown
- 2013-11-07 IL IL229318A patent/IL229318A0/en unknown
- 2013-11-15 MA MA36452A patent/MA35128B1/fr unknown
- 2013-11-15 ZA ZA2013/08609A patent/ZA201308609B/en unknown
- 2013-11-22 DO DO2013000276A patent/DOP2013000276A/es unknown
- 2013-11-22 CO CO13275568A patent/CO6811858A2/es not_active Application Discontinuation
- 2013-11-25 EC ECSP13013047 patent/ECSP13013047A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| TW201311658A (zh) | 2013-03-16 |
| PH12013502435A1 (en) | 2014-01-13 |
| IL229318A0 (en) | 2014-01-30 |
| AU2012259234A1 (en) | 2013-11-14 |
| CN103562200A (zh) | 2014-02-05 |
| CO6811858A2 (es) | 2013-12-16 |
| KR20130143138A (ko) | 2013-12-30 |
| ECSP13013047A (es) | 2014-01-31 |
| CA2836240A1 (fr) | 2012-11-29 |
| EA201391568A1 (ru) | 2014-04-30 |
| US8648200B2 (en) | 2014-02-11 |
| EP2714679A1 (fr) | 2014-04-09 |
| JP2014518886A (ja) | 2014-08-07 |
| TN2013000434A1 (en) | 2015-03-30 |
| DOP2013000276A (es) | 2014-03-31 |
| ZA201308609B (en) | 2015-05-27 |
| MX2013013859A (es) | 2014-05-28 |
| AR086254A1 (es) | 2013-11-27 |
| WO2012161965A1 (fr) | 2012-11-29 |
| SG195020A1 (en) | 2013-12-30 |
| US20120302608A1 (en) | 2012-11-29 |
| BR112013029692A2 (pt) | 2017-01-17 |
| CR20130534A (es) | 2014-03-12 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA35128B1 (fr) | Nouveaux dérivés d'imidazole utiles pour le traitement de l'arthrite | |
| MA38227A1 (fr) | Nouveaux composés bicycliques et leur utilisation en tant qu'agents antibactériens et inhibiteurs de ?-lactamase | |
| TN2009000450A1 (fr) | Derives de pyridine | |
| TN2014000147A1 (fr) | Derives de (4-phenylimidazol-2-yl) ethylamine utiles comme modulateurs de canal sodique | |
| MA42239B1 (fr) | Nouveaux dérivés d'hydroxyester, leur procédé de préparation et compositions pharmaceutiques les contenant | |
| MA43639B1 (fr) | Nouveaux dérivés d'ammonium, procédé de préparation de ceux-ci et compositions pharmaceutiques les contenant | |
| MA42231B1 (fr) | Nouveaux dérivés d'hydroxyacide, leur procédé de préparation, et compositions pharmaceutiques les contenant | |
| MA41134B1 (fr) | Composés substitués de 5-amino-6h-thiazolo[4,5-d]pyrimidine-2,7-dione pour le traitement et la prophylaxie des infections virales | |
| MA45223A (fr) | Nouveaux dérivés de pipéridinyle subsitués par (hétéro)aryle, leur procédé de préparation et compositions pharmaceutiques les contenant | |
| MA32727B1 (fr) | Pyrazolylaminopyridines au titre d'inhibiteurs de fak | |
| MA42230B1 (fr) | Dérivés bicycliques, leur procédé de préparation, et compositions pharmaceutiques les contenant | |
| MA37866B1 (fr) | Dérivés de type aza-indazole ou diaza-indazole pour le traitement de la douleur | |
| MA33662B1 (fr) | Composés de spiropipéridine et leur utilisation pharmaceutique pour le traitement du diabète | |
| MA40225B1 (fr) | Composés dihydroisoquinolinone substitués | |
| MA30932B1 (fr) | Spirocetones servant d'inhibiteurs d'acetyl-coa -carboxylase | |
| MA34727B1 (fr) | Imidazolylimidazoles condensés utilisés comme composés antiviraux | |
| MA35275B1 (fr) | Composés de tétrahydropyridopyridine et tétrahydropyridopyrimidine et utilisation de ceux-ci en tant que modulateurs de récepteur c5a | |
| MA35351B1 (fr) | Nouveau dérivé 1,2,3,4- tétrahydroquinoléine utile pour le traitement du diabète. | |
| MA35826B1 (fr) | Triazolopyridines substituées et leur utilisation à titre d'inhibiteurs de ttk | |
| MA32965B1 (fr) | Derives de sulfonamides | |
| MA33840B1 (fr) | Nouveau composé de spiropipéridine | |
| TNSN07022A1 (fr) | Derives de pyridine | |
| MA29926B1 (fr) | Derives de pyrazine | |
| MA38323A1 (fr) | Dérivés pyrimidone et leur utilisation dans le traitement, l'amélioration ou la prévention d'une maladie virale | |
| MA38260A1 (fr) | Nouveaux dérivés de cyclohexyl et quinuclidinyl carbamate ayant une activité d'agoniste adrénergique beta2 et une activité d'antagoniste muscarinique m3 |