TN2009000331A1 - Derives de 3-amino-pyrrolo [3,4-c]pyrazole -5- (1h,4h,6h) carbaldehyde servant d'inhibiteurs de pkc - Google Patents
Derives de 3-amino-pyrrolo [3,4-c]pyrazole -5- (1h,4h,6h) carbaldehyde servant d'inhibiteurs de pkcInfo
- Publication number
- TN2009000331A1 TN2009000331A1 TNP2009000331A TN2009000331A TN2009000331A1 TN 2009000331 A1 TN2009000331 A1 TN 2009000331A1 TN P2009000331 A TNP2009000331 A TN P2009000331A TN 2009000331 A TN2009000331 A TN 2009000331A TN 2009000331 A1 TN2009000331 A1 TN 2009000331A1
- Authority
- TN
- Tunisia
- Prior art keywords
- pyrrolo
- pyrazole
- amino
- disease
- pkc inhibitors
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/4162—1,2-Diazoles condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- 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
- A61P25/28—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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- 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
- 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
- A61P3/08—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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Urology & Nephrology (AREA)
- Heart & Thoracic Surgery (AREA)
- Obesity (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Pain & Pain Management (AREA)
- Hospice & Palliative Care (AREA)
- Rheumatology (AREA)
- Virology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Oncology (AREA)
- Vascular Medicine (AREA)
- Ophthalmology & Optometry (AREA)
- Communicable Diseases (AREA)
- Psychiatry (AREA)
- Dermatology (AREA)
- Gastroenterology & Hepatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
La présente invention concerne des composés et sels pharmaceutiquement acceptables de formules A et B : dans lesquelles A, B, R1, R2, R3, R4, R5, R6, R7, R8, R9 et R10 répondent aux définitions précitées. L'invention concerne en outre des compositions pharmaceutiques comprenant les composés et sels pharmaceutiquement acceptables et des méthodes de traitement du diabète sucré et de ses complications, du cancer, d'une ischémie, de l'inflammation, de troubles du système nerveux central, d'une maladie cardiovasculaire, de la maladie d'Alzheimer et d'une maladie dermatologique, de maladies virales, de troubles inflammatoires, ou de maladies dans lesquelles le foie est un organe cible.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US88874907P | 2007-02-07 | 2007-02-07 | |
US98908607P | 2007-11-19 | 2007-11-19 | |
US2096508P | 2008-01-14 | 2008-01-14 | |
PCT/IB2008/000297 WO2008096260A1 (fr) | 2007-02-07 | 2008-02-04 | Nouveaux dérivés de 3-amino-pyrrolo[3,4-c]pyrazole-5(1h,4h,6h) carbaldéhyde |
Publications (1)
Publication Number | Publication Date |
---|---|
TN2009000331A1 true TN2009000331A1 (fr) | 2010-12-31 |
Family
ID=39493354
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TNP2009000331A TN2009000331A1 (fr) | 2007-02-07 | 2009-08-05 | Derives de 3-amino-pyrrolo [3,4-c]pyrazole -5- (1h,4h,6h) carbaldehyde servant d'inhibiteurs de pkc |
Country Status (20)
Country | Link |
---|---|
US (6) | US8183255B2 (fr) |
EP (1) | EP2118112B1 (fr) |
JP (1) | JP5161245B2 (fr) |
KR (1) | KR101060892B1 (fr) |
AP (1) | AP2009004958A0 (fr) |
AU (1) | AU2008212625B2 (fr) |
BR (1) | BRPI0807346B8 (fr) |
CA (1) | CA2677572C (fr) |
CR (1) | CR10968A (fr) |
DO (1) | DOP2009000201A (fr) |
EA (1) | EA017937B1 (fr) |
EC (1) | ECSP099569A (fr) |
HK (1) | HK1139130A1 (fr) |
IL (1) | IL200270A (fr) |
MA (1) | MA31178B1 (fr) |
MX (1) | MX2009008546A (fr) |
NZ (1) | NZ578876A (fr) |
TN (1) | TN2009000331A1 (fr) |
WO (1) | WO2008096260A1 (fr) |
ZA (1) | ZA200906032B (fr) |
Families Citing this family (38)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008096260A1 (fr) | 2007-02-07 | 2008-08-14 | Pfizer Inc. | Nouveaux dérivés de 3-amino-pyrrolo[3,4-c]pyrazole-5(1h,4h,6h) carbaldéhyde |
US9180127B2 (en) | 2009-12-29 | 2015-11-10 | Dana-Farber Cancer Institute, Inc. | Type II Raf kinase inhibitors |
WO2011107494A1 (fr) | 2010-03-03 | 2011-09-09 | Sanofi | Nouveaux dérivés aromatiques de glycoside, médicaments contenants ces composés, et leur utilisation |
US8933024B2 (en) | 2010-06-18 | 2015-01-13 | Sanofi | Azolopyridin-3-one derivatives as inhibitors of lipases and phospholipases |
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 |
TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
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 |
WO2012112674A2 (fr) * | 2011-02-15 | 2012-08-23 | The Johns Hopkins University | Composés et procédés d'utilisation de ceux-ci dans le traitement de troubles neurodégénératifs |
CN102093366B (zh) * | 2011-03-04 | 2012-11-28 | 中国医学科学院医药生物技术研究所 | 双环氨基吡唑类化合物及其在抗柯萨奇病毒中的应用 |
WO2013037390A1 (fr) | 2011-09-12 | 2013-03-21 | Sanofi | Dérivés amides d'acide 6-(4-hydroxyphényl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylique en tant qu'inhibiteurs de kinase |
EP2567959B1 (fr) | 2011-09-12 | 2014-04-16 | Sanofi | Dérivés d'amide d'acide 6-(4-hydroxy-phényl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylique en tant qu'inhibiteurs de kinase |
EP2760862B1 (fr) | 2011-09-27 | 2015-10-21 | Sanofi | Dérivés d'amide d'acide 6-(4-hydroxyphényl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylique utilisés comme inhibiteurs de kinase |
WO2013074986A1 (fr) | 2011-11-17 | 2013-05-23 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de la kinase c-jun-n-terminale (jnk) |
JP6113828B2 (ja) * | 2012-04-04 | 2017-04-12 | ライジェル ファーマシューティカルズ, インコーポレイテッド | プロテインキナーゼc阻害剤およびその使用 |
EP2844658B1 (fr) * | 2012-05-03 | 2019-03-20 | Genentech, Inc. | Dérivés de pyrazole aminopyrimidine en tant que modulateurs de lrrk2 destinés à être utilisés dans le traitement de la maladie de parkinson |
EP2909194A1 (fr) | 2012-10-18 | 2015-08-26 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de cycline-dépendante kinase 7 (cdk7) |
US9758522B2 (en) | 2012-10-19 | 2017-09-12 | Dana-Farber Cancer Institute, Inc. | Hydrophobically tagged small molecules as inducers of protein degradation |
WO2014063054A1 (fr) | 2012-10-19 | 2014-04-24 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de kinase moelle osseuse sur chromosome x (bmx) et leurs utilisations |
US10154988B2 (en) | 2012-11-14 | 2018-12-18 | The Johns Hopkins University | Methods and compositions for treating schizophrenia |
CA2904610A1 (fr) | 2013-03-14 | 2014-09-25 | Rigel Pharmaceuticals, Inc. | Inhibiteurs de proteine kinase c et leurs utilisations |
AU2014337044A1 (en) | 2013-10-18 | 2016-05-05 | Dana-Farber Cancer Institute, Inc. | Polycyclic inhibitors of cyclin-dependent kinase 7 (CDK7) |
CA2927917C (fr) | 2013-10-18 | 2022-08-09 | Syros Pharmaceuticals, Inc. | Composes heteroaromatiques utiles pour le traitement des maladies proliferatives |
WO2015164614A1 (fr) | 2014-04-23 | 2015-10-29 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de janus kinase et leurs utilisations |
WO2015164604A1 (fr) | 2014-04-23 | 2015-10-29 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de janus kinase marqués de manière hydrophobe et utilisations associées |
CN105377852B (zh) * | 2014-05-23 | 2018-08-28 | 深圳明赛瑞霖药业有限公司 | 自身免疫疾病的治疗 |
CA2972239A1 (fr) * | 2014-12-23 | 2016-06-30 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de la kinase cycline-dependante 7 (cdk7) |
EP3273966B1 (fr) | 2015-03-27 | 2023-05-03 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de kinases cycline-dépendantes |
AU2016276963C1 (en) | 2015-06-12 | 2021-08-05 | Dana-Farber Cancer Institute, Inc. | Combination therapy of transcription inhibitors and kinase inhibitors |
WO2017044858A2 (fr) | 2015-09-09 | 2017-03-16 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de kinases cycline-dépendantes |
AU2016355303B2 (en) * | 2015-11-20 | 2021-10-07 | Mingsight Pharmaceuticals, Inc. | Treatment of autoimmune disease |
CN106727582B (zh) * | 2015-11-20 | 2020-06-12 | 深圳明赛瑞霖药业有限公司 | 自身免疫疾病的治疗 |
EP3484477B1 (fr) * | 2016-07-14 | 2023-09-13 | Mingsight Pharmaceuticals, Inc. | Traitement du cancer |
WO2018218205A1 (fr) * | 2017-05-25 | 2018-11-29 | Mingsight Pharmaceuticals, Inc. | Formes à l'état solide d'inhibiteur de pkc |
MA50356A (fr) | 2017-10-11 | 2021-04-21 | Hoffmann La Roche | Composés bicycliques destinés à être utilisés en tant qu'inhibiteurs de la kinase rip1 |
WO2019143818A1 (fr) * | 2018-01-17 | 2019-07-25 | Mingsight Pharmaceuticals, Inc. | Polythérapie pour le traitement du cancer |
US20220089611A1 (en) * | 2018-12-28 | 2022-03-24 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinase 7 and uses thereof |
WO2022261214A1 (fr) * | 2021-06-09 | 2022-12-15 | Mingsight Pharmaceuticals, Inc. | Compositions comprenant des inhibiteurs de pkc-bêta et procédés de préparation associés |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2001287654B2 (en) * | 2000-08-10 | 2006-12-14 | Pfizer Italia S.R.I. | Bicyclo-pyrazoles active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them |
UA81790C2 (uk) | 2002-12-19 | 2008-02-11 | Фармация Италия С.П.А. | Заміщені піролопіразольні похідні як інгібітори кінази |
EP1838718B1 (fr) | 2005-01-10 | 2011-06-15 | Pfizer Inc. | Pyrrolopyrazoles, puissants inhibiteurs de kinases |
WO2008096260A1 (fr) | 2007-02-07 | 2008-08-14 | Pfizer Inc. | Nouveaux dérivés de 3-amino-pyrrolo[3,4-c]pyrazole-5(1h,4h,6h) carbaldéhyde |
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2008
- 2008-02-04 WO PCT/IB2008/000297 patent/WO2008096260A1/fr active Application Filing
- 2008-02-04 JP JP2009548766A patent/JP5161245B2/ja active Active
- 2008-02-04 BR BRPI0807346A patent/BRPI0807346B8/pt active IP Right Grant
- 2008-02-04 KR KR1020097018673A patent/KR101060892B1/ko active IP Right Grant
- 2008-02-04 MX MX2009008546A patent/MX2009008546A/es active IP Right Grant
- 2008-02-04 NZ NZ578876A patent/NZ578876A/xx unknown
- 2008-02-04 US US12/523,965 patent/US8183255B2/en active Active
- 2008-02-04 EA EA200970670A patent/EA017937B1/ru not_active IP Right Cessation
- 2008-02-04 CA CA2677572A patent/CA2677572C/fr active Active
- 2008-02-04 AP AP2009004958A patent/AP2009004958A0/xx unknown
- 2008-02-04 EP EP08702370.1A patent/EP2118112B1/fr active Active
- 2008-02-04 AU AU2008212625A patent/AU2008212625B2/en active Active
-
2009
- 2009-08-05 TN TNP2009000331A patent/TN2009000331A1/fr unknown
- 2009-08-06 IL IL200270A patent/IL200270A/en not_active IP Right Cessation
- 2009-08-06 CR CR10968A patent/CR10968A/es unknown
- 2009-08-07 DO DO2009000201A patent/DOP2009000201A/es unknown
- 2009-08-07 EC EC2009009569A patent/ECSP099569A/es unknown
- 2009-08-07 MA MA32158A patent/MA31178B1/fr unknown
- 2009-08-31 ZA ZA2009/06032A patent/ZA200906032B/en unknown
-
2010
- 2010-05-14 HK HK10104719.0A patent/HK1139130A1/xx unknown
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2012
- 2012-04-18 US US13/450,388 patent/US8877761B2/en active Active
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2014
- 2014-10-03 US US14/506,470 patent/US9518060B2/en active Active
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2016
- 2016-12-12 US US15/376,279 patent/US10316045B2/en active Active
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2019
- 2019-04-17 US US16/387,369 patent/US11220518B2/en active Active
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2021
- 2021-12-01 US US17/539,948 patent/US11780853B2/en active Active
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