MA34655B1 - 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 - Google Patents
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'angiogenèseInfo
- Publication number
- MA34655B1 MA34655B1 MA35889A MA35889A MA34655B1 MA 34655 B1 MA34655 B1 MA 34655B1 MA 35889 A MA35889 A MA 35889A MA 35889 A MA35889 A MA 35889A MA 34655 B1 MA34655 B1 MA 34655B1
- Authority
- MA
- Morocco
- Prior art keywords
- treatment
- quinazolein
- dihydroimidazo
- aminoalcool
- substituted
- Prior art date
Links
Classifications
-
- 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
-
- 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
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5386—1,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged ring 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
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/541—Non-condensed thiazines containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/08—Bridged systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Immunology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Oncology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
CETTE INVENTION CONCERNE DE NOUVEAUX COMPOSÉS DE 2,3-DIHYDROIMIDAZO[1,2-C]-QUINAZOLÉINE, LES COMPOSITIONS PHARMACEUTIQUES CONTENANT CES COMPOSÉS ET L'UTILISATION DE CES COMPOSÉS OU COMPOSITIONS POUR L'INHIBITION DE LA PHOSPHOTIDYLINOSITOL-3-KINASE (PI3K) ET LE TRAITEMENT DE MALADIES ASSOCIÉES À L'ACTIVITÉ DE LA PHOSPHOTIDYLINOSITOL-3-KINASE (PI3K), EN PARTICULIER LE TRAITEMENT DES TROUBLES HYPERPROLIFÉRATIFS ET/OU DE L'ANGIOGENÈSE, COMME SEUL AGENT OU EN COMBINAISON AVEC D'AUTRES INGRÉDIENTS ACTIFS.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US41255610P | 2010-11-11 | 2010-11-11 | |
| PCT/EP2011/069637 WO2012062748A1 (fr) | 2010-11-11 | 2011-11-08 | 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 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA34655B1 true MA34655B1 (fr) | 2013-11-02 |
Family
ID=44999756
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA35889A MA34655B1 (fr) | 2010-11-11 | 2011-11-08 | 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 |
Country Status (31)
| Country | Link |
|---|---|
| US (2) | US8895549B2 (fr) |
| EP (1) | EP2638045B1 (fr) |
| JP (1) | JP6196156B2 (fr) |
| KR (1) | KR20140003436A (fr) |
| CN (1) | CN102906094B (fr) |
| AP (1) | AP3337A (fr) |
| AR (1) | AR083842A1 (fr) |
| AU (1) | AU2011328192B2 (fr) |
| BR (1) | BR112013011634A2 (fr) |
| CA (1) | CA2817317C (fr) |
| CL (1) | CL2013001295A1 (fr) |
| CO (1) | CO6761350A2 (fr) |
| CR (1) | CR20130213A (fr) |
| CU (1) | CU20130069A7 (fr) |
| DO (1) | DOP2013000105A (fr) |
| EA (1) | EA024406B1 (fr) |
| EC (1) | ECSP13012618A (fr) |
| GT (1) | GT201300121A (fr) |
| IL (1) | IL226066A0 (fr) |
| MA (1) | MA34655B1 (fr) |
| MX (1) | MX2013005305A (fr) |
| MY (1) | MY164730A (fr) |
| NZ (1) | NZ610018A (fr) |
| PE (1) | PE20140411A1 (fr) |
| PH (1) | PH12013500938A1 (fr) |
| SG (1) | SG190100A1 (fr) |
| TW (1) | TW201305170A (fr) |
| UA (1) | UA113280C2 (fr) |
| UY (1) | UY33719A (fr) |
| WO (1) | WO2012062748A1 (fr) |
| ZA (1) | ZA201304244B (fr) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9730943B2 (en) * | 2010-11-11 | 2017-08-15 | Bayer Intellectual Property Gmbh | Alkoxy-substituted 2,3-dihydroimidazo[1,2-C]quinazolines |
| UA113280C2 (xx) * | 2010-11-11 | 2017-01-10 | АМІНОСПИРТЗАМІЩЕНІ ПОХІДНІ 2,3-ДИГІДРОІМІДАЗО$1,2-c]ХІНАЗОЛІНУ, ПРИДАТНІ ДЛЯ ЛІКУВАННЯ ГІПЕРПРОЛІФЕРАТИВНИХ ПОРУШЕНЬ І ЗАХВОРЮВАНЬ, ПОВ'ЯЗАНИХ З АНГІОГЕНЕЗОМ | |
| CN103370320B (zh) * | 2010-11-11 | 2016-04-27 | 拜耳知识产权有限责任公司 | 芳基氨基醇取代的2,3-二氢咪唑并[1,2-c]喹啉 |
| EP2508525A1 (fr) | 2011-04-05 | 2012-10-10 | Bayer Pharma Aktiengesellschaft | Sels de 2,3-dihydroimidazo[1,2-C]quinazoline substitutés |
| JO3733B1 (ar) | 2011-04-05 | 2021-01-31 | Bayer Ip Gmbh | استخدام 3,2-دايهيدروايميدازو[1, 2 -c]كوينازولينات مستبدلة |
| CN103214489B (zh) * | 2013-02-25 | 2016-10-26 | 中国人民解放军第二军医大学 | 一类具有抗肿瘤活性的多靶点激酶抑制剂及其制备方法 |
| UA119537C2 (uk) * | 2013-04-08 | 2019-07-10 | Байєр Фарма Акцієнгезелльшафт | ЗАСТОСУВАННЯ ЗАМІЩЕНИХ 2,3-ДИГІДРОІМІДАЗО[1,2-c]ХІНАЗОЛІНІВ ДЛЯ ЛІКУВАННЯ ЛІМФОМ |
| WO2015082376A2 (fr) | 2013-12-03 | 2015-06-11 | Bayer Pharma Aktiengesellschaft | Utilisation d'inhibiteurs de pi3k |
| US10124007B2 (en) | 2013-12-03 | 2018-11-13 | Bayer Pharma Aktiengesellschaft | Combination of PI3K-inhibitors |
| JP6499657B2 (ja) | 2013-12-03 | 2019-04-10 | バイエル ファーマ アクチエンゲゼルシャフト | Pi3k阻害剤の組み合わせ |
| WO2016071380A1 (fr) * | 2014-11-07 | 2016-05-12 | Bayer Pharma Aktiengesellschaft | Synthèse d'inhibiteur de pi3k et ses sels |
| WO2016071382A1 (fr) * | 2014-11-07 | 2016-05-12 | Bayer Pharma Aktiengesellschaft | Synthèse d'un inhibiteur de pi3k et de ses sels |
| WO2016087488A1 (fr) * | 2014-12-03 | 2016-06-09 | Bayer Pharma Aktiengesellschaft | Régime d'administration de dérivés de 2,3-dihydroimidazo[1,2-c]quinazoline substitués par un amino-alcool |
| WO2016087490A1 (fr) * | 2014-12-03 | 2016-06-09 | Bayer Pharma Aktiengesellschaft | Combinaison d'inhibiteurs de la voie pi3k |
| AU2016349632A1 (en) | 2015-11-07 | 2018-05-24 | Multivir Inc. | Compositions comprising tumor suppressor gene therapy and immune checkpoint blockade for the treatment of cancer |
| CA3037626A1 (fr) | 2016-09-23 | 2018-03-29 | Bayer Pharma Aktiengesellschaft | Combinaison d'inhibiteurs de la pi3k |
| CN110381997A (zh) | 2016-12-12 | 2019-10-25 | 茂体外尔公司 | 用于治疗和预防癌症和感染性疾病的包含病毒基因治疗和免疫检查点抑制剂的方法和组合物 |
| WO2018215282A1 (fr) | 2017-05-26 | 2018-11-29 | Bayer Pharma Aktiengesellschaft | Combinaison d'inhibiteurs de bub1 et de pi3k |
| EP3645005A1 (fr) | 2017-06-28 | 2020-05-06 | Bayer Consumer Care AG | Combinaison d'un inhibiteur de pi3k et d'un antagoniste du récepteur des androgènes |
| KR20200135986A (ko) | 2018-03-19 | 2020-12-04 | 멀티비르 인코포레이티드 | 종양 억제인자 유전자 치료 및 cd122/cd132 작용제를 포함하는 암 치료를 위한 방법 및 조성물 |
| CN108383849B (zh) * | 2018-04-26 | 2020-11-06 | 浙江大学 | 咪唑并喹唑啉衍生物及其在抗肿瘤抗炎中的应用 |
| MX2021010669A (es) * | 2019-03-07 | 2021-09-28 | BioNTech SE | Proceso para la preparacion de una imidazoquinolina sustituida. |
| US20230029385A1 (en) * | 2019-10-15 | 2023-01-26 | Bayer Aktiengesellschaft | 2-methyl-aza-quinazolines |
| WO2021113644A1 (fr) | 2019-12-05 | 2021-06-10 | Multivir Inc. | Combinaisons comprenant un activateur de lymphocytes t cd8+, un inhibiteur de point de contrôle immunitaire et une radiothérapie en vue d'obtenir des effets ciblés et abscopal pour le traitement du cancer |
| WO2021260443A1 (fr) | 2020-06-24 | 2021-12-30 | Bayer Aktiengesellschaft | Associations de 2,3-dihydroimidazo[1,2-c]quinazolines |
| CN115572256B (zh) * | 2021-06-21 | 2025-01-24 | 武汉睿健医药科技有限公司 | Oct4高选择性活化剂 |
| CN113512040B (zh) * | 2021-08-25 | 2023-10-13 | 河南牧业经济学院 | 一种血根碱仿生化合物及其制备方法 |
| TW202404968A (zh) * | 2022-04-20 | 2024-02-01 | 美商思諾維新醫藥公司 | PI3Kα抑制劑 |
| US20250346603A1 (en) * | 2022-05-26 | 2025-11-13 | Pikavation Therapeutics, Inc. | Tricyclic compounds as pi3kalpha inhibitors |
| AU2024361550A1 (en) * | 2023-10-17 | 2026-04-09 | Pikavation Therapeutics, Inc. | 5-oxo-4,5-dihydroimidazo[1,5-a]quinazoline compounds as pi3k[alpha] inhibitors |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5023252A (en) | 1985-12-04 | 1991-06-11 | Conrex Pharmaceutical Corporation | Transdermal and trans-membrane delivery of drugs |
| US5011472A (en) | 1988-09-06 | 1991-04-30 | Brown University Research Foundation | Implantable delivery system for biological factors |
| GB9400680D0 (en) | 1994-01-14 | 1994-03-09 | Sandoz Ltd | Improvements in or relating to organic compounds |
| US5792766A (en) | 1996-03-13 | 1998-08-11 | Neurogen Corporation | Imidazo 1,5-c! quinazolines; a new class of GABA brain receptor ligands |
| AU2003293310B2 (en) * | 2002-09-30 | 2010-04-01 | Bayer Intellectual Property Gmbh | Fused azole-pyrimidine derivatives |
| MXPA06003113A (es) | 2003-09-19 | 2006-06-20 | Astrazeneca Ab | Derivados de quinazolina. |
| EP1673087B1 (fr) * | 2003-10-03 | 2015-05-13 | 3M Innovative Properties Company | Imidazoquinolines a substitution alcoxy |
| US7842701B2 (en) * | 2004-02-19 | 2010-11-30 | Takeda Pharmaceutical Company Limited | Pyrazoloquinolone derivative and use thereof |
| AU2006346931B2 (en) | 2006-08-03 | 2012-07-19 | Rottapharm Biotech S.R.L. | 6-1H-imidazo-quinazoline and quinolines derivatives, new potent analgesics and anti-inflammatory agents |
| AR064106A1 (es) * | 2006-12-05 | 2009-03-11 | Bayer Schering Pharma Ag | Derivados de 2,3-dihidroimidazo [1,2-c] quinazolina sustituida utiles para el tratamiento de enfermedades y trastornos hiper-proliferativos asociados con la angiogenesis |
| GB2454549B (en) * | 2007-09-25 | 2009-09-23 | Medical & Pharm Ind Tech & Dev | Uses of 2-[piperidinyl]methyl-2,3-dihydroimidazo[1,2-c]quinazolin-5(6H)-one for providing an anti-allergic effect and histamine H1 receptor antagonism effect |
| BRPI0822462A2 (pt) | 2008-06-20 | 2015-10-13 | Rottapharm Spa | derivados de 6-1h-imidazo-quinazolina e de quinolinas, novos inibidores de mao e ligantes a receptor de imidazolina. |
| AU2009264431B2 (en) | 2008-06-26 | 2013-11-07 | Nerviano Medical Sciences S.R.L. | Pyrazolo-quinazolines |
| EP2168583A1 (fr) * | 2008-09-24 | 2010-03-31 | Bayer Schering Pharma Aktiengesellschaft | Utilisation de 2,3-dihydroimidazo[1,2-c]quinazolines substituées pour le traitement du myélome |
| PE20130191A1 (es) | 2010-04-16 | 2013-02-21 | Bayer Ip Gmbh | Combinaciones que contienen 2, 3-dihidroimidazo[1, 2-c]quinazolina sustituida |
| CN103370320B (zh) * | 2010-11-11 | 2016-04-27 | 拜耳知识产权有限责任公司 | 芳基氨基醇取代的2,3-二氢咪唑并[1,2-c]喹啉 |
| UA113280C2 (xx) * | 2010-11-11 | 2017-01-10 | АМІНОСПИРТЗАМІЩЕНІ ПОХІДНІ 2,3-ДИГІДРОІМІДАЗО$1,2-c]ХІНАЗОЛІНУ, ПРИДАТНІ ДЛЯ ЛІКУВАННЯ ГІПЕРПРОЛІФЕРАТИВНИХ ПОРУШЕНЬ І ЗАХВОРЮВАНЬ, ПОВ'ЯЗАНИХ З АНГІОГЕНЕЗОМ | |
| US9730943B2 (en) * | 2010-11-11 | 2017-08-15 | Bayer Intellectual Property Gmbh | Alkoxy-substituted 2,3-dihydroimidazo[1,2-C]quinazolines |
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2011
- 2011-08-11 UA UAA201307179A patent/UA113280C2/uk unknown
- 2011-11-08 CA CA2817317A patent/CA2817317C/fr active Active
- 2011-11-08 CN CN201180023122.7A patent/CN102906094B/zh not_active Expired - Fee Related
- 2011-11-08 MA MA35889A patent/MA34655B1/fr unknown
- 2011-11-08 KR KR1020137014882A patent/KR20140003436A/ko not_active Ceased
- 2011-11-08 MY MYPI2013700753A patent/MY164730A/en unknown
- 2011-11-08 MX MX2013005305A patent/MX2013005305A/es unknown
- 2011-11-08 NZ NZ610018A patent/NZ610018A/en not_active IP Right Cessation
- 2011-11-08 PE PE2013001051A patent/PE20140411A1/es not_active Application Discontinuation
- 2011-11-08 US US13/885,122 patent/US8895549B2/en active Active
- 2011-11-08 AU AU2011328192A patent/AU2011328192B2/en not_active Ceased
- 2011-11-08 BR BR112013011634A patent/BR112013011634A2/pt not_active IP Right Cessation
- 2011-11-08 SG SG2013033634A patent/SG190100A1/en unknown
- 2011-11-08 JP JP2013538163A patent/JP6196156B2/ja active Active
- 2011-11-08 AP AP2013006921A patent/AP3337A/xx active
- 2011-11-08 WO PCT/EP2011/069637 patent/WO2012062748A1/fr not_active Ceased
- 2011-11-08 PH PH1/2013/500938A patent/PH12013500938A1/en unknown
- 2011-11-08 EA EA201300556A patent/EA024406B1/ru not_active IP Right Cessation
- 2011-11-08 EP EP11784978.6A patent/EP2638045B1/fr active Active
- 2011-11-10 UY UY0001033719A patent/UY33719A/es not_active Application Discontinuation
- 2011-11-11 TW TW100141328A patent/TW201305170A/zh unknown
- 2011-11-11 AR ARP110104216A patent/AR083842A1/es unknown
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2013
- 2013-04-30 IL IL226066A patent/IL226066A0/en unknown
- 2013-05-10 EC ECSP13012618 patent/ECSP13012618A/es unknown
- 2013-05-10 CU CU2013000069A patent/CU20130069A7/es unknown
- 2013-05-10 GT GT201300121A patent/GT201300121A/es unknown
- 2013-05-10 CO CO13117697A patent/CO6761350A2/es not_active Application Discontinuation
- 2013-05-10 CL CL2013001295A patent/CL2013001295A1/es unknown
- 2013-05-10 CR CR20130213A patent/CR20130213A/es unknown
- 2013-05-10 DO DO2013000105A patent/DOP2013000105A/es unknown
- 2013-06-10 ZA ZA2013/04244A patent/ZA201304244B/en unknown
-
2014
- 2014-11-25 US US14/553,280 patent/US9902727B2/en not_active Expired - Fee Related
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