TN2009000137A1 - Substituted 2,3-dihydroimidazo[1,2-c]quinazoline derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis - Google Patents
Substituted 2,3-dihydroimidazo[1,2-c]quinazoline derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesisInfo
- Publication number
- TN2009000137A1 TN2009000137A1 TNP2009000137A TN2009000137A TN2009000137A1 TN 2009000137 A1 TN2009000137 A1 TN 2009000137A1 TN P2009000137 A TNP2009000137 A TN P2009000137A TN 2009000137 A TN2009000137 A TN 2009000137A TN 2009000137 A1 TN2009000137 A1 TN 2009000137A1
- Authority
- TN
- Tunisia
- Prior art keywords
- dihydroimidazo
- diseases associated
- angiogenesis
- substituted
- proliferative disorders
- Prior art date
Links
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title abstract 4
- NTTQCLSBWRKUIJ-UHFFFAOYSA-N 2,3-dihydroimidazo[1,2-c]quinazoline Chemical class C1=CC=C2C3=NCCN3C=NC2=C1 NTTQCLSBWRKUIJ-UHFFFAOYSA-N 0.000 title abstract 2
- 230000033115 angiogenesis Effects 0.000 title abstract 2
- 201000010099 disease Diseases 0.000 title abstract 2
- 230000003463 hyperproliferative effect Effects 0.000 title abstract 2
- 208000035475 disorder Diseases 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 239000004480 active ingredient Substances 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
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
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- 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
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
-
- 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
- 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
- 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
- A61P17/06—Antipsoriatics
-
- 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
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- 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
- 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
- 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
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- 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
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- 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
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Cardiology (AREA)
- Diabetes (AREA)
- Heart & Thoracic Surgery (AREA)
- Hematology (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Ophthalmology & Optometry (AREA)
- Hospice & Palliative Care (AREA)
- Obesity (AREA)
- Rheumatology (AREA)
- Urology & Nephrology (AREA)
- Psychiatry (AREA)
- Oncology (AREA)
- Pulmonology (AREA)
- Transplantation (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US87309006P | 2006-12-05 | 2006-12-05 | |
| PCT/US2007/024985 WO2008070150A1 (fr) | 2006-12-05 | 2007-12-05 | Produits dérivés de 2,3-dihydroimidazo[1,2-c]quinazoline substitués, utiles pour le traitement de troubles hyperlifératifs et de maladies associées à une angiogénèse |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TN2009000137A1 true TN2009000137A1 (en) | 2010-10-18 |
Family
ID=39492563
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TNP2009000137A TN2009000137A1 (en) | 2006-12-05 | 2009-04-13 | Substituted 2,3-dihydroimidazo[1,2-c]quinazoline derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis |
Country Status (41)
| Country | Link |
|---|---|
| US (3) | USRE46856E1 (fr) |
| EP (1) | EP2096919B1 (fr) |
| JP (1) | JP5326092B2 (fr) |
| KR (1) | KR101501785B1 (fr) |
| CN (4) | CN108774232B (fr) |
| AR (1) | AR064106A1 (fr) |
| AU (1) | AU2007328008B2 (fr) |
| BR (1) | BRPI0720178B8 (fr) |
| CA (1) | CA2671614C (fr) |
| CL (1) | CL2007003508A1 (fr) |
| CO (1) | CO6220908A2 (fr) |
| CR (1) | CR10838A (fr) |
| CU (1) | CU23796B7 (fr) |
| DK (1) | DK2096919T3 (fr) |
| DO (1) | DOP2009000135A (fr) |
| EA (1) | EA018839B1 (fr) |
| EC (1) | ECSP099387A (fr) |
| ES (1) | ES2572189T3 (fr) |
| GT (1) | GT200900154A (fr) |
| HN (1) | HN2009001131A (fr) |
| HU (1) | HUE028773T2 (fr) |
| IL (1) | IL198273A (fr) |
| JO (1) | JO3147B1 (fr) |
| MA (1) | MA31283B1 (fr) |
| MX (1) | MX2009006001A (fr) |
| MY (1) | MY157944A (fr) |
| NO (1) | NO342348B1 (fr) |
| NZ (1) | NZ577342A (fr) |
| PA (1) | PA8759601A1 (fr) |
| PE (1) | PE20081444A1 (fr) |
| PL (1) | PL2096919T3 (fr) |
| RS (1) | RS56045B1 (fr) |
| SG (1) | SG177170A1 (fr) |
| SI (1) | SI2096919T1 (fr) |
| SV (1) | SV2009003288A (fr) |
| TN (1) | TN2009000137A1 (fr) |
| TW (1) | TWI406662B (fr) |
| UA (1) | UA96965C2 (fr) |
| UY (1) | UY30761A1 (fr) |
| WO (1) | WO2008070150A1 (fr) |
| ZA (1) | ZA200904691B (fr) |
Families Citing this family (68)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8859572B2 (en) * | 2008-01-14 | 2014-10-14 | Bayer Intellectual Property Gmbh | Sulfone substituted 2,3-dihydroimidazo [1,2-C] quinazoline derivatives useful for treating hyper-proliferative disorders and diseases with angiogenesis |
| EP2168582A1 (fr) | 2008-09-24 | 2010-03-31 | Bayer Schering Pharma Aktiengesellschaft | Combinaisons de 2,3-dihydroimidazo[1,2-c]quinazolines substituées |
| 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 |
| US8791131B2 (en) * | 2008-09-30 | 2014-07-29 | Pfizer Inc. | Imidazo[1,5]naphthyridine compounds, their pharmaceutical use and compositions |
| EP2184276A1 (fr) | 2008-11-07 | 2010-05-12 | Universite Paul Cezanne Aix-Marseille Iii | Procédé de préparation de nouvelles 1H-benzo(d) imidazol-2(3h)-ones substituées, de nouveaux intermédiaires et leur utilisation en tant qu'inhibiteurs de bace 1 |
| WO2010082627A1 (fr) | 2009-01-16 | 2010-07-22 | ダイソー株式会社 | Procédé de production d'un sel de la 2-hydroxyméthylmorpholine |
| WO2011107494A1 (fr) | 2010-03-03 | 2011-09-09 | Sanofi | Nouveaux dérivés aromatiques de glycoside, médicaments contenants ces composés, et leur utilisation |
| US20130184270A1 (en) | 2010-04-16 | 2013-07-18 | Bayer Intellectual Property Gmbh | Substituted 2,3-dihydroimidazo[1,2-c]quinazoline-containing combinations |
| WO2011157827A1 (fr) | 2010-06-18 | 2011-12-22 | Sanofi | Dérivés d'azolopyridin-3-one en tant qu'inhibiteurs de lipases et de 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 |
| 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 |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| CN103298469A (zh) | 2010-08-31 | 2013-09-11 | 首尔大学校产学协力财团 | PPARδ激动剂的胎儿重编程的用途 |
| US9675616B2 (en) | 2010-11-11 | 2017-06-13 | Bayer Intellectual Property Gmbh | Arylaminoalcohol-substituted 2,3-dihydroimidazo[1,2-C]quinolines |
| 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 | |
| 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 |
| 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 |
| 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 |
| WO2013045413A1 (fr) | 2011-09-27 | 2013-04-04 | Sanofi | Dérivés d'amide d'acide 6-(4-hydroxyphényl)-3-alkyl-1h-pyrazolo[3,4-b] pyridine-4-carboxylique utilisés comme inhibiteurs de kinase |
| EP2861256B1 (fr) | 2012-06-15 | 2019-10-23 | The Brigham and Women's Hospital, Inc. | Compositions pour le traitement du cancer et leurs procédés de préparation |
| WO2014068070A1 (fr) | 2012-10-31 | 2014-05-08 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Procédés pour prévenir le syndrome des antiphospholipides (sapl) |
| JP6437441B2 (ja) * | 2012-11-02 | 2018-12-12 | ティージー セラピューティクス インコーポレイテッド | 抗cd20抗体およびpi3キナーゼ選択的阻害剤の組み合わせ |
| 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 |
| UA122822C2 (uk) * | 2013-04-08 | 2021-01-06 | Байєр Фарма Акцієнгезелльшафт | ЗАСТОСУВАННЯ ЗАМІЩЕНИХ 2,3-ДИГІДРОІМІДАЗО[1,2-c]ХІНАЗОЛІНІВ ДЛЯ ЛІКУВАННЯ ЛІМФОМ |
| CN104557955B (zh) * | 2013-10-23 | 2017-05-03 | 上海汇伦生命科技有限公司 | 作为PI3K/mTOR抑制剂的三环类化合物,其制备方法和用途 |
| CA2931615A1 (fr) * | 2013-11-26 | 2015-06-04 | Gilead Sciences, Inc. | Therapies pour le traitement de troubles myeloproliferatifs |
| EP3077003A1 (fr) | 2013-12-03 | 2016-10-12 | Bayer Pharma Aktiengesellschaft | Combinaison d'inhibiteurs de la pi3k |
| CN105934256B (zh) * | 2013-12-03 | 2019-12-27 | 拜耳制药股份公司 | Pi3k-抑制剂的组合产品 |
| TWI533871B (zh) | 2014-03-11 | 2016-05-21 | 國立中央大學 | 萘并[2,3-f]喹喔啉-7,12-二酮化合物緩解疼痛的應用 |
| TWI533869B (zh) | 2014-03-11 | 2016-05-21 | 國立中央大學 | 蒽醌[2,1-c][1,2,5]噻二唑-6,11-二酮化合物緩解疼痛的應用 |
| FR3018813B1 (fr) * | 2014-03-18 | 2016-04-15 | Maco Pharma Sa | Procede de synthese d'un derive de psoralene |
| WO2016059220A1 (fr) | 2014-10-16 | 2016-04-21 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Agents d'activation du tcr à utiliser dans le traitement de la lla-t |
| EP3018131A1 (fr) | 2014-11-07 | 2016-05-11 | Bayer Pharma Aktiengesellschaft | Synthèse de copanlisib et son sel de dichlorhydrate |
| EP3018127A1 (fr) * | 2014-11-07 | 2016-05-11 | Bayer Pharma Aktiengesellschaft | Synthèse de copanlisib et son sel de dichlorhydrate |
| EA201791974A1 (ru) | 2015-03-09 | 2018-05-31 | Байер Фарма Акциенгезельшафт | Комбинации, содержащие замещенный 2,3-дигидроимидазо[1,2-с]хиназолин |
| HK1250645A1 (zh) * | 2015-03-09 | 2019-01-11 | Bayer Pharma Aktiengesellschaft | 取代的2,3-二氢咪唑并[1,2-c]喹唑啉类化合物的用途 |
| FR3033499A1 (fr) * | 2015-03-11 | 2016-09-16 | Centre Leon-Berard | Composition pour le traitement des tumeurs neuroendocrines pancreatiques |
| ES2764497T3 (es) * | 2015-07-02 | 2020-06-03 | Hoffmann La Roche | Compuestos de benzoxazepina oxazolidinona y procedimientos de uso |
| CN105130998B (zh) * | 2015-09-25 | 2017-07-28 | 苏州立新制药有限公司 | 库潘尼西的制备方法 |
| CN105130997B (zh) * | 2015-09-25 | 2017-12-05 | 苏州明锐医药科技有限公司 | 一种库潘尼西的制备方法 |
| CA3016584A1 (fr) * | 2016-03-08 | 2017-09-14 | Bayer Pharma Aktiengesellschaft | 2-amino-n-[7-methoxy-2,3-dihydroimidazo-[1,2-c]quinazolin-5-yl]pyrimidine-5-carboxamides |
| EP3219329A1 (fr) | 2016-03-17 | 2017-09-20 | Bayer Pharma Aktiengesellschaft | Combinaisons de copanlisib |
| KR102434879B1 (ko) | 2016-05-26 | 2022-08-22 | 유니버시티 오브 피츠버그 - 오브 더 커먼웰쓰 시스템 오브 하이어 에듀케이션 | 폐혈관 질환 치료용 조성물 및 방법 |
| WO2017211248A1 (fr) * | 2016-06-08 | 2017-12-14 | 深圳市塔吉瑞生物医药有限公司 | Composé d'imidazoquinazoline substitué et composition pharmaceutique correspondante |
| JP2019532922A (ja) | 2016-09-23 | 2019-11-14 | 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 |
| CN106177918A (zh) * | 2016-09-30 | 2016-12-07 | 广州赛莱拉干细胞科技股份有限公司 | 一种间充质干细胞注射液及其制备方法和应用 |
| WO2018112176A1 (fr) | 2016-12-14 | 2018-06-21 | Tarveda Therapeutics, Inc. | Conjugués ciblant hsp90 et formulations de ces derniers |
| CA3054249A1 (fr) | 2017-02-24 | 2018-08-30 | Bayer Pharma Aktiengesellschaft | Combinaisons de copanlisib avec un anticorps anti-pd-1 |
| WO2018215282A1 (fr) | 2017-05-26 | 2018-11-29 | Bayer Pharma Aktiengesellschaft | Combinaison d'inhibiteurs de bub1 et de pi3k |
| CA3068324A1 (fr) | 2017-06-28 | 2019-01-03 | Bayer Consumer Care Ag | Combinaison d'un inhibiteur de pi3k et d'un antagoniste du recepteur des androgenes |
| US11253594B2 (en) * | 2017-07-07 | 2022-02-22 | University Of Pittsburgh-Of The Commonwealth System Of Higher Education | Drug combinations for protecting against neuronal cell death |
| ES2930081T3 (es) * | 2017-08-11 | 2022-12-07 | Teligene Ltd | Pirazolopirimidinas sustituidas útiles como inhibidores de quinasas |
| JP2020533292A (ja) | 2017-09-08 | 2020-11-19 | バイエル・コンシューマー・ケア・アクチェンゲゼルシャフトBayer Consumer Care AG | コパンリシブの製剤 |
| EP3498266A1 (fr) | 2017-12-15 | 2019-06-19 | Bayer Consumer Care AG | Formulations de copanlisib |
| WO2019105734A1 (fr) | 2017-11-28 | 2019-06-06 | Bayer Consumer Care Ag | Combinaisons de copanlisib |
| WO2019105835A1 (fr) | 2017-11-29 | 2019-06-06 | Bayer Consumer Care Ag | Combinaisons de copanlisib et d'anetumab ravtansine |
| WO2019197269A1 (fr) | 2018-04-11 | 2019-10-17 | Bayer Aktiengesellschaft | Combinaisons de copanlisib et de dérivés de triazolone ainsi que leur utilisation dans le traitement du cancer |
| 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 |
| CN108841318A (zh) * | 2018-07-12 | 2018-11-20 | 中国科学院海洋研究所 | 一种自修复壳聚糖水凝胶防腐涂料及其合成方法 |
| CA3110754A1 (fr) | 2018-08-28 | 2020-03-05 | Bayer As | Combinaison d'inhibiteurs de pi3k et de conjugues de thorium cibles |
| EP3866805A1 (fr) | 2018-10-16 | 2021-08-25 | Bayer Aktiengesellschaft | Combinaison d'inhibiteurs de kinase atr avec des composés de 2,3-dihydro-imidazo[1,2-c]quinazoline |
| CN109516961B (zh) * | 2018-12-25 | 2021-01-01 | 浙江大学 | 氨基喹唑啉酮和氨基异喹啉酮衍生物及其应用 |
| WO2020164997A1 (fr) | 2019-02-12 | 2020-08-20 | Bayer Aktiengesellschaft | Combinaison d'inhibiteurs de la pi3k |
| WO2023139125A1 (fr) | 2022-01-18 | 2023-07-27 | Synthon B.V. | Procédé amélioré de préparation de copanlisib |
| WO2023218032A1 (fr) | 2022-05-13 | 2023-11-16 | Synthon B.V. | Formes solides de sels de copanlisib |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3644354A (en) | 1968-09-16 | 1972-02-22 | Sandoz Ag | 5-substituted-2 3-dihydroimidazo(1 2-c)quinazolines |
| US4146718A (en) * | 1978-04-10 | 1979-03-27 | Bristol-Myers Company | Alkyl 5,6-dichloro-3,4-dihydro-2(1h)-iminoquinazoline-3-acetate hydrohalides |
| US6608053B2 (en) * | 2000-04-27 | 2003-08-19 | Yamanouchi Pharmaceutical Co., Ltd. | Fused heteroaryl derivatives |
| DE60112272T2 (de) * | 2000-04-27 | 2006-05-24 | Astellas Pharma Inc. | Imidazopyridin-derivate |
| PA8578001A1 (es) * | 2002-08-07 | 2004-05-07 | Warner Lambert Co | Combinaciones terapeuticas de inhibidores de quinasa de erb b y terapias antineoplasicas |
| NZ539062A (en) * | 2002-09-30 | 2007-05-31 | Bayer Pharmaceuticals Corp | Fused azole-pyrimidine derivatives exhibiting enhanced potency for phosphotidylinositol-3-kinase (P13K) inhibition |
| AU2004249138B2 (en) * | 2003-06-12 | 2008-07-17 | Merck Sharp & Dohme Corp. | Mitotic kinesin inhibitors |
| AT412873B (de) | 2004-02-20 | 2005-08-25 | Aop Orphan Pharmaceuticals Ag | Verfahren zur herstellung von anagrelid hydrochlorid |
| WO2007143483A2 (fr) | 2006-06-01 | 2007-12-13 | Smithkline Beecham Corporation | Procédé de traitement du cancer |
| WO2008002039A1 (fr) | 2006-06-28 | 2008-01-03 | Hanmi Pharm. Co., Ltd. | Dérivés de quinazoline destinés à inhiber le développement de cellules cancéreuses |
| EP2508525A1 (fr) | 2011-04-05 | 2012-10-10 | Bayer Pharma Aktiengesellschaft | Sels de 2,3-dihydroimidazo[1,2-C]quinazoline substitutés |
-
2007
- 2007-12-03 AR ARP070105390A patent/AR064106A1/es active IP Right Grant
- 2007-12-04 PE PE2007001709A patent/PE20081444A1/es active IP Right Grant
- 2007-12-04 PA PA20078759601A patent/PA8759601A1/es unknown
- 2007-12-04 TW TW096145999A patent/TWI406662B/zh not_active IP Right Cessation
- 2007-12-04 JO JOP/2007/0517A patent/JO3147B1/ar active
- 2007-12-04 UY UY30761A patent/UY30761A1/es not_active Application Discontinuation
- 2007-12-05 HU HUE07862580A patent/HUE028773T2/en unknown
- 2007-12-05 RS RS20170561A patent/RS56045B1/sr unknown
- 2007-12-05 JP JP2009540293A patent/JP5326092B2/ja not_active Expired - Fee Related
- 2007-12-05 EA EA200900733A patent/EA018839B1/ru not_active IP Right Cessation
- 2007-12-05 DK DK07862580.3T patent/DK2096919T3/en active
- 2007-12-05 ES ES07862580T patent/ES2572189T3/es active Active
- 2007-12-05 CN CN201810535933.9A patent/CN108774232B/zh active Active
- 2007-12-05 PL PL07862580T patent/PL2096919T3/pl unknown
- 2007-12-05 SG SG2011088887A patent/SG177170A1/en unknown
- 2007-12-05 US US15/398,916 patent/USRE46856E1/en not_active Expired - Fee Related
- 2007-12-05 BR BRPI0720178A patent/BRPI0720178B8/pt not_active IP Right Cessation
- 2007-12-05 CN CN201510632842.3A patent/CN105254634B/zh active Active
- 2007-12-05 US US12/517,875 patent/US8466283B2/en not_active Ceased
- 2007-12-05 CA CA2671614A patent/CA2671614C/fr active Active
- 2007-12-05 UA UAA200906701A patent/UA96965C2/ru unknown
- 2007-12-05 CL CL200703508A patent/CL2007003508A1/es unknown
- 2007-12-05 CN CN202211453281.7A patent/CN115724847A/zh active Pending
- 2007-12-05 CN CN200780044849.7A patent/CN101631464B/zh active Active
- 2007-12-05 NZ NZ577342A patent/NZ577342A/en not_active IP Right Cessation
- 2007-12-05 MY MYPI20092044A patent/MY157944A/en unknown
- 2007-12-05 MX MX2009006001A patent/MX2009006001A/es active IP Right Grant
- 2007-12-05 SI SI200731771A patent/SI2096919T1/sl unknown
- 2007-12-05 KR KR1020097011551A patent/KR101501785B1/ko not_active Expired - Fee Related
- 2007-12-05 WO PCT/US2007/024985 patent/WO2008070150A1/fr not_active Application Discontinuation
- 2007-12-05 AU AU2007328008A patent/AU2007328008B2/en not_active Ceased
- 2007-12-05 EP EP07862580.3A patent/EP2096919B1/fr active Active
-
2009
- 2009-04-13 TN TNP2009000137A patent/TN2009000137A1/fr unknown
- 2009-04-21 IL IL198273A patent/IL198273A/en active IP Right Grant
- 2009-06-04 CO CO09057915A patent/CO6220908A2/es active IP Right Grant
- 2009-06-04 EC EC2009009387A patent/ECSP099387A/es unknown
- 2009-06-04 HN HN2009001131A patent/HN2009001131A/es unknown
- 2009-06-05 SV SV2009003288A patent/SV2009003288A/es unknown
- 2009-06-05 CU CU20090103A patent/CU23796B7/es active IP Right Grant
- 2009-06-05 DO DO2009000135A patent/DOP2009000135A/es unknown
- 2009-06-05 CR CR10838A patent/CR10838A/es unknown
- 2009-06-05 GT GT200900154A patent/GT200900154A/es unknown
- 2009-06-29 MA MA32057A patent/MA31283B1/fr unknown
- 2009-07-03 NO NO20092529A patent/NO342348B1/no unknown
- 2009-07-03 ZA ZA200904691A patent/ZA200904691B/xx unknown
-
2013
- 2013-06-03 US US13/908,566 patent/US20130261113A1/en not_active Abandoned
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| TN2009000137A1 (en) | Substituted 2,3-dihydroimidazo[1,2-c]quinazoline derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis | |
| PH12013500938A1 (en) | Aminoalcohol substituted 2,3-dihydroimidazo[1,2-c]quinazoline derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis | |
| WO2009091550A8 (fr) | Dérivés de 2,3-dihydroimidazo [1,2-c] quinazoline à substitution sulfone utilisés pour traiter des troubles hyperproliférants et des maladies associées à l'angiogénèse | |
| WO2007064931A3 (fr) | Derives substitues de 4-amino-pyrrolotriazine utiles dans le traitement de troubles hyperproliferatifs et de maladies associees a l'angiogenese | |
| MY143795A (en) | Tetrahydropyridoindole derivatives | |
| MY144992A (en) | Substituted 1,2,3,4-tetrahydroisoquinoline derivatives. | |
| WO2005004818A3 (fr) | Composes heterocycliques et leur utilisation comme agents anticancereux | |
| MX2009012000A (es) | Derivados de pirazol heteroarilo sustituidos utiles para el tratamiento de trastornos hiperproliferativos y enfermedades asociadas a la angiogenesis. | |
| MY191349A (en) | New pharmaceutical compositions for the treatment of hyper-proliferative disorders | |
| MX2009004745A (es) | Derivados de 1,2,3-triazol como inhibidores del receptor sigma. | |
| DE602005021770D1 (de) | Indol-1-yl-essigsäurederivate | |
| MY144897A (en) | 2,3,4,9-tetrahydro-1h-carbazole derivatives as crth2 receptor antagonists | |
| WO2007075650A3 (fr) | Derives substitues de la pyrimidine utilisables dans le traitement du cancer et d'autres affections | |
| TW200628468A (en) | Bicyclononene derivatives | |
| MY148611A (en) | Imino-imidazo-pyridine derivatives having antithrombotic activity | |
| TN2013000204A1 (en) | Aminoalcohol substituted 2,3-dihydroimidazo[1,2-c]quinazoline derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis | |
| WO2006110447A3 (fr) | Derives de pyrimidine | |
| TH85706B (th) | อนุพันธ์ 2,3-ไดไฮโดรอิมิดาโซ[1,2-c]ควินาโซลีนถูกแทนที่ (Substituted 2,3-dihydromidazo[1,2-c]quinazoline Derivatives) ซึ่งเป็นประโยชน์สำหรับการรักษาความผิดปกติด้านงอกขยายเกินปกติ และ โรคที่มีส่วนสัมพันธ์กับการก่อเกิดหลอดเลือดใหม่ | |
| TH149016A (th) | อนุพันธ์ 2,3-ไดไฮโดรอิมิดาโซ[1,2-c]ควินาโซลีนถูกแทนที่ (Substituted 2,3-dihydromidazo[1,2-c]quinazoline Derivatives) ซึ่งเป็นประโยชน์สำหรับการรักษาความผิดปกติด้านงอกขยายเกินปกติ และ โรคที่มีส่วนสัมพันธ์กับการก่อเกิดหลอดเลือดใหม่ | |
| TW200603791A (en) | Compounds and compositions as cathepsin S inhibitors | |
| CY1117512T1 (el) | Υποκατεστημενα παραγωγα 2,3-δiυδpoϊmiδazo[1,2-c] κιναζολινης χρησιμα στη θεραπευτικη αντιμετωπιση υπερ-πολλαπλασιαστικων διαταραχων και παθησεων που σχετιζονται με την αγγειογενεση |