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
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- 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
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- 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
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- 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
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- 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
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- A—HUMAN NECESSITIES
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- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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- A—HUMAN NECESSITIES
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- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
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- 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
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- 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)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pest Control & Pesticides (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Ophthalmology & Optometry (AREA)
- Biomedical Technology (AREA)
- Rheumatology (AREA)
- Urology & Nephrology (AREA)
- Obesity (AREA)
- Hospice & Palliative Care (AREA)
- Physical Education & Sports Medicine (AREA)
- Endocrinology (AREA)
- Dermatology (AREA)
- Pain & Pain Management (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 |
|---|---|---|---|---|
| WO2009091550A2 (fr) * | 2008-01-14 | 2009-07-23 | Bayer Healthcare Llc | 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 |
| 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 |
| EP2168582A1 (fr) | 2008-09-24 | 2010-03-31 | Bayer Schering Pharma Aktiengesellschaft | Combinaisons de 2,3-dihydroimidazo[1,2-c]quinazolines substituées |
| CA2735932C (fr) * | 2008-09-30 | 2013-07-09 | Pfizer Inc. | Composes d'imidazo[1,5]naphtyridine, leur utilisation pharmaceutique et compositions associees |
| 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 |
| US8648190B2 (en) | 2009-01-16 | 2014-02-11 | Daiso Co., Ltd. | Process for producing 2-hydroxymethylmorpholine salt |
| WO2011107494A1 (fr) | 2010-03-03 | 2011-09-09 | Sanofi | Nouveaux dérivés aromatiques de glycoside, médicaments contenants ces composés, et leur utilisation |
| MA34158B1 (fr) * | 2010-04-16 | 2013-04-03 | Bayer Ip Gmbh | Combinaisons contenant une 2,3-dihydroimidazo{1,2-c]quinazoline substituée |
| EP2582709B1 (fr) | 2010-06-18 | 2018-01-24 | 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 |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, 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 |
| CA2809958A1 (fr) | 2010-08-31 | 2012-03-08 | Snu R & Db Foundation | Utilisation de la reprogrammation ftale d'un agoniste des ppar ? |
| CA2817287A1 (fr) | 2010-11-11 | 2012-05-18 | Bayer Intellectual Property Gmbh | 2,3-dihydroimidazo[1,2-c]quinolines a substitution arylaminoalcool |
| 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 | |
| CA2817312A1 (fr) | 2010-11-11 | 2012-05-18 | Bayer Intellectual Property Gmbh | 2,3-dihydroimidazo[1,2-c]quinazolines a substitution alcoxy |
| 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 |
| WO2013188763A1 (fr) * | 2012-06-15 | 2013-12-19 | The Brigham And Women's Hospital, Inc. | Compositions pour le traitement du cancer et leurs procédés de préparation |
| US20150258127A1 (en) | 2012-10-31 | 2015-09-17 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for preventing antiphospholipid syndrome (aps) |
| WO2014071125A1 (fr) * | 2012-11-02 | 2014-05-08 | Tg Therapeutics, Inc. | Association d'un anticorps anti-cd20 et d'un inhibiteur sélectif de la pi3 kinase |
| 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 |
| EP2983669B1 (fr) * | 2013-04-08 | 2018-10-24 | Bayer Pharma Aktiengesellschaft | Utilisation de 2,3-dihydroimidazo[1,2-c]quinazolines substituées pour traiter les lymphomes |
| 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 |
| EP3077002B1 (fr) | 2013-12-03 | 2020-04-22 | Bayer Pharma Aktiengesellschaft | Combinaisons d'inhibiteurs de pi3k |
| EP3077003A1 (fr) | 2013-12-03 | 2016-10-12 | Bayer Pharma Aktiengesellschaft | Combinaison d'inhibiteurs de la pi3k |
| 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 |
| 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 |
| FR3018813B1 (fr) * | 2014-03-18 | 2016-04-15 | Maco Pharma Sa | Procede de synthese d'un derive de psoralene |
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| AU2017376766A1 (en) | 2016-12-14 | 2019-06-06 | Tva (Abc), Llc | HSP90-targeting conjugates and formulations thereof |
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| 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 |
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