MA33053B1 - Inhibiteurs de la poly(adp-ribose) polymerase (parp) - Google Patents
Inhibiteurs de la poly(adp-ribose) polymerase (parp)Info
- Publication number
- MA33053B1 MA33053B1 MA34106A MA34106A MA33053B1 MA 33053 B1 MA33053 B1 MA 33053B1 MA 34106 A MA34106 A MA 34106A MA 34106 A MA34106 A MA 34106A MA 33053 B1 MA33053 B1 MA 33053B1
- Authority
- MA
- Morocco
- Prior art keywords
- parp
- compounds
- adp
- ribose
- polymerase
- Prior art date
Links
- 229920000776 Poly(Adenosine diphosphate-ribose) polymerase Polymers 0.000 title abstract 3
- 102000012338 Poly(ADP-ribose) Polymerases Human genes 0.000 title 2
- 108010061844 Poly(ADP-ribose) Polymerases Proteins 0.000 title 2
- 239000003112 inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 3
- 238000000034 method Methods 0.000 abstract 2
- 201000010099 disease Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 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
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains three hetero rings
- C07D513/14—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
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic 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
- A61K31/495—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
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further 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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- 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
- A61K31/5383—1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with heterocyclic 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
- A61K31/542—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 ortho- or peri-condensed with heterocyclic 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
- A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
- A61K31/5517—1,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
-
- 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
- A61K31/63—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide
- A61K31/635—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide having a heterocyclic ring, e.g. sulfadiazine
-
- 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
- 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
- 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
- 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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/08—Plasma substitutes; Perfusion solutions; Dialytics or haemodialytics; Drugs for electrolytic or acid-base disorders, e.g. hypovolemic shock
-
- 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
- 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
- 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
- C07D471/12—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 three hetero rings
- C07D471/14—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
- C07D498/12—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 three hetero rings
- C07D498/14—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Hospice & Palliative Care (AREA)
- Urology & Nephrology (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Obesity (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Epoxy Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
LA PRÉSENTE INVENTION CONCERNE DES COMPOSÉS DE FORMULE (I) SUIVANTE DANS LAQUELLE R1, R2, R3, R4, R5, R6, R7, X ET T SONT TELS QUE DÉFINIS DANS LE MÉMOIRE DESCRIPTIF. L'INVENTION CONCERNE ÉGALEMENT DES COMPOSITIONS PHARMACEUTIQUES, DES NÉCESSAIRES ET DES ARTICLES MANUFACTURÉS IMPLIQUANT LES COMPOSÉS, LES PROCÉDÉS ET LES INTERMÉDIAIRES UTILISABLES POUR LA FABRICATION DESDITS COMPOSÉS, AINSI QUE DES PROCÉDÉS D'UTILISATION DESDITS COMPOSÉS EN VUE DU TRAITEMENT DE MALADIES, D'AFFECTIONS ET DE TROUBLES ASSOCIÉS À L'ACTIVITÉ DE LA PARP.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US14674009P | 2009-01-23 | 2009-01-23 | |
| US22887909P | 2009-07-27 | 2009-07-27 | |
| PCT/US2010/021669 WO2010085570A1 (fr) | 2009-01-23 | 2010-01-21 | Inhibiteurs de la poly(adp-ribose)polymérase (parp) |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA33053B1 true MA33053B1 (fr) | 2012-02-01 |
Family
ID=42271897
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA34106A MA33053B1 (fr) | 2009-01-23 | 2010-01-21 | Inhibiteurs de la poly(adp-ribose) polymerase (parp) |
Country Status (23)
| Country | Link |
|---|---|
| US (5) | US7928105B2 (fr) |
| EP (1) | EP2389379A1 (fr) |
| JP (1) | JP5567599B2 (fr) |
| KR (1) | KR101779137B1 (fr) |
| CN (1) | CN102341394B (fr) |
| AU (1) | AU2010206744B2 (fr) |
| BR (1) | BRPI1007358A2 (fr) |
| CA (1) | CA2750106A1 (fr) |
| CL (1) | CL2011001754A1 (fr) |
| CO (1) | CO6410305A2 (fr) |
| CR (1) | CR20110452A (fr) |
| DO (1) | DOP2011000237A (fr) |
| EA (1) | EA020301B1 (fr) |
| EC (1) | ECSP11011284A (fr) |
| IL (1) | IL213993A (fr) |
| MA (1) | MA33053B1 (fr) |
| MX (1) | MX2011007741A (fr) |
| MY (1) | MY152386A (fr) |
| NZ (1) | NZ594322A (fr) |
| PE (1) | PE20120418A1 (fr) |
| SG (1) | SG172958A1 (fr) |
| TN (1) | TN2011000339A1 (fr) |
| WO (1) | WO2010085570A1 (fr) |
Families Citing this family (68)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MA33053B1 (fr) * | 2009-01-23 | 2012-02-01 | Tadeka Pharmaceutical Company Ltd | Inhibiteurs de la poly(adp-ribose) polymerase (parp) |
| JP5715625B2 (ja) | 2009-07-30 | 2015-05-07 | 武田薬品工業株式会社 | ポリ(adp−リボース)ポリメラーゼ(parp)阻害剤 |
| US8247436B2 (en) | 2010-03-19 | 2012-08-21 | Novartis Ag | Pyridine and pyrazine derivative for the treatment of CF |
| US9301962B2 (en) | 2010-05-14 | 2016-04-05 | Baylor College Of Medicine | Male contraceptive compositions and methods of use |
| MX373121B (es) | 2010-05-14 | 2020-04-30 | Dana Farber Cancer Inst Inc | Composiciones y metodos para el tratamiento de leucemia. |
| MX384074B (es) | 2010-05-14 | 2025-03-12 | Dana Farber Cancer Inst Inc | Composiciones y métodos para tratar neoplasias, enfermedades inflamatorias y otros trastornos. |
| CA2848154C (fr) | 2011-09-30 | 2020-04-28 | C&C Research Laboratories | Nouveaux derives heterocycliques et leurs utilisations |
| MX385227B (es) | 2012-01-20 | 2025-03-14 | Del Mar Pharmaceuticals | Uso de hexitoles sustituidos que incluyen dianhidrogalactitol y análogos para tratar enfermedad neoplásica y células madre de cáncer que incluyen glioblastoma multiforme y meduloblastoma. |
| US20150344444A1 (en) * | 2012-12-20 | 2015-12-03 | Bayer Pharma Aktiengesellschaft | Bet-protein-inhibiting dihydroxyquinoxalinones |
| CN103923088B (zh) * | 2013-01-11 | 2016-09-07 | 上海汇伦生命科技有限公司 | 2,5-二氮杂双环[2.2.1]庚烷类化合物和制备方法、其药用组合物及其在医药上的应用 |
| US9714946B2 (en) | 2013-03-14 | 2017-07-25 | Dana-Farber Cancer Institute, Inc. | Bromodomain binding reagents and uses thereof |
| EP2983674A4 (fr) | 2013-04-08 | 2017-05-10 | Dennis M. Brown | Bénéfice thérapeutique de composés chimiques administrés de façon sous-optimale |
| US20160176867A1 (en) * | 2013-07-09 | 2016-06-23 | Bayer Pharma Aktiengesellschaft | Modified bet-protein-inhibiting dihydroquinoxalinones and dihydropyridopyrazinones |
| WO2015013635A2 (fr) | 2013-07-25 | 2015-01-29 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs des facteurs de transcription et leurs utilisations |
| CA2928568A1 (fr) | 2013-07-26 | 2015-01-29 | Update Pharma Inc. | Procedes combinatoires permettant d'ameliorer l'avantage therapeutique du bisantrene |
| EP3066101B1 (fr) | 2013-11-08 | 2020-07-29 | Dana-Farber Cancer Institute, Inc. | Polythérapie pour le traitement du cancer utilisant des inhibiteurs de protéine à bromodomaine et à domaine extra-terminal (bet) |
| EP3099677A4 (fr) | 2014-01-31 | 2017-07-26 | Dana-Farber Cancer Institute, Inc. | Dérivés de diaminopyrimidine benzènesulfone et leurs utilisations |
| JP2017504650A (ja) * | 2014-01-31 | 2017-02-09 | ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド | ジアゼパン誘導体およびその使用 |
| WO2015117087A1 (fr) | 2014-01-31 | 2015-08-06 | Dana-Farber Cancer Institute, Inc. | Utilisations des dérivés de diazépane |
| KR20160130778A (ko) | 2014-02-28 | 2016-11-14 | 텐샤 세러퓨틱스 인코포레이티드 | 고인슐린혈증과 관련된 질환의 치료 |
| JP6783224B2 (ja) | 2014-04-04 | 2020-11-11 | デル マー ファーマシューティカルズ | 肺の非小細胞癌腫及び卵巣癌を処置するためのジアンヒドロガラクチトール及びその類縁体又は誘導体の使用 |
| KR102310128B1 (ko) * | 2014-07-14 | 2021-10-06 | 주식회사 포스코 | 트리아진-피페라진 골격을 갖는 알파-헬릭스 유사체 및 이의 제조방법 |
| EP3177626A4 (fr) | 2014-08-08 | 2017-12-27 | Dana Farber Cancer Institute, Inc. | Dérivés de diazépane et leurs utilisations |
| MX2017001757A (es) | 2014-08-08 | 2017-05-30 | Dana Farber Cancer Inst Inc | Derivados de dihidropteridinona y sus usos. |
| AU2015339511B2 (en) | 2014-10-27 | 2020-05-14 | Tensha Therapeutics, Inc. | Bromodomain inhibitors |
| EP3307728A4 (fr) | 2015-06-12 | 2019-07-17 | Dana Farber Cancer Institute, Inc. | Thérapie d'association utilisant des inhibiteurs de transcription et des inhibiteurs de kinases |
| PE20181287A1 (es) | 2015-09-11 | 2018-08-07 | Dana Farber Cancer Inst Inc | Ciano tienotriazolpirazinas y usos de las mismas |
| UA123946C2 (uk) | 2015-09-11 | 2021-06-30 | Дана-Фарбер Кенсер Інстітьют, Інк. | Ацетамідтієнотриазолодіазепіни й шляхи їх застосування |
| CA3003288A1 (fr) | 2015-11-25 | 2017-06-01 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de bromodomaines bivalents et leurs utilisations |
| EP3440052B1 (fr) | 2016-04-06 | 2023-10-25 | University Of Oulu | Composés pour utilisation dans le traitement du cancer |
| DE102017005089A1 (de) | 2016-05-30 | 2017-11-30 | Bayer Pharma Aktiengesellschaft | Substitulerte 3,4-Dihydrochinoxalin-2(1H)-one |
| DE102017005091A1 (de) | 2016-05-30 | 2017-11-30 | Bayer Pharma Aktiengesellschaft | Substituierte 3,4-Dihydropyrido[2,3-b]pyrazin-2(1H)-one |
| EP3267192B1 (fr) * | 2016-07-07 | 2020-08-19 | Alpha M.O.S. | Chromatographe en phase gazeuse comprenant des capteurs a oxyde metallique |
| CN106883232B (zh) * | 2017-03-31 | 2019-01-22 | 苏州康润医药有限公司 | 一种氮杂非那烯-3-酮的衍生物及其制备方法与应用 |
| HUE071067T2 (hu) * | 2019-07-19 | 2025-07-28 | Astrazeneca Ab | PARP1 inhibitorok |
| CN111097386B (zh) * | 2019-12-26 | 2022-01-11 | 江苏大学 | 一种二维层状水稳定染料吸附剂及制备方法 |
| US11795158B2 (en) | 2020-06-25 | 2023-10-24 | Astrazeneca Ab | Chemical compounds |
| CA3216373A1 (fr) | 2021-04-19 | 2022-10-27 | Lynnie TRZOSS | Inhibiteurs de parp1 et leurs utilisations |
| AU2022261011A1 (en) * | 2021-04-22 | 2023-11-16 | Wigen Biomedicine Technology (shanghai) Co., Ltd. | Parp inhibitor containing piperazine structure, preparation method therefor and pharmaceutical use thereof |
| WO2022222966A1 (fr) * | 2021-04-23 | 2022-10-27 | 成都百裕制药股份有限公司 | Inhibiteur sélectif de parp1 et son application |
| CN115702156A (zh) * | 2021-04-23 | 2023-02-14 | 南京明德新药研发有限公司 | 吡啶酰胺类化合物 |
| CN117083274A (zh) * | 2021-04-23 | 2023-11-17 | 四川海思科制药有限公司 | 一种并环杂环衍生物及其在医药上的应用 |
| CN115403595A (zh) * | 2021-05-27 | 2022-11-29 | 江苏恒瑞医药股份有限公司 | 含氮杂环类化合物、其制备方法及其在医药上的应用 |
| CN117980307A (zh) * | 2021-08-27 | 2024-05-03 | 上海瑛派药业有限公司 | 取代的三环类化合物作为parp抑制剂及其应用 |
| WO2023046034A1 (fr) * | 2021-09-22 | 2023-03-30 | 明慧医药(杭州)有限公司 | Composé hétérocyclique contenant de l'azote, son procédé de préparation, intermédiaire de celui-ci et application de celui-ci |
| WO2023046158A1 (fr) * | 2021-09-26 | 2023-03-30 | 张文燕 | Composé d'azaquinolinone et son utilisation médicale |
| WO2023046149A1 (fr) * | 2021-09-26 | 2023-03-30 | 张文燕 | Composé quinoxaline et son utilisation médicinale |
| EP4410791A4 (fr) * | 2021-09-30 | 2025-10-22 | Xizang Haisco Pharmaceutical Co Ltd | Inhibiteur de parp dérivé bicyclique et son utilisation |
| CN118043322A (zh) * | 2021-09-30 | 2024-05-14 | 西藏海思科制药有限公司 | 含氮杂环衍生物parp抑制剂及其用途 |
| US20240400586A1 (en) * | 2021-09-30 | 2024-12-05 | Haisco Pharmaceutical Group Co., Ltd. | Heteroaryl derivative parp inhibitor and use thereof |
| CR20240144A (es) | 2021-10-01 | 2024-05-24 | Xinthera Inc | Inhibidores de parp1 de azetidina y pirrolidina y usos de estos |
| WO2023061406A1 (fr) * | 2021-10-12 | 2023-04-20 | 微境生物医药科技(上海)有限公司 | Inhibiteur de parp contenant une structure tricyclique condensée, son procédé de préparation et son utilisation médicale |
| JP7762306B2 (ja) * | 2021-11-19 | 2025-10-29 | 康百達(四川)生物医薬科技有限公司 | 選択的parp1阻害剤およびその用途 |
| WO2023096915A1 (fr) * | 2021-11-24 | 2023-06-01 | Slap Pharmaceuticals Llc | Composés multicycliques |
| JP7804371B2 (ja) * | 2021-12-17 | 2026-01-22 | キーセラ(スーチョウ)バイオ-ファーマスーティカルズ カンパニー,リミテッド | Parp阻害剤、それを含む医薬組成物及びそれらの使用 |
| WO2023134647A1 (fr) * | 2022-01-13 | 2023-07-20 | 优领医药科技(香港)有限公司 | Dérivé contenant un cycle pipérazino, sel pharmaceutiquement acceptable de celui-ci, son procédé de préparation et son utilisation |
| AU2023209820B2 (en) | 2022-01-21 | 2024-10-10 | Xinthera, Inc. | Parp1 inhibitors and uses thereof |
| IL315586A (en) * | 2022-03-11 | 2024-11-01 | Impact Therapeutics Shanghai Inc | Substituted tricyclic compounds as parp inhibitors and the use thereof |
| CA3250945A1 (fr) | 2022-04-28 | 2023-11-02 | Xinthera, Inc. | Inhibiteurs de parp1 tricycliques et leurs utilisations |
| WO2023207284A1 (fr) * | 2022-04-28 | 2023-11-02 | Ningbo Newbay Technology Development Co., Ltd | Dérivés de pipérazine utilisés comme inhibiteurs de parp1 |
| CN117263943A (zh) * | 2022-09-09 | 2023-12-22 | 轩竹生物科技股份有限公司 | 聚(adp核糖)聚合酶选择性抑制剂 |
| CN117917407A (zh) * | 2022-10-20 | 2024-04-23 | 成都赜灵生物医药科技有限公司 | 并杂环类化合物及其用途 |
| JP2025538192A (ja) * | 2022-11-10 | 2025-11-26 | 上海海和薬物研究開発股▲ふん▼有限公司 | 縮合三環式parp1阻害剤、その調製方法、および使用 |
| JP2025537520A (ja) * | 2022-11-10 | 2025-11-18 | チア タイ ティエンチン ファーマシューティカル グループ カンパニー リミテッド | 縮合二環化合物 |
| EP4665724A1 (fr) * | 2023-02-16 | 2025-12-24 | Ohio State Innovation Foundation | Inhibiteurs de topoisomérase de type ii et leurs procédés de fabrication et d'utilisation |
| KR20250154499A (ko) * | 2023-03-01 | 2025-10-28 | 임팩트 테라퓨틱스 (상하이), 인코포레이티드 | Parp 억제제로서의 치환된 질소-함유 트리시클릭 화합물 및 이의 용도 |
| CN120677162A (zh) * | 2023-06-13 | 2025-09-19 | 中国医药研究开发中心有限公司 | 含氮杂环类化合物及其医药用途 |
| US12258345B1 (en) | 2023-12-12 | 2025-03-25 | King Faisal University | Pyrrolo[3,2-c]isoquinoline-2,3-dione compounds as CK2 inhibitors |
Family Cites Families (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4138564A (en) | 1977-08-03 | 1979-02-06 | American Home Products Corporation | Tetrahydro[1H]pyrazino[1,2-a]azaquinoxalin-5(6H)-ones and derivatives thereof |
| US4446323A (en) * | 1983-05-23 | 1984-05-01 | American Home Products Corporation | Tetra- and hexa-hydropyrrolo(1,2-a)quinoxaline and azaquinoxaline derivatives |
| US5055465A (en) | 1989-05-31 | 1991-10-08 | Berlex Laboratories, Inc. | Imidazoquinoxalinones, their aza analogs and process for their preparation |
| US5166344A (en) | 1989-05-31 | 1992-11-24 | Berlex Laboratories, Inc. | Process for the preparation of imidazoquinoxalinones |
| DE4228095A1 (de) | 1992-08-24 | 1994-03-03 | Asta Medica Ag | Neue 4,5-Dihydro-4-oxo-pyrrolo[1,2-a]chinoxaline und entsprechende Aza-analoga und Verfahren zu deren Herstellung |
| US5306819A (en) | 1992-08-27 | 1994-04-26 | Neurogen Corporation | Certain aryl a cycloalkyl fused imidazopyrazinols; and new class of GABA brain receptor ligands |
| TW274550B (fr) | 1992-09-26 | 1996-04-21 | Hoechst Ag | |
| US6121278A (en) | 1997-09-03 | 2000-09-19 | Guilford Pharmaceuticals, Inc. | Di-n-heterocyclic compounds, methods, and compositions for inhibiting parp activity |
| US6635642B1 (en) * | 1997-09-03 | 2003-10-21 | Guilford Pharmaceuticals Inc. | PARP inhibitors, pharmaceutical compositions comprising same, and methods of using same |
| US6197785B1 (en) | 1997-09-03 | 2001-03-06 | Guilford Pharmaceuticals Inc. | Alkoxy-substituted compounds, methods, and compositions for inhibiting PARP activity |
| MXPA03004832A (es) | 2000-12-01 | 2004-05-04 | Guilford Pharm Inc | Compuestos y sus usos. |
| GB0206219D0 (en) * | 2002-03-15 | 2002-05-01 | Ferring Bv | Non-Peptide GnRH antagonists |
| US7160888B2 (en) * | 2003-08-22 | 2007-01-09 | Warner Lambert Company Llc | [1,8]naphthyridin-2-ones and related compounds for the treatment of schizophrenia |
| WO2005058843A1 (fr) * | 2003-12-10 | 2005-06-30 | Janssen Pharmaceutica N.V. | 2-quinolinones substitues 6-cyclohexylalkyl substitues et 2-quinoxalinones utilises en tant qu'inhibiteurs de la poly(adp-ribose) polymerase |
| WO2006009734A1 (fr) | 2004-06-17 | 2006-01-26 | Wyeth | Antagonistes de récepteurs de l'hormone de libération de gonadotrophines |
| CA2586080A1 (fr) | 2004-11-01 | 2006-08-31 | University Of Southern California | Nouveaux composes utiles pour le traitement du cancer et des troubles associes a la fonction d'angiogenese |
| US20090093489A1 (en) | 2004-12-29 | 2009-04-09 | University Of Southern California | Novel compounds for treatment of cancer and disorders associated with angiogenesis function |
| US7947682B2 (en) | 2004-12-29 | 2011-05-24 | University Of Southern California | Substituted N′-pyrrolo[1,2-a]quinoxalin-4-yl-hydrazides as anti-cancer agents |
| JP2008528448A (ja) * | 2005-01-03 | 2008-07-31 | ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン | 新規化合物に関連する組成物および方法、ならびにその標的 |
| WO2006125179A1 (fr) | 2005-05-19 | 2006-11-23 | Xenon Pharmaceuticals Inc. | Composes tricycliques: utilisation comme agents therapeutiques |
| US7601716B2 (en) * | 2006-05-01 | 2009-10-13 | Cephalon, Inc. | Pyridopyrazines and derivatives thereof as ALK and c-Met inhibitors |
| GB0615809D0 (en) | 2006-08-09 | 2006-09-20 | Istituto Di Ricerche D Biolog | Therapeutic compounds |
| EP2123301A4 (fr) | 2006-12-13 | 2010-11-03 | Aska Pharm Co Ltd | Utilisation d'un agent thérapeutique dans les affections du tractus urinaire |
| WO2008072779A1 (fr) | 2006-12-13 | 2008-06-19 | Aska Pharmaceutical Co., Ltd. | Dérivé de quinoxaline |
| PT2698062E (pt) | 2006-12-28 | 2015-10-19 | Abbvie Inc | Inibidores da poli (adp-ribose) polimerase |
| US8466150B2 (en) | 2006-12-28 | 2013-06-18 | Abbott Laboratories | Inhibitors of poly(ADP-ribose)polymerase |
| CN101302214B (zh) * | 2007-05-11 | 2012-06-20 | 江苏国华投资有限公司 | 芳烷基哌啶(嗪)衍生物及在治疗精神神经疾病中的应用 |
| US8642660B2 (en) | 2007-12-21 | 2014-02-04 | The University Of Rochester | Method for altering the lifespan of eukaryotic organisms |
| MA33053B1 (fr) | 2009-01-23 | 2012-02-01 | Tadeka Pharmaceutical Company Ltd | Inhibiteurs de la poly(adp-ribose) polymerase (parp) |
| WO2010096426A2 (fr) | 2009-02-20 | 2010-08-26 | Emory University | Composés, compositions, procédés de synthèse et procédés de traitement |
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- 2010-01-21 KR KR1020117019556A patent/KR101779137B1/ko not_active Expired - Fee Related
- 2010-01-21 WO PCT/US2010/021669 patent/WO2010085570A1/fr not_active Ceased
- 2010-01-21 MX MX2011007741A patent/MX2011007741A/es active IP Right Grant
- 2010-01-21 JP JP2011548104A patent/JP5567599B2/ja not_active Expired - Fee Related
- 2010-01-21 CN CN201080009854.6A patent/CN102341394B/zh not_active Expired - Fee Related
- 2010-01-21 EA EA201170963A patent/EA020301B1/ru not_active IP Right Cessation
- 2010-01-21 BR BRPI1007358-2A patent/BRPI1007358A2/pt not_active Application Discontinuation
- 2010-01-21 EP EP10703547A patent/EP2389379A1/fr not_active Withdrawn
- 2010-01-21 CA CA2750106A patent/CA2750106A1/fr not_active Abandoned
- 2010-01-21 SG SG2011050630A patent/SG172958A1/en unknown
- 2010-01-21 AU AU2010206744A patent/AU2010206744B2/en not_active Ceased
- 2010-01-21 US US12/691,668 patent/US7928105B2/en not_active Expired - Fee Related
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- 2011-07-07 IL IL213993A patent/IL213993A/en not_active IP Right Cessation
- 2011-07-08 TN TN2011000339A patent/TN2011000339A1/fr unknown
- 2011-07-19 CL CL2011001754A patent/CL2011001754A1/es unknown
- 2011-07-22 DO DO2011000237A patent/DOP2011000237A/es unknown
- 2011-08-11 CO CO11102248A patent/CO6410305A2/es active IP Right Grant
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