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
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
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 (58)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SG172958A1 (en) | 2009-01-23 | 2011-08-29 | Takeda Pharmaceutical | Poly (adp-ribose) polymerase (parp) inhibitors |
WO2011014681A1 (fr) | 2009-07-30 | 2011-02-03 | Takeda Pharmaceutical Company Limited | Inhibiteurs de la poly (adp-ribose) polymérase (parp) |
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 |
WO2011143660A2 (fr) | 2010-05-14 | 2011-11-17 | Dana-Farber Cancer Institute, Inc. | Compositions et méthodes de traitement de la leucémie |
KR101857599B1 (ko) | 2010-05-14 | 2018-05-14 | 다나-파버 캔서 인스티튜트 인크. | 종양형성, 염증성 질환 및 다른 장애를 치료하기 위한 조성물 및 방법 |
FI3461825T3 (fi) | 2011-09-30 | 2023-08-17 | C&C Res Lab | Uusia heterosyklisiä johdannaisia ja niiden käyttöjä |
MX367614B (es) | 2012-01-20 | 2019-08-28 | Del Mar Pharmaceuticals | Uso de hexitoles sustituidos que incluyen dianhidrogalactitol y analogos para tratar enfermedad neoplasica y celulas madre de cancer que incluyen glioblastoma multiforme y meduloblastoma. |
CN104995190A (zh) * | 2012-12-20 | 2015-10-21 | 拜耳医药股份有限公司 | Bet蛋白抑制剂二氢喹喔啉酮 |
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 |
CN105492011A (zh) | 2013-04-08 | 2016-04-13 | 丹尼斯·M·布朗 | 不理想给药化学化合物的治疗增效 |
WO2015004075A1 (fr) * | 2013-07-09 | 2015-01-15 | Bayer Pharma Aktiengesellschaft | Dihydroquinoxalinones et dihydropyridopyrazinones inhibitrices de protéine bet modifiées |
BR112016001457A2 (pt) | 2013-07-25 | 2017-08-29 | Dana Farber Cancer Inst Inc | Inibidores de fatores de transcrição e usos dos mesmos |
CN105764501A (zh) | 2013-07-26 | 2016-07-13 | 现代化制药公司 | 改善比生群治疗效益的组合物 |
US11446309B2 (en) | 2013-11-08 | 2022-09-20 | Dana-Farber Cancer Institute, Inc. | Combination therapy for cancer using bromodomain and extra-terminal (BET) protein inhibitors |
JP2017504651A (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 | ジアゼパン誘導体の使用 |
US9695172B2 (en) | 2014-01-31 | 2017-07-04 | Dana-Farber Cancer Institute, Inc. | Diazepane derivatives and uses thereof |
JP2017504653A (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 | ジアミノピリミジンベンゼンスルホン誘導体およびその使用 |
US10925881B2 (en) | 2014-02-28 | 2021-02-23 | Tensha Therapeutics, Inc. | Treatment of conditions associated with hyperinsulinaemia |
AU2015240465B2 (en) | 2014-04-04 | 2020-02-27 | Del Mar Pharmaceuticals | Use of dianhydrogalactitol and analogs or derivatives thereof to treat non-small-cell carcinoma of the lung and ovarian cancer |
KR102310128B1 (ko) | 2014-07-14 | 2021-10-06 | 주식회사 포스코 | 트리아진-피페라진 골격을 갖는 알파-헬릭스 유사체 및 이의 제조방법 |
WO2016022902A1 (fr) | 2014-08-08 | 2016-02-11 | Dana-Farber Cancer Institute, Inc. | Dérivés de diazépane et leurs utilisations |
CA2955077A1 (fr) | 2014-08-08 | 2016-02-11 | Dana-Farber Cancer Institute, Inc. | Derives de dihydropteridinone et leurs utilisations |
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 |
KR20180051576A (ko) | 2015-09-11 | 2018-05-16 | 다나-파버 캔서 인스티튜트 인크. | 아세트아미드 티에노트리아졸로디아제핀 및 그의 용도 |
RU2750164C2 (ru) | 2015-09-11 | 2021-06-22 | Дана-Фарбер Кэнсер Инститьют, Инк. | Цианотиенотриазолодиазепины и пути их применения |
WO2017091673A2 (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 |
DE102017005091A1 (de) | 2016-05-30 | 2017-11-30 | Bayer Pharma Aktiengesellschaft | Substituierte 3,4-Dihydropyrido[2,3-b]pyrazin-2(1H)-one |
DE102017005089A1 (de) | 2016-05-30 | 2017-11-30 | Bayer Pharma Aktiengesellschaft | Substitulerte 3,4-Dihydrochinoxalin-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 |
CA3145644A1 (fr) * | 2019-07-19 | 2021-01-28 | Astrazeneca Ab | Inhibiteurs de parp1 |
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 |
WO2022222921A1 (fr) * | 2021-04-22 | 2022-10-27 | 微境生物医药科技(上海)有限公司 | Inhibiteur de parp contenant une structure de pipérazine, son procédé de préparation et son utilisation pharmaceutique |
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 |
WO2022222995A1 (fr) * | 2021-04-23 | 2022-10-27 | 南京明德新药研发有限公司 | Composé picolinamide |
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 |
AU2022334408A1 (en) * | 2021-08-27 | 2024-02-15 | Impact Therapeutics (Shanghai), Inc. | Substituted tricyclic compounds as parp inhibitors and use thereof |
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 |
WO2023051807A1 (fr) * | 2021-09-30 | 2023-04-06 | 海思科医药集团股份有限公司 | Inhibiteur de parp dérivé bicyclique et son utilisation |
WO2023051812A1 (fr) * | 2021-09-30 | 2023-04-06 | 海思科医药集团股份有限公司 | Dérivé hétérocyclique contenant de l'azote à utiliser en tant qu'inhibiteur de parp et son utilisation |
WO2023051716A1 (fr) * | 2021-09-30 | 2023-04-06 | 海思科医药集团股份有限公司 | Inhibiteur de parp dérivé d'hétéroaryle et son utilisation |
TW202322807A (zh) | 2021-10-01 | 2023-06-16 | 美商辛瑟拉股份有限公司 | 吖丁啶及吡咯啶parp1抑制劑及其用途 |
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 |
WO2023096915A1 (fr) * | 2021-11-24 | 2023-06-01 | Slap Pharmaceuticals Llc | Composés multicycliques |
WO2023109521A1 (fr) * | 2021-12-17 | 2023-06-22 | 凯复(苏州)生物医药有限公司 | Inhibiteur de parp, composition pharmaceutique le comprenant et son utilisation |
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 |
US11939329B2 (en) | 2022-01-21 | 2024-03-26 | Xinthera, Inc. | PARP1 inhibitors and uses thereof |
WO2023169226A1 (fr) * | 2022-03-11 | 2023-09-14 | Impact Therapeutics (Shanghai), Inc | Composés tricycliques substitués utilisés en tant qu'inhibiteurs de parp et leur utilisation |
TW202400596A (zh) | 2022-04-28 | 2024-01-01 | 美商辛瑟拉股份有限公司 | 三環parp1抑制劑及其用途 |
WO2023207284A1 (fr) * | 2022-04-28 | 2023-11-02 | Ningbo Newbay Technology Development Co., Ltd | Dérivés de pipérazine utilisés comme inhibiteurs de parp1 |
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 | |
US6197785B1 (en) | 1997-09-03 | 2001-03-06 | Guilford Pharmaceuticals Inc. | Alkoxy-substituted compounds, methods, and compositions for inhibiting PARP activity |
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 |
EP1339402B1 (fr) | 2000-12-01 | 2010-08-25 | Eisai Inc. | Derives d'azaphenanthridone et leur utilisation comme inhibiteurs de parp |
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 |
UA91007C2 (ru) | 2003-12-10 | 2010-06-25 | Янссен Фармацевтика Н.В. | Замещенные 6-циклогексилалкилом замещенные 2-хинолиноны и 2-хиноксалиноны как ингибиторы поли-(адф-рибоза)полимеразы |
KR20070027584A (ko) | 2004-06-17 | 2007-03-09 | 와이어쓰 | 고나도트로핀 방출 호르몬 수용체 길항제 |
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 |
US20090093489A1 (en) | 2004-12-29 | 2009-04-09 | University Of Southern California | Novel compounds for treatment of cancer and disorders associated with angiogenesis function |
EP1816913A4 (fr) | 2004-11-01 | 2010-02-24 | Univ Southern California | Nouveaux composes utiles pour le traitement du cancer et des troubles associes a la fonction d'angiogenese |
EP1845996A4 (fr) * | 2005-01-03 | 2009-04-29 | Univ Michigan | Compositions et procedes concernant de nouveaux composes et leurs cibles |
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 |
ES2566774T3 (es) | 2006-12-13 | 2016-04-15 | Aska Pharmaceutical Co., Ltd. | Derivado de quinoxalina |
CA2672591A1 (fr) | 2006-12-13 | 2008-06-19 | Aska Pharmaceutical Co., Ltd. | Agent therapeutique de l'uropathie |
HUE027641T2 (en) | 2006-12-28 | 2016-11-28 | Abbvie Inc | Poly (ADP-ribose) polymerase inhibitors |
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 |
WO2009086303A2 (fr) | 2007-12-21 | 2009-07-09 | University Of Rochester | Procédé permettant de modifier la durée de vie d'organismes eucaryotes |
SG172958A1 (en) | 2009-01-23 | 2011-08-29 | Takeda Pharmaceutical | Poly (adp-ribose) polymerase (parp) inhibitors |
US8551996B2 (en) | 2009-02-20 | 2013-10-08 | Emory University | Compounds, compositions, methods of synthesis, and methods of treatment |
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