MA35036B1 - Composés bis(fluoroalkyl)-1,4-benzodiazépinone - Google Patents
Composés bis(fluoroalkyl)-1,4-benzodiazépinoneInfo
- Publication number
- MA35036B1 MA35036B1 MA36323A MA36323A MA35036B1 MA 35036 B1 MA35036 B1 MA 35036B1 MA 36323 A MA36323 A MA 36323A MA 36323 A MA36323 A MA 36323A MA 35036 B1 MA35036 B1 MA 35036B1
- Authority
- MA
- Morocco
- Prior art keywords
- compounds
- benzodiazepinone
- fluoroalkyl
- ch2ch2cf3
- ch2cf3
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D243/00—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
- C07D243/06—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
- C07D243/10—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D243/14—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines
- C07D243/16—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals
- C07D243/18—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals substituted in position 2 by nitrogen, oxygen or sulfur atoms
- C07D243/24—Oxygen atoms
-
- 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
- A61K31/13—Amines
- A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
- A61K31/138—Aryloxyalkylamines, e.g. propranolol, tamoxifen, phenoxybenzamine
-
- 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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/337—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
-
- 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
-
- 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
- A61K31/555—Heterocyclic compounds containing heavy metals, e.g. hemin, hematin, melarsoprol
-
- 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
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/57—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
- A61K31/573—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone substituted in position 21, e.g. cortisone, dexamethasone, prednisone or aldosterone
-
- 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
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
L'INVENTION CONCERNE DES COMPOSÉS DE FORMULE (I) OU LEURS PROMÉDICAMENTS ; DANS LAQUELLE R1 REPRÉSENTE CH2CF3 OU CH2CH2CF3 ; R2 REPRÉSENTE CH2CF3, CH2CH2CF3, OU CH2CH2CH2CF3 ; R3 REPRÉSENTE H OU CH3; CHAQUE RA REPRÉSENTE INDÉPENDAMMENT F, CL, -CN, -OCH3 ET/OU NHCH2CH2OCH3 ; ET Z VAUT ZÉRO, 1 OU 2. ELLE CONCERNE ÉGALEMENT DES PROCÉDÉS D'UTILISATION DE CES COMPOSÉS POUR INHIBER LE RÉCEPTEUR NOTCH, ET DES COMPOSITIONS PHARMACEUTIQUES COMPRENANT CES COMPOSÉS. CES COMPOSÉS SONT UTILES DANS LE TRAITEMENT, LA PRÉVENTION OU LE RALENTISSEMENT DE L'ÉVOLUTION DE MALADIES OU DE TROUBLES DANS DIVERS DOMAINES THÉRAPEUTIQUES, COMME LE TRAITEMENT DU CANCER.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161466238P | 2011-03-22 | 2011-03-22 | |
PCT/US2012/030021 WO2012129353A1 (fr) | 2011-03-22 | 2012-03-22 | Composés bis(fluoroalkyl)-1,4-benzodiazépinone |
Publications (1)
Publication Number | Publication Date |
---|---|
MA35036B1 true MA35036B1 (fr) | 2014-04-03 |
Family
ID=45894701
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA36323A MA35036B1 (fr) | 2011-03-22 | 2012-03-22 | Composés bis(fluoroalkyl)-1,4-benzodiazépinone |
Country Status (32)
Country | Link |
---|---|
US (2) | US8629136B2 (fr) |
EP (1) | EP2688873B1 (fr) |
JP (1) | JP5873923B2 (fr) |
KR (1) | KR101948347B1 (fr) |
CN (1) | CN103717576B (fr) |
AR (1) | AR085471A1 (fr) |
AU (1) | AU2012230904B2 (fr) |
BR (1) | BR112013024059B1 (fr) |
CA (1) | CA2830902C (fr) |
CL (1) | CL2013002690A1 (fr) |
CO (1) | CO6771446A2 (fr) |
CY (1) | CY1116423T1 (fr) |
DK (1) | DK2688873T3 (fr) |
EA (1) | EA022530B1 (fr) |
ES (1) | ES2534080T3 (fr) |
HK (1) | HK1189218A1 (fr) |
HR (1) | HRP20150273T1 (fr) |
IL (1) | IL228534A (fr) |
MA (1) | MA35036B1 (fr) |
MX (1) | MX2013010420A (fr) |
MY (1) | MY161233A (fr) |
PE (1) | PE20140626A1 (fr) |
PL (1) | PL2688873T3 (fr) |
PT (1) | PT2688873E (fr) |
RS (1) | RS53843B1 (fr) |
SG (1) | SG193555A1 (fr) |
SI (1) | SI2688873T1 (fr) |
SM (1) | SMT201500091B (fr) |
TN (1) | TN2013000372A1 (fr) |
TW (1) | TWI530489B (fr) |
UY (1) | UY33961A (fr) |
WO (1) | WO2012129353A1 (fr) |
Families Citing this family (57)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TR201818814T4 (tr) | 2009-10-16 | 2019-01-21 | Oncomed Pharm Inc | Dll4 antagonist antikorlarının ve anti-hipertansif ajanların terapötik kombinasyonu ve kullanımı. |
EP3485903B1 (fr) | 2011-09-23 | 2022-11-16 | Mereo BioPharma 5, Inc. | Agents de liaison à vegf/dll4 et leurs utilisations |
EP2897938B1 (fr) | 2012-09-21 | 2017-03-15 | Bristol-Myers Squibb Company | Composés fluoroalkyl benzodiazépinones |
TWI614238B (zh) | 2012-09-21 | 2018-02-11 | 必治妥美雅史谷比公司 | 雙(氟烷基)-1,4-苯并二氮呯酮化合物及其前藥 |
JP2015534553A (ja) | 2012-09-21 | 2015-12-03 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | 置換1,5−ベンゾジアゼピノン化合物 |
EP2897954B1 (fr) * | 2012-09-21 | 2016-10-26 | Bristol-Myers Squibb Company | Composés fluoroalkyl-1,4-benzodiazépinones |
CN104822665A (zh) * | 2012-09-21 | 2015-08-05 | 百时美施贵宝公司 | 用作Notch抑制剂的氟烷基和氟环烷基1,4-苯并二氮杂*酮化合物 |
JP2015533811A (ja) * | 2012-09-21 | 2015-11-26 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | N−置換ビス(フルオロアルキル)1,4−ベンゾジアゼピノン化合物 |
JP2015531792A (ja) | 2012-09-21 | 2015-11-05 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | 1,4−ベンゾジアゼピノン化合物のプロドラッグ |
WO2014047390A1 (fr) | 2012-09-21 | 2014-03-27 | Bristol-Myers Squibb Company | Composés hétérocycliques tricycliques utilisables en tant qu'inhibiteurs du récepteur notch |
JP2015534554A (ja) | 2012-09-21 | 2015-12-03 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | アルキル,フルオロアルキル−1,4−ベンゾジアゼピノン化合物 |
JP6371294B2 (ja) | 2012-10-31 | 2018-08-08 | オンコメッド ファーマシューティカルズ インコーポレイテッド | Dll4アンタゴニストによる処置の方法およびモニタリング |
WO2014165718A1 (fr) * | 2013-04-04 | 2014-10-09 | Bristol-Myers Squibb Company | Traitement combiné pour le traitement de maladies prolifératives |
US9993460B2 (en) | 2013-07-26 | 2018-06-12 | Race Oncology Ltd. | Compositions to improve the therapeutic benefit of bisantrene and analogs and derivatives thereof |
CN103435562B (zh) * | 2013-08-26 | 2016-02-24 | 华东理工大学 | 6-取代苯并二氮卓-2,4-二酮类化合物及其用途 |
US10174015B2 (en) | 2014-10-31 | 2019-01-08 | Xiamen University | Substituted heterocyclic derivative, preparation method and use thereof |
CA2966042A1 (fr) | 2014-10-31 | 2016-05-06 | Oncomed Pharmaceuticals, Inc. | Therapie combinee pour le traitement d'une maladie |
CN104352488B (zh) * | 2014-10-31 | 2016-08-31 | 厦门大学 | 一类取代杂环衍生物在制备治疗疼痛药物中的应用 |
CN104356082B (zh) * | 2014-10-31 | 2016-07-13 | 厦门大学 | 一类取代杂环衍生物及其制备方法 |
CN104892532B (zh) * | 2015-05-20 | 2017-09-08 | 成都理工大学 | 手性3‑取代1,3,4,5‑四氢‑1,4‑苯二氮*‑2‑酮的合成工艺 |
DK3324977T3 (da) | 2015-07-22 | 2022-10-17 | Enanta Pharm Inc | Benzodiazepinderivater som rsv-inhibitorer |
CN109071644B (zh) | 2015-09-23 | 2023-09-19 | 昂考梅德药品有限公司 | 治疗癌症的方法和组合物 |
CN108699077B (zh) | 2016-01-15 | 2021-03-02 | 英安塔制药有限公司 | 作为rsv抑制剂的杂环化合物 |
CN109195593A (zh) | 2016-03-15 | 2019-01-11 | 奥莱松基因组股份有限公司 | 用于治疗实体瘤的lsd1抑制剂的组合 |
EP3582784B1 (fr) | 2017-02-16 | 2022-06-08 | Enanta Pharmaceuticals, Inc. | Procédés pour la préparation de dérivés de benzodiazépine |
US20200055948A1 (en) | 2017-04-28 | 2020-02-20 | Novartis Ag | Cells expressing a bcma-targeting chimeric antigen receptor, and combination therapy with a gamma secretase inhibitor |
EP3615068A1 (fr) | 2017-04-28 | 2020-03-04 | Novartis AG | Agent ciblant le bcma et polythérapie incluant un inhibiteur de gamma-sécrétase |
WO2018226801A1 (fr) | 2017-06-07 | 2018-12-13 | Enanta Pharmaceuticals, Inc. | Dérivés d'aryldiazépine utilisés en tant qu'inhibiteurs du vrs |
US11091501B2 (en) | 2017-06-30 | 2021-08-17 | Enanta Pharmaceuticals, Inc. | Heterocyclic compounds as RSV inhibitors |
WO2019006291A1 (fr) | 2017-06-30 | 2019-01-03 | Enanta Pharmaceuticals, Inc. | Composés hétérocycliques utilisés en tant qu'inhibiteurs du vrs |
EP3438128B1 (fr) * | 2017-08-04 | 2020-05-20 | Alzheimur 2012 S.L. | Anticorps anti preseniline pour une utilisation dans la prévention et/ou le traitement du cancer |
WO2019067864A1 (fr) | 2017-09-29 | 2019-04-04 | Enanta Pharmaceuticals, Inc. | Agents pharmaceutiques en combinaison en tant qu'inhibiteurs de rsv |
WO2019094920A1 (fr) | 2017-11-13 | 2019-05-16 | Enanta Pharmaceuticals, Inc. | Dérivés d'azépin-2-one en tant qu'inhibiteurs du vrs |
KR102634720B1 (ko) * | 2017-11-13 | 2024-02-06 | 이난타 파마슈티칼스, 인코포레이티드 | 벤조디아제핀-2-온 및 벤조아제핀-2-온 유도체의 분할 방법 |
WO2019199908A1 (fr) | 2018-04-11 | 2019-10-17 | Enanta Pharmaceuticals, Inc. | Composés hétérocycliques en tant qu'inhibiteurs de vrs |
EP3790553A4 (fr) | 2018-05-06 | 2022-04-20 | Ayala Pharmaceuticals Inc. | Compositions comprenant des inhibiteurs de cd20 et des composés de bisfluoroalkyl-1,4-benzodiazépinone et leurs procédés d'utilisation |
US20210244745A1 (en) * | 2018-05-06 | 2021-08-12 | Ayala Pharmaceuticals Inc. | Combination compositions comprising bisfluoroalkyl-1,4-benzodiazepinone compounds and methods of use thereof |
AU2019271044A1 (en) | 2018-05-15 | 2021-01-14 | Ayala Pharmaceuticals Inc. | Compositions comprising bisfluoroalkyl-l,4-benzodiazepinone compounds for treating adenoid cystic carcinoma |
MX2020012281A (es) * | 2018-05-15 | 2021-01-29 | Bristol Myers Squibb Co | Composiciones que comprenden compuestos de bisfluoroalquil-1,4-ben zodiacepinona y metodos de uso de las mismas. |
JP2021526517A (ja) | 2018-05-24 | 2021-10-07 | アヤラ ファーマシューティカルズ インコーポレイテッド | ビスフルオロアルキル−1,4−ベンゾジアゼピノン化合物および免疫療法剤を含む組成物ならびにそれらの使用方法 |
KR20210016390A (ko) | 2018-06-01 | 2021-02-15 | 노파르티스 아게 | Bcma에 대한 결합 분자 및 이의 용도 |
KR20210138684A (ko) | 2019-03-18 | 2021-11-19 | 이난타 파마슈티칼스, 인코포레이티드 | Rsv 억제제로서의 벤조디아제핀 유도체 |
WO2020210246A1 (fr) | 2019-04-09 | 2020-10-15 | Enanta Pharmaceuticals, Inc, | Composés hétérocycliques utilisés comme inhibiteurs du vrs |
US20220241294A1 (en) * | 2019-05-15 | 2022-08-04 | Ayala Pharmaceuticals Inc. | Bisfluoroalkyl-1,4-benzodiazepinone compounds for treating notch-activated breast cancer |
KR20220024729A (ko) | 2019-06-24 | 2022-03-03 | 노파르티스 아게 | B-세포 성숙 항원을 표적으로 하는 다중특이성 항체에 대한 투여 요법 및 병용 요법 |
CN114761016A (zh) | 2019-10-04 | 2022-07-15 | 英安塔制药有限公司 | 抗病毒杂环化合物 |
US11505558B1 (en) | 2019-10-04 | 2022-11-22 | Enanta Pharmaceuticals, Inc. | Antiviral heterocyclic compounds |
UY39032A (es) | 2020-01-24 | 2021-07-30 | Enanta Pharm Inc | Compuestos heterocíclicos como agentes antivirales |
US11534439B2 (en) | 2020-07-07 | 2022-12-27 | Enanta Pharmaceuticals, Inc. | Dihydroquinoxaline and dihydropyridopyrazine derivatives as RSV inhibitors |
WO2022051442A1 (fr) | 2020-09-03 | 2022-03-10 | Bristol-Myers Squibb Company | Polymorphes de composés de bis(fluoroalkyl)-1,4-benzodiazépinone et leurs utilisations |
WO2022086840A1 (fr) | 2020-10-19 | 2022-04-28 | Enanta Pharmaceuticals, Inc. | Composés hétérocycliques en tant qu'agents antiviraux |
EP4008324A1 (fr) | 2020-12-07 | 2022-06-08 | Cellestia Biotech AG | Combinaisons comprenant un inhibiteur d'une protéine anti-apoptotique, telle que bcl-2, bcl-xl, bclw ou mcl-1, et un inhibiteur de voie de signalisation notch pour le traitement du cancer |
EP4255409A1 (fr) | 2020-12-07 | 2023-10-11 | Cellestia Biotech AG | Combinaisons pharmaceutiques pour le traitement du cancer |
MX2023009961A (es) | 2021-02-26 | 2023-09-05 | Enanta Pharm Inc | Compuestos heterociclicos antivirales. |
TW202313020A (zh) | 2021-06-02 | 2023-04-01 | 瑞士商西萊絲蒂亞生物科技股份有限公司 | 自體免疫及發炎性疾病的治療方法 |
WO2023079132A1 (fr) | 2021-11-08 | 2023-05-11 | Cellestia Biotech Ag | Combinaisons pharmaceutiques pour le traitement du cancer |
EP4223292A1 (fr) | 2022-02-07 | 2023-08-09 | Cellestia Biotech AG | Combinaisons pharmaceutiques pour le traitement du cancer |
Family Cites Families (38)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5324726A (en) | 1989-12-18 | 1994-06-28 | Merck & Co., Inc. | Benzodiazepine analogs |
US5852010A (en) * | 1996-04-03 | 1998-12-22 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
EP0891337A1 (fr) | 1996-04-03 | 1999-01-20 | Merck & Co., Inc. | Inhibiteurs de transferase de farnesyl-proteine |
US6635632B1 (en) | 1996-12-23 | 2003-10-21 | Athena Neurosciences, Inc. | Cycloalkyl, lactam, lactone and related compounds, pharmaceutical compositions comprising same, and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds |
NZ509241A (en) | 1998-08-07 | 2003-08-29 | Du Pont Pharm Co | Succinoylamino lactams as inhibitors of alpha-beta protein production |
HRP990246A2 (en) | 1998-08-07 | 2000-06-30 | Du Pont Pharm Co | Succinoylamino benzodiazepines as inhibitors of a beta protein production |
US6331408B1 (en) | 1998-11-12 | 2001-12-18 | Robert Zaczek | Use of small molecule radioligands to discover inhibitors of amyloid-beta peptide production |
US6737038B1 (en) | 1998-11-12 | 2004-05-18 | Bristol-Myers Squibb Company | Use of small molecule radioligands to discover inhibitors of amyloid-beta peptide production and for diagnostic imaging |
CN1636011A (zh) * | 1998-12-24 | 2005-07-06 | 杜邦药品公司 | 作为Aβ蛋白产生抑制剂的琥珀酰氨基苯并二氮杂䓬 |
EP2062583B1 (fr) | 1999-04-30 | 2012-12-26 | The Regents of the University of Michigan | Applications thérapeutiques de benzodiazépines pro-apoptotiques |
US6503902B2 (en) | 1999-09-13 | 2003-01-07 | Bristol-Myers Squibb Pharma Company | Hydroxyalkanoylaminolactams and related structures as inhibitors of a β protein production |
US6960576B2 (en) | 1999-09-13 | 2005-11-01 | Bristol-Myers Squibb Pharma Company | Hydroxyalkanoylaminolactams and related structures as inhibitors of Aβ protein production |
AU7997600A (en) | 1999-10-08 | 2001-04-23 | Du Pont Pharmaceuticals Company | Amino lactam sulfonamides as inhibitors of abeta protein production |
KR20020071931A (ko) * | 2000-01-07 | 2002-09-13 | 트렌스폼 파마수티컬스 인코퍼레이티드 | 다양한 고체-형태들의 고도의 자료 처리 편성, 확인 및분석 |
AU779875B2 (en) | 2000-01-24 | 2005-02-17 | Merck Sharp & Dohme Limited | Gamma-secretase inhibitors |
WO2001060826A2 (fr) | 2000-02-17 | 2001-08-23 | Bristol-Myers Squibb Pharma Company | CARBOCYCLES ET HETEROCYCLES SUCCINOYLAMINO UTILISES EN TANT QU'INHIBITEURS DE LA PRODUCTION DE LA PROTEINE A$g(b) |
US6495540B2 (en) | 2000-03-28 | 2002-12-17 | Bristol - Myers Squibb Pharma Company | Lactams as inhibitors of A-β protein production |
AU2001251147A1 (en) | 2000-03-31 | 2001-10-15 | Dupont Pharmaceuticals Company | Succinoylamino heterocycles as inhibitors of abeta protein production |
JP2004508289A (ja) | 2000-04-03 | 2004-03-18 | デュポン ファーマシューティカルズ カンパニー | Aβタンパク質産生の阻害剤としての環状ラクタム |
BR0107532A (pt) | 2000-04-03 | 2004-11-03 | Bristol Myers Squibb Pharma Co | Composto, uso do composto, método para o tratamento de disfunções neurológicas associadas com a produção de b-amilóide, método de inibição da atividade de y-secretase e composição farmacêutica |
GB0008710D0 (en) | 2000-04-07 | 2000-05-31 | Merck Sharp & Dohme | Therapeutic compounds |
US6632812B2 (en) | 2000-04-11 | 2003-10-14 | Dupont Pharmaceuticals Company | Substituted lactams as inhibitors of Aβ protein production |
WO2001087354A2 (fr) | 2000-05-17 | 2001-11-22 | Bristol-Myers Squibb Pharma Company | Utilisation de radioligands a petites molecules en vue de rechercher des inhibiteurs de production d'amyloide-beta et destine a l'imagerie diagnostique |
GB0012671D0 (en) * | 2000-05-24 | 2000-07-19 | Merck Sharp & Dohme | Therapeutic agents |
CA2379445C (fr) | 2000-06-01 | 2007-08-21 | Bristol-Myers Squibb Pharma Company | Lactames substitues par des succinates cycliques en tant qu'inhibiteurs de la production de la proteine .beta. |
US7001901B2 (en) | 2002-08-27 | 2006-02-21 | Bristol-Myers Squibb Company | Tetrazolylpropionamides as inhibitors of Aβ protein production |
BR0314595A (pt) | 2002-09-20 | 2005-08-09 | Arrow Therapeutics Ltd | Uso de um derivado de benzodiazepina ou um sal farmaceuticamente aceitável deste, inalador ou nebulisador, produto, usos de um produto e de um composto ou sal farmaceuticamente aceitável deste, derivado de benzodiazepina, composto, e, composição farmacêutica |
EP1592684B1 (fr) | 2003-02-04 | 2008-07-30 | F. Hoffmann-La Roche Ag | Derives de malonamide utilises comme inhibiteurs de la gamma-secretase |
GB0312365D0 (en) | 2003-05-30 | 2003-07-02 | Univ Aston | Novel 3-substituted-1, 4-benzodiazepines |
PT1711470E (pt) | 2003-09-09 | 2009-05-21 | Hoffmann La Roche | Derivados de malonamida que bloqueiam a actividade de gama-secretase |
EP1795198A1 (fr) | 2005-12-09 | 2007-06-13 | Hubrecht Laboratorium | Traitement de l'esophage de Barret |
CA2644136A1 (fr) | 2006-02-27 | 2007-09-07 | The Johns Hopkins University | Traitement anticancereux utilisant des inhibiteurs de gamma-secretases |
RU2440342C2 (ru) | 2006-03-27 | 2012-01-20 | Ф.Хоффманн-Ля Рош Аг | МАЛОНАМИДНЫЕ ПРОИЗВОДНЫЕ В КАЧЕСТВЕ ИНГИБИТОРОВ γ-СЕКРЕТАЗЫ |
KR101096476B1 (ko) | 2006-09-20 | 2011-12-20 | 에프. 호프만-라 로슈 아게 | 4-옥소-2,3,4,5-테트라히드로-벤조[b][1,4]디아제핀 유도체 |
KR101136260B1 (ko) | 2007-08-14 | 2012-04-19 | 일라이 릴리 앤드 캄파니 | 감마-세크레타제 억제제로서의 아제핀 유도체 |
EP2244713A1 (fr) | 2008-01-11 | 2010-11-03 | F. Hoffmann-La Roche AG | Utilisation d'un inhibiteur de la gamma-sécrétase pour le traitement du cancer |
US8637493B2 (en) | 2009-11-12 | 2014-01-28 | University Of Massachusetts | Methods for treating glioblastoma |
US20120225860A1 (en) | 2011-03-02 | 2012-09-06 | John Frederick Boylan | Method for administration of a gamma secretase inhibitor |
-
2012
- 2012-02-24 TW TW101106426A patent/TWI530489B/zh active
- 2012-03-21 AR ARP120100932A patent/AR085471A1/es not_active Application Discontinuation
- 2012-03-21 UY UY0001033961A patent/UY33961A/es active IP Right Grant
- 2012-03-22 DK DK12711102T patent/DK2688873T3/en active
- 2012-03-22 SI SI201230162T patent/SI2688873T1/sl unknown
- 2012-03-22 PL PL12711102T patent/PL2688873T3/pl unknown
- 2012-03-22 WO PCT/US2012/030021 patent/WO2012129353A1/fr active Application Filing
- 2012-03-22 ES ES12711102.9T patent/ES2534080T3/es active Active
- 2012-03-22 BR BR112013024059-8A patent/BR112013024059B1/pt active IP Right Grant
- 2012-03-22 CA CA2830902A patent/CA2830902C/fr active Active
- 2012-03-22 JP JP2014501220A patent/JP5873923B2/ja active Active
- 2012-03-22 US US13/426,730 patent/US8629136B2/en active Active
- 2012-03-22 SG SG2013070743A patent/SG193555A1/en unknown
- 2012-03-22 KR KR1020137027347A patent/KR101948347B1/ko active IP Right Grant
- 2012-03-22 PE PE2013002083A patent/PE20140626A1/es active IP Right Grant
- 2012-03-22 MX MX2013010420A patent/MX2013010420A/es active IP Right Grant
- 2012-03-22 AU AU2012230904A patent/AU2012230904B2/en active Active
- 2012-03-22 PT PT127111029T patent/PT2688873E/pt unknown
- 2012-03-22 EA EA201391324A patent/EA022530B1/ru not_active IP Right Cessation
- 2012-03-22 MA MA36323A patent/MA35036B1/fr unknown
- 2012-03-22 RS RS20150150A patent/RS53843B1/en unknown
- 2012-03-22 MY MYPI2013003410A patent/MY161233A/en unknown
- 2012-03-22 CN CN201280025022.2A patent/CN103717576B/zh active Active
- 2012-03-22 EP EP12711102.9A patent/EP2688873B1/fr active Active
-
2013
- 2013-09-17 CL CL2013002690A patent/CL2013002690A1/es unknown
- 2013-09-17 IL IL228534A patent/IL228534A/en active IP Right Grant
- 2013-09-19 TN TNP2013000372A patent/TN2013000372A1/fr unknown
- 2013-09-20 CO CO13224494A patent/CO6771446A2/es unknown
- 2013-12-09 US US14/100,896 patent/US8822454B2/en active Active
-
2014
- 2014-01-30 HK HK14101033.1A patent/HK1189218A1/xx unknown
-
2015
- 2015-03-10 HR HRP20150273TT patent/HRP20150273T1/hr unknown
- 2015-04-13 SM SM201500091T patent/SMT201500091B/xx unknown
- 2015-04-17 CY CY20151100355T patent/CY1116423T1/el unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
MA35036B1 (fr) | Composés bis(fluoroalkyl)-1,4-benzodiazépinone | |
MA37929A1 (fr) | Composés bis(fluoroalkyl) -1,4-benzodiazépinones en tant qu'inhibiteurs de notch | |
MA31683B1 (fr) | Composes et procedes pour moduler fxr | |
MA42410A (fr) | Oxystérols et leurs méthodes d'utilisation | |
MA47043A1 (fr) | Composés indole carboxamides utiles comme inhibiteurs de kinase | |
MA37762A1 (fr) | Composés n-aryltriazole utilisés comme antagonistes de lpar | |
MA37764A1 (fr) | Composés n-alkyltriazole utilisés comme antagonistes de lpar | |
MA43979B1 (fr) | Dérivés de 1h-indazole-3-carboxamide et composés similaires en tant qu'inhibiteurs du facteur d pour le traitement de maladies characterisés par une activité aberrante du système complémentaire, comme p.E. Troubles immunologiques | |
MA40225A (fr) | Composés dihydroisoquinolinone substitués | |
MA37142A3 (fr) | Dérivés de dihydro-benzo-oxazine et de dihydro-pyrido-oxazine | |
MA32729B1 (fr) | Derives d'acide 1-amino-2-cyclobutylethylboronique | |
MA34474B1 (fr) | Agonistes de gpr40 | |
MA31117B1 (fr) | Composes tricycliques et leur utilisation comme modulateurs du recepteur de glucocorticoïdes | |
MA35716B1 (fr) | Formulations pharmaceutiques | |
MA37891B1 (fr) | Alcoxypyrazoles comme activateurs de guanylate cyclase soluble | |
MA37990B1 (fr) | Benzamides | |
MA37765A1 (fr) | Composés de pyrazole substitués utilisés comme antagonistes de lpar | |
MA38425B1 (fr) | Composés bicycliques pour une utilisation comme agonistes selectifs pour le recepteur s1p1 | |
MA46229A (fr) | Composés d'hétéroaryle carboxamide en tant qu'inhibiteurs de ripk2 | |
MA43913B1 (fr) | Modulateurs allostériques positifs du récepteur m1 muscarinique | |
MA40149A1 (fr) | Dérivés de nucléoside 4'-vinyle substitués utiles en tant qu'inhibiteurs de la réplication due l'arn du virus respiratoire syncytial | |
MA38009B1 (fr) | Composes d'azaindoline substitues qui ont une activite inhibitrice de la proteine d'apoptose pour leurs utilisations dans le traitement et/ou la prophylaxie du cancer | |
MA39750B1 (fr) | Dérivés d'acide aza-indol-acétique et leur utilisation comme modulateurs des récepteurs de la prostaglandine d2 | |
MA30267B1 (fr) | Derives amides en tant que ligands de canal ionique et compositions pharmaceutiques et procedes d'utilisation de tels derives | |
MA52370B1 (fr) | Dérivés de la pyridine et leurs utilisations thérapeutiques comme inhibiteurs du trpc6 |