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
- 150000001875 compounds Chemical class 0.000 title abstract 5
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 102000005650 Notch Receptors Human genes 0.000 abstract 1
- 108010070047 Notch Receptors Proteins 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 230000001225 therapeutic effect Effects 0.000 abstract 1
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)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (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 (2) | 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) |
| HR (1) | HRP20150273T1 (fr) |
| IL (1) | IL228534A (fr) |
| MA (1) | MA35036B1 (fr) |
| MX (1) | MX2013010420A (fr) |
| MY (1) | MY161233A (fr) |
| PE (1) | PE20140626A1 (fr) |
| PH (1) | PH12013501738B1 (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) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3072526B1 (fr) | 2009-10-16 | 2018-09-26 | Oncomed Pharmaceuticals, Inc. | Combinaison thérapeutique et utilisation d'anticorps antagonistes de dll4 et d'agents anti-hypertenseurs |
| EP2758073B1 (fr) | 2011-09-23 | 2018-10-31 | OncoMed Pharmaceuticals, Inc. | Agents de liaison à vegf/dll4 et leurs utilisations |
| CN104854094A (zh) * | 2012-09-21 | 2015-08-19 | 百时美施贵宝公司 | 氟烷基二苯并二氮杂*酮化合物 |
| CN104797569A (zh) | 2012-09-21 | 2015-07-22 | 百时美施贵宝公司 | 取代的1,5-苯并二氮杂*酮化合物 |
| 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 |
| WO2014047397A1 (fr) * | 2012-09-21 | 2014-03-27 | Bristol-Myers Squibb Company | Composés de fluoralkyl- et de fluorocycloalkyl-1,4-benzodiazépinone utilisables en tant qu'inhibiteurs du récepteur notch |
| CN104822677A (zh) * | 2012-09-21 | 2015-08-05 | 百时美施贵宝公司 | 氟烷基-1,4-苯并二氮杂*酮化合物 |
| CN105308030A (zh) | 2012-09-21 | 2016-02-03 | 百时美施贵宝公司 | 烷基、氟烷基-1,4-苯并二氮杂*酮化合物 |
| US9273075B2 (en) | 2012-09-21 | 2016-03-01 | Bristol-Myers Squibb Company | Prodrugs of 1,4-benzodiazepinone compounds |
| US9249157B2 (en) | 2012-09-21 | 2016-02-02 | Bristol-Myers Squibb Company | Tricyclic heterocycle compounds |
| US9242940B2 (en) | 2012-09-21 | 2016-01-26 | Bristol-Myers Squibb Company | N-substituted bis(fluoroalkyl)-1,4-benzodiazepinone compounds |
| EP2914961A4 (fr) | 2012-10-31 | 2016-04-20 | Oncomed Pharm Inc | Méthodes et surveillance d'un traitement par un antagoniste de dll4 |
| JP2016515625A (ja) * | 2013-04-04 | 2016-05-30 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | 増殖性疾患を治療するための併用療法 |
| AU2014293011A1 (en) | 2013-07-26 | 2016-03-17 | Race Oncology Ltd. | Compositions to improve the therapeutic benefit of bisantrene |
| 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 |
| 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 |
| CN107530419B (zh) | 2014-10-31 | 2021-05-18 | 昂考梅德药品有限公司 | 治疗疾病的组合疗法 |
| WO2016066115A1 (fr) * | 2014-10-31 | 2016-05-06 | 厦门大学 | Dérivé hétérocyclique substitué, son procédé de préparation et son utilisation |
| 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 |
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| JP6967003B2 (ja) | 2015-09-23 | 2021-11-17 | メレオ バイオファーマ 5 インコーポレイテッド | がんの処置のための方法および組成物 |
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| IL301060A (en) | 2020-09-03 | 2023-05-01 | Bristol Myers Squibb Co | Polymorphs of bis(fluoroalkyl)-1,4-benzodiazepine compounds and their uses |
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| US6495540B2 (en) | 2000-03-28 | 2002-12-17 | Bristol - Myers Squibb Pharma Company | Lactams as inhibitors of A-β protein production |
| EP1268454A1 (fr) | 2000-03-31 | 2003-01-02 | Bristol-Myers Squibb Pharma Company | Heterocycles succinoylamino en tant qu'inhibiteurs de la production de la beta-proteine |
| BR0110051A (pt) | 2000-04-03 | 2004-12-07 | Bristol Myers Squibb Pharma Co | Composto, uso do composto, composição farmacêutica e método de tratamento do mal de alzheimer |
| EP1268433A1 (fr) | 2000-04-03 | 2003-01-02 | Bristol-Myers Squibb Pharma Company | Lactames cycliques utilises comme inhibiteurs de la production de la proteine beta-amyloide |
| 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 |
| AU2001261728A1 (en) | 2000-05-17 | 2001-11-26 | Bristol-Myers Squibb Pharma Company | Use of small molecule radioligands for diagnostic imaging |
| GB0012671D0 (en) | 2000-05-24 | 2000-07-19 | Merck Sharp & Dohme | Therapeutic agents |
| WO2001092235A1 (fr) | 2000-06-01 | 2001-12-06 | 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 |
| KR101125899B1 (ko) | 2002-09-20 | 2012-04-12 | 애로우 쎄라퓨틱스 리미티드 | 벤조디아제핀 유도체 및 이를 함유하는 약학 조성물 |
| 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 |
| KR100838852B1 (ko) | 2003-09-09 | 2008-06-16 | 에프. 호프만-라 로슈 아게 | 감마-세크리테이즈의 활성을 차단하는 말론아미드 유도체 |
| EP1795198A1 (fr) | 2005-12-09 | 2007-06-13 | Hubrecht Laboratorium | Traitement de l'esophage de Barret |
| US20080058316A1 (en) | 2006-02-27 | 2008-03-06 | The Johns Hopkins University | Cancer treatment with gama-secretase inhibitors |
| EP2018368B1 (fr) | 2006-03-27 | 2012-12-05 | F. Hoffmann-La Roche AG | Dérivés de malonamide en tant qu'inhibiteurs de la gamma secrétase |
| BRPI0717587A2 (pt) | 2006-09-20 | 2013-10-29 | Hoffmann La Roche | Derivados de 4-oxo-2,3,4,5-tetra-hidro-benzo[b][1,4]diazepina |
| US8188069B2 (en) | 2007-08-14 | 2012-05-29 | Eli Lilly And Company | Azepine derivatives as gamma-secretase inhibitors |
| RU2010133489A (ru) | 2008-01-11 | 2012-02-20 | Ф.Хоффманн-Ля Рош Аг (Ch) | Применение ингибиторов гамма-секретазы для лечения рака |
| WO2011060051A1 (fr) | 2009-11-12 | 2011-05-19 | University Of Massachusetts | Méthodes de traitement du glioblastome |
| US20120225860A1 (en) | 2011-03-02 | 2012-09-06 | John Frederick Boylan | Method for administration of a gamma secretase inhibitor |
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