MA35036B1 - Composés bis(fluoroalkyl)-1,4-benzodiazépinone - Google Patents

Composés bis(fluoroalkyl)-1,4-benzodiazépinone

Info

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
Application number
MA36323A
Other languages
English (en)
Inventor
Claude Quesnelle
Soong-Hoon Kim
Francis Lee
Ashvinikumar Gavai
Original Assignee
Bristol Myers Squibb Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=45894701&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA35036(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of MA35036B1 publication Critical patent/MA35036B1/fr

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)
  • 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.
MA36323A 2011-03-22 2012-03-22 Composés bis(fluoroalkyl)-1,4-benzodiazépinone MA35036B1 (fr)

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)

Families Citing this family (63)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3485908B1 (fr) 2009-10-16 2021-08-18 Mereo BioPharma 5, Inc. Combinaison thérapeutique et utilisation d'anticorps antagonistes de dll4 et d'agents anti-hypertenseurs
TWI583699B (zh) 2011-09-23 2017-05-21 安可美德藥物股份有限公司 Ｖｅｇｆ／ｄｌｌ４結合劑類及彼等之用途
WO2014047393A1 (fr) * 2012-09-21 2014-03-27 Bristol-Myers Squibb Company Composés bis(fluoroalkyl)-1,4-benzodiazépinone n-substitués utilisés comme inhibiteurs de notch
US9133126B2 (en) 2012-09-21 2015-09-15 Bristol-Myers Squibb Company Fluoroalkyl dibenzoazepinone compounds
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
WO2014047374A1 (fr) 2012-09-21 2014-03-27 Bristol-Myers Squibb Company Composés alkyl, 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
EP2897954B1 (fr) * 2012-09-21 2016-10-26 Bristol-Myers Squibb Company Composés fluoroalkyl-1,4-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
US9187434B2 (en) 2012-09-21 2015-11-17 Bristol-Myers Squibb Company Substituted 1,5-benzodiazepinones compounds
CN104797584A (zh) 2012-09-21 2015-07-22 百时美施贵宝公司 作为notch抑制剂的三环杂环化合物
CA2889638A1 (fr) 2012-10-31 2014-05-08 Oncomed Pharmaceuticals, Inc. Methodes et surveillance d'un traitement par un antagoniste de dll4
CN105101968A (zh) * 2013-04-04 2015-11-25 百时美施贵宝公司 治疗增殖性疾病的组合疗法
AU2014293013A1 (en) 2013-07-26 2016-03-17 Race Oncology Ltd. Combinatorial methods 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
CN107074788B (zh) * 2014-10-31 2019-09-20 厦门大学 取代杂环衍生物、其制备方法和用途
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
EP3212233B1 (fr) * 2014-10-31 2020-06-24 Oncomed Pharmaceuticals, Inc. Thérapie combinée pour le traitement d'une maladie
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
MY197231A (en) 2015-07-22 2023-06-06 Enanta Pharm Inc Benzodiazepine derivatives as rsv inhibitors
US11339213B2 (en) 2015-09-23 2022-05-24 Mereo Biopharma 5, Inc. Methods and compositions for treatment of cancer
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
CN120661674A (zh) 2016-03-15 2025-09-19 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
WO2018152413A1 (fr) 2017-02-16 2018-08-23 Enanta Pharmaceuticals, Inc. Procédés pour la préparation de dérivés de benzodiazépine
EP3615055A1 (fr) 2017-04-28 2020-03-04 Novartis AG Cellules exprimant un récepteur antigénique chimérique ciblant le bcma, et polythérapie comprenant un inhibiteur de gamma sécrétase
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
WO2019006295A1 (fr) 2017-06-30 2019-01-03 Enanta Pharmaceuticals, Inc. Composés hétérocycliques utilisés en tant qu'inhibiteurs du vrs
US10851115B2 (en) 2017-06-30 2020-12-01 Enanta Pharmaceuticals, Inc. Heterocyclic compounds as RSV inhibitors
ES2817910T3 (es) * 2017-08-04 2021-04-08 Alzheimur 2012 S L Uso de un anticuerpo antipresenilina para la prevención y/o tratamiento del cáncer
CN111386118B (zh) 2017-09-29 2023-05-09 英安塔制药有限公司 作为rsv抑制剂的组合药物剂
US11066475B2 (en) 2017-11-01 2021-07-20 Juno Therapeutics, Inc. Chimeric antigen receptors specific for B-cell maturation antigen and encoding polynucleotides
AU2018359907A1 (en) 2017-11-06 2020-05-07 Fred Hutchinson Cancer Center Combination of a cell therapy and a gamma secretase inhibitor
MX394621B (es) * 2017-11-13 2025-03-24 Enanta Pharm Inc Procesos para la resolucion de los derivados de la benzodiazepina-2-ona y de la benzoazepin-2-ona
WO2019094920A1 (fr) 2017-11-13 2019-05-16 Enanta Pharmaceuticals, Inc. Dérivés d'azépin-2-one en tant qu'inhibiteurs du vrs
WO2019199908A1 (fr) 2018-04-11 2019-10-17 Enanta Pharmaceuticals, Inc. Composés hétérocycliques en tant qu'inhibiteurs de vrs
US20210379079A1 (en) 2018-05-06 2021-12-09 Ayala Pharmaceuticals Inc. Compositions comprising cd20 inhibitors and bisfluoroalkyl-1,4-benzodiazepinone compounds and methods of use thereof
EP3790552A4 (fr) 2018-05-06 2022-06-15 Ayala Pharmaceuticals Inc. Compositions de combinaison comprenant des composés de bisfluoroalkyle-1,4-benzodiazépinone et leurs procédés d'utilisation
EP3793564A4 (fr) * 2018-05-15 2022-03-30 Ayala Pharmaceuticals Inc. Compositions comprenant des composés de bisfluoroalkyl-1,4-benzodiazépinone pour traiter le carcinome adénoïde kystique
EP3793563A4 (fr) * 2018-05-15 2022-02-23 Bristol-Myers Squibb Company Compositions comprenant des composés de bisfluoroalkyl-1,4-benzodiazépinone et méthodes d'utilisation associées
BR112020023975A2 (pt) * 2018-05-24 2021-02-23 Ayala Pharmaceuticals Inc. composições que compreendem os compostos de bisfluoroalquil-1,4-benzodiazepinona e imunoterapêuticos e métodos de uso das mesmas
PE20210320A1 (es) 2018-06-01 2021-02-16 Novartis Ag Moleculas de union contra bcma y usos de las mismas
WO2020190935A1 (fr) 2019-03-18 2020-09-24 Enanta Pharmaceuticals, Inc. Dérivés de benzodiazépine en tant qu'inhibiteurs de rsv
US11179400B2 (en) 2019-04-09 2021-11-23 Enanta Pharmaceuticals, Inc. Heterocyclic compounds as RSV inhibitors
JP2022533100A (ja) * 2019-05-15 2022-07-21 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 Ｎｏｔｃｈ活性化乳がんを治療するためのビスフルオロアルキル－１，４－ベンゾジアゼピノン化合物
AU2020307471A1 (en) 2019-06-24 2022-01-27 Novartis Ag Dosing regimen and combination therapies for multispecific antibodies targeting B-cell maturation antigen
PH12022550783A1 (en) 2019-10-04 2023-07-31 Enanta Pharm Inc Antiviral heterocyclic compounds
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
WO2022010882A1 (fr) 2020-07-07 2022-01-13 Enanta Pharmaceuticals, Inc, Dérivés de dihydroquinoxaline et de dihydropyridopyrazine utilisés comme inhibiteurs de rsv
CA3193737A1 (fr) * 2020-09-03 2022-03-10 Bristol-Myers Squibb Company Polymorphes de composes de bis(fluoroalkyl)-1,4-benzodiazepinone et leurs utilisations
WO2022086840A1 (fr) 2020-10-19 2022-04-28 Enanta Pharmaceuticals, Inc. Composés hétérocycliques en tant qu'agents antiviraux
EP4255409A1 (fr) 2020-12-07 2023-10-11 Cellestia Biotech AG Combinaisons pharmaceutiques pour le traitement du cancer
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
US12612412B2 (en) 2021-02-26 2026-04-28 Enanta Pharmaceuticals, Inc. Antiviral heterocyclic compounds
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
AR129003A1 (es) 2022-04-07 2024-07-03 Enanta Pharm Inc Compuestos heterocíclicos antivirales
WO2023211997A1 (fr) 2022-04-27 2023-11-02 Enanta Pharmaceuticals, Inc. Composés antiviraux
US20260028319A1 (en) * 2022-12-28 2026-01-29 Immunome, Inc. Intermediate salt for the preparation of bis(fluoroalkyl) benzodiazepinone compounds

Family Cites Families (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5324726A (en) 1989-12-18 1994-06-28 Merck & Co., Inc. Benzodiazepine analogs
JP2000507587A (ja) * 1996-04-03 2000-06-20 メルク エンド カンパニー インコーポレーテッド ファルネシルタンパク質トランスフェラーゼ阻害剤
US5852010A (en) * 1996-04-03 1998-12-22 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
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
NZ525513A (en) 1998-08-07 2004-09-24 Pont Pharmaceuticals Du Succinoylamino lactams as inhibitors of Abeta protein production
HRP990246A2 (en) 1998-08-07 2000-06-30 Du Pont Pharm Co Succinoylamino benzodiazepines as inhibitors of a beta protein production
EP1129355B1 (fr) 1998-11-12 2005-07-20 Bristol-Myers Squibb Pharma Company Utilisation de radioligands pour detecter des inhibiteurs de la production de peptides beta-amyloides
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
MXPA01011052A (es) 1999-04-30 2002-11-22 Univ Michigan Aplicaciones terapeuticas de benzodiazepinas pro-apoctoticas.
US6960576B2 (en) 1999-09-13 2005-11-01 Bristol-Myers Squibb Pharma Company Hydroxyalkanoylaminolactams and related structures as inhibitors of Aβ protein production
US6503902B2 (en) 1999-09-13 2003-01-07 Bristol-Myers Squibb Pharma Company Hydroxyalkanoylaminolactams and related structures as inhibitors of a β protein production
EP1222176A1 (fr) 1999-10-08 2002-07-17 Bristol-Myers Squibb Pharma Company AMINO SULFONAMIDES DE LACTAME UTILISES COMME INHIBITEURS DE LA PRODUCTION DE PROTEINE A$g(b)
IL150524A0 (en) * 2000-01-07 2003-02-12 Transform Pharmaceuticals Inc High-throughput formation, identification, and analysis of diverse solid-forms
AU779875B2 (en) 2000-01-24 2005-02-17 Merck Sharp & Dohme Limited Gamma-secretase inhibitors
EP1261610A2 (fr) 2000-02-17 2002-12-04 Bristol-Myers Squibb Pharma Company CARBOCYCLES ET HETEROCYCLES SUCCINOYLAMINO UTILISES EN TANT QU'INHIBITEURS DE LA PRODUCTION DE LA PROTEINE A$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
MXPA02009755A (es) 2000-04-03 2003-03-27 Bristol Myers Squibb Pharma Co Lactamas ciclicas como inhibidores de la produccion de proteina a-beta.
EP1268434A1 (fr) 2000-04-03 2003-01-02 Bristol-Myers Squibb Pharma Company Lactames cycliques utiles en tant qu'inhibiteurs de la production de proteine a-beta
GB0008710D0 (en) 2000-04-07 2000-05-31 Merck Sharp & Dohme Therapeutic compounds
WO2001077086A1 (fr) 2000-04-11 2001-10-18 Dupont Pharmaceuticals Company LACTAMES SUBSTITUES UTILISES EN TANT QU'INHIBITEURS DE PRODUCTION DE PROTEINE A$g(b)
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
IL147629A0 (en) 2000-06-01 2002-08-14 Bristol Myers Squibb Pharma Co LACTAMS SUBSTITUTED BY CYCLIC SUCCINATES AS INHIBITORS OF Aβ PROTEIN PRODUCTION
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
CN100480248C (zh) 2003-02-04 2009-04-22 弗·哈夫曼-拉罗切有限公司 用作γ-分泌酶抑制剂的丙二酰胺衍生物
GB0312365D0 (en) 2003-05-30 2003-07-02 Univ Aston Novel 3-substituted-1, 4-benzodiazepines
BRPI0413533A (pt) 2003-09-09 2006-10-10 Hoffmann La Roche derivados de malonamida que bloqueiam a atividade de gama-secretase
EP1795198A1 (fr) 2005-12-09 2007-06-13 Hubrecht Laboratorium Traitement de l'esophage de Barret
EP2198863A1 (fr) 2006-02-27 2010-06-23 The Johns Hopkins University Traitement anticancéreux utilisant des inhibiteurs de gamma-sécrétases
WO2007110335A1 (fr) 2006-03-27 2007-10-04 F. Hoffmann-La Roche Ag Dérivés de malonamide en tant qu'inhibiteurs de la gamma secrétase
WO2008034735A2 (fr) 2006-09-20 2008-03-27 F. Hoffmann-La Roche Ag Dérivés 4-oxo-2,3,4,5-tetrahydro-benzo[b][1,4]diazépine
KR101136260B1 (ko) 2007-08-14 2012-04-19 일라이 릴리 앤드 캄파니 감마-세크레타제 억제제로서의 아제핀 유도체
US20090181944A1 (en) 2008-01-11 2009-07-16 John Frederick Boylan Method for cancer therapy
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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BR112013024059B1 (pt) 2022-01-25
HK1189218A1 (en) 2014-05-30
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RS53843B1 (sr) 2015-08-31
TW201309656A (zh) 2013-03-01
KR101948347B1 (ko) 2019-02-14
EP2688873B1 (fr) 2015-01-21
NZ616876A (en) 2014-08-29
MY161233A (en) 2017-04-14
TWI530489B (zh) 2016-04-21
AU2012230904A1 (en) 2013-11-07
UY33961A (es) 2012-09-28
PH12013501738B1 (en) 2019-03-13
US8629136B2 (en) 2014-01-14
SG193555A1 (en) 2013-11-29
US20120245151A1 (en) 2012-09-27
CA2830902A1 (fr) 2012-09-27
IL228534A (en) 2017-02-28
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PE20140626A1 (es) 2014-05-30
KR20140027956A (ko) 2014-03-07
US20140100365A1 (en) 2014-04-10
PL2688873T3 (pl) 2015-06-30
HRP20150273T1 (hr) 2015-06-19
AR129859A2 (es) 2024-10-02
EP2688873A1 (fr) 2014-01-29
CA2830902C (fr) 2019-10-29
SI2688873T1 (sl) 2015-04-30
MX2013010420A (es) 2013-10-01
JP5873923B2 (ja) 2016-03-01
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CN103717576B (zh) 2015-11-25
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CN103717576A (zh) 2014-04-09
IL228534A0 (en) 2013-12-31
AU2012230904B2 (en) 2016-03-31
PH12013501738A1 (en) 2013-10-07
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