ES2570569T3 - Compuestos de benzoxazepina como inhibidores de la PI3K y métodos de uso - Google Patents

Compuestos de benzoxazepina como inhibidores de la PI3K y métodos de uso

Info

Publication number
ES2570569T3
ES2570569T3 ES13193562T ES13193562T ES2570569T3 ES 2570569 T3 ES2570569 T3 ES 2570569T3 ES 13193562 T ES13193562 T ES 13193562T ES 13193562 T ES13193562 T ES 13193562T ES 2570569 T3 ES2570569 T3 ES 2570569T3
Authority
ES
Spain
Prior art keywords
methods
pi3k inhibitors
benzoxazepine compounds
benzoxazepine
compounds
Prior art date
Legal status (The legal status 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 status listed.)
Active
Application number
ES13193562T
Other languages
English (en)
Inventor
Nicole Blaquiere
Steven Do
Danette Dudley
Adrian J Folkes
Robert Heald
Timothy Heffron
Mark Jones
Aleksandr Kolesnikov
Chudi Ndubaku
Alan G Olivero
Stephen Price
Steven Staben
Lan Wang
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
F Hoffmann La Roche AG
Original Assignee
F Hoffmann La Roche AG
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=43037239&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ES2570569(T3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by F Hoffmann La Roche AG filed Critical F Hoffmann La Roche AG
Application granted granted Critical
Publication of ES2570569T3 publication Critical patent/ES2570569T3/es
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic 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 two hetero rings
    • C07D498/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
    • A61K31/41621,2-Diazoles condensed with heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • A61K31/41881,3-Diazoles condensed with other heterocyclic ring systems, e.g. biotin, sorbinil
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41961,2,4-Triazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/553Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/04Immunostimulants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • C07D491/044Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/12Heterocyclic 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
    • C07D498/14Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

Abstract

Un compuesto que tiene la estructura:**Fórmula**
ES13193562T 2009-09-28 2010-09-27 Compuestos de benzoxazepina como inhibidores de la PI3K y métodos de uso Active ES2570569T3 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US24638109P 2009-09-28 2009-09-28
US33068510P 2010-05-03 2010-05-03

Publications (1)

Publication Number Publication Date
ES2570569T3 true ES2570569T3 (es) 2016-05-19

Family

ID=43037239

Family Applications (2)

Application Number Title Priority Date Filing Date
ES13193562T Active ES2570569T3 (es) 2009-09-28 2010-09-27 Compuestos de benzoxazepina como inhibidores de la PI3K y métodos de uso
ES10757213.3T Active ES2444779T3 (es) 2009-09-28 2010-09-27 Compuestos de benzoxazepina inhibidores de la PI3K y su utilización en el tratamiento de cáncer

Family Applications After (1)

Application Number Title Priority Date Filing Date
ES10757213.3T Active ES2444779T3 (es) 2009-09-28 2010-09-27 Compuestos de benzoxazepina inhibidores de la PI3K y su utilización en el tratamiento de cáncer

Country Status (32)

Country Link
US (7) US8242104B2 (es)
EP (3) EP2845592A1 (es)
JP (2) JP5540101B2 (es)
KR (1) KR101428346B1 (es)
CN (2) CN104744491B (es)
AR (1) AR078187A1 (es)
AU (1) AU2010299816C1 (es)
BR (1) BR112012006807A2 (es)
CA (1) CA2772691C (es)
CL (1) CL2012000754A1 (es)
CO (1) CO6491026A2 (es)
CR (1) CR20120121A (es)
DK (1) DK2483278T3 (es)
EC (1) ECSP12011755A (es)
ES (2) ES2570569T3 (es)
HK (2) HK1211929A1 (es)
HR (1) HRP20140229T1 (es)
IL (2) IL217558A (es)
MA (1) MA33531B1 (es)
MX (1) MX2012003591A (es)
MY (2) MY184074A (es)
NZ (1) NZ597833A (es)
PE (1) PE20121025A1 (es)
PL (1) PL2483278T3 (es)
PT (1) PT2483278E (es)
RS (1) RS53164B (es)
RU (2) RU2600927C2 (es)
SG (1) SG10201405049RA (es)
SI (1) SI2483278T1 (es)
TW (1) TWI423980B (es)
WO (1) WO2011036280A1 (es)
ZA (1) ZA201202199B (es)

Families Citing this family (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RS56410B1 (sr) * 2009-07-27 2018-01-31 Gilead Sciences Inc Fuzionisana heterociklična jedinjenja kao modulatori jonskih kanala
US8263633B2 (en) * 2009-09-28 2012-09-11 F. Hoffman-La Roche Ag Benzoxepin PI3K inhibitor compounds and methods of use
KR101428346B1 (ko) * 2009-09-28 2014-08-07 에프. 호프만-라 로슈 아게 벤즈옥사제핀 pi3k 억제 화합물 및 사용 방법
JP5858586B2 (ja) 2010-07-02 2016-02-10 ギリアード サイエンシーズ, インコーポレイテッド イオンチャネルモジュレーターとしての縮合複素環式化合物
BR112013024122A2 (pt) * 2011-03-21 2019-09-24 Hoffmann La Roche compostos de benzoxazepina seletivos para p110 delta pi3k e métodos de uso
US9115096B2 (en) 2011-05-10 2015-08-25 Gilead Sciences, Inc. Fused heterocyclic compounds as ion channel modulators
WO2012156379A1 (en) 2011-05-13 2012-11-22 Universität Zürich PIK3/P110α INHIBITORS FOR PREVENTION OF RESTENOSIS BY APPLICATION AS AN IMPLANT COATING
TWI549944B (zh) 2011-07-01 2016-09-21 吉李德科學股份有限公司 作為離子通道調節劑之稠合雜環化合物
NO3175985T3 (es) * 2011-07-01 2018-04-28
RU2014136578A (ru) 2012-02-17 2016-04-10 Ф. Хоффманн-Ля Рош Аг Трициклические соединения и способы их применения
SG10201706196XA (en) * 2012-06-08 2017-08-30 Hoffmann La Roche Mutant selectivity and combinations of a phosphoinositide 3 kinase inhibitor compound and chemotherapeutic agents for the treatment of cancer
CN104797267A (zh) 2012-06-26 2015-07-22 德玛医药 使用卫康醇、二乙酰二脱水卫矛醇、二溴卫矛醇或类似物或其衍生物治疗具有基因多型性或ahi1失调或突变患者的抗酪氨酸激酶抑制剂的恶性肿瘤的方法
CN102775395A (zh) * 2012-07-12 2012-11-14 江苏七洲绿色化工股份有限公司 一种丙环唑的制备方法及丙环唑中间体
WO2014025675A1 (en) * 2012-08-07 2014-02-13 Janssen Pharmaceutica Nv Process for the preparation of heterocyclic ester derivatives
JP6363120B2 (ja) * 2013-03-13 2018-07-25 エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト ベンゾオキサゼピン化合物の作製方法
WO2014168986A1 (en) 2013-04-08 2014-10-16 Brown Dennis M Therapeutic benefit of suboptimally administered chemical compounds
KR101902664B1 (ko) * 2013-12-16 2018-09-28 에프. 호프만-라 로슈 아게 2-(4-(2-(1-이소프로필-3-메틸-1H-1,2,4-트라이아졸-5-일)-5,6-다이하이드로벤조[f]이미다조[1,2-d][1,4]옥사제핀-9-일)-1H-피라졸-1-일)-2-메틸프로판아미드의 다형체, 이의 제조 방법 및 이의 약학적 용도
AU2015228859A1 (en) 2014-03-13 2016-07-07 F. Hoffmann-La Roche Ag Therapeutic combinations with estrogen receptor modulators
CN107873023B (zh) 2015-02-02 2021-07-23 福马治疗股份有限公司 作为hdac抑制剂的3-烷基-4-酰氨基-双环[4,5,0]异羟肟酸
TW201636329A (zh) 2015-02-02 2016-10-16 佛瑪治療公司 作為hdac抑制劑之雙環[4,6,0]異羥肟酸
AR104068A1 (es) 2015-03-26 2017-06-21 Hoffmann La Roche Combinaciones de un compuesto inhibidor de fosfoinosítido 3-cinasa y un compuesto inhibidor de cdk4/6 para el tratamiento del cáncer
JP6691552B2 (ja) * 2015-04-30 2020-04-28 ノバルティス アーゲー ファルネソイドx受容体をモジュレートするのに有用である縮合三環式ピラゾール誘導体
JP6698712B2 (ja) 2015-06-29 2020-05-27 エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト Taselisibを用いた治療方法
CN111848643A (zh) * 2015-07-02 2020-10-30 豪夫迈·罗氏有限公司 苯并氧氮杂*噁唑烷酮化合物及其使用方法
LT3317284T (lt) 2015-07-02 2020-01-27 F. Hoffmann-La Roche Ag Benzoksazepino oksazolidinono junginiai ir jų naudojimo būdai
WO2017042182A1 (en) * 2015-09-08 2017-03-16 F. Hoffmann-La Roche Ag Tricyclic pi3k inhibitor compounds and methods of use
US9721369B2 (en) * 2015-09-15 2017-08-01 Facebook, Inc. Systems and methods for utilizing multiple map portions from multiple map data sources
EP3472131B1 (en) 2016-06-17 2020-02-19 Forma Therapeutics, Inc. 2-spiro-5- and 6-hydroxamic acid indanes as hdac inhibitors
TW201825465A (zh) 2016-09-23 2018-07-16 美商基利科學股份有限公司 磷脂醯肌醇3-激酶抑制劑
TW201813963A (zh) 2016-09-23 2018-04-16 美商基利科學股份有限公司 磷脂醯肌醇3-激酶抑制劑
TW201815787A (zh) 2016-09-23 2018-05-01 美商基利科學股份有限公司 磷脂醯肌醇3-激酶抑制劑
CA3038407A1 (en) 2016-09-29 2018-04-05 Bayer Cropscience Aktiengesellschaft Novel 5-substituted imidazolylmethyl derivatives
PL3851441T3 (pl) 2016-12-15 2023-11-06 F. Hoffmann-La Roche Ag Proces otrzymywania (S)-2-((2-((S)-4-(difluorometylo)-2-oksooksazolidyn-3-ylo)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oksazepin-9-ylo)amino)propanamidu
US11077189B2 (en) 2017-03-02 2021-08-03 Genentech Inc. Adjuvant treatment of HER2-positive breast cancer
KR102342776B1 (ko) * 2017-04-28 2021-12-23 에프. 호프만-라 로슈 아게 (S)-2-((2-((S)-4-(다이플루오로메틸)-2-옥소옥사졸리딘-3-일)-5,6-다이하이드로벤조[f]이미다조[1,2-d][1,4]옥사제핀-9-일)아미노)프로판아미드의 다형체 및 고체 형태, 및 이의 제조 방법
WO2019084459A1 (en) * 2017-10-26 2019-05-02 Xynomic Pharmaceuticals, Inc. CRYSTALLINE SALTS AND FORMS OF B-RAF KINASE INHIBITOR
JP7456945B2 (ja) * 2018-05-30 2024-03-27 江▲蘇▼豪森▲薬▼▲業▼集▲団▼有限公司 三環式誘導体を含む阻害剤、その製造方法、及び使用
CN111909157B (zh) * 2019-05-07 2023-02-03 南京药石科技股份有限公司 Ezh2抑制剂及其用途
WO2021088845A1 (zh) * 2019-11-04 2021-05-14 贝达药业股份有限公司 咪唑烷酮类化合物及其制备方法与应用
IL292592A (en) * 2019-11-04 2022-07-01 Betta Pharmaceuticals Co Ltd Imidazoline compound, process for its preparation and use
CA3159094A1 (en) * 2019-11-25 2021-06-03 Shanghai Hansoh Biomedical Co., Ltd. Three fused ring derivative-containing salt or crystal form and pharmaceutical composition thereof
WO2022237871A1 (zh) * 2021-05-13 2022-11-17 贝达药业股份有限公司 咪唑烷酮类化合物的多晶型物、制备方法及其用途
IL308457A (en) 2021-05-28 2024-01-01 Genentech Inc A process for preparing benzoxazepine oxazolidinone compounds

Family Cites Families (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3773919A (en) 1969-10-23 1973-11-20 Du Pont Polylactide-drug mixtures
GB8504702D0 (en) * 1985-02-23 1985-03-27 Zyma Sa Tricyclic compounds
US5583024A (en) 1985-12-02 1996-12-10 The Regents Of The University Of California Recombinant expression of Coleoptera luciferase
FR2677356B1 (fr) * 1991-06-05 1995-03-17 Sanofi Sa Derives heterocycliques d'acylamino-2 thiazoles-5 substitues, leur preparation et compositions pharmaceutiques en contenant.
EP0638071B1 (en) * 1992-12-28 1997-04-09 Eisai Co., Ltd. Heterocyclic carbonic acid derivatives which bind to retinoid receptors (rar)
AU678503B2 (en) * 1993-09-24 1997-05-29 Takeda Chemical Industries Ltd. Condensed heterocyclic compounds and their use as squalene synthetase inhibitors
US5543523A (en) 1994-11-15 1996-08-06 Regents Of The University Of Minnesota Method and intermediates for the synthesis of korupensamines
JPH08336393A (ja) 1995-04-13 1996-12-24 Mitsubishi Chem Corp 光学活性なγ−置換−β−ヒドロキシ酪酸エステルの製造法
BR9611731A (pt) * 1995-11-17 1999-02-23 Du Pont Composto mistura composição herbicida e método para controlar o crescimento de vegetação indesejada
US6602677B1 (en) 1997-09-19 2003-08-05 Promega Corporation Thermostable luciferases and methods of production
DE19908535A1 (de) * 1999-02-26 2000-08-31 Aventis Pharma Gmbh Verwendung von polycyclischen Thiazol-Systemen zur Herstellung von Medikamenten zur Prophylaxe oder Behandlung von Obesitas
DE19908533A1 (de) * 1999-02-26 2000-08-31 Aventis Pharma Gmbh Polycyclische Thiazol-Systeme, Verfahren zu ihrer Herstellung und Arzneimittel enthaltend diese Verbindungen
DE19908538A1 (de) * 1999-02-26 2000-08-31 Aventis Pharma Gmbh Polycyclische 2-Amino-Thiazol Systeme, Verfahren zu ihrer Herstellung und Arzneimittel enthaltend diese Verbindungen
DE19908537A1 (de) * 1999-02-26 2000-08-31 Aventis Pharma Gmbh Verwendung von polycyclischen 2-Amino-Thiazol Systemen zur Herstellung von Medikamenten zur Prophylaxe oder Behandlung von Obesitas
US7273880B2 (en) * 1999-06-30 2007-09-25 H. Lunbeck A/S Selective NPY (Y5) antagonists
AU2001246494A1 (en) 2000-03-03 2001-09-12 Novartis Ag Condensed thiazolamines and their use as neuropeptide y5 antagonists
SK9782003A3 (en) 2001-02-02 2004-01-08 Schering Corp 3,4-Di-substituted cyclobutene-1,2-diones as CXC chemokine receptor antagonists
TWI232863B (en) * 2001-06-11 2005-05-21 Akzo Nobel Nv Benzoxazepine derivatives
MXPA05000381A (es) * 2002-07-19 2005-03-31 Pharmacia Corp Compuestos de carboxamida tiofeno sustituido para el tratamiento de inflamacion.
WO2004069245A1 (en) * 2003-02-07 2004-08-19 Warner-Lambert Company Llc Oxazolidinone derivates n-substituted by a tricyclic ring, for use as antibacterial agents
TW200510356A (en) * 2003-08-01 2005-03-16 Takeda Chemical Industries Ltd Benzoxaepine compounds
US20050239767A1 (en) * 2003-10-28 2005-10-27 Chan Michael K Intermolecular SNAr of the heterocycle-activated nitro and fluoro groups-application in the synthesis of polyazamacrocyclic ligands
EP1765830B1 (en) * 2004-07-01 2010-09-22 Merck Sharp & Dohme Corp. Mitotic kinesin inhibitors
MX2007004051A (es) * 2004-10-07 2007-05-24 Boehringer Ingelheim Int Pi3-quinasas.
CA3052368A1 (en) 2005-10-07 2007-04-19 Exelixis, Inc. Azetidines as mek inhibitors
US20070238746A1 (en) * 2006-04-06 2007-10-11 Trixi Brandl Thiazolyl-dihydro-chinazoline
US20070238718A1 (en) * 2006-04-06 2007-10-11 Matthias Grauert Thiazolyl-dihydro-indazole
GB0610866D0 (en) * 2006-06-02 2006-07-12 Hammersmith Imanet Ltd Novel in vivo imaging compounds
US20080026171A1 (en) * 2006-07-28 2008-01-31 Alcan Packaging Flexible France Coextruded film with polylactic acid (PLA) and Ethylene Vinyl Acetate (EVA)
ES2614931T3 (es) 2006-08-04 2017-06-02 Beth Israel Deaconess Medical Center Inhibidores de la piruvato cinasa y métodos de tratamiento de enfermedad
US8779154B2 (en) * 2006-09-26 2014-07-15 Qinglin Che Fused ring compounds for inflammation and immune-related uses
RU2485114C2 (ru) * 2006-12-29 2013-06-20 Эбботт Гмбх Унд Ко.Кг Карбоксамидные соединения и их применение в качестве ингибиторов кальпаинов
EP2200658B1 (en) 2007-09-19 2014-12-03 The Regents of The University of California Positron emission tomography probes for imaging immune activation and selected cancers
CN102333779B (zh) * 2008-03-31 2015-12-09 吉宁特有限公司 苯并吡喃和苯并氧杂*pi3k抑制剂化合物和使用方法
US8653097B2 (en) * 2008-10-17 2014-02-18 Boehringer Ingelheim International Gmbh Tetra-aza-heterocycles as phosphatidylinositol-3-kinases (P13-kinases) inhibitor
KR101428346B1 (ko) * 2009-09-28 2014-08-07 에프. 호프만-라 로슈 아게 벤즈옥사제핀 pi3k 억제 화합물 및 사용 방법
US8263633B2 (en) * 2009-09-28 2012-09-11 F. Hoffman-La Roche Ag Benzoxepin PI3K inhibitor compounds and methods of use

Also Published As

Publication number Publication date
IL239081B (en) 2018-05-31
ZA201202199B (en) 2013-01-30
WO2011036280A1 (en) 2011-03-31
BR112012006807A2 (pt) 2020-11-03
SI2483278T1 (sl) 2014-03-31
EP2845592A1 (en) 2015-03-11
US8586574B2 (en) 2013-11-19
HRP20140229T1 (hr) 2014-04-11
US9198918B2 (en) 2015-12-01
IL217558A0 (en) 2012-02-29
PT2483278E (pt) 2014-03-05
CN102762576A (zh) 2012-10-31
AU2010299816C1 (en) 2018-02-01
CN102762576B (zh) 2015-04-22
ECSP12011755A (es) 2012-05-30
EP2483278B1 (en) 2013-12-25
US8343955B2 (en) 2013-01-01
HK1211929A1 (en) 2016-06-03
US20120244149A1 (en) 2012-09-27
US20110076292A1 (en) 2011-03-31
CL2012000754A1 (es) 2012-09-07
CA2772691C (en) 2017-10-03
JP2014070075A (ja) 2014-04-21
US8242104B2 (en) 2012-08-14
US20160052933A1 (en) 2016-02-25
SG10201405049RA (en) 2014-10-30
ES2444779T3 (es) 2014-02-26
CN104744491A (zh) 2015-07-01
JP5540101B2 (ja) 2014-07-02
US20130079331A1 (en) 2013-03-28
AU2010299816A1 (en) 2012-02-02
RU2012117398A (ru) 2013-11-10
JP2013505917A (ja) 2013-02-21
CR20120121A (es) 2012-06-01
IL239081A0 (en) 2015-07-30
IL217558A (en) 2015-06-30
HK1174629A1 (en) 2013-06-14
PL2483278T3 (pl) 2014-05-30
NZ597833A (en) 2014-01-31
TWI423980B (zh) 2014-01-21
RU2600927C2 (ru) 2016-10-27
US20140288047A1 (en) 2014-09-25
KR20120065431A (ko) 2012-06-20
PE20121025A1 (es) 2012-08-06
AR078187A1 (es) 2011-10-19
CO6491026A2 (es) 2012-07-31
DK2483278T3 (da) 2014-01-13
US9546178B2 (en) 2017-01-17
MX2012003591A (es) 2012-04-19
MY160064A (en) 2017-02-15
AU2010299816B2 (en) 2015-11-12
CA2772691A1 (en) 2011-03-31
RS53164B (en) 2014-06-30
US8785626B2 (en) 2014-07-22
MA33531B1 (fr) 2012-08-01
CN104744491B (zh) 2017-07-11
JP5625101B2 (ja) 2014-11-12
US9670228B2 (en) 2017-06-06
MY184074A (en) 2021-03-17
KR101428346B1 (ko) 2014-08-07
RU2654068C1 (ru) 2018-05-16
EP2711368A1 (en) 2014-03-26
US20170081341A1 (en) 2017-03-23
EP2483278A1 (en) 2012-08-08
TW201127844A (en) 2011-08-16
EP2711368B1 (en) 2016-03-23
US20140058098A1 (en) 2014-02-27

Similar Documents

Publication Publication Date Title
ES2570569T3 (es) Compuestos de benzoxazepina como inhibidores de la PI3K y métodos de uso
CR20120295A (es) Triazolopiridinas
CR20140180A (es) Inhibidores macrocíclicos de serina proteasas de hepatitis c
CL2016001732A1 (es) Métodos sintéticos para compuestos espiro-oxoindol (div. sol. 3633-13).
CR20120348A (es) Nuevos compuestos tricíclicos
SMT201600135B (it) Nuovi inibitori della s-nitrosoglutatione riduttasi
SMT201400008B (it) Uso di betanecolo per il trattamento di xerostomia
CR20140501A (es) Nuevos diazaespirocicloalcanos y azaespirocicloalcanos
CR20120334A (es) Derivados de imidazopiridina como inhibidores de jak
BR112013025353A2 (pt) combinações de compostos de inibidores de akt e erlotinibe e métodos de uso
DK2448938T3 (da) Pyrimidinoner som pi3k-inhibitorer
UY34216A (es) Nuevos compuestos que inhiben la actividad de la Lp-PLA2
CR20120637A (es) Triazolopiridinas sustituidas
UY33958A (es) Inhibidores de la glucosilceramida sintasa
CR20130539A (es) Triazolopiridinas
CR20130045A (es) Compuestos terapéuticos
CR20120011A (es) Inhibidores de bace
CR20110467A (es) Derivados de benzofuranilo como inhibidores de la glucoquinasa
UY33929A (es) Compuestos de ciclohexilo tetrasustituido como inhibidores de quinasas
BRPI1010795A2 (pt) compostos antivirais
CR20120283A (es) Inhibidor de bromodominio de benzodiazepina
UA110338C2 (en) Chemical compounds
ME01665B (me) Analozi buprenorfina
CR20120297A (es) Espironucleósidos uracílicos oxetánicos
CR20130001A (es) Derivados de indolizina, su procedimiento de preparación y su aplicación en terapéutica