PT3033343T - Compostos e composições como inibidores de mek - Google Patents
Compostos e composições como inibidores de mekInfo
- Publication number
- PT3033343T PT3033343T PT14792587T PT14792587T PT3033343T PT 3033343 T PT3033343 T PT 3033343T PT 14792587 T PT14792587 T PT 14792587T PT 14792587 T PT14792587 T PT 14792587T PT 3033343 T PT3033343 T PT 3033343T
- Authority
- PT
- Portugal
- Prior art keywords
- mek
- inhibitors
- compositions
- compounds
- Prior art date
Links
Classifications
-
- 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
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
-
- 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
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines 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
- A61K31/495—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
- A61K31/495—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
- A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
-
- 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
- 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
- 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)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN2418DE2013 | 2013-08-14 | ||
IN1686DE2014 | 2014-06-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
PT3033343T true PT3033343T (pt) | 2019-03-21 |
Family
ID=51844790
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PT14792587T PT3033343T (pt) | 2013-08-14 | 2014-08-14 | Compostos e composições como inibidores de mek |
Country Status (33)
Country | Link |
---|---|
US (3) | US9227969B2 (pt) |
EP (1) | EP3033343B1 (pt) |
JP (1) | JP6473453B2 (pt) |
KR (1) | KR102354208B1 (pt) |
CN (1) | CN105473588B (pt) |
AP (1) | AP2016008981A0 (pt) |
AU (1) | AU2014307593C1 (pt) |
BR (1) | BR112016001783B1 (pt) |
CA (1) | CA2921300C (pt) |
CL (1) | CL2016000150A1 (pt) |
CR (1) | CR20160072A (pt) |
CU (1) | CU20160020A7 (pt) |
DO (1) | DOP2016000047A (pt) |
EA (1) | EA029093B1 (pt) |
ES (1) | ES2714718T3 (pt) |
GE (1) | GEP201706725B (pt) |
HK (1) | HK1219271A1 (pt) |
IL (1) | IL243349A0 (pt) |
MX (1) | MX359401B (pt) |
NI (1) | NI201600014A (pt) |
PE (1) | PE20160204A1 (pt) |
PH (1) | PH12016500003A1 (pt) |
PL (1) | PL3033343T3 (pt) |
PT (1) | PT3033343T (pt) |
SG (1) | SG11201510727VA (pt) |
SV (1) | SV2016005153A (pt) |
TN (1) | TN2015000574A1 (pt) |
TR (1) | TR201902709T4 (pt) |
TW (1) | TW201536782A (pt) |
UA (1) | UA116566C2 (pt) |
UY (1) | UY35704A (pt) |
WO (1) | WO2015022662A1 (pt) |
ZA (1) | ZA201509337B (pt) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9227969B2 (en) | 2013-08-14 | 2016-01-05 | Novartis Ag | Compounds and compositions as inhibitors of MEK |
CA2946538A1 (en) | 2014-04-04 | 2015-10-08 | Del Mar Pharmaceuticals | Use of dianhydrogalactitol and analogs or derivatives thereof to treat non-small-cell carcinoma of the lung and ovarian cancer |
AU2016211246B2 (en) | 2015-01-30 | 2020-08-27 | Biomed Valley Discoveries, Inc. | Crystalline forms of C21H22CI2N4O2 |
WO2016123581A1 (en) * | 2015-01-30 | 2016-08-04 | Biomed Valley Discoveries, Inc. | Crystalline c21h22c12n4o2 malonate |
EP3842429B1 (en) * | 2015-06-15 | 2022-09-07 | Asana BioSciences, LLC | Heterocyclic inhibitors of erk1 and erk2 and their use in the treatment of cancer |
TWI674261B (zh) | 2017-02-17 | 2019-10-11 | 美商英能腫瘤免疫股份有限公司 | Nlrp3 調節劑 |
US20210380683A1 (en) * | 2018-04-12 | 2021-12-09 | The Methodist Hospital System | Modulation of irf-4 and uses thereof |
CN114364798A (zh) | 2019-03-21 | 2022-04-15 | 欧恩科斯欧公司 | 用于治疗癌症的Dbait分子与激酶抑制剂的组合 |
CN110141657B (zh) * | 2019-05-17 | 2023-01-17 | 温州医科大学附属第二医院、温州医科大学附属育英儿童医院 | 一种表皮生长因子脂质体及其制备方法 |
UY38880A (es) | 2019-09-16 | 2021-04-30 | Novartis Ag | Degradadores bifuncionales de brd9 y sus métodos de uso |
WO2021089791A1 (en) | 2019-11-08 | 2021-05-14 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for the treatment of cancers that have acquired resistance to kinase inhibitors |
WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
AU2023238106A1 (en) * | 2022-03-24 | 2024-09-26 | Biomed Valley Discoveries, Inc. | Deuterated analogs of pyrrole inhibitors of erk, synthesis thereof and intermediates thereto |
Family Cites Families (85)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH445129A (fr) | 1964-04-29 | 1967-10-15 | Nestle Sa | Procédé pour la préparation de composés d'inclusion à poids moléculaire élevé |
US3459731A (en) | 1966-12-16 | 1969-08-05 | Corn Products Co | Cyclodextrin polyethers and their production |
US3453257A (en) | 1967-02-13 | 1969-07-01 | Corn Products Co | Cyclodextrin with cationic properties |
US3426011A (en) | 1967-02-13 | 1969-02-04 | Corn Products Co | Cyclodextrins with anionic properties |
US3453259A (en) | 1967-03-22 | 1969-07-01 | Corn Products Co | Cyclodextrin polyol ethers and their oxidation products |
GB1524747A (en) | 1976-05-11 | 1978-09-13 | Ici Ltd | Polypeptide |
US4235871A (en) | 1978-02-24 | 1980-11-25 | Papahadjopoulos Demetrios P | Method of encapsulating biologically active materials in lipid vesicles |
ATE28864T1 (de) | 1982-07-23 | 1987-08-15 | Ici Plc | Amide-derivate. |
GB8327256D0 (en) | 1983-10-12 | 1983-11-16 | Ici Plc | Steroid derivatives |
ZA848968B (en) | 1983-11-18 | 1986-06-25 | Riker Laboratories Inc | 1h-imidazo(4,5-c)quinolines and 1h-imidazo(4,5-c)quinolin-4-amines |
US4737323A (en) | 1986-02-13 | 1988-04-12 | Liposome Technology, Inc. | Liposome extrusion method |
US5093330A (en) | 1987-06-15 | 1992-03-03 | Ciba-Geigy Corporation | Staurosporine derivatives substituted at methylamino nitrogen |
EP0385630B1 (en) | 1989-02-27 | 1996-11-27 | Riker Laboratories, Inc. | 1H-imidazo(4,5-c)Quinolin-4-amines as antivirals |
US5010099A (en) | 1989-08-11 | 1991-04-23 | Harbor Branch Oceanographic Institution, Inc. | Discodermolide compounds, compositions containing same and method of preparation and use |
GB8928281D0 (en) | 1989-12-14 | 1990-02-21 | Smith Kline French Lab | Compounds |
KR0166088B1 (ko) | 1990-01-23 | 1999-01-15 | . | 수용해도가 증가된 시클로덱스트린 유도체 및 이의 용도 |
US5395855A (en) | 1990-05-07 | 1995-03-07 | Ciba-Geigy Corporation | Hydrazones |
NZ243082A (en) | 1991-06-28 | 1995-02-24 | Ici Plc | 4-anilino-quinazoline derivatives; pharmaceutical compositions, preparatory processes, and use thereof |
AU661533B2 (en) | 1992-01-20 | 1995-07-27 | Astrazeneca Ab | Quinazoline derivatives |
TW225528B (pt) | 1992-04-03 | 1994-06-21 | Ciba Geigy Ag | |
DE69233803D1 (de) | 1992-10-28 | 2011-03-31 | Genentech Inc | Verwendung von vaskulären Endothelwachstumsfaktor-Antagonisten |
GB9314893D0 (en) | 1993-07-19 | 1993-09-01 | Zeneca Ltd | Quinazoline derivatives |
IL115849A0 (en) | 1994-11-03 | 1996-01-31 | Merz & Co Gmbh & Co | Tangential filtration preparation of liposomal drugs and liposome product thereof |
EP3103799B1 (en) | 1995-03-30 | 2018-06-06 | OSI Pharmaceuticals, LLC | Quinazoline derivatives |
GB9508538D0 (en) | 1995-04-27 | 1995-06-14 | Zeneca Ltd | Quinazoline derivatives |
US5747498A (en) | 1996-05-28 | 1998-05-05 | Pfizer Inc. | Alkynyl and azido-substituted 4-anilinoquinazolines |
US5880141A (en) | 1995-06-07 | 1999-03-09 | Sugen, Inc. | Benzylidene-Z-indoline compounds for the treatment of disease |
US5843901A (en) | 1995-06-07 | 1998-12-01 | Advanced Research & Technology Institute | LHRH antagonist peptides |
CA2224435C (en) | 1995-07-06 | 2008-08-05 | Novartis Ag | Pyrrolopyrimidines and processes for the preparation thereof |
US5760041A (en) | 1996-02-05 | 1998-06-02 | American Cyanamid Company | 4-aminoquinazoline EGFR Inhibitors |
GB9603095D0 (en) | 1996-02-14 | 1996-04-10 | Zeneca Ltd | Quinazoline derivatives |
IL126351A0 (en) | 1996-04-12 | 1999-05-09 | Warner Lambert Co | Irreversible inhibitors of tyrosine kinases |
JP2000512990A (ja) | 1996-06-24 | 2000-10-03 | ファイザー・インク | 過増殖性疾患を処置するためのフェニルアミノ置換三環式誘導体 |
NZ334821A (en) | 1996-08-30 | 2000-12-22 | Novartis Ag | Method for producing epothilones |
DE69724269T2 (de) | 1996-09-06 | 2004-06-09 | Obducat Ab | Verfahren für das anisotrope ätzen von strukturen in leitende materialien |
DE19638745C2 (de) | 1996-09-11 | 2001-05-10 | Schering Ag | Monoklonale Antikörper gegen die extrazelluläre Domäne des menschlichen VEGF - Rezeptorproteins (KDR) |
CA2265630A1 (en) | 1996-09-13 | 1998-03-19 | Gerald Mcmahon | Use of quinazoline derivatives for the manufacture of a medicament in the treatment of hyperproliferative skin disorders |
EP0837063A1 (en) | 1996-10-17 | 1998-04-22 | Pfizer Inc. | 4-Aminoquinazoline derivatives |
DK1367057T3 (da) | 1996-11-18 | 2009-01-19 | Biotechnolog Forschung Gmbh | Epothiloner E og F |
US6441186B1 (en) | 1996-12-13 | 2002-08-27 | The Scripps Research Institute | Epothilone analogs |
CO4950519A1 (es) | 1997-02-13 | 2000-09-01 | Novartis Ag | Ftalazinas, preparaciones farmaceuticas que las comprenden y proceso para su preparacion |
CO4940418A1 (es) | 1997-07-18 | 2000-07-24 | Novartis Ag | Modificacion de cristal de un derivado de n-fenil-2- pirimidinamina, procesos para su fabricacion y su uso |
GB9721069D0 (en) | 1997-10-03 | 1997-12-03 | Pharmacia & Upjohn Spa | Polymeric derivatives of camptothecin |
US6194181B1 (en) | 1998-02-19 | 2001-02-27 | Novartis Ag | Fermentative preparation process for and crystal forms of cytostatics |
CA2322157C (en) | 1998-02-25 | 2012-05-29 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues thereof |
BR9912938B1 (pt) | 1998-08-11 | 2011-06-28 | derivados de isoquinolina, composição que os compreende, processo para preparação e uso dos mesmos. | |
JP2000119271A (ja) * | 1998-08-12 | 2000-04-25 | Hokuriku Seiyaku Co Ltd | 1h―イミダゾピリジン誘導体 |
UA71587C2 (uk) | 1998-11-10 | 2004-12-15 | Шерінг Акцієнгезелльшафт | Аміди антранілової кислоти та їхнє застосування як лікарських засобів |
GB9824579D0 (en) | 1998-11-10 | 1999-01-06 | Novartis Ag | Organic compounds |
EP1135470A2 (en) | 1998-11-20 | 2001-09-26 | Kosan Biosciences, Inc. | Recombinant methods and materials for producing epothilone and epothilone derivatives |
EP2016953A3 (en) | 1998-12-22 | 2009-04-15 | Genentech, Inc. | Vascular endothelial cell growth factor antagonists and uses thereof |
PT1165085E (pt) | 1999-03-30 | 2006-10-31 | Novartis Ag | Derivados de ftalazina para tratar doencas inflamatorias |
AU2001278790A1 (en) | 2000-08-22 | 2002-03-04 | Hokuriku Seiyaku Co. Ltd | 1h-imidazopyridine derivatives |
PE20020354A1 (es) | 2000-09-01 | 2002-06-12 | Novartis Ag | Compuestos de hidroxamato como inhibidores de histona-desacetilasa (hda) |
AR035885A1 (es) | 2001-05-14 | 2004-07-21 | Novartis Ag | Derivados de 4-amino-5-fenil-7-ciclobutilpirrolo (2,3-d)pirimidina, un proceso para su preparacion, una composicion farmaceutica y el uso de dichos derivados para la preparacion de una composicion farmaceutica |
GB0119249D0 (en) | 2001-08-07 | 2001-10-03 | Novartis Ag | Organic compounds |
GB0211649D0 (en) | 2002-05-21 | 2002-07-03 | Novartis Ag | Organic compounds |
JP2004161662A (ja) | 2002-11-13 | 2004-06-10 | Abbott Japan Co Ltd | 1h−イミダゾキノリン誘導体 |
CN1747953A (zh) * | 2002-12-20 | 2006-03-15 | 3M创新有限公司 | 芳基/杂芳基取代的咪唑并喹啉 |
EP1590348A1 (en) * | 2002-12-20 | 2005-11-02 | 3M Innovative Properties Company | Aryl / hetaryl substituted imidazoquinolines |
CA2517655A1 (en) * | 2003-03-07 | 2004-09-23 | 3M Innovative Properties Company | 1-amino 1h-imidazoquinolines |
WO2005005423A1 (en) | 2003-07-02 | 2005-01-20 | F. Hoffmann-La Roche Ag | Indolyl derivatives substituted with a thiazole ring and their use as ppar modulators |
AR046845A1 (es) | 2003-11-21 | 2005-12-28 | Novartis Ag | Derivados de 1h-imidazo[4,5-c]quinolina para tratamiento de enfermedades dependientes de las proteino-quinasas |
KR20060117329A (ko) * | 2003-11-21 | 2006-11-16 | 노파르티스 아게 | 단백질 키나제 저해제로서의 1h-이미다조퀴놀린 유도체 |
CA2559863A1 (en) | 2004-03-24 | 2005-10-13 | 3M Innovative Properties Company | Amide substituted imidazopyridines, imidazoquinolines, and imidazonaphthyridines |
US8658666B2 (en) | 2005-02-11 | 2014-02-25 | 3M Innovative Properties Company | Substituted imidazoquinolines and imidazonaphthyridines |
GB0510390D0 (en) | 2005-05-20 | 2005-06-29 | Novartis Ag | Organic compounds |
KR20080048551A (ko) | 2005-09-23 | 2008-06-02 | 콜레이 파마시티컬 그룹, 인코포레이티드 | 1H-이미다조[4,5-c]피리딘 및 그의 유사체의 제조법 |
CN101330916A (zh) | 2005-12-16 | 2008-12-24 | 科勒制药集团公司 | 经取代的咪唑并喹啉、咪唑并萘啶和咪唑并吡啶、其组合物及其方法 |
WO2007079086A1 (en) | 2005-12-28 | 2007-07-12 | Coley Pharmaceutical Group, Inc. | Pyrazoloalkyl substituted imidazo ring compounds and methods |
US9370508B2 (en) | 2007-02-20 | 2016-06-21 | Novartis Ag | Imidazoquinolines as dual lipid kinase and mTOR inhibitors |
AU2009266956B2 (en) | 2008-07-01 | 2014-03-20 | Genentech, Inc. | Bicyclic heterocycles as MEK kinase inhibitors |
MX336723B (es) | 2008-07-11 | 2016-01-28 | Novartis Ag | Combinacion de (a) un inhibidor de fosfoinositido 3-cinasa y (b) un modulador de la ruta de ras/raf/mek. |
US8791131B2 (en) * | 2008-09-30 | 2014-07-29 | Pfizer Inc. | Imidazo[1,5]naphthyridine compounds, their pharmaceutical use and compositions |
PE20121471A1 (es) | 2009-11-04 | 2012-11-01 | Novartis Ag | Derivados de sulfonamida heterociclicos utiles como inhibidores de mek |
JP5863058B2 (ja) * | 2010-05-17 | 2016-02-16 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 1H−イミダゾ[4,5−c]キノリン |
AU2011277935B2 (en) | 2010-07-16 | 2015-01-22 | Piramal Enterprises Limited | Substituted imidazoquinoline derivatives as kinase inhibitors |
KR20130087020A (ko) | 2010-09-16 | 2013-08-05 | 허치슨 메디파르마 리미티드 | 축합 헤테로아릴 및 그 용도 |
AU2011340167A1 (en) * | 2010-12-06 | 2013-07-18 | Piramal Enterprises Limited | Substituted imidazoquinoline derivatives |
EP2763677B1 (en) | 2011-10-04 | 2020-02-26 | Janus Biotherapeutics, Inc. | Novel imidazole quinoline-based immune system modulators |
GB201205669D0 (en) | 2012-03-30 | 2012-05-16 | Agency Science Tech & Res | Bicyclic heterocyclic derivatives as mnk2 and mnk2 modulators and uses thereof |
MX2014014097A (es) | 2012-05-31 | 2015-04-13 | Bayer Pharma AG | Biomarcadores para determinar la respuesta eficaz de tratamientos en pacientes de carcinoma hepatocelular (chc). |
US9227969B2 (en) | 2013-08-14 | 2016-01-05 | Novartis Ag | Compounds and compositions as inhibitors of MEK |
WO2015022663A1 (en) | 2013-08-14 | 2015-02-19 | Novartis Ag | Compounds and compositions as inhibitors of mek |
WO2015022664A1 (en) | 2013-08-14 | 2015-02-19 | Novartis Ag | Compounds and compositions as inhibitors of mek |
-
2014
- 2014-08-05 US US14/451,563 patent/US9227969B2/en active Active
- 2014-08-13 UY UY35704A patent/UY35704A/es not_active Application Discontinuation
- 2014-08-13 TW TW103127830A patent/TW201536782A/zh unknown
- 2014-08-14 CA CA2921300A patent/CA2921300C/en active Active
- 2014-08-14 EP EP14792587.9A patent/EP3033343B1/en active Active
- 2014-08-14 WO PCT/IB2014/063916 patent/WO2015022662A1/en active Application Filing
- 2014-08-14 EA EA201690386A patent/EA029093B1/ru not_active IP Right Cessation
- 2014-08-14 TN TN2015000574A patent/TN2015000574A1/en unknown
- 2014-08-14 MX MX2016001980A patent/MX359401B/es active IP Right Grant
- 2014-08-14 UA UAA201600270A patent/UA116566C2/uk unknown
- 2014-08-14 PE PE2016000238A patent/PE20160204A1/es active IP Right Grant
- 2014-08-14 AP AP2016008981A patent/AP2016008981A0/xx unknown
- 2014-08-14 JP JP2016533987A patent/JP6473453B2/ja active Active
- 2014-08-14 TR TR2019/02709T patent/TR201902709T4/tr unknown
- 2014-08-14 GE GEAP201414059A patent/GEP201706725B/en unknown
- 2014-08-14 PL PL14792587T patent/PL3033343T3/pl unknown
- 2014-08-14 PT PT14792587T patent/PT3033343T/pt unknown
- 2014-08-14 SG SG11201510727VA patent/SG11201510727VA/en unknown
- 2014-08-14 KR KR1020167003386A patent/KR102354208B1/ko active IP Right Grant
- 2014-08-14 AU AU2014307593A patent/AU2014307593C1/en active Active
- 2014-08-14 ES ES14792587T patent/ES2714718T3/es active Active
- 2014-08-14 CN CN201480044367.1A patent/CN105473588B/zh active Active
- 2014-08-14 BR BR112016001783-8A patent/BR112016001783B1/pt active IP Right Grant
-
2015
- 2015-11-13 US US14/940,717 patent/US9629836B2/en active Active
- 2015-12-22 ZA ZA2015/09337A patent/ZA201509337B/en unknown
- 2015-12-24 IL IL243349A patent/IL243349A0/en unknown
-
2016
- 2016-01-04 PH PH12016500003A patent/PH12016500003A1/en unknown
- 2016-01-20 CL CL2016000150A patent/CL2016000150A1/es unknown
- 2016-01-21 NI NI201600014A patent/NI201600014A/es unknown
- 2016-02-10 DO DO2016000047A patent/DOP2016000047A/es unknown
- 2016-02-11 CU CUP2016000020A patent/CU20160020A7/es unknown
- 2016-02-12 SV SV2016005153A patent/SV2016005153A/es unknown
- 2016-02-12 CR CR20160072A patent/CR20160072A/es unknown
- 2016-06-22 HK HK16107241.4A patent/HK1219271A1/zh unknown
-
2017
- 2017-03-16 US US15/460,633 patent/US10011599B2/en active Active
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
HK1219271A1 (zh) | 作爲 抑制劑的化合物和組合物 | |
HK1220409A1 (zh) | 用於抑制 的新型化合物及組合物 | |
HK1222329A1 (zh) | 抑制劑的製劑 | |
EP2964235A4 (en) | ANTIMICROBIAL-ANTIBIOFILM COMPOSITIONS AND METHODS OF USE | |
SG11201507867RA (en) | Antimicrobial compositions and methods of use | |
EP2968244A4 (en) | COMPOSITIONS AND METHODS FOR USING ALIGAL COMPOUNDS | |
HK1215657A1 (zh) | 抗微生物組合物及相關使用方法 | |
EP3632467C0 (en) | INHIBITORS OF COMPLEMENT FACTOR H | |
HK1223275A1 (zh) | 用於預防過敏反應的方法和組合物 | |
HK1222339A1 (zh) | 金屬-β-內酰胺酶的抑制劑 | |
IL240763A0 (en) | The halopyrazoles as thrombin inhibitors | |
EP2906041A4 (en) | COMPOSITIONS AND METHODS OF USING INAPPETENCE COMPOUND | |
IL245588A0 (en) | Solid compositions of triglycerides and their use | |
HRP20182110T1 (hr) | Sastav spojeva tiakumicina | |
HK1204865A1 (en) | Composition for elimination of troublesome varmints | |
HUE057170T2 (hu) | Poliészter-kompozíciók alkalmazása | |
GB201310349D0 (en) | Composition and method of use thereof | |
GB201301928D0 (en) | Composition and method of use thereof |