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AU2001262723A1 - 1,2-dihydropyridine compounds, process for preparation of the same and use thereof - Google Patents

1,2-dihydropyridine compounds, process for preparation of the same and use thereof

Info

Publication number
AU2001262723A1
AU2001262723A1 AU2001262723A AU2001262723A AU2001262723A1 AU 2001262723 A1 AU2001262723 A1 AU 2001262723A1 AU 2001262723 A AU2001262723 A AU 2001262723A AU 2001262723 A AU2001262723 A AU 2001262723A AU 2001262723 A1 AU2001262723 A1 AU 2001262723A1
Authority
AU
Australia
Prior art keywords
preparation
same
dihydropyridine compounds
dihydropyridine
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.)
Granted
Application number
AU2001262723A
Other versions
AU2001262723C1 (en
AU2001262723B2 (en
Inventor
Hiroyuki Amino
Anthony John Groom
Takahisa Hanada
Shinji Hatakeyama
Koichi Ito
Koki Kawano
Satoshi Nagato
Hiroyuki Naka
Yoshihiko Norimine
Makoto Ogo
Leanne Rivers
Terence Smith
Kohshi Ueno
Masataka Ueno
Yoshio Urawa
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.)
Eisai R&D Management Co Ltd
Original Assignee
Eisai R&D Management Co Ltd
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
Priority claimed from GB0022483A external-priority patent/GB0022483D0/en
Application filed by Eisai R&D Management Co Ltd filed Critical Eisai R&D Management Co Ltd
Priority claimed from PCT/JP2001/004857 external-priority patent/WO2001096308A1/en
Publication of AU2001262723A1 publication Critical patent/AU2001262723A1/en
Application granted granted Critical
Publication of AU2001262723B2 publication Critical patent/AU2001262723B2/en
Publication of AU2001262723C1 publication Critical patent/AU2001262723C1/en
Assigned to EISAI R&D MANAGEMENT CO., LTD. reassignment EISAI R&D MANAGEMENT CO., LTD. Request for Assignment Assignors: EISAI CO., LTD.
Active legal-status Critical Current
Adjusted expiration legal-status Critical

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AU2001262723A 2000-06-12 2001-06-08 1,2-dihydropyridine compounds, process for preparation of the same and use thereof Active 2026-06-08 AU2001262723C1 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
JP2000-175966 2000-06-12
JP2000175966 2000-06-12
GB0022483A GB0022483D0 (en) 2000-09-13 2000-09-13 1 2 Dihydropyridine compounds manufacturing method thereof and use thereof
GB0022483 2000-09-13
PCT/JP2001/004857 WO2001096308A1 (en) 2000-06-12 2001-06-08 1,2-dihydropyridine compounds, process for preparation of the same and use thereof

Publications (3)

Publication Number Publication Date
AU2001262723A1 true AU2001262723A1 (en) 2002-03-14
AU2001262723B2 AU2001262723B2 (en) 2005-05-12
AU2001262723C1 AU2001262723C1 (en) 2006-05-11

Family

ID=26244997

Family Applications (2)

Application Number Title Priority Date Filing Date
AU2001262723A Active 2026-06-08 AU2001262723C1 (en) 2000-06-12 2001-06-08 1,2-dihydropyridine compounds, process for preparation of the same and use thereof
AU6272301A Pending AU6272301A (en) 2000-06-12 2001-06-08 1,2-dihydropyridine compounds, process for preparation of the same and use thereof

Family Applications After (1)

Application Number Title Priority Date Filing Date
AU6272301A Pending AU6272301A (en) 2000-06-12 2001-06-08 1,2-dihydropyridine compounds, process for preparation of the same and use thereof

Country Status (26)

Country Link
US (3) US6949571B2 (en)
EP (3) EP1300396B1 (en)
JP (3) JP3922368B2 (en)
KR (3) KR100850728B1 (en)
CN (1) CN1245386C (en)
AT (1) ATE420862T1 (en)
AU (2) AU2001262723C1 (en)
BE (1) BE2013C003I2 (en)
BR (1) BRPI0111596B8 (en)
CA (1) CA2412172C (en)
CY (2) CY1108969T1 (en)
DE (1) DE60137426D1 (en)
DK (1) DK1300396T3 (en)
ES (1) ES2320973T3 (en)
FR (1) FR12C0074I2 (en)
HU (2) HU1300187D0 (en)
IL (5) IL152848A0 (en)
LU (1) LU92113I2 (en)
MX (1) MXPA02012314A (en)
NL (1) NL300565I1 (en)
NO (2) NO325160B1 (en)
NZ (1) NZ522773A (en)
PT (1) PT1300396E (en)
TW (2) TW200815402A (en)
WO (1) WO2001096308A1 (en)
ZA (1) ZA200209270B (en)

Families Citing this family (148)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1300396B1 (en) * 2000-06-12 2009-01-14 Eisai R&D Management Co., Ltd. 1,2-dihydropyridine compounds, process for preparation of the same and use thereof
CA2436854A1 (en) * 2000-11-20 2002-05-23 Bristol-Myers Squibb Company Pyridone derivatives as ap2 inhibitors
US20030105144A1 (en) 2001-04-17 2003-06-05 Ping Gao Stabilized oral pharmaceutical composition
JP4119114B2 (en) * 2001-11-28 2008-07-16 広栄化学工業株式会社 Novel dihydroxy (3-pyridyl) boranes
GB0129260D0 (en) * 2001-12-06 2002-01-23 Eisai London Res Lab Ltd Pharmaceutical compositions and their uses
US7482366B2 (en) 2001-12-21 2009-01-27 X-Ceptor Therapeutics, Inc. Modulators of LXR
WO2003059884A1 (en) 2001-12-21 2003-07-24 X-Ceptor Therapeutics, Inc. Modulators of lxr
AU2003220401A1 (en) 2002-03-18 2003-10-08 Bristol-Myers Squibb Company Uracil derivatives as inhibitors of tnf-alpha converting enzyme (tace) and matrix metalloproteinases
US20050203079A1 (en) * 2002-04-19 2005-09-15 Glaxo Group Limited Compounds having affinity at 5ht2C receptor and use thereof in therapy
JP4208512B2 (en) * 2002-07-23 2009-01-14 株式会社クラレ Process for producing 5- (2'-pyridyl) -2-pyridone derivative
AU2003274022A1 (en) * 2002-10-17 2004-05-04 Syngenta Participations Ag 3-heterocyclylpyridine derivatives useful as herbicides
CA2510170C (en) * 2002-12-16 2011-05-24 Mitsubishi Pharma Corporation 3-substituted-4-pyrimidone derivatives
EP1581539A4 (en) 2003-01-03 2007-09-19 Bristol Myers Squibb Co Novel tyrosine kinase inhibitors
GB0305024D0 (en) * 2003-03-05 2003-04-09 Glaxo Group Ltd Compounds
SE0302324D0 (en) * 2003-08-28 2003-08-28 Astrazeneca Ab Novel compounds
SE0302323D0 (en) * 2003-08-28 2003-08-28 Astrazeneca Ab Novel compounds
SE0302486D0 (en) 2003-09-18 2003-09-18 Astrazeneca Ab Novel compounds
WO2005099688A2 (en) 2004-04-07 2005-10-27 Takeda Pharmaceutical Company Limited Cyclic compounds
MY148809A (en) 2004-07-06 2013-05-31 Eisai R&D Man Co Ltd Crystals of 1,2-dihydropyridine compound and their production process
JP2007099781A (en) * 2004-07-06 2007-04-19 Eisai R & D Management Co Ltd Method for producing crystal of 1,2-dihydropyridine compound
GB0420722D0 (en) * 2004-09-17 2004-10-20 Addex Pharmaceuticals Sa Novel allosteric modulators
US20060069260A1 (en) * 2004-09-28 2006-03-30 Huiping Zhang Preparation of N-aryl pyridones
JP2008524233A (en) * 2004-12-16 2008-07-10 バーテックス ファーマシューティカルズ インコーポレイテッド Pyrid-2-ones useful as inhibitors of TEC family protein kinases for the treatment of inflammatory, proliferative and immune-mediated diseases
EP1858325A4 (en) * 2005-01-07 2010-06-30 Roskamp Res Llc Compounds for inhibiting beta-amyloid production and methods of identifying the compounds
TW200700392A (en) * 2005-03-16 2007-01-01 Astrazeneca Ab Novel compounds
RS51822B (en) * 2005-04-04 2012-02-29 Eisai R. &D. Management Co. Ltd. DIHYDROPYRIDINE COMPOUNDS FOR TREATMENT OF NEURODEGENERATIVE DISEASES AND Dementia
CN101180056A (en) * 2005-04-08 2008-05-14 卫材R&D管理有限公司 Therapeutic agent for dyskinesia
US7728013B2 (en) 2005-05-10 2010-06-01 Intermune, Inc. Method of modulating stress-activated protein kinase system
GB0510141D0 (en) * 2005-05-18 2005-06-22 Addex Pharmaceuticals Sa Novel compounds B3
US8153804B2 (en) * 2005-08-02 2012-04-10 Lexicon Pharmaceuticals, Inc. Aryl pyridines and methods of their use
AU2006285038A1 (en) * 2005-08-29 2007-03-08 Vertex Pharmaceuticals Incorporated 3,5-disubstituted pyrid-2-ones useful as inhibitors of Tec family of non-receptor tyrosine kinases
EP1919906B1 (en) 2005-08-29 2011-10-12 Vertex Pharmaceuticals Incorporated 3, 5-disubstituted pyrid-2-ones useful as inhibitors of tec family of non-receptor tyrosine kinases
DE602006020293D1 (en) 2005-08-29 2011-04-07 Vertex Pharma 3,5-DISUBSTITUTED PYRID-2-ONE, WHICH ARE USES AS INHIBITORS OF THE TEC FAMILY OF NON-RECEPTOR TYROSINE KINASES
EP1932840B1 (en) 2005-10-03 2014-04-09 Ono Pharmaceutical Co., Ltd. Nitrogen-containing heterocyclic compound and pharmaceutical application thereof
JPWO2007072868A1 (en) * 2005-12-21 2009-06-04 エーザイ・アール・アンド・ディー・マネジメント株式会社 Crystals of 1,2-dihydropyridine compounds (type IV)
US7803818B2 (en) * 2005-12-21 2010-09-28 Eisai R&D Management Co., Ltd. Amorphous form of 1,2-dihydropyridine compound
JP4865337B2 (en) * 2006-01-24 2012-02-01 富士フイルムファインケミカルズ株式会社 Process for producing 2,3'-bipyridyl-6'-one
TWI417095B (en) 2006-03-15 2013-12-01 Janssen Pharmaceuticals Inc 1,4-disubstituted 3-cyano-pyridone derivatives and their use as positive allosteric modulators of mglur2-receptors
WO2007126060A1 (en) * 2006-04-28 2007-11-08 Eisai R & D Management Co., Ltd Salt of 1,2-dihydropyridine compound
TW200808763A (en) 2006-05-08 2008-02-16 Astrazeneca Ab Novel compounds I
TW200808771A (en) 2006-05-08 2008-02-16 Astrazeneca Ab Novel compounds II
US20080108603A1 (en) * 2006-10-19 2008-05-08 Eisenach James C Combination therapy for the treatment of pain
US20080108622A1 (en) * 2006-10-19 2008-05-08 Eisenach James C Combination therapy for the treatment of pain
JP2010520154A (en) * 2007-03-05 2010-06-10 エーザイ・アール・アンド・ディー・マネジメント株式会社 AMPA receptor antagonists and NMDA receptor antagonists for neurodegenerative diseases
TW200845978A (en) 2007-03-07 2008-12-01 Janssen Pharmaceutica Nv 3-cyano-4-(4-tetrahydropyran-phenyl)-pyridin-2-one derivatives
TW200900065A (en) 2007-03-07 2009-01-01 Janssen Pharmaceutica Nv 3-cyano-4-(4-pyridinyloxy-phenyl)-pyridin-2-one derivatives
EP2148673A1 (en) * 2007-04-26 2010-02-03 Eisai R&D Management Co., Ltd. Cinnamide compounds for dementia
EP2164488A1 (en) * 2007-07-13 2010-03-24 Eisai R&D Management Co., Ltd. Ampa receptor antagonists and aldose reductase inhibitors for neuropathic pain
JP2010533126A (en) * 2007-07-13 2010-10-21 エーザイ・アール・アンド・ディー・マネジメント株式会社 Combination of AMPA receptor antagonist and acetylcholinesterase inhibitor for the treatment of neuropathic pain
CA2697399C (en) 2007-09-14 2016-01-19 Ortho-Mcneil-Janssen Pharmaceuticals, Inc. 1,3-disubstituted 4-(aryl-x-phenyl)-1h-pyridin-2-ones
NZ584148A (en) 2007-09-14 2011-05-27 Ortho Mcneil Janssen Pharm 1,3-disubstituted-4-phenyl-1 h-pyridin-2-ones
MY152078A (en) 2007-09-14 2014-08-15 Ortho Mcneil Janssen Pharm 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h,1'h-[1,4']bipyridinyl-2'-ones
WO2009054544A1 (en) * 2007-10-26 2009-04-30 Eisai R & D Management Co., Ltd. Ampa receptor antagonists for parkinson's disease and movement disorders
JP2011502982A (en) * 2007-11-06 2011-01-27 アストラゼネカ・アクチエボラーグ Certain 2-pyrazinone derivatives and their use as inhibitors of neutrophil elastase
RU2492170C9 (en) 2007-11-14 2013-12-27 Орто-Макнейл-Янссен Фармасьютикалз, Инк. Imidazo[1,2-a]pyridine derivatives and their application as positive allosteric modulators of mglur2 receptors
US8742127B2 (en) 2007-12-21 2014-06-03 Kuraray Co., Ltd. Production method of 6-halogeno-3-arylpyridine derivative
WO2009082038A2 (en) * 2007-12-26 2009-07-02 Eisai R & D Management Co., Ltd. Ampa receptor antagonists and zonisamide for epilepsy
US20100297181A1 (en) * 2007-12-26 2010-11-25 Eisai R&D Management Co., Ltd. AMPA Receptor Antagonists for Epilepsy, Mental Disorders or Deficits in Sensory Organ
EP2300427A1 (en) * 2008-05-05 2011-03-30 Amgen Inc. Urea compounds as gamma secretase modulators
ES2567283T3 (en) * 2008-06-03 2016-04-21 Intermune, Inc. Compounds and methods to treat inflammatory and fibrotic disorders
US8859760B2 (en) 2008-07-29 2014-10-14 Frontier Scientific, Inc. Compositions for killing or preventing the growth of microbes
AU2009289784B2 (en) 2008-09-02 2012-03-22 Addex Pharma S.A. 3-azabicyclo[3.1.0]hexyl derivatives as modulators of metabotropic glutamate receptors
ES2466341T3 (en) 2008-10-16 2014-06-10 Janssen Pharmaceuticals, Inc. Indole and benzomorpholine derivatives as modulators of metabotropic glutamate receptors
ES2534199T3 (en) * 2008-10-31 2015-04-20 Merck Sharp & Dohme Corp. P2X3 receptor antagonists for pain management
WO2010060589A1 (en) 2008-11-28 2010-06-03 Ortho-Mcneil-Janssen Pharmaceuticals, Inc. Indole and benzoxazine derivatives as modulators of metabotropic glutamate receptors
US8153808B2 (en) 2008-12-23 2012-04-10 Roche Palo Alto Llc Dihydropyridone amides as P2X7 modulators
SG172382A1 (en) 2008-12-23 2011-07-28 Hoffmann La Roche Dihydropyridone ureas as p2x7 modulators
SG172385A1 (en) 2008-12-23 2011-08-29 Hoffmann La Roche Dihydropyridone amides as p2x7 modulators
CA2745864A1 (en) 2008-12-23 2010-07-01 F.Hoffmann-La Roche Ag Dihydropyridone amides as p2x7 modulators
MX2011006245A (en) 2008-12-23 2011-07-13 Hoffmann La Roche Dihydropyridone amides as p2x7 modulators.
TW201036957A (en) 2009-02-20 2010-10-16 Astrazeneca Ab Novel salt 628
TW201100398A (en) 2009-03-31 2011-01-01 Arqule Inc Substituted indolo-pyridinone compounds
AU2010246609B2 (en) 2009-05-12 2013-09-05 Addex Pharma S.A. 1,2,4-triazolo [4,3-a] pyridine derivatives and their use for the treatment or prevention of neurological and psychiatric disorders
MY153913A (en) 2009-05-12 2015-04-15 Janssen Pharmaceuticals Inc 7-aryl-1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors
NZ596053A (en) 2009-05-12 2013-05-31 Janssen Pharmaceuticals Inc 1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors
EP2483244A1 (en) 2009-10-02 2012-08-08 AstraZeneca AB 2-pyridone compounds used as inhibitors of neutrophil elastase
JP2013234123A (en) * 2010-09-03 2013-11-21 Taisho Pharmaceutical Co Ltd 3-pyrazolyl-2-pyridone derivative
CN103298810B (en) 2010-11-08 2016-03-16 杨森制药公司 The purposes of 1,2,4-triazolo [4,3-a] pyridine derivate and the positive allosteric modulators as MGLUR2 acceptor thereof
EP2643320B1 (en) 2010-11-08 2015-03-04 Janssen Pharmaceuticals, Inc. 1,2,4-TRIAZOLO[4,3-a]PYRIDINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS
EP2661435B1 (en) 2010-11-08 2015-08-19 Janssen Pharmaceuticals, Inc. 1,2,4-TRIAZOLO[4,3-a]PYRIDINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS
ES2873029T3 (en) * 2010-12-06 2021-11-03 Aclaris Therapeutics Inc Substituted pyridinone-pyridinyl compounds
MX382066B (en) 2011-03-04 2025-03-12 Univ Yale (--)- huperzine a processes and related compositions and methods of treatment
ITMI20111952A1 (en) 2011-10-27 2013-04-28 Italiana Sint Spa PROCEDURE FOR THE PREPATION OF 2-METHOXY-5- (PIRIDIN-2-IL) PYRIDINE, AN INTERMEDIATE OF THE PERAMPANEL
WO2013102897A1 (en) * 2012-01-03 2013-07-11 Mapi Pharma Ltd. Polymorphs of perampanel
US9650360B2 (en) 2012-03-31 2017-05-16 University Of Georgia Research Foundation, Inc. Anti-mycobacterial drugs against tuberculosis
EP2875001B1 (en) * 2012-07-18 2019-01-09 Sunshine Lake Pharma Co., Ltd. Nitrogenous heterocyclic derivatives and their application in drugs
ITMI20121390A1 (en) 2012-08-06 2014-02-07 F I S Fabbrica Italiana Sint P A PROCEDURE FOR THE PREPARATION OF 2-CYANOPHENYLBORONIC ACID AND ITS ESTERS, INTERMEDIATE OF THE PERAMPANEL OR E2040
AR092742A1 (en) 2012-10-02 2015-04-29 Intermune Inc ANTIFIBROTIC PYRIDINONES
JO3225B1 (en) * 2012-11-27 2018-03-08 Lilly Co Eli 6-((s)-1-{1-[5-(2-hydroxy-ethoxy)-pyridin-2-yl]-1h-pyrazol-3-yl}-ethyl)-3h-1,3-benzothiazol-2-one as a tarp-gamma 8 dependent ampa receptor antagonist
TW201441193A (en) 2012-12-06 2014-11-01 Kyowa Hakko Kirin Co Ltd Pyridone compound
US9242969B2 (en) 2013-03-14 2016-01-26 Novartis Ag Biaryl amide compounds as kinase inhibitors
JP2016522786A (en) * 2013-04-04 2016-08-04 エーザイ・アール・アンド・ディー・マネジメント株式会社 [11C] and [18F] labeled 1,3-diphenyl-5- (pyrimidin-2-yl) -pyridin-2 (1H) -one derivatives and their use for PET imaging of AMPA receptors
JO3368B1 (en) 2013-06-04 2019-03-13 Janssen Pharmaceutica Nv 6, 7- dihydropyrazolu [5,1-a] pyrazine-4 (5 hands) -on compounds and their use as negative excretory regulators of Miglore 2 receptors.
CN103274993A (en) * 2013-06-13 2013-09-04 南京工业大学 New synthesis method of dihydropyridine and pyrrole heterocycles
EA031384B1 (en) * 2013-07-25 2018-12-28 Тева Фармасьютикалз Интернэшнл Гмбх Improved processes for the preparation of perampanel
JO3367B1 (en) 2013-09-06 2019-03-13 Janssen Pharmaceutica Nv 1,2,4-TRIAZOLO[4,3-a]PYRIDINE COMPOUNDS AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS
LT3063139T (en) 2013-10-29 2019-02-25 Takeda Pharmaceutical Company Limited Heterocyclic compound
CN103664756A (en) * 2013-11-26 2014-03-26 苏州晶云药物科技有限公司 Perampanel new type crystal A and preparation method thereof
CN104706604A (en) * 2013-12-12 2015-06-17 北京星昊医药股份有限公司 Perampanel freeze-dried oral disintegrating tablet and preparation method thereof
CN104725301A (en) * 2013-12-20 2015-06-24 北京蓝贝望生物医药科技股份有限公司 Preparation method of 1,2-dihydropyridin-2-one derivative
KR20220038826A (en) 2014-01-21 2022-03-29 얀센 파마슈티카 엔.브이. Combinations comprising positive allosteric modulators or orthosteric agonists of metabotropic glutamatergic receptor subtype 2 and their use
DK3096790T3 (en) 2014-01-21 2019-10-07 Janssen Pharmaceutica Nv COMBINATIONS INCLUDING POSITIVE ALLOSTERIC MODULATORS OR ORTHOSTERIC AGONISTS OF METABOTROP GLUTAMATERG SUBTYPE 2 RECEPTOR AND APPLICATION OF THESE
CA2943363A1 (en) 2014-04-02 2015-10-08 Intermune, Inc. Anti-fibrotic pyridinones
CN105085382B (en) * 2014-05-14 2019-10-18 江苏豪森药业集团有限公司 Pyrrole Lun Panai isomers crystal form and its preparation method and application
TW201609719A (en) 2014-05-28 2016-03-16 美國禮來大藥廠 6-substituted-3H-1,3-benzothiazol-2-one compounds as TARP-gamma 8 dependent AMPA receptor antagonists
CN103980188B (en) * 2014-05-30 2016-01-27 浙江永宁药业股份有限公司 The synthetic method of a kind of pyrrole Lun Panai and the synthetic method of intermediate and intermediate thereof
UY36294A (en) 2014-09-12 2016-04-29 Novartis Ag COMPOUNDS AND COMPOSITIONS AS QUINASA INHIBITORS
DK3255042T3 (en) 2015-02-04 2021-02-08 Beyondbio Inc HETEROCYCLIC COMPOUND AND PHARMACEUTICAL COMPOSITION INCLUDING THE SAME
US10111867B2 (en) 2015-02-17 2018-10-30 Mapi Pharma Ltd. Process and intermediates for the preparation of perampanel
AR104259A1 (en) * 2015-04-15 2017-07-05 Celgene Quanticel Res Inc BROMODOMINUM INHIBITORS
WO2016172333A1 (en) 2015-04-21 2016-10-27 Teva Pharmaceuticals International Gmbh A solid state form of perampanel
CN107922328B (en) 2015-07-06 2020-05-19 公立大学法人横滨市立大学 Novel compounds that specifically bind to AMPA receptors
CN105085383B (en) * 2015-08-19 2017-09-01 四川大学 5-methyl-2 (1H) pyridone derivatives and their preparation methods and uses
PE20181008A1 (en) * 2015-11-13 2018-06-26 Eisai Randd Man Co Ltd PYRANODIPYRIDINIC COMPOUND
KR101652750B1 (en) * 2015-12-03 2016-08-31 김종선 Purification method of pyridine and pyridine derivatives
ES2974991T3 (en) 2016-09-19 2024-07-02 Novartis Ag Therapeutic combinations comprising a RAF inhibitor and an ERK inhibitor
CN110099898B (en) 2016-10-24 2023-07-25 优曼尼蒂治疗公司 Compounds and uses thereof
US10669237B2 (en) 2016-11-18 2020-06-02 Dow Agrosciences Llc 4-((6-bromopyridin-3-yl)oxy)benzonitrile and processes of preparation
US11826492B2 (en) * 2016-12-22 2023-11-28 Biotronik Ag Intratumoral drug delivery materials and methods for treating breast cancer
WO2018129403A1 (en) 2017-01-06 2018-07-12 Yumanity Therapeutics Methods for the treatment of neurological disorders
JP6241974B1 (en) 2017-01-11 2017-12-06 公立大学法人横浜市立大学 Imaging method, program and screening method for AMPA receptor in brain of primate organism
GB201702221D0 (en) 2017-02-10 2017-03-29 Univ Of Sussex Compounds
FI3618875T3 (en) 2017-05-02 2023-07-04 Novartis Ag COMBINATION THERAPY WITH A RAF INHIBITOR AND TRAMETINIB
WO2019028062A1 (en) 2017-07-31 2019-02-07 Washington University Pirfenidone derivatives for modulation of b lymphocyte activity and organ protection
EP3700934A4 (en) 2017-10-24 2021-10-27 Yumanity Therapeutics, Inc. COMPOUNDS AND USES OF THESE COMPOUNDS
CN110028442B (en) * 2018-01-11 2020-07-17 新发药业有限公司 Simple preparation method of Perampanel
GB201803340D0 (en) 2018-03-01 2018-04-18 Univ Of Sussex Compounds
CN112312913B (en) 2018-03-23 2024-03-08 詹森药业有限公司 Compounds and their uses
EP3560934A1 (en) 2018-04-26 2019-10-30 F.I.S.- Fabbrica Italiana Sintetici S.p.A. Process for the preparation of pure 2-cyanophenylboronic acid and esters thereof, intermediates of perampanel or of e2040
MA54460A (en) 2018-12-14 2021-10-20 Eisai R&D Man Co Ltd WATER-BASED PHARMACEUTICAL FORMULATIONS OF 1,2-DIHYDROPYRIDINE COMPOUNDS
AU2020212034A1 (en) 2019-01-24 2021-09-16 Janssen Pharmaceutica Nv Compounds and uses thereof
MX2021013817A (en) 2019-05-13 2021-12-14 Novartis Ag NEW CRYSTALLINE FORMS OF N-(3-(2-(2-HYDROXYETOXY)-6-MORPHOLINOP IRIDIN-4-IL)-4-METHYLPHENYL)-2-(TRIFLUOROMETHYL)SONICOTINAMIDE AS RAF INHIBITORS FOR THE TREATMENT OF CANCER.
CN110483563B (en) * 2019-09-06 2021-12-28 山西医科大学 Preparation method and application of novel ionic beta-naphthoic aldehyde Schiff base zirconium complex
JP7646643B2 (en) * 2019-10-04 2025-03-17 アンスティトゥート・ナシオナル・ドゥ・ラ・サンテ・エ・ドゥ・ラ・ルシャルシュ・メディカル・（インセルム） Novel pyridin-2(1H)one derivatives, their preparation and their use for treating pain - Patents.com
EA202192047A1 (en) 2019-11-13 2021-12-08 Юманити Терапьютикс, Инк. COMPOUNDS AND THEIR APPLICATIONS
KR102392825B1 (en) 2020-02-18 2022-04-29 명인제약주식회사 Co-crystal compound of 2-(2-oxo-1-phenyl-5-pyridin-2-ylpyridin-3-yl)benzonitrile and L-malic acid, and manufacturing method thereof
CN111362930B (en) * 2020-04-15 2023-02-03 安徽医科大学 1,2,4-oxadiazole-pyridine compound and application thereof
US20240092759A1 (en) * 2021-01-08 2024-03-21 Yale University Non-Covalent Inhibitors of the Main Protease of SARS-CoV-2 and Methods of Use
US12378229B2 (en) 2021-02-02 2025-08-05 Liminal Biosciences Limited GPR84 antagonists and uses thereof
JPWO2023042887A1 (en) 2021-09-15 2023-03-23
EP4403185A4 (en) 2021-09-15 2025-10-08 Univ Of The Ryukyus Pharmaceutical composition for the treatment of cognitive decline or for the treatment of overweight or obesity
CN116265440B (en) * 2021-12-16 2024-09-27 贵州大学 A salicylic acid spliced pyridone compound and its preparation method and application
CN114057630B (en) * 2021-12-23 2023-06-02 郑州大学 Pirfenidone derivatives and their synthetic methods and applications
AU2023276599A1 (en) 2022-05-25 2024-12-05 Imagenebio, Inc. Mek inhibitors and uses thereof
US20250312345A1 (en) * 2022-07-07 2025-10-09 Yale University Non-covalent inhibitors of the main protease of sars-cov-2 and methods of use
KR102768044B1 (en) * 2022-07-12 2025-02-17 이화여자대학교 산학협력단 Method of preparing perampanel derivatives including a continuous flow process
US11958832B1 (en) 2023-10-12 2024-04-16 King Faisal University 2-alkoxy[4,3:6,3-terpyridine]-3-carbonitriles as antimicrobial compounds
KR20250129557A (en) 2024-02-22 2025-08-29 단국대학교 천안캠퍼스 산학협력단 Composition for preventing or treating neurological disease comprising doxazosin

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5283761A (en) * 1976-01-01 1977-07-12 Yamanouchi Pharmaceut Co Ltd Novel pyridone derivative
JPS5531072A (en) * 1979-07-30 1980-03-05 Rikagaku Kenkyusho Preparation of 2-pyridone compound
DE4003541C1 (en) 1990-02-06 1991-08-08 Alter S.A., Madrid, Es
US5356902A (en) 1992-11-06 1994-10-18 Eli Lilly And Company Decahydroisoquinoline compounds as excitatory amino acid receptor antagonists
IL109397A0 (en) 1993-04-28 1994-07-31 Schering Ag Quinoxalinedione derivatives, processes for the preparation thereof and pharmaceutical compositions containing the same
HU219777B (en) 1993-07-02 2001-07-30 Gyógyszerkutató Intézet Kft. Optical active 1-(4-nitrophenyl)-4-methyl-7,8-methylen dioxi-3,4-dihydro-5h-2,3-benzodiazepine and process for producing it
CN1067387C (en) 1994-09-27 2001-06-20 山之内制药株式会社 1,2,3,4-tetrahydroquinoxalindione derivative
DE69634122D1 (en) * 1995-04-27 2005-02-03 Mitsubishi Pharma Corp Heterocyclic amide compounds and their use in medicine
US5935551A (en) 1995-11-15 1999-08-10 California Institute Of Technology Synthesis of zeolites by hydrothermal reaction of zeolite P1
DE19604920A1 (en) 1996-02-01 1997-08-07 Schering Ag New 2,3-benzodiazepine derivatives, their production and use as medicines
US5891871A (en) 1996-03-21 1999-04-06 Cocensys, Inc. Substituted 2,3-benzodiazepin-4-ones and the use thereof
HU9600871D0 (en) 1996-04-04 1996-05-28 Gyogyszerkutato Intezet New 2,3-benzodiazepine derivatives
EA002905B1 (en) 1996-05-15 2002-10-31 Пфайзер Инк. 2,3 disubstituted -4 (3h)-quinazolinones and pharmaceutcal composition comprising thereon
DE19643037A1 (en) 1996-10-18 1998-04-23 Boehringer Ingelheim Kg New oxadiazoles, processes for their preparation and their use as medicines
NZ335992A (en) 1996-12-05 2001-09-28 Amgen Inc Substituted pyrimidinone and pyridone compounds and methods of use
CN1248248A (en) 1997-02-28 2000-03-22 辉瑞产品公司 Atropisomers of 3-aryl-4(3H)-quinazolinones and their use as AMPA-receptor antagonists
GB9708945D0 (en) 1997-05-01 1997-06-25 Merck Sharp & Dohme Therapeutic agents
GB9711753D0 (en) 1997-06-06 1997-08-06 Merck Sharp & Dohme Therapeutic agents
JP4321737B2 (en) * 1997-12-17 2009-08-26 塩野義製薬株式会社 New pyridine compounds
EP1100504A2 (en) 1998-07-02 2001-05-23 Eisai Co., Ltd. Pharmaceutical compositions and their uses for treatment of demyelinating disorders
DE19835918A1 (en) 1998-08-07 2000-02-10 Dresden Arzneimittel New anticonvulsant 4-amino-1-aryl-pyridin-2-ones and process for their preparation
EP1300396B1 (en) 2000-06-12 2009-01-14 Eisai R&D Management Co., Ltd. 1,2-dihydropyridine compounds, process for preparation of the same and use thereof
GB0129260D0 (en) 2001-12-06 2002-01-23 Eisai London Res Lab Ltd Pharmaceutical compositions and their uses

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