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AU2003248122A8 - Sodium channel inhibitor - Google Patents

Sodium channel inhibitor

Info

Publication number
AU2003248122A8
AU2003248122A8AU2003248122AAU2003248122AAU2003248122A8AU 2003248122 A8AU2003248122 A8AU 2003248122A8AU 2003248122 AAU2003248122 AAU 2003248122AAU 2003248122 AAU2003248122 AAU 2003248122AAU 2003248122 A8AU2003248122 A8AU 2003248122A8
Authority
AU
Australia
Prior art keywords
sodium channel
channel inhibitor
inhibitor
sodium
channel
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.)
Withdrawn
Application number
AU2003248122A
Other versions
AU2003248122A1 (en
Inventor
Toshihiro Watanabe
Yukinori Nagakura
Hiroshi Tomiyama
Motoharu Sonegawa
Kazuo Tokuzaki
Yoshinori Iwai
Kazumi Kikuchi
Makoto Oku
Takeshi Hondo
Tetsuya Kimizuka
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.)
Kotobuki Seiyaku Co Ltd
Yamanouchi Pharmaceutical Co Ltd
Original Assignee
Kotobuki Seiyaku Co Ltd
Yamanouchi Pharmaceutical 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
Application filed by Kotobuki Seiyaku Co Ltd, Yamanouchi Pharmaceutical Co LtdfiledCriticalKotobuki Seiyaku Co Ltd
Publication of AU2003248122A1publicationCriticalpatent/AU2003248122A1/en
Publication of AU2003248122A8publicationCriticalpatent/AU2003248122A8/en
Abandonedlegal-statusCriticalCurrent

Links

Classifications

Landscapes

AU2003248122A2002-07-252003-07-25Sodium channel inhibitorAbandonedAU2003248122A1 (en)

Applications Claiming Priority (3)

Application NumberPriority DateFiling DateTitle
JP20022161872002-07-25
JP2002-2161872002-07-25
PCT/JP2003/009474WO2004011430A1 (en)2002-07-252003-07-25Sodium channel inhibitor

Publications (2)

Publication NumberPublication Date
AU2003248122A1 AU2003248122A1 (en)2004-02-16
AU2003248122A8true AU2003248122A8 (en)2004-02-16

Family

ID=31184572

Family Applications (1)

Application NumberTitlePriority DateFiling Date
AU2003248122AAbandonedAU2003248122A1 (en)2002-07-252003-07-25Sodium channel inhibitor

Country Status (3)

CountryLink
JP (1)JPWO2004011430A1 (en)
AU (1)AU2003248122A1 (en)
WO (1)WO2004011430A1 (en)

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ZA200507486B (en)2003-03-072007-03-28Astellas Pharma IncNitrogenous heterocyclic derivative having 2,6-disubstituted styryl
EP1680408A2 (en)*2003-10-242006-07-19F. Hoffmann-La Roche AgCcr3 receptor antagonists
MX2007002541A (en)*2004-09-012007-05-09Astellas Pharma IncPiperidine derivative or pharmaceutically acceptable salt thereof.
WO2006101521A2 (en)2004-09-202006-09-28Xenon Pharmaceuticals Inc.Heterocyclic derivatives and their use as stearoyl-coa desaturase inhibitors
JP2008513515A (en)2004-09-202008-05-01ゼノン・ファーマシューティカルズ・インコーポレイテッド Heterocyclic derivatives and their use as therapeutic agents
US20080167321A1 (en)*2004-09-202008-07-10Xenon Pharmaceuticals Inc.Pyridine Derivatives For Inhibiting Human Stearoyl-Coa-Desaturase
GB0503646D0 (en)*2005-02-222005-03-30Novartis AgOrganic compounds
GB0508319D0 (en)2005-04-252005-06-01Novartis AgOrganic compounds
AU2006343359A1 (en)2005-06-032007-11-15Xenon Pharmaceuticals Inc.Aminothiazole derivatives as human stearoyl-coa desaturase inhibitors
GB0514615D0 (en)2005-07-152005-08-24Novartis AgOrganic compounds
DOP2006000210A (en)*2005-10-042007-06-15Aventis Pharma Inc AMIDA PYRIMIDINE COMPOUNDS AS PGDS INHIBITORS
EP1963276B9 (en)*2005-12-212012-09-26Decode Genetics EHFN-linked aryl heteroaryl inhibitors of lta4h for treating inflammation
RU2364597C1 (en)2007-12-142009-08-20Андрей Александрович ИващенкоHETEROCYCLIC INHIBITORS OF Hh-SYGNAL CASCADE, BASED ON THEM MEDICINAL COMPOSITIONS AND METHOD OF TREATING DISEASES INDUCED BY ABBARANT ACTIVITY OF Hh-SIGNAL SYSTEM
JP5592388B2 (en)*2008-10-312014-09-17メルク・シャープ・アンド・ドーム・コーポレーション Technical field of P2X3 receptor antagonist for the treatment of pain
US8809380B2 (en)2009-08-042014-08-19Raqualia Pharma Inc.Picolinamide derivatives as TTX-S blockers
UY33755A (en)2010-11-302012-06-29Astrazeneca Ab NEW IKACH BLOCKERS
RU2018104472A (en)*2011-03-182019-02-22Джензим Корпорейшн Glucosylceramide synthase inhibitors
MA37975B2 (en)2012-09-112021-03-31Genzyme Corp Glucosylceramide synthase inhibitors
ES2983048T3 (en)2017-09-222024-10-21Jubilant Epipad LLC Heterocyclic compounds as PAD inhibitors
US11426412B2 (en)2017-10-182022-08-30Jubilant Epipad LLCImidazo-pyridine compounds as PAD inhibitors
AU2018362046B2 (en)2017-11-062023-04-13Jubilant Prodel LLCPyrimidine derivatives as inhibitors of PD1/PD-L1 activation
RS65576B1 (en)2017-11-242024-06-28Jubilant Episcribe LlcHeterocyclic compounds as prmt5 inhibitors
GB201801355D0 (en)2018-01-262018-03-14Enterprise Therapeutics LtdCompounds
AU2019234185B2 (en)2018-03-132024-08-01Jubilant Prodel LLC.Bicyclic compounds as inhibitors of PD1/PD-L1 interaction/activation
KR20210082473A (en)2018-10-232021-07-05바스프 에스이 tricyclic insecticidal compounds
AU2021215396A1 (en)2020-02-032022-09-29Genzyme CorporationMethods for treating neurological symptoms associated with lysosomal storage diseases
BR112023000798A2 (en)2020-07-242023-02-07Genzyme Corp PHARMACEUTICAL COMPOSITIONS COMPRISING VENGLUTAT

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GB925429A (en)*1960-04-011963-05-08Irwin Neisler & CoIndole derivatives
DE3643666A1 (en)*1986-12-201988-06-30Thomae Gmbh Dr K NEW CONDENSED DIAZEPINONE, METHOD FOR THE PRODUCTION THEREOF, AND MEDICINAL PRODUCTS CONTAINING THESE COMPOUNDS
DE3735895A1 (en)*1987-10-231989-05-03Thomae Gmbh Dr K CONDENSED DIAZEPINONE, METHOD FOR THE PRODUCTION THEREOF AND MEDICAMENT CONTAINING THESE COMPOUNDS
DE3819444A1 (en)*1988-06-081989-12-14Thomae Gmbh Dr K NEW CONDENSED DIAZEPINONE, PROCESS FOR THEIR MANUFACTURE AND MEDICAMENTS CONTAINING THESE COMPOUNDS
FR2668149B1 (en)*1990-10-181994-09-23Synthelabo 1- (3,4-DIHYDRO-2-OXO-1H-QUINOLEIN-6-YL) -2- [4- (2-PHENYL-ETHYL) PIPERIDIN-1-YL] ETHANOL, ITS PREPARATION AND THERAPEUTIC APPLICATION .
WO1998035957A1 (en)*1997-02-141998-08-20Bayer CorporationAmide derivatives as selective neuropeptide y receptor antagonists
US6048900A (en)*1998-02-132000-04-11Bayer CorporationAmide derivatives and methods for using the same as selective neuropeptide Y receptor antagonists
CA2232147A1 (en)*1997-04-031998-10-03F. Hoffmann-La Roche AgPhenoxymethyl piperidine derivatives
DE19756235A1 (en)*1997-12-171999-07-01Klinge Co Chem Pharm Fab New piperidinyl-substituted pyridylalkane alkene and alkane carboxylic acid amides
FR2803298A1 (en)*1999-12-302001-07-06Adir NOVEL LINEAR OR CYCLIC UREAS, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
JP4282048B2 (en)*2000-01-202009-06-17エーザイ・アール・アンド・ディー・マネジメント株式会社 Novel piperidine compounds and pharmaceuticals thereof

Also Published As

Publication numberPublication date
JPWO2004011430A1 (en)2005-11-24
AU2003248122A1 (en)2004-02-16
WO2004011430A1 (en)2004-02-05

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Legal Events

DateCodeTitleDescription
MK6Application lapsed section 142(2)(f)/reg. 8.3(3) - pct applic. not entering national phase
THCorrigenda

Free format text:IN VOL 18, NO 12, PAGE(S) 3443 UNDER THE HEADING APPLICATIONS OPI - NAME INDEX UNDER THE NAME YAMANOUCHI PHARMACEUTICAL CO., LTD., APPLICATION NO. 2003248122, UNDER INID (71) CORRECT THE NAME TO READ KOTOBUKI PHARMACEUTICAL CO., LTD.; YAMANOUCHI PHARMACEUTICAL CO., LTD.


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