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MA30268B1 - Derive polycyclique de cinnamide - Google Patents

Derive polycyclique de cinnamide

Info

Publication number
MA30268B1
MA30268B1 MA31220A MA31220A MA30268B1 MA 30268 B1 MA30268 B1 MA 30268B1 MA 31220 A MA31220 A MA 31220A MA 31220 A MA31220 A MA 31220A MA 30268 B1 MA30268 B1 MA 30268B1
Authority
MA
Morocco
Prior art keywords
cinnamide
polycyclic derivative
novel pharmaceutical
polycyclic
derivative
Prior art date
Application number
MA31220A
Other languages
English (en)
Inventor
Teiji Kimura
Noritaka Kitazawa
Toshihiko Kaneko
Nobuaki Sato
Koki Kawano
Koichi Ito
Eriko Doi
Mamoru Takaishi
Takeo Sasaki
Takashi Doko
Takehiko Miyagawa
Hiroaki Hagiwara
Original Assignee
Eisai R&D Man 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 Eisai R&D Man Co Ltd filed Critical Eisai R&D Man Co Ltd
Publication of MA30268B1 publication Critical patent/MA30268B1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/64Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/90Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/10Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Neurosurgery (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

«Composition pharmaceutique nouvelle» Il est révélé des compositions pharmaceutiques nouvelles contenant de l'acide 3'-[(2Z)-[1-(3,4-diméthylphényl)-1,5-dihydro-3-méthyl-5-oxo-4H-pyrazole-4-ylidène]hydrazino]-2'-hydroxy-[1,1'-biphényl]-3-carboxylique bis-(monoéthanolamine) (eltrombopag olamine) et des procédés pour leur préparation.
MA31220A 2006-03-09 2008-09-08 Derive polycyclique de cinnamide MA30268B1 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US78051706P 2006-03-09 2006-03-09
JP2006063562 2006-03-09
US86170206P 2006-11-30 2006-11-30
JP2006322728 2006-11-30

Publications (1)

Publication Number Publication Date
MA30268B1 true MA30268B1 (fr) 2009-03-02

Family

ID=38474999

Family Applications (1)

Application Number Title Priority Date Filing Date
MA31220A MA30268B1 (fr) 2006-03-09 2008-09-08 Derive polycyclique de cinnamide

Country Status (15)

Country Link
EP (1) EP1992618B1 (fr)
KR (1) KR101464651B1 (fr)
AR (1) AR059955A1 (fr)
AU (1) AU2007223158B2 (fr)
CA (1) CA2643796A1 (fr)
CY (1) CY1112767T1 (fr)
EA (1) EA016464B1 (fr)
GE (1) GEP20115139B (fr)
HN (1) HN2008001374A (fr)
HR (1) HRP20120174T1 (fr)
IL (1) IL193770A (fr)
MA (1) MA30268B1 (fr)
MX (1) MX2008011221A (fr)
PL (1) PL1992618T3 (fr)
WO (1) WO2007102580A1 (fr)

Families Citing this family (58)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1757591A4 (fr) 2004-05-26 2010-05-05 Eisai R&D Man Co Ltd Composé de cinnamide
CN100577657C (zh) 2004-10-26 2010-01-06 卫材R&D管理有限公司 肉桂酰胺化合物的无定形物
TWI370130B (en) 2005-11-24 2012-08-11 Eisai R&D Man Co Ltd Two cyclic cinnamide compound
MY144960A (en) 2005-11-24 2011-11-30 Eisai R&D Man Co Ltd Morpholine type cinnamide compound
TWI378091B (en) 2006-03-09 2012-12-01 Eisai R&D Man Co Ltd Multi-cyclic cinnamide derivatives
AR062095A1 (es) 2006-07-28 2008-10-15 Eisai R&D Man Co Ltd Profarmaco de compuesto cinamida
WO2008097538A1 (fr) * 2007-02-08 2008-08-14 Merck & Co., Inc. Agents thérapeutiques
TW200848054A (en) 2007-02-28 2008-12-16 Eisai R&D Man Co Ltd Two cyclic oxomorpholine derivatives
CA2686754C (fr) 2007-05-11 2014-10-28 F. Hoffmann-La Roche Ag Hetarylanilines en tant que modulateurs de l'amyloide beta
EP2152695A2 (fr) * 2007-06-01 2010-02-17 Schering Corporation Modulateurs de sécrétase gamma
US7935815B2 (en) * 2007-08-31 2011-05-03 Eisai R&D Management Co., Ltd. Imidazoyl pyridine compounds and salts thereof
MY150507A (en) 2007-08-31 2014-01-30 Eisai R&D Man Co Ltd Polycyclic compound
WO2009061699A1 (fr) * 2007-11-05 2009-05-14 Schering Corporation Modulateurs de gamma-secrétase
US20100298372A1 (en) * 2007-12-11 2010-11-25 Schering Corporation Gamma secretase modulators
WO2009086277A1 (fr) 2007-12-20 2009-07-09 Envivo Pharmaceuticals, Inc. Benzènes tétrasubstitués
BRPI0821141A2 (pt) 2007-12-21 2015-06-16 Hoffmann La Roche Derivados de heteroarila como antagonistas do receptor de orexina
US7923450B2 (en) 2008-01-11 2011-04-12 Hoffmann-La Roche Inc. Modulators for amyloid beta
MX2010008700A (es) 2008-02-22 2010-08-30 Hoffmann La Roche Moduladores de beta-amiloide.
EP2324009A1 (fr) * 2008-08-27 2011-05-25 Eisai R&D Management Co., Ltd. Procédé de préparation de certains composés de cinnamide
EP2334665B1 (fr) 2008-10-09 2013-07-10 F. Hoffmann-La Roche AG Modulateurs pour l'amyloïde bêta
US20110263529A1 (en) * 2008-11-06 2011-10-27 Ruo Xu Gamma secretase modulators
AU2009313527A1 (en) * 2008-11-06 2010-05-14 Merck Sharp & Dohme Corp. Gamma secretase modulators
CN102209537A (zh) 2008-11-10 2011-10-05 弗·哈夫曼-拉罗切有限公司 杂环γ分泌酶调节剂
CA2742472A1 (fr) * 2008-11-13 2010-05-20 Schering Corporation Modulateurs de gamma secretase
JP2012513399A (ja) 2008-12-22 2012-06-14 シェーリング コーポレイション γ−セクレターゼ調節剤
TW201030002A (en) 2009-01-16 2010-08-16 Bristol Myers Squibb Co Bicyclic compounds for the reduction of beta-amyloid production
CA2749702A1 (fr) 2009-02-26 2010-09-02 Eisai R&D Management Co., Ltd. Sel de derive de tetrahydrotriazolopyridine et ses cristaux
JP2012051805A (ja) 2009-02-26 2012-03-15 Eisai R & D Management Co Ltd テトラヒドロトリアゾロピリジン誘導体の製造方法
JP2012051807A (ja) * 2009-02-26 2012-03-15 Eisai R & D Management Co Ltd アリールイミダゾール化合物
JP2012121809A (ja) * 2009-02-26 2012-06-28 Eisai R & D Management Co Ltd 多環式化合物の製造法およびその中間体
US8754100B2 (en) * 2009-02-26 2014-06-17 Eisai R&D Management Co., Ltd. Nitrogen-containing fused heterocyclic compounds and their use as beta amyloid production inhibitors
WO2011007756A1 (fr) 2009-07-13 2011-01-20 武田薬品工業株式会社 Composé hétérocyclique et son utilisation
US8871760B2 (en) * 2009-09-21 2014-10-28 Roche Palo Alto Llc [1,2,4]triazolo[3,4-C][1,4]oxazines as P2X7 modulators
EP2523955B1 (fr) 2010-01-15 2014-07-16 Janssen Pharmaceuticals, Inc. Nouveaux dérivés de triazole en tant que modulateurs de la secrétase gamma
US8486967B2 (en) 2010-02-17 2013-07-16 Hoffmann-La Roche Inc. Heteroaryl substituted piperidines
US8513230B2 (en) 2010-03-05 2013-08-20 Karyopharm Therapeutics, Inc. Nuclear transport modulators and uses thereof
US8901309B2 (en) * 2010-09-02 2014-12-02 Takeda Pharmaceutical Company Limited Fused triazoles for the treatment or prophylaxis of mild cognitive impairment
JP2014012641A (ja) * 2010-10-29 2014-01-23 Dainippon Sumitomo Pharma Co Ltd 新規ピリジン誘導体
JP6106605B2 (ja) * 2011-01-17 2017-04-05 カリオファーム セラピューティクス,インコーポレイテッド オレフィン含有核輸送調節剤およびその使用
CN110372673B (zh) 2011-07-29 2023-10-03 卡尔约药物治疗公司 含酰肼的核运输调节剂及其用途
SG10201609097PA (en) 2011-07-29 2016-12-29 Karyopharm Therapeutics Inc Nuclear transport modulators and uses thereof
WO2013055793A1 (fr) 2011-10-12 2013-04-18 University Of Pittsburg-Of The Commonwealth System Of Higher Education Petites molécules ciblant la localisation et/ou le niveau nucléaire des récepteurs de l'androgène dans le cancer de la prostate
SG11201407268SA (en) 2012-05-09 2015-01-29 Karyopharm Therapeutics Inc Nuclear transport modulators and uses thereof
CN104583208B (zh) 2012-05-16 2016-09-28 杨森制药公司 可用于治疗(尤其是)阿尔茨海默病的取代的3,4-二氢-2H-吡啶并[1,2-a]吡嗪-1,6-二酮衍生物
EP2687528A1 (fr) * 2012-07-17 2014-01-22 Ares Trading S.A. Dérivés de triazole fusionnés comme modulateurs de gamma-sécrétase
WO2014096212A1 (fr) 2012-12-20 2014-06-26 Janssen Pharmaceutica Nv Dérivés d'un nouveau type de 3,4-dihydro-2h-pyrido[1,2-α]pyrazine-1,6-dione tricyclique en tant que modulateurs de la gamma sécrétase
KR102171710B1 (ko) 2013-01-17 2020-10-30 얀센 파마슈티카 엔.브이. 감마 세크레타제 조절 인자로서의 신규 치환 피리도-피페라지논 유도체
EP2968278B8 (fr) 2013-03-15 2019-05-22 Karyopharm Therapeutics Inc. Procédés de promotion de la cicatrisation d'une plaie à l'aide d'inhibiteurs de crm1
ES2724275T3 (es) 2013-06-21 2019-09-09 Karyopharm Therapeutics Inc 1,2,4-triazoles como moduladores del transporte nuclear y usos de los mismos
CA2924527C (fr) 2013-09-20 2022-07-12 University Of Pittsburgh - Of The Commonwealth System Of Higher Education Composes destines au traitement du cancer de la prostate
US20160257657A1 (en) 2013-09-20 2016-09-08 University Of Pittsburgh - Of The Commonwealth System Of Higher Education Small molecule inhibitors of the nuclear translocation of androgen receptor for the treatment of castration-resistant prostate cancer
US10562897B2 (en) 2014-01-16 2020-02-18 Janssen Pharmaceutica Nv Substituted 3,4-dihydro-2H-pyrido[1,2-a]pyrazine-1,6-diones as gamma secretase modulators
KR102608259B1 (ko) 2014-08-15 2023-11-29 카리오팜 쎄라퓨틱스, 인코포레이티드 셀리넥소의 다형태
EP3397633A1 (fr) 2015-12-31 2018-11-07 Karyopharm Therapeutics, Inc. Modulateurs de transport nucléaire et leurs utilisations
WO2017117535A1 (fr) 2015-12-31 2017-07-06 Karyopharm Therapeutics Inc. Modulateurs de transport nucléaire et leurs utilisations
CN113332292A (zh) * 2016-02-23 2021-09-03 辉瑞公司 6,7-二氢-5H-吡唑并[5,1-b][1,3]噁嗪-2-甲酰胺化合物
US10980806B2 (en) 2016-03-24 2021-04-20 University of Pittsburgh—of the Commonwealth System of Higher Education Small molecule inhibitors of the nuclear translocation of androgen receptor for the treatment of castration-resistant prostate cancer
WO2018098472A1 (fr) 2016-11-28 2018-05-31 Karyopharm Therapeutics Inc. Inhibiteurs de crm1 pour le traitement de l'épilepsie

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ525917A (en) * 2000-12-04 2005-11-25 F Phenylethenyl or phenylethinyl derivatives as glutamate receptor antagonists and their use in treating mGLuR5 receptor mediated disorders
US20040192743A1 (en) * 2003-02-12 2004-09-30 Mjalli Adnan M.M. Substituted azole derivatives as therapeutic agents
AU2005214349B2 (en) * 2004-02-12 2011-11-03 Transtech Pharma, Inc. Substituted azole derivatives, compositions, and methods of use
EP1757591A4 (fr) * 2004-05-26 2010-05-05 Eisai R&D Man Co Ltd Composé de cinnamide

Also Published As

Publication number Publication date
GEP20115139B (en) 2011-01-10
AU2007223158B2 (en) 2012-04-12
EA016464B1 (ru) 2012-05-30
IL193770A0 (en) 2009-05-04
IL193770A (en) 2012-10-31
AU2007223158A1 (en) 2007-09-13
KR101464651B1 (ko) 2014-11-24
CY1112767T1 (el) 2016-02-10
HN2008001374A (es) 2011-03-15
WO2007102580A1 (fr) 2007-09-13
CA2643796A1 (fr) 2007-09-13
PL1992618T3 (pl) 2012-06-29
AR059955A1 (es) 2008-05-14
EP1992618A1 (fr) 2008-11-19
HK1122027A1 (en) 2009-05-08
EA200870336A1 (ru) 2009-02-27
KR20080108481A (ko) 2008-12-15
EP1992618B1 (fr) 2012-01-18
HRP20120174T1 (hr) 2012-03-31
EP1992618A4 (fr) 2010-11-10
HK1128085A1 (en) 2009-10-16
MX2008011221A (es) 2008-09-11

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