Nothing Special   »   [go: up one dir, main page]

PE20071029A1 - Compuestos de cinamida no peptidicos biciclicos como inhibidores de beta amiloides - Google Patents

Compuestos de cinamida no peptidicos biciclicos como inhibidores de beta amiloides

Info

Publication number
PE20071029A1
PE20071029A1 PE2006001479A PE2006001479A PE20071029A1 PE 20071029 A1 PE20071029 A1 PE 20071029A1 PE 2006001479 A PE2006001479 A PE 2006001479A PE 2006001479 A PE2006001479 A PE 2006001479A PE 20071029 A1 PE20071029 A1 PE 20071029A1
Authority
PE
Peru
Prior art keywords
compounds
inhibitors
cyane
benzyliden
metoxy
Prior art date
Application number
PE2006001479A
Other languages
English (en)
Inventor
Teiji Kimura
Koki Kawano
Eriko Doi
Noritaka Kitazawa
Mamoru Takaishi
Koichi Ito
Toshihiko Kaneko
Takeo Sasaki
Takehiko Miyagawa
Hiroaki Hagiwara
Yu Yoshida
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 PE20071029A1 publication Critical patent/PE20071029A1/es

Links

Classifications

    • 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
    • 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
    • A61K31/41781,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
    • 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
    • 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
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-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)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

REFERIDA A UN COMPUESTO CINAMIDA DE FORMULA (I), DONDE LA LINEA PUNTEADA REPRESENTA UN ENLACE SIMPLE O UN ENLACE DOBLE; Ar1 ES FENILO O PIRIDINILO OPCIONALMENTE SUSTITUIDOS CON HALOGENO, HIDROXILO, CIANO, CICLOALQUILO C3-C8, ENTRE OTROS; R1 Y R2 SON HALOGENO, CIANO, OH, CICLOALQUILO C3-C8, CICLOALCOXI C3-C8, ENTRE OTROS; Z1 ES METILENO O VIVNILENO OPCIONALMENTE SUSTITUIDOS CON HALO, CIANO, OH, CICLOALQUILO C3-C8, ENTRE OTROS; p, q Y r SON UN NUMERO ENTERO DE 0 A 2. SON COMPUESTOS PREFERIDOS: (E)-(3S)-(3,4,5-TRIFLUOROFENIL)-6-[3-METOXI-4-(4-METIL-1H-IMIDAZOL-1-IL)-BENCILIDEN]-(9R)-HEXAHIDROINDOLIZIN-5-ONA, (E)-(3S)-(3,4-DIFLUOROFENIL)-6-[3-METOXI-4-(4-METIL-1H-IMIDAZOL-1-IL)-BENCILIDEN]-(9R)-HEXAHIDROINDOLIZIN-5-ONA, (E)-(6R,9aS)-6-(4-FLUOROFENIL)-3-[3-METOXI-4-(4-METIL-1H-IMIDAZOL-1-IL)-BENCILIDEN]OCTAHIDROQUINOLIZIN-4-ONA, ENTRE OTROS. TAMBIEN ESTA REFERIDA A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA PRODUCCION DE BETA AMILOIDE Y SON UTILES EN EL TRATAMIENTO DE ENFERMEDADES NEURODEGENERATIVAS TALES COMO LA ENFERMEDAD DE ALZHEIMER Y EL SINDROME DE DOWN
PE2006001479A 2005-11-24 2006-11-21 Compuestos de cinamida no peptidicos biciclicos como inhibidores de beta amiloides PE20071029A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2005337963 2005-11-24
JP2006205538 2006-07-28

Publications (1)

Publication Number Publication Date
PE20071029A1 true PE20071029A1 (es) 2007-11-17

Family

ID=38067057

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2006001479A PE20071029A1 (es) 2005-11-24 2006-11-21 Compuestos de cinamida no peptidicos biciclicos como inhibidores de beta amiloides

Country Status (26)

Country Link
US (1) US8048878B2 (es)
EP (1) EP1953158B1 (es)
JP (1) JP5178203B2 (es)
KR (1) KR101296239B1 (es)
AR (1) AR057915A1 (es)
AU (1) AU2006317468B2 (es)
BR (1) BRPI0618890A2 (es)
CA (1) CA2629512C (es)
CR (1) CR9983A (es)
EA (1) EA014427B1 (es)
EC (1) ECSP088466A (es)
ES (1) ES2394364T3 (es)
GE (1) GEP20115172B (es)
HK (1) HK1122806A1 (es)
HN (1) HN2008000792A (es)
MA (1) MA29968B1 (es)
ME (1) ME00040B (es)
MY (1) MY144596A (es)
NO (1) NO20082805L (es)
NZ (1) NZ568422A (es)
PE (1) PE20071029A1 (es)
PL (1) PL1953158T3 (es)
RS (1) RS20080242A (es)
SA (1) SA06270432B1 (es)
TW (1) TWI370130B (es)
WO (1) WO2007060821A1 (es)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI335816B (en) 2004-05-26 2011-01-11 Eisai R&D Man Co Ltd Cinnamide compound
JPWO2006046575A1 (ja) 2004-10-26 2008-05-22 エーザイ・アール・アンド・ディー・マネジメント株式会社 シンナミド化合物の非晶質体
TWI386207B (zh) 2005-11-24 2013-02-21 Eisai R&D Man Co Ltd 味啉類型之肉桂醯胺化合物
TWI370130B (en) 2005-11-24 2012-08-11 Eisai R&D Man Co Ltd Two cyclic cinnamide compound
US7482345B2 (en) * 2005-12-05 2009-01-27 Meng-Hsin Chen P38 kinase inhibiting agents
TWI378091B (en) 2006-03-09 2012-12-01 Eisai R&D Man Co Ltd Multi-cyclic cinnamide derivatives
SA07280403B1 (ar) * 2006-07-28 2010-12-01 إيساي أر أند دي منجمنت كو. ليمتد ملح رباعي لمركب سيناميد
US20080207900A1 (en) * 2007-02-28 2008-08-28 Teiji Kimura Two cyclic oxomorphorin derivatives
EP2152695A2 (en) * 2007-06-01 2010-02-17 Schering Corporation Gamma secretase modulators
JP5121346B2 (ja) * 2007-08-07 2013-01-16 国立大学法人 長崎大学 光学活性プロリンエステル誘導体およびn−ホルミル光学活性プロリン誘導体の製造方法
US7935815B2 (en) * 2007-08-31 2011-05-03 Eisai R&D Management Co., Ltd. Imidazoyl pyridine compounds and salts thereof
TW200916469A (en) 2007-08-31 2009-04-16 Eisai R & Amp D Man Co Ltd Multi-cyclic compounds
US20100280243A1 (en) * 2007-12-26 2010-11-04 Akio Kayano Process for production of 4- (substituted phenyl) hexahydropyrido [2,1-c] [1,4] oxazin-6-one
MX2010008700A (es) 2008-02-22 2010-08-30 Hoffmann La Roche Moduladores de beta-amiloide.
EP2334665B1 (en) 2008-10-09 2013-07-10 F. Hoffmann-La Roche AG Modulators for amyloid beta
CA2742500A1 (en) * 2008-11-06 2010-05-14 Schering Corporation Gamma secretase modulators
JP2012508181A (ja) * 2008-11-06 2012-04-05 シェーリング コーポレイション γ−セクレターゼ調節剤
EP2355817A1 (en) 2008-11-10 2011-08-17 F. Hoffmann-La Roche AG Heterocyclic gamma secretase modulators
JP5503663B2 (ja) * 2008-11-13 2014-05-28 メルク・シャープ・アンド・ドーム・コーポレーション ガンマセクレターゼモジュレータ
JP5580816B2 (ja) 2009-02-26 2014-08-27 エーザイ・アール・アンド・ディー・マネジメント株式会社 テトラヒドロトリアゾロピリジン誘導体の塩およびその結晶
JP2012519152A (ja) 2009-02-26 2012-08-23 エーザイ・アール・アンド・ディー・マネジメント株式会社 含窒素縮合複素環化合物及びベータアミロイド産生阻害剤としてのその使用
JP2012176901A (ja) * 2009-09-25 2012-09-13 Eisai R & D Management Co Ltd 新規ベンゾニトリル化合物およびその製造方法
US8486967B2 (en) 2010-02-17 2013-07-16 Hoffmann-La Roche Inc. Heteroaryl substituted piperidines
CN102939284A (zh) * 2010-06-15 2013-02-20 卫材R&D管理有限公司 Hcv感染症治疗剂
JP6095208B2 (ja) * 2012-12-04 2017-03-15 学校法人慶應義塾 環化化合物の製造方法、及び、環化化合物を含有する溶液の発光方法
PL3552017T3 (pl) * 2016-12-09 2022-08-08 Denali Therapeutics Inc. Związki użyteczne jako inhibitory RIPK1
BR112019023979A2 (pt) * 2017-05-17 2020-06-09 Denali Therapeutics Inc compostos, composições e métodos
WO2021071832A1 (en) * 2019-10-07 2021-04-15 D.E. Shaw Research, Llc Aryl heterobicyclic compounds as kv1.3 potassium shaker channel blockers

Family Cites Families (66)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4508718A (en) 1984-01-16 1985-04-02 Warner-Lambert Company Cardiotonic and antihypertensive oxadiazinone compounds
DE3689506D1 (de) 1985-10-09 1994-02-17 Shell Int Research Neue Acrylsäureamide.
US4783463A (en) 1985-10-23 1988-11-08 Rorer Pharmaceutical Corporation Pyridyl-pyridazinone and pyridyl-pyrazolinone compounds and their use in the treatment of congestive heart failure
DE3541716A1 (de) 1985-11-26 1987-05-27 Celamerck Gmbh & Co Kg Neue acrylsaeureamide
FI91754C (fi) 1986-12-02 1994-08-10 Tanabe Seiyaku Co Analogiamenetelmä lääkeaineena käyttökelpoisen imidatsolijohdannaisen valmistamiseksi
IT1205834B (it) * 1987-04-22 1989-03-31 Elbart Derivati tiodiossolanici ad attivita' mucolitica a procedimento per la loro preparazione
FI902321A0 (fi) 1989-05-19 1990-05-09 Eisai Co Ltd Butensyraderivat.
JPH03206042A (ja) 1990-01-06 1991-09-09 Takeda Chem Ind Ltd 降圧剤
JP3176365B2 (ja) 1990-02-08 2001-06-18 エーザイ株式会社 ベンゼンスルホンアミド誘導体
AU680870B2 (en) 1993-04-28 1997-08-14 Astellas Pharma Inc. New heterocyclic compounds
GB9402807D0 (en) 1994-02-14 1994-04-06 Xenova Ltd Pharmaceutical compounds
CA2200981A1 (en) 1994-10-04 1996-04-11 Hisashi Takasugi Urea derivatives and their use as acat-inhibitors
JPH08283219A (ja) 1995-04-07 1996-10-29 Eisai Co Ltd アラルキルアミノアルキルアミド誘導体
ES2175404T3 (es) * 1996-05-10 2002-11-16 Icos Corp Derivados de carbolina.
CN1238688A (zh) 1996-07-22 1999-12-15 孟山都公司 硫羟磺酰胺金属蛋白酶抑制剂
JP2001508767A (ja) 1996-12-02 2001-07-03 藤沢薬品工業株式会社 5―ht拮抗作用を有するインドール―ウレア誘導体
JP3108997B2 (ja) 1997-03-31 2000-11-13 武田薬品工業株式会社 アゾール化合物、その製造法および用途
EP0973768B1 (en) 1997-03-31 2003-07-09 Takeda Chemical Industries, Ltd. Azole compounds, their production and their use
TW379224B (en) 1997-12-02 2000-01-11 Fujisawa Pharmaceutical Co Urea derivatives
WO1999033846A2 (en) * 1997-12-31 1999-07-08 The University Of Kansas Water soluble prodrugs of secondary and tertiary amine containing drugs and methods of making thereof
GB9816984D0 (en) 1998-08-05 1998-09-30 Smithkline Beecham Plc Novel compounds
US6235728B1 (en) * 1999-02-19 2001-05-22 Bristol-Myers Squibb Company Water-soluble prodrugs of azole compounds
MXPA01008606A (es) 1999-02-26 2003-05-05 Merck & Co Inc Compuestos de sulfonamida novedosos y uso de los mismos.
AU2899400A (en) * 1999-03-04 2000-09-21 Nortran Pharmaceuticals Inc. Aminocycloalkyl cinnamide compounds for arrhythmia and as analgesics and anesthetics
AU2001241128A1 (en) * 2000-03-14 2001-09-24 Fujisawa Pharmaceutical Co. Ltd. Novel amide compounds
US20010051642A1 (en) * 2000-04-17 2001-12-13 Kyunghye Ahn Method for treating Alzheimer's disease
WO2001081312A2 (en) 2000-04-24 2001-11-01 Merck Frosst Canada & Co. Method of treatment using phenyl and biaryl derivatives as prostaglandin e inhibitors and compounds useful therefore
SI1349839T1 (es) 2000-12-04 2005-08-31 Hoffmann La Roche
GB0108770D0 (en) 2001-04-06 2001-05-30 Eisai London Res Lab Ltd Inhibitors
JP2005503400A (ja) 2001-09-13 2005-02-03 ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド サイトカイン媒介病の治療方法
US7879893B2 (en) 2001-09-14 2011-02-01 Novo Nordisk A/S Ligands for the HisB10 Zn2 + sites of the R-state insulin hexamer
MXPA04005427A (es) 2001-12-10 2005-04-19 Amgen Inc Ligandos de receptor vainilloide y su uso en tratamientos.
HUP0500173A3 (en) * 2001-12-20 2009-03-30 Bristol Myers Squibb Co Alpha-sulphonamido-acetamide derivatives as beta-amyloid inhibitors and pharmaceutical compositions containing them
JP2003206280A (ja) 2001-12-28 2003-07-22 Takeda Chem Ind Ltd ビアリール化合物およびその用途
EP1509505A2 (en) 2002-01-23 2005-03-02 Arena Pharmaceuticals, Inc. SMALL MOLECULE MODULATORS OF THE 5−HT2A SEROTONIN RECEPTOR USEFUL FOR THE PROPHYLAXIS AND TREATMENT OF DISORDERS RELATED THERETO
GB0207436D0 (en) 2002-03-28 2002-05-08 Glaxo Group Ltd Novel compounds
PL375552A1 (en) * 2002-05-22 2005-11-28 Amgen Inc. Vanilloid receptor ligands and their medical applications
SI2527315T1 (sl) * 2002-05-31 2014-06-30 Proteotech Inc., Spojine, sestavki in metode za zdravljenje amiloidnih bolezni in sinukleinopatij, kot so Alzheimerjeva bolezen, diabetes tipa 2 in Parkinsonova bolezen
AU2003247758A1 (en) * 2002-06-27 2004-01-19 Elan Pharmaceuticals, Inc. Methods for treating alzheimer's disease using hydroxyethylene compounds containing a heterocyclic amide bond isostere
RS20050019A (en) 2002-07-12 2007-09-21 Sanofi - Aventis Pharma Deutschland Gmbh., Heterocyclically substituted benzoylureas,method for their production and their use as medicaments
US6900354B2 (en) 2002-07-15 2005-05-31 Hoffman-La Roche Inc. 3-phenyl-propionamido, 3-phenyl-acrylamido and 3-phenyl-propynamido derivatives
EP1594847A2 (en) * 2003-02-12 2005-11-16 Transtech Pharma, Inc. Substituted azole derivatives as therapeutic agents
US7244739B2 (en) * 2003-05-14 2007-07-17 Torreypines Therapeutics, Inc. Compounds and uses thereof in modulating amyloid beta
JP5010917B2 (ja) * 2003-08-29 2012-08-29 エグゼリクシス, インコーポレイテッド c−Kit調節因子および使用方法
WO2005063754A1 (en) 2003-12-22 2005-07-14 Pfizer Limited Triazole derivatives as vasopressin antagonists
WO2005072731A1 (en) 2004-01-29 2005-08-11 X-Ceptor Therapeutics, Inc. 3-phenyl-n- ((1, 3, 4) thiadiazol-2-yl) -acrylamide derivatives and related compounds as modulators of estrogen-related receptors for the treatment of e.g. cancer, rheumatoid arthritis or neurological disorders
CN1922151A (zh) 2004-02-12 2007-02-28 特兰斯泰克制药公司 取代的吡咯衍生物、组合物和使用方法
TWI335816B (en) * 2004-05-26 2011-01-11 Eisai R&D Man Co Ltd Cinnamide compound
WO2006018662A2 (en) 2004-08-16 2006-02-23 Prosidion Limited Aryl urea derivatives for treating obesity
JPWO2006046575A1 (ja) * 2004-10-26 2008-05-22 エーザイ・アール・アンド・ディー・マネジメント株式会社 シンナミド化合物の非晶質体
US20060241038A1 (en) 2005-04-20 2006-10-26 Eisai Co., Ltd. Therapeutic agent for Abeta related disorders
WO2007034282A2 (en) 2005-09-19 2007-03-29 Pfizer Products Inc. Diaryl-imidazole compounds condensed with a heterocycle as c3a receptor antagonists
KR20080076907A (ko) * 2005-11-18 2008-08-20 에자이 알앤드디 매니지먼트 가부시키가이샤 신나미드 유도체의 제조 방법
EP1953151A4 (en) 2005-11-18 2010-06-02 Eisai R&D Man Co Ltd SALTS FROM A CYNNAMIDE COMPOUND OR SOLVATE THEREOF
US20070117839A1 (en) * 2005-11-24 2007-05-24 Eisai R&D Management Co., Ltd. Two cyclic cinnamide compound
TWI386207B (zh) 2005-11-24 2013-02-21 Eisai R&D Man Co Ltd 味啉類型之肉桂醯胺化合物
TWI370130B (en) 2005-11-24 2012-08-11 Eisai R&D Man Co Ltd Two cyclic cinnamide compound
AU2007223158B2 (en) 2006-03-09 2012-04-12 Eisai R & D Management Co., Ltd. Polycyclic cinnamide derivative
TWI378091B (en) * 2006-03-09 2012-12-01 Eisai R&D Man Co Ltd Multi-cyclic cinnamide derivatives
SA07280403B1 (ar) 2006-07-28 2010-12-01 إيساي أر أند دي منجمنت كو. ليمتد ملح رباعي لمركب سيناميد
JP2010518080A (ja) 2007-02-08 2010-05-27 メルク・シャープ・エンド・ドーム・コーポレイション 治療薬
WO2008137102A2 (en) 2007-05-04 2008-11-13 Torreypines Therapeutics, Inc. Methods of modulating amyloid beta and compounds useful therefor
CA2686589A1 (en) 2007-05-07 2008-11-13 Schering Corporation Gamma secretase modulators
DE602008004769D1 (en) * 2007-05-11 2011-03-10 Hoffmann La Roche Hetarylaniline als modulatoren für amyloid beta
US8242150B2 (en) 2007-06-13 2012-08-14 Merck Sharp & Dohme Corp. Triazole derivatives for treating alzheimer'S disease and related conditions
US20110009392A1 (en) 2007-08-06 2011-01-13 Schering Corporation Gamma secretase modulators

Also Published As

Publication number Publication date
TW200804372A (en) 2008-01-16
CA2629512A1 (en) 2007-05-31
AU2006317468B2 (en) 2011-10-13
AR057915A1 (es) 2007-12-26
MY144596A (en) 2011-10-14
GEP20115172B (en) 2011-03-10
EP1953158B1 (en) 2012-09-12
ES2394364T3 (es) 2013-01-31
RS20080242A (xx) 2009-09-08
WO2007060821A1 (ja) 2007-05-31
EP1953158A4 (en) 2010-09-01
EP1953158A1 (en) 2008-08-06
KR101296239B1 (ko) 2013-08-13
EA200801417A1 (ru) 2009-02-27
KR20080072057A (ko) 2008-08-05
HN2008000792A (es) 2010-09-17
AU2006317468A1 (en) 2007-05-31
PL1953158T3 (pl) 2013-02-28
EA014427B1 (ru) 2010-12-30
NO20082805L (no) 2008-08-20
TWI370130B (en) 2012-08-11
BRPI0618890A2 (pt) 2013-01-08
CR9983A (es) 2008-08-21
SA06270432B1 (ar) 2011-06-22
MA29968B1 (fr) 2008-11-03
JP5178203B2 (ja) 2013-04-10
JPWO2007060821A1 (ja) 2009-05-07
NZ568422A (en) 2010-09-30
US8048878B2 (en) 2011-11-01
ECSP088466A (es) 2008-08-29
CA2629512C (en) 2014-04-22
ME00040B (me) 2010-06-10
US20090181945A1 (en) 2009-07-16
HK1122806A1 (en) 2009-05-29

Similar Documents

Publication Publication Date Title
PE20071029A1 (es) Compuestos de cinamida no peptidicos biciclicos como inhibidores de beta amiloides
ECSP088871A (es) Derivados de triazolopirazina
TW200612939A (en) Antibiotics containing borinic acid complexes and methods of use
NO20074044L (no) Meleimidderivater, farmasoytiske preparater og fremgangsmater for behandling av kreft
WO2006086562A3 (en) Phenylazetidinone derivatives
DK1505973T3 (da) Kombinationer til behandling af multipelt myelom
ECSP077239A (es) Formulación farmacéutica
NO20074703L (no) Antibakterielle piperidinderivater
ATE504565T1 (de) Azetidine als mek-inhibitoren bei der behandlung proliferativer erkrankungen
DE60331056D1 (de) 6-11 bicyclische ketolidderivate
PE20081374A1 (es) Combinacion que comprende un agente antipsicotico y (2s)-(4e)-n-metil-5-[3-(5-isopropoxipiridin)il]-4-penten-2-amina
TW200728276A (en) Oxindole derivatives
NO20055894L (no) Fremgangsmater og blandinger for behandling av amyloidrelatertere sykdommer
NO20061245L (no) Farmasoytiske sammensetninger og fremgangsmater omfattende kombinasjoner av 2-alkyliden-19-nor-vitamin D derivater og en bisfosfon
GEP20084439B (en) Nitrogen-containing heterocyclic derivatives and pharmaceutical use thereof
ATE523495T1 (de) Substituierte pyrazolinverbindungen, deren herstellung und verwendung als medikamente
UY29414A1 (es) Derivados de pirimidina para el tratamiento de trastornos hiperproliferativos
ATE499372T1 (de) Azabenzimidalzolderivate, ihre herstellung und ihre verwendung als antikrebsmittel
EA201001196A1 (ru) Соединения 4-пиридинона и их применение для лечения рака
GT200600160A (es) Tratamiento del dolor
MX2021014029A (es) Formulaciones, fabricación y usos de imatinib.
CR8574A (es) Compuestos silinano como inhibidores de cisteina proteasa
ZA200409379B (en) Cationically substituted diphenyl azetidinones, method for their production, medicaments containing said compounds and use thereof
BRPI0511874A (pt) derivados da pirrolopiridina
DE60317098D1 (de) Carbostyril-derivate mit selektiven serotonin-aufnahme inhibitoren, zur behandlung von gemütskrankheiten

Legal Events

Date Code Title Description
FG Grant, registration
FD Application declared void or lapsed