ATE303387T1 - Kondensierte imidazolderivate und arzneimittel gegen diabetes mellitus - Google Patents

Kondensierte imidazolderivate und arzneimittel gegen diabetes mellitus

Info

Publication number
ATE303387T1
ATE303387T1 AT00940909T AT00940909T ATE303387T1 AT E303387 T1 ATE303387 T1 AT E303387T1 AT 00940909 T AT00940909 T AT 00940909T AT 00940909 T AT00940909 T AT 00940909T AT E303387 T1 ATE303387 T1 AT E303387T1
Authority
AT
Austria
Prior art keywords
group
diabetes mellitus
alkyl group
adenosine
substituted
Prior art date
Application number
AT00940909T
Other languages
English (en)
Inventor
Osamu Asano
Hitoshi Harada
Seiji Yoshikawa
Nobuhisa Watanabe
Takashi Inoue
Tatsuo Horizoe
Nobuyuki Yasuda
Kaya Ohashi
Hiroe Minami
Junsaku Nagaoka
Manabu Murakami
Seiichi Kobayashi
Isao Tanaka
Tsutomu Kawata
Naoyuki Shimomura
Hiroshi Akamatsu
Naoki Ozeki
Toshikazu Shimizu
Kenji Hayashi
Toyokazu Haga
Shigeto Negi
Toshihiko Naito
Original Assignee
Eisai 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 Co Ltd filed Critical Eisai Co Ltd
Application granted granted Critical
Publication of ATE303387T1 publication Critical patent/ATE303387T1/de

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/26Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
    • C07D473/32Nitrogen atom
    • C07D473/34Nitrogen atom attached in position 6, e.g. adenine
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • 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
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/18Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 one oxygen and one nitrogen atom, e.g. guanine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/40Heterocyclic compounds containing purine ring systems with halogen atoms or perhalogeno-alkyl radicals directly attached in position 2 or 6

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Diabetes (AREA)
  • General Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Veterinary Medicine (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyridine Compounds (AREA)
AT00940909T 1999-07-02 2000-06-30 Kondensierte imidazolderivate und arzneimittel gegen diabetes mellitus ATE303387T1 (de)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP18848499 1999-07-02
JP2000143495 2000-05-16
JP2000182786 2000-06-19
PCT/JP2000/004358 WO2001002400A1 (en) 1999-07-02 2000-06-30 Fused imidazole compounds and remedies for diabetes mellitus

Publications (1)

Publication Number Publication Date
ATE303387T1 true ATE303387T1 (de) 2005-09-15

Family

ID=27326046

Family Applications (1)

Application Number Title Priority Date Filing Date
AT00940909T ATE303387T1 (de) 1999-07-02 2000-06-30 Kondensierte imidazolderivate und arzneimittel gegen diabetes mellitus

Country Status (14)

Country Link
US (1) US6841549B1 (de)
EP (1) EP1221444B1 (de)
JP (1) JP4324338B2 (de)
KR (1) KR100694684B1 (de)
CN (1) CN1166666C (de)
AT (1) ATE303387T1 (de)
AU (1) AU778450B2 (de)
CA (1) CA2376835C (de)
DE (1) DE60022366T2 (de)
DK (1) DK1221444T3 (de)
ES (1) ES2246867T3 (de)
NZ (1) NZ516260A (de)
PT (1) PT1221444E (de)
WO (1) WO2001002400A1 (de)

Families Citing this family (70)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9915437D0 (en) 1999-07-01 1999-09-01 Cerebrus Ltd Chemical compounds III
AU5260601A (en) 2000-04-26 2001-11-07 Eisai Co Ltd Medicinal compositions promoting bowel movement
GB0100624D0 (en) 2001-01-10 2001-02-21 Vernalis Res Ltd Chemical compounds VII
GB0100620D0 (en) 2001-01-10 2001-02-21 Vernalis Res Ltd Chemical cokpounds V
GB0100623D0 (en) * 2001-01-10 2001-02-21 Vernalis Res Ltd Chemical compounds IV
TWI301834B (en) 2001-10-22 2008-10-11 Eisai R&D Man Co Ltd Pyrimidone compound and pharmaceutical composition including the same
TWI330183B (de) 2001-10-22 2010-09-11 Eisai R&D Man Co Ltd
ES2279903T3 (es) * 2001-12-18 2007-09-01 Cv Therapeutics, Inc. Antagonistas del receptor a2a de adenosina.
KR101098209B1 (ko) 2002-01-28 2011-12-23 교와 핫꼬 기린 가부시키가이샤 운동성 질환에 걸린 환자의 치료 방법
US7129239B2 (en) 2002-10-28 2006-10-31 Pfizer Inc. Purine compounds and uses thereof
WO2004092170A2 (en) 2003-04-09 2004-10-28 Biogen Idec Ma Inc. Triazolotriazines and pyrazolotriazines useful as a2a adenosine receptor antagon ists
WO2004092177A1 (en) 2003-04-09 2004-10-28 Biogen Idec Ma Inc. Triazolopyrazines and methods of making and using the same
WO2004092173A2 (en) 2003-04-09 2004-10-28 Biogen Idec Ma Inc. A2a adenosine receptor antagonists
KR100710453B1 (ko) * 2003-05-13 2007-04-24 에프. 호프만-라 로슈 아게 아데노신 수용체 리간드로서의 2-이미다조-벤조싸이아졸
US20080280926A1 (en) * 2003-12-16 2008-11-13 Palle Venkata P Phosphodiesterase Inhibitors
CA2565037A1 (en) * 2004-04-28 2005-11-10 Cv Therapeutics, Inc. Purine derivatives as a1 adenosine receptor antagonists
PE20060272A1 (es) * 2004-05-24 2006-05-22 Glaxo Group Ltd (2r,3r,4s,5r,2'r,3'r,4's,5's)-2,2'-{trans-1,4-ciclohexanodiilbis-[imino(2-{[2-(1-metil-1h-imidazol-4-il)etil]amino}-9h-purin-6,9-diil)]}bis[5-(2-etil-2h-tetrazol-5-il)tetrahidro-3,4-furanodiol] como agonista a2a
KR20070027584A (ko) 2004-06-17 2007-03-09 와이어쓰 고나도트로핀 방출 호르몬 수용체 길항제
AU2005264998A1 (en) * 2004-06-17 2006-01-26 Wyeth The present invention relates to methods of making Gonadotropin Releasing Hormone ('GnRH') (also known as Leutinizing Hormone Releasing Hormone) receptor antagonists
GB0423551D0 (en) * 2004-10-22 2004-11-24 Novartis Ag Organic compounds
GT200500281A (es) * 2004-10-22 2006-04-24 Novartis Ag Compuestos organicos.
CA2587853A1 (en) * 2004-11-23 2006-06-01 Wyeth Gonadotropin releasing hormone receptor antagonists
US7582634B2 (en) * 2005-02-18 2009-09-01 Wyeth 7-substituted imidazo[4,5-c]pyridine antagonists of gonadotropin releasing hormone receptor
US7538113B2 (en) * 2005-02-18 2009-05-26 Wyeth 4-substituted imidazo[4,5-c]pyridine antagonists of gonadotropin releasing hormone receptor
US7534796B2 (en) * 2005-02-18 2009-05-19 Wyeth Imidazo[4,5-b]pyridine antagonists of gonadotropin releasing hormone receptor
US20060189619A1 (en) * 2005-02-24 2006-08-24 Wyeth 3-({4-[2-(4-Tert-butylphenyl)-1h-benzimidazol-4-yl]piperazin-1-yl}methyl)pyrido[2,3-b]]pyrazi ne compounds
US7531542B2 (en) 2005-05-18 2009-05-12 Wyeth Benzooxazole and benzothiazole antagonists of gonadotropin releasing hormone receptor
US7582636B2 (en) * 2005-05-26 2009-09-01 Wyeth Piperazinylimidazopyridine and piperazinyltriazolopyridine antagonists of Gonadotropin Releasing Hormone receptor
GB0514809D0 (en) 2005-07-19 2005-08-24 Glaxo Group Ltd Compounds
ES2270715B1 (es) 2005-07-29 2008-04-01 Laboratorios Almirall S.A. Nuevos derivados de pirazina.
JP2007063225A (ja) * 2005-09-01 2007-03-15 Takeda Chem Ind Ltd イミダゾピリジン化合物
US20090023723A1 (en) * 2005-09-21 2009-01-22 Pharmacopeia Drug Discovery, Inc. Purinone derivatives for treating neurodegenerative diseases
ES2274712B1 (es) * 2005-10-06 2008-03-01 Laboratorios Almirall S.A. Nuevos derivados imidazopiridina.
ES2273599B1 (es) 2005-10-14 2008-06-01 Universidad De Barcelona Compuestos para el tratamiento de la fibrilacion auricular.
US7989459B2 (en) 2006-02-17 2011-08-02 Pharmacopeia, Llc Purinones and 1H-imidazopyridinones as PKC-theta inhibitors
US7919490B2 (en) 2006-10-04 2011-04-05 Wyeth Llc 6-substituted 2-(benzimidazolyl)purine and purinone derivatives for immunosuppression
TW200837064A (en) 2006-10-04 2008-09-16 Pharmacopeia Inc 8-substituted 2-(benzimidazolyl)purine derivatives for immunosuppression
US7902187B2 (en) 2006-10-04 2011-03-08 Wyeth Llc 6-substituted 2-(benzimidazolyl)purine and purinone derivatives for immunosuppression
ES2303776B1 (es) * 2006-12-29 2009-08-07 Laboratorios Almirall S.A. Derivados de 5-fenil-6-piridin-4-il-1,3-dihidro-2h-imidazo(4,5-b)piridin-2-ona utiles como antagonistas del receptor de adenosina a2b.
KR101313804B1 (ko) 2007-03-20 2013-10-01 쿠리스 인코퍼레이션 Hsp90 억제제로서의 융합된 아미노 피리딘
GB0906579D0 (en) 2009-04-16 2009-05-20 Vernalis R&D Ltd Pharmaceuticals, compositions and methods of making and using the same
CA2738429C (en) * 2008-09-26 2016-10-25 Intellikine, Inc. Heterocyclic kinase inhibitors
EP2348860B1 (de) 2008-10-31 2015-05-27 Genentech, Inc. Pyrazolopyrimidin-jak-hemmer-verbindungen und entsprechende verfahren
EP2246335A1 (de) 2009-02-17 2010-11-03 Bayer CropScience AG Aminopyrimidinamide als Schädlingsbekämpfungsmittel
EP2408775B1 (de) * 2009-03-20 2015-06-17 SIGMA-TAU Industrie Farmaceutiche Riunite S.p.A. Oxidierte derivate von triazolylpurinen, die als liganden von adenosin a2a-rezeptor nützlich sind, und die verwendung davon als medikamente
UA110324C2 (en) 2009-07-02 2015-12-25 Genentech Inc Jak inhibitory compounds based on pyrazolo pyrimidine
WO2011074658A1 (ja) 2009-12-18 2011-06-23 田辺三菱製薬株式会社 新規抗血小板薬
US20130096104A1 (en) * 2010-03-17 2013-04-18 Genentech, Inc. Imidazopyridine compounds, compositions and methods of use
ES2365960B1 (es) 2010-03-31 2012-06-04 Palobiofarma, S.L Nuevos antagonistas de los receptores de adenosina.
TW201217387A (en) 2010-09-15 2012-05-01 Hoffmann La Roche Azabenzothiazole compounds, compositions and methods of use
BR112013011520A2 (pt) 2010-11-19 2019-09-24 Hoffmann La Roche pirazolo piridinas e pirazolo piridinas e seu uso como inibidores de tyk2
JP5714602B2 (ja) * 2010-11-24 2015-05-07 ヤマサ醤油株式会社 新規な2−アルキニル−n9−プロパギルアデニンおよびその医薬用途
MX2013010513A (es) 2011-03-16 2013-10-07 Hoffmann La Roche Compuestos de alcohol 6,5-heterociclil-propargilico y usos de los mismos.
CN103044337A (zh) * 2011-10-13 2013-04-17 南京理工大学 2-(n-烷基)氨基咪唑衍生物的合成方法
CN103664704B (zh) * 2012-08-31 2016-05-18 南京理工大学 一种合成n,n’-二取代基脲的方法
EP2818472A1 (de) * 2013-06-27 2014-12-31 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. Imidazo[4,5-c]pyridin- und Pyrrolo[3,2-c]pyridinverbindungen als Modulatoren der G-Protein-Gekoppelte Rezeptoren Kinase 5 (GRK5)
BR112016005199B1 (pt) 2013-08-23 2022-02-22 Neupharma, Inc Certos compostos químicos, composições, e métodos
JP2017516850A (ja) 2014-05-23 2017-06-22 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft Jak阻害剤である5−クロロ−2−ジフルオロメトキシフェニルピラゾロピリミジン化合物
JP6964072B2 (ja) * 2016-04-26 2021-11-10 大日本住友製薬株式会社 置換プリン誘導体
WO2018035061A1 (en) 2016-08-15 2018-02-22 Neupharma, Inc. Certain chemical entities, compositions, and methods
WO2018195155A1 (en) 2017-04-18 2018-10-25 Celgene Quanticel Research, Inc. Therapeutic compounds
MX387969B (es) 2017-05-22 2025-03-19 Hoffmann La Roche Composiciones y compuestos terapéuticos, y métodos para su uso.
PT3661941T (pt) 2017-08-01 2023-03-16 Merck Patent Gmbh Derivados tiazolopiridina como antagonistas do recetor de adenosina
TWI791593B (zh) 2017-08-21 2023-02-11 德商馬克專利公司 做為腺苷受體拮抗劑之苯并咪唑衍生物
EP3672951B1 (de) 2017-08-21 2023-08-30 Merck Patent GmbH Chinoxalinderivate als adenosinrezeptor-antagonisten
KR20210083293A (ko) 2018-10-25 2021-07-06 메르크 파텐트 게엠베하 아데노신 수용체 안타고니스트로서의 5-아자인다졸 유도체
KR20210083287A (ko) 2018-10-25 2021-07-06 메르크 파텐트 게엠베하 아데노신 수용체 안타고니스트로서의 5-아자인다졸 유도체
AR117844A1 (es) 2019-01-22 2021-09-01 Merck Patent Gmbh Derivados de tiazolopiridina como antagonistas del receptor de adenosina
KR20210061202A (ko) * 2019-11-19 2021-05-27 일동제약(주) 벤조나이트릴이 치환된 축합 피리미딘 유도체 및 그의 의약 용도
US11806350B2 (en) 2020-11-19 2023-11-07 Ildong Pharmaceutical Co., Ltd. Prevention and/or treatment of CNS disorders

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL264338A (de) * 1960-05-04
GB1004073A (en) * 1962-08-13 1965-09-08 Merck & Co Inc Veterinary antihelmintic compositions comprising benzimidazole derivatives
JPS5441331A (en) * 1977-06-29 1979-04-02 Sandoz Ag Antiistout agent
US4212876A (en) 1978-06-21 1980-07-15 Sandoz, Inc. Substituted or unsubstituted 2-phenylbenzimidazoles as anti-obesity agents
JPS60260579A (ja) 1984-01-13 1985-12-23 Yoshitomi Pharmaceut Ind Ltd プリン誘導体
JPS61158983A (ja) * 1984-12-28 1986-07-18 Yoshitomi Pharmaceut Ind Ltd プリン誘導体
SU1282506A1 (ru) * 1985-05-11 1997-12-10 Институт физико-органической химии и углехимии АН УССР 2-(3',4',5'-триметоксифенил)-1-метилимидазо (4,5-с)пиридингидрохлорид, обладающий спазмолитической и гипотензивной активностью
US4772600A (en) 1986-06-09 1988-09-20 A. H. Robins Company, Inc. Fused imidazoheterocyclic compounds and pharmaceutical compositions
US4714762A (en) 1986-10-31 1987-12-22 Warner-Lambert Company Antiarteriosclerotic substituted benzimidazol-2-yl-and 3H-imidazo[4,5-b]pyridin-2-yl-phenoxy-alkanoic acids and salts and esters thereof
JP2869561B2 (ja) * 1989-05-22 1999-03-10 大塚製薬株式会社 血小板粘着抑制剤
US5117830A (en) * 1990-11-08 1992-06-02 Whitby Research, Inc. Method of determining viability of tissue
GB9125001D0 (en) 1991-11-25 1992-01-22 Ici Plc Heterocyclic compounds
CN1046724C (zh) 1993-12-29 1999-11-24 藤泽药品工业株式会社 吡唑并吡啶化合物、含有它们的药物组合物、及其制法与用途
JPH07243069A (ja) * 1994-03-08 1995-09-19 Murata:Kk 金属表面の電解処理方法
US5552426A (en) * 1994-04-29 1996-09-03 Eli Lilly And Company Methods for treating a physiological disorder associated with β-amyloid peptide
JPH11508267A (ja) 1995-06-26 1999-07-21 藤沢薬品工業株式会社 ピラゾール化合物および医薬組成物
AU2207897A (en) * 1996-03-11 1997-10-01 Eli Lilly And Company Methods of treating or preventing interstitial cystitis
WO1997037072A1 (en) * 1996-04-02 1997-10-09 Microfibres, Inc. Improved printed flocked pile fabric and method for making same
WO1998001459A1 (en) 1996-07-05 1998-01-15 Novo Nordisk A/S Novel n-alkoxyadenine derivatives acting as cytokine inhibitors
AUPO111096A0 (en) 1996-07-18 1996-08-08 Fujisawa Pharmaceutical Co., Ltd. New compound
JP4021964B2 (ja) * 1996-12-26 2007-12-12 トーアエイヨー株式会社 ピリダジノン誘導体、その製造法およびそれを含有するアデノシンa1拮抗剤
US6284748B1 (en) 1997-03-07 2001-09-04 Metabasis Therapeutics, Inc. Purine inhibitors of fructose 1,6-bisphosphatase
AU1688599A (en) * 1998-01-05 1999-07-26 Eisai Co. Ltd. Purine derivatives and adenosine a2 receptor antagonists serving as preventives/remedies for diabetes
JP3990061B2 (ja) * 1998-01-05 2007-10-10 エーザイ・アール・アンド・ディー・マネジメント株式会社 プリン誘導体および糖尿病の予防・治療剤としてのアデノシンa2受容体拮抗剤
AU3538899A (en) * 1998-04-30 1999-11-23 Nippon Chemiphar Co. Ltd. Condensed imidazole derivative and therapeutic agent for liver disease

Also Published As

Publication number Publication date
DK1221444T3 (da) 2005-11-14
EP1221444A1 (de) 2002-07-10
US6841549B1 (en) 2005-01-11
DE60022366T2 (de) 2006-06-14
AU5571700A (en) 2001-01-22
WO2001002400A1 (en) 2001-01-11
NZ516260A (en) 2004-08-27
DE60022366D1 (de) 2005-10-06
KR100694684B1 (ko) 2007-03-13
WO2001002400A8 (en) 2001-04-05
EP1221444A4 (de) 2003-05-07
CN1166666C (zh) 2004-09-15
JP4324338B2 (ja) 2009-09-02
ES2246867T3 (es) 2006-03-01
CA2376835C (en) 2009-09-15
EP1221444B1 (de) 2005-08-31
CA2376835A1 (en) 2001-01-11
KR20020015060A (ko) 2002-02-27
PT1221444E (pt) 2005-11-30
AU778450B2 (en) 2004-12-09
CN1365361A (zh) 2002-08-21

Similar Documents

Publication Publication Date Title
ATE303387T1 (de) Kondensierte imidazolderivate und arzneimittel gegen diabetes mellitus
EE200300403A (et) N-asendatud mittearomaatne heterotsükliline ühend, seda sisaldav ravimkompositsioon ning ühendi kasutamine ravimina
ATE388958T1 (de) 4'-c-substituierte 2-haloadenosinderivate
DK1213296T3 (da) Glucopyranosyloxpyrazolderivater, lægemidler indeholdende samme samt mellemprodukter til fremstilling heraf
WO2004048345A3 (en) 2,5-diketopiperazines for the treatment of obesity
PT976748E (pt) Derivados de pirrolidina com actividade inibidora de fosfolipase a2
NO985518L (no) Morfinanderivater og medisinsk anvendelse derav
ATE316089T1 (de) Isoindolderivate
NO20052074L (no) Substituerte benzoksazinoner og anvendelser derav.
ATE503746T1 (de) Neue imidazolidinderivate
NO20025035D0 (no) Oksadiazolderivater som har anticancer-effekter
DE60032016D1 (de) Zyklische aminverbindungen als ccr5-rezeptor antagonisten
DK1454903T3 (da) Thiadiazolinderivater til behandling af cancer
DE60330758D1 (de) Bestimmte pharmazeutisch wertvolle substituierte aminoalkyl-heterocyclen
ATE402151T1 (de) 2-(arylphenyl)amino-imidazolin-derivate
WO2004080411A3 (en) Melanin-concentrating hormone receptor antagonists and compositions and methods related thereto
IL169577A0 (en) Oligosaccharide derivatives and pharmaceutical compostions containing the same
ATE319452T1 (de) Arzneimittel gegen essstörungen
WO2007000392A3 (en) Chloro-substituted guanidines
DE60238847D1 (de) Pyrimidinderivate enthaltendes medikament
ATE262522T1 (de) Benzimidazolverbindungen

Legal Events

Date Code Title Description
UEP Publication of translation of european patent specification

Ref document number: 1221444

Country of ref document: EP

EEIH Change in the person of patent owner
REN Ceased due to non-payment of the annual fee