ES2141137T3 - Agentes terapeuticos para la enfermedad de parkinson. - Google Patents

Agentes terapeuticos para la enfermedad de parkinson.

Info

Publication number
ES2141137T3
ES2141137T3 ES93307654T ES93307654T ES2141137T3 ES 2141137 T3 ES2141137 T3 ES 2141137T3 ES 93307654 T ES93307654 T ES 93307654T ES 93307654 T ES93307654 T ES 93307654T ES 2141137 T3 ES2141137 T3 ES 2141137T3
Authority
ES
Spain
Prior art keywords
straight
alkoxy
branched chain
naphthyl
halogen
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.)
Expired - Lifetime
Application number
ES93307654T
Other languages
English (en)
Inventor
Fumio Suzuki
Junichi Shimada
Nobuaki Koike
Joji Nakamura
Shizuo Shiozaki
Shunji Ichikawa
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.)
KH Neochem Co Ltd
Original Assignee
Kyowa Hakko Kogyo 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 Kyowa Hakko Kogyo Co Ltd filed Critical Kyowa Hakko Kogyo Co Ltd
Application granted granted Critical
Publication of ES2141137T3 publication Critical patent/ES2141137T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D473/00—Heterocyclic compounds containing purine ring systems
    • C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/04—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
    • C07D473/06—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/08—Bronchodilators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/24—Antidepressants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/26—Psychostimulants, e.g. nicotine, cocaine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D473/00—Heterocyclic compounds containing purine ring systems
    • C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/04—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
    • C07D473/06—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
    • C07D473/08—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3 with methyl radicals in positions 1 and 3, e.g. theophylline
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D473/00—Heterocyclic compounds containing purine ring systems
    • C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/04—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
    • C07D473/06—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
    • C07D473/12—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3 with methyl radicals in positions 1, 3, and 7, e.g. caffeine

Landscapes

  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Hospice & Palliative Care (AREA)
  • Pulmonology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Radar Systems Or Details Thereof (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

SE PRESENTAN DERIVADOS DE LA XANTINA COMO AGENTES TERAPEUTICOS PARA LA ENFERMEDAD DE PARKINSON, QUE TIENEN LA FORMULA: EN QUE: R1 Y R2 REPRESENTAN CADA UNO METILO O ETILO; R3 REPRESENTA HIDROGENO, ALKILO C1-C6 DE CADENA RECTA O RAMIFICADA O ALKINILO O ALKELINO C2-C6 DE CADENA RECTA O RAMIFICADA; R4 REPRESENTA CICLOALKILO C3-C8; UN GRUPO -(CH2)N-R5 DONDE N ES 0 O UN ENTERO DE 1 A 4 Y R5 REPRESENTA FENILO, NAFTILO O UN GRUPO HETEROCICLICO O UN GRUPO FENILO, NAFTILO O HETEROCICLICO SUSTITUIDO QUE CONTIENE DE 1 A 4 SUSTITUYENTES SELECCIONADOS DEL ALKILO C1-C6, ALCOXI C1-C6, HIDROXI, HALOGENO, NITRO, AMINO, MONO O DIALKILAMINO C1-C6, TIFLUOROMETILO, BENCILOXI, FENILO, FENOXI O ALCOXI C1-C6 SUSTITUIDO POR HIDROXI, ALCOXI C1-C6, HALOGENO, NITRO, AZIDA, CARBOXI O (C1-C6 ALCOXI)CARBONILO; O UN GRUPO DONDE Y1 E Y2 REPRESENTAN CADA UNO HIDROGENO, HALOGENO O ALKILO C1-C6 DE CADENA RECTA O RAMIFICADA; Y Z REPRESENTA UN GRUPO EN QUE R6 REPRESENTA HIDROGENO, HIDROXI, ALKILO C1-C6 DE CADENA RECTA O RAMIFICADA, ALCOXI C1-C6 DE CADENA RECTA O RAMIFICADA, HALOGENO, NITRO O AMINO Y M REPRESENTA UN ENTERO DE 1 A 4; UN GRUPO FENILO, NAFTILO O HETEROCICLICO O UN GRUPO FENILO, NAFTILO O HETEROCICLICO SUSTITUIDO IGUAL A COMO SE HA DEFINIDO EN R5; Y X1 Y X2 REPRESENTA CADA UNO O O S; O UNA SAL FARMACEUTICAMENTE ACEPTABLE DE LOS MISMOS.
ES93307654T 1992-09-28 1993-09-28 Agentes terapeuticos para la enfermedad de parkinson. Expired - Lifetime ES2141137T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP25783492 1992-09-28

Publications (1)

Publication Number Publication Date
ES2141137T3 true ES2141137T3 (es) 2000-03-16

Family

ID=17311787

Family Applications (1)

Application Number Title Priority Date Filing Date
ES93307654T Expired - Lifetime ES2141137T3 (es) 1992-09-28 1993-09-28 Agentes terapeuticos para la enfermedad de parkinson.

Country Status (10)

Country Link
EP (1) EP0590919B1 (es)
JP (1) JP2613355B2 (es)
AT (1) ATE188216T1 (es)
CA (1) CA2107014C (es)
DE (1) DE69327438T2 (es)
DK (1) DK0590919T3 (es)
ES (1) ES2141137T3 (es)
GR (1) GR3032972T3 (es)
NO (1) NO304946B1 (es)
PT (1) PT590919E (es)

Families Citing this family (44)

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AU6781194A (en) * 1993-05-03 1994-11-21 United States Of America, Represented By The Secretary, Department Of Health And Human Services, The 8-substituted 1,3,7-trialkyl-xanthine derivatives as a2-selective adenosine receptor antagonists
GB9312853D0 (en) 1993-06-22 1993-08-04 Euro Celtique Sa Chemical compounds
DE69526822T2 (de) * 1994-02-23 2003-01-23 Kyowa Hakko Kogyo K.K., Tokio/Tokyo Xanthin-derivate
US5620676A (en) * 1994-03-08 1997-04-15 The United States Of America As Represented By The Department Of Health And Human Services Biologically active ATP analogs
US5591776A (en) 1994-06-24 1997-01-07 Euro-Celtique, S.A. Pheynl or benzyl-substituted rolipram-based compounds for and method of inhibiting phosphodiesterase IV
US5922751A (en) 1994-06-24 1999-07-13 Euro-Celtique, S.A. Aryl pyrazole compound for inhibiting phosphodiesterase IV and methods of using same
GB9415529D0 (en) * 1994-08-01 1994-09-21 Wellcome Found Phenyl xanthine derivatives
EP0814809B1 (en) 1994-12-13 2003-08-13 Euroceltique S.A. Aryl thioxanthines
JP2001523213A (ja) 1994-12-13 2001-11-20 ユーロ−セルティーク，エス．エイ． 三置換チオキサンチン類
US6166041A (en) 1995-10-11 2000-12-26 Euro-Celtique, S.A. 2-heteroaryl and 2-heterocyclic benzoxazoles as PDE IV inhibitors for the treatment of asthma
US6075016A (en) 1996-04-10 2000-06-13 Euro-Celtique S.A. 6,5-fused aromatic ring systems having enhanced phosphodiesterase IV inhibitory activity
US5864037A (en) * 1996-06-06 1999-01-26 Euro-Celtique, S.A. Methods for the synthesis of chemical compounds having PDE-IV inhibitory activity
GB9703044D0 (en) 1997-02-14 1997-04-02 Glaxo Group Ltd Phenyl xanthine esters and amides
DE69834500T2 (de) * 1997-09-05 2007-05-03 Kyowa Hakko Kogyo Co., Ltd. Xanthinderivative zur behandlung von hirnischämie
AU1507099A (en) * 1997-12-15 1999-07-05 Kyowa Hakko Kogyo Co. Ltd. Preventives/remedies for sleep disturbance
GB9817623D0 (en) 1998-08-13 1998-10-07 Glaxo Group Ltd Pharmaceutical compounds
WO2000069464A1 (en) * 1999-05-12 2000-11-23 Fujisawa Pharmaceutical Co., Ltd. Novel use
ATE319452T1 (de) * 1999-10-29 2006-03-15 Kyowa Hakko Kogyo Kk Arzneimittel gegen essstörungen
EE05643B1 (et) * 2001-02-24 2013-04-15 Boehringer Ingelheim Pharma Gmbh & Co. Kg Ksantiini derivaadid, nende valmistamine ja kasutamine ravimina
TWI330183B (es) 2001-10-22 2010-09-11 Eisai R&D Man Co Ltd
US20060106040A1 (en) * 2002-12-19 2006-05-18 Michael Grzelak Adenosine A2a receptor antagonists for the treatment of extra-pyramidal syndrome and other movement disorders
EP1626049B1 (en) * 2003-05-09 2012-02-22 Kyowa Hakko Kirin Co., Ltd. Microcrystal of (E)-8-(3,4-dimethoxystyryl)-1,3-diethyl-7-methyl-3,7-dihydro-1H-purine-2,6-dione
TW200507882A (en) * 2003-07-17 2005-03-01 Kyowa Hakko Kogyo Kk Solid formulations
TWI346114B (en) * 2003-09-29 2011-08-01 Method for stabilization of diarylvinylene compounds
CA2554426C (en) 2004-01-28 2012-10-16 Kyowa Kirin Co., Ltd. Agents for treating migraine
JP5188066B2 (ja) * 2004-12-03 2013-04-24 協和発酵キリン株式会社 薬物依存症の予防および／または治療剤
MX2009006346A (es) * 2006-12-22 2010-03-03 Sanol Arznei Schwarz Gmbh Derivados de 8-etinilxantina como antagonistas de receptores de a2a selectivos.
US8871751B2 (en) 2008-01-18 2014-10-28 The Board Of Trustees Of The University Of Illinois Compositions and methods relating to nuclear hormone and steroid hormone receptors including inhibitors of estrogen receptor alpha-mediated gene expression and inhibition of breast cancer
EP2657236A4 (en) * 2010-11-24 2014-02-26 Yamasa Corp NEW 2-ALKYNYL-N9-PROPARGYLADENINE AND ITS MEDICAL USE
RU2477726C1 (ru) * 2011-10-18 2013-03-20 Общество С Ограниченной Ответственностью "Ньювак" (Ооо "Ньювак") Замещенные феноксиуксусные кислоты, их эфиры и амиды, включающие 2,6-диоксо-2,3,6,7-тетрагидро-1н-пурин-8-иловый фрагмент, - антагонисты аденозинового a2a рецептора и их применение
RU2480469C1 (ru) * 2012-02-03 2013-04-27 Общество С Ограниченной Ответственностью "Ньювак" (Ооо "Ньювак") Замещенные 1,3-диэтил-8-винил-7-метил-3,7-дигидро-пурин-2,6-дионы-антагонисты аденозинового a2a рецептора и их применение
CN103554109A (zh) * 2013-11-15 2014-02-05 南京华威医药科技开发有限公司 伊曲茶碱多晶型
CN105884776A (zh) * 2014-11-05 2016-08-24 南京瑞天医药科技有限公司 一种伊曲茶碱的新晶型及其制备方法
WO2016148260A1 (ja) * 2015-03-17 2016-09-22 協和発酵キリン株式会社 医薬組成物
KR20170129818A (ko) * 2015-03-19 2017-11-27 교와 핫꼬 기린 가부시키가이샤 레비소체병의 치료 및/또는 예방제
CN110981876B (zh) * 2018-12-21 2021-10-01 广东东阳光药业有限公司 8-取代的苯乙烯基黄嘌呤衍生物及其用途
CN111333648B (zh) * 2019-04-24 2021-05-11 东莞市东阳光新药研发有限公司 8-取代的芳香环乙烯基黄嘌呤衍生物及其用途
CN110041331B (zh) * 2019-05-17 2020-08-07 广东东阳光药业有限公司 苯乙烯基黄嘌呤衍生物及其用途
CN112300165B (zh) * 2019-11-11 2022-03-04 广东东阳光药业有限公司 8-取代的苯乙烯基黄嘌呤衍生物及其用途
CN111018856B (zh) * 2019-12-12 2021-10-01 广东东阳光药业有限公司 8-取代的苯乙烯基黄嘌呤衍生物及其用途
CN111072663B (zh) * 2019-12-12 2021-10-01 广东东阳光药业有限公司 8-取代的苯乙烯基黄嘌呤衍生物及其用途
EP4118083A4 (en) * 2020-03-10 2024-07-03 Marvel Biotechnology PURIN COMPOUNDS FOR THE TREATMENT OF DISEASES
CN111548351B (zh) * 2020-06-22 2021-03-12 连云港贵科药业有限公司 一种伊曲茶碱的合成方法
CN113248505B (zh) * 2021-06-09 2021-09-21 南京安杰新生物医药有限公司 伊曲茶碱去甲基杂质的制备方法

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CA2093403C (en) * 1992-04-08 1999-08-10 Fumio Suzuki Therapeutic agent for parkinson's disease

Also Published As

Publication number Publication date
GR3032972T3 (en) 2000-07-31
JP2613355B2 (ja) 1997-05-28
EP0590919A1 (en) 1994-04-06
NO933452L (no) 1994-03-29
CA2107014A1 (en) 1994-03-29
NO933452D0 (no) 1993-09-27
CA2107014C (en) 2000-06-13
DE69327438T2 (de) 2000-06-21
NO304946B1 (no) 1999-03-08
JPH06211856A (ja) 1994-08-02
EP0590919B1 (en) 1999-12-29
DE69327438D1 (de) 2000-02-03
PT590919E (pt) 2000-04-28
ATE188216T1 (de) 2000-01-15
DK0590919T3 (da) 2000-04-17

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