NO20002696L - Nye forbindelser med cGMP-PDE-inhibitoreffekt - Google Patents

Nye forbindelser med cGMP-PDE-inhibitoreffekt

Info

Publication number
NO20002696L
NO20002696L NO20002696A NO20002696A NO20002696L NO 20002696 L NO20002696 L NO 20002696L NO 20002696 A NO20002696 A NO 20002696A NO 20002696 A NO20002696 A NO 20002696A NO 20002696 L NO20002696 L NO 20002696L
Authority
NO
Norway
Prior art keywords
cgmp
pde inhibitor
compounds
new compounds
pde
Prior art date
Application number
NO20002696A
Other languages
English (en)
Other versions
NO20002696D0 (no
Inventor
Masayuki Ohashi
Hidemitsu Nishida
Toshiyuki Shudo
Original Assignee
Mochida Pharm 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 Mochida Pharm Co Ltd filed Critical Mochida Pharm Co Ltd
Publication of NO20002696D0 publication Critical patent/NO20002696D0/no
Publication of NO20002696L publication Critical patent/NO20002696L/no

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic 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
    • C07D498/06—Peri-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic 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
    • C07D471/02—Heterocyclic 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
    • C07D471/06—Peri-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/06—Peri-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Nye, kondenserte, tetra- sykliske, heterosykliske forbindelser med en sterk og svært selektiv virk- ning på inhibering av syklisk GMP- fosfodiesterase (cGMP-PDE) og en høy sikkerhet; fremgangsmåte for frem- stilling av de samme; legemidler som er kjennetegnet ved å inneholde minst en av disse forbindelsene som den aktive bestanddel, særlig preventive og/eller behandlende midler for pul- monal hypertensjon, iskemiske hjerte- sykdommer, erektil insuffisiens, kvinnelig seksuell dysfunksjon eller sykdommer som cGMP-PDE-inhibitorvirk- ninger er virkningsfulle mot; og mellomprodukter som kan anvendes ved fremstilling av de ovenfor nevnte forbindelser.
NO20002696A 1997-11-28 2000-05-26 Nye forbindelser med cGMP-PDE-inhibitoreffekt NO20002696L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP34416497 1997-11-28
PCT/JP1998/005350 WO1999028319A1 (en) 1997-11-28 1998-11-27 NOVEL COMPOUNDS HAVING cGMP-PDE INHIBITORY EFFECT

Publications (2)

Publication Number Publication Date
NO20002696D0 NO20002696D0 (no) 2000-05-26
NO20002696L true NO20002696L (no) 2000-07-24

Family

ID=18367131

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20002696A NO20002696L (no) 1997-11-28 2000-05-26 Nye forbindelser med cGMP-PDE-inhibitoreffekt

Country Status (14)

Country Link
US (1) US6476021B1 (no)
EP (1) EP1048666A4 (no)
KR (1) KR20010032546A (no)
CN (1) CN1284075A (no)
AU (1) AU746883B2 (no)
BR (1) BR9815070A (no)
CA (1) CA2311947A1 (no)
HU (1) HUP0100083A3 (no)
IL (1) IL136340A0 (no)
MX (1) MXPA00005190A (no)
NO (1) NO20002696L (no)
PL (1) PL340789A1 (no)
WO (1) WO1999028319A1 (no)
ZA (1) ZA9810766B (no)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3933870B2 (ja) 1998-06-23 2007-06-20 グラクソ グループ リミテッド ２−（プリン−９−イル）−テトラヒドロフラン−３，４−ジオール誘導体
AU5204800A (en) * 1999-06-21 2001-01-09 Biochemical Pharmaceutical Factory of Zhuhai Sez, The Process for preparing sildenafil, and troche which comprises sildenafil and apomorphine
DE19954707A1 (de) * 1999-11-13 2001-05-17 Merck Patent Gmbh Imidazolverbindungen als Phosphodiesterase VII-Hemmer
HK1054039B (zh) 2000-03-15 2010-04-16 萨诺费－阿文蒂斯德国有限公司 取代的β-咔啉
EP1268477B1 (en) * 2000-03-15 2010-04-21 Sanofi-Aventis Deutschland GmbH Substituted beta-carbolines with ikb-kinase inhibiting activity
US20020006926A1 (en) 2000-04-19 2002-01-17 Roylance H. H. Use of cyclic GMP-specific phosphodiesterase inhibitors for treatment of parkinson's disease
US6271228B1 (en) * 2000-04-28 2001-08-07 Pfizer Inc. Blood pressure stabilization during hemodialysis
UA80258C2 (en) * 2001-09-06 2007-09-10 Biogen Inc Methods of treating pulmonary disease
US20050107394A1 (en) * 2001-12-17 2005-05-19 Ardeschir Ghofrani Novel use of selective pde5 inhibitors
GB0202254D0 (en) * 2002-01-31 2002-03-20 Pfizer Ltd Prevention of scarring
US8133903B2 (en) 2003-10-21 2012-03-13 Los Angeles Biomedical Research Institute at Harbor—UCLA Medical Center Methods of use of inhibitors of phosphodiesterases and modulators of nitric oxide, reactive oxygen species, and metalloproteinases in the treatment of peyronie's disease, arteriosclerosis and other fibrotic diseases
US7662831B2 (en) * 2006-07-27 2010-02-16 Wyeth Llc Tetracyclic indoles as potassium channel modulators
US7601856B2 (en) 2006-07-27 2009-10-13 Wyeth Benzofurans as potassium ion channel modulators
WO2017168174A1 (en) 2016-04-02 2017-10-05 N4 Pharma Uk Limited New pharmaceutical forms of sildenafil
CN115872991B (zh) * 2021-09-26 2024-08-23 深圳大学 β-咔伯啉生物碱类化合物及其药用组合物、制备方法和应用

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CS261338B1 (cs) * 1987-09-17 1989-06-15 Viktor Zikan Způsob přípravy 10-nitro-4-oxo-4H-chino/2,3,4-i,j//1,4/benzoxazinových derivátů
GB9126260D0 (en) * 1991-12-11 1992-02-12 Pfizer Ltd Therapeutic agents
PH31122A (en) * 1993-03-31 1998-02-23 Eisai Co Ltd Nitrogen-containing fused-heterocycle compounds.
JPH0710843A (ja) * 1993-03-31 1995-01-13 Eisai Co Ltd 含窒素縮合複素環化合物
DE69533057T2 (de) * 1994-08-09 2005-06-16 Eisai Co., Ltd. Kondensierte pyridazinverbindungen
GB9423910D0 (en) * 1994-11-26 1995-01-11 Pfizer Ltd Therapeutic agents
JP3713783B2 (ja) * 1995-01-20 2005-11-09 大正製薬株式会社 １Ｈ−ピラゾロ［３，４−ｄ］ピリミジン−４−オン誘導体
EP0985671B1 (en) * 1996-05-31 2003-04-02 Mochida Pharmaceutical Co., Ltd. PYRIDOCARBAZOLE DERIVATIVES HAVING cGMP-PDE INHIBITORY EFFECT
WO1998053819A1 (en) * 1997-05-29 1998-12-03 Mochida Pharmaceutical Co., Ltd. Therapeutic agent for erection failure
WO1999026946A1 (en) * 1997-11-26 1999-06-03 Mochida Pharmaceutical Co., Ltd. PYRIDOCARBAZOLE DERIVATIVES WITH cGMP-PDE INHIBITORY ACTIVITY

Also Published As

Publication number Publication date
AU1261799A (en) 1999-06-16
BR9815070A (pt) 2000-10-03
MXPA00005190A (es) 2002-04-24
KR20010032546A (ko) 2001-04-25
PL340789A1 (en) 2001-02-26
CA2311947A1 (en) 1999-06-10
US6476021B1 (en) 2002-11-05
EP1048666A4 (en) 2001-10-31
ZA9810766B (en) 1999-05-25
IL136340A0 (en) 2001-05-20
HUP0100083A2 (hu) 2001-08-28
CN1284075A (zh) 2001-02-14
WO1999028319A1 (en) 1999-06-10
EP1048666A1 (en) 2000-11-02
AU746883B2 (en) 2002-05-02
HUP0100083A3 (en) 2002-01-28
NO20002696D0 (no) 2000-05-26

Similar Documents

Publication Publication Date Title
NO20002696L (no) Nye forbindelser med cGMP-PDE-inhibitoreffekt
WO2003000343A3 (en) Administration of phosphodiesterase inhibitors for the treatment of premature ejaculation
BR0313743A (pt) Benzimidazol quinolinonas e usos destas
MXPA04012965A (es) Inhibidores virales.
EA200400735A1 (ru) 3-β-D-РИБОФУРАНОЗИЛТИАЗОЛО[4,5-d]ПИРИМИДИННУКЛЕОЗИДЫ И ИХ ПРИМЕНЕНИЯ
BG106762A (en) Polycycloalkylpurines as adenosine receptor antagonists
NO20072548L (no) Xantinderivater med HM74A reseptoraktivitet
WO2005000298A3 (en) 5-membered heterocycle-based p-38 inhibitors
WO2004013300A3 (en) Compounds with the bicyclo[4.2.1]nonane system for the treatment of flaviviridae infections
NO20012514D0 (no) Fremgangsmåte for fremstilling av partikler med en omdannet amorf og/eller meta-stabil krystallinsk region til krystallinsktilstand
EP1254899A3 (en) Piperazine derivatives and their use as anti-inflammatory agents
EP0668863A1 (en) CHINUCLIDINE DERIVATIVE AS SUBSTANCE P ANTAGONIST.
WO2002060392A3 (en) Use of gal3 receptor antagonists for the treatment of depression and/or anxiety and compounds useful in such methods
NO20022442D0 (no) Legemidler for sykdommer i forbindelse med reduksjon i benmasse
NO990433L (no) Nye forbindelser og blandinger for behandling av sykdommer i forbindelse med tryptase-aktivitet
WO2002028865A3 (en) Condensed pyridoindole derivatives
EA200000355A2 (ru) Промышленные изделия
BR9809508A (pt) Agente terapêutico para disfunção de ereção
ATE457177T1 (de) Kombinationstherapie zur behandlung respiratorischer krankheiten mittels antikörper und anti-entzündungs wirkstoffe
WO2002079169A8 (en) Cyano-substituted dihydropyrimidine compounds and their use to treat diseases
DK531089A (da) Bicycliske imidazolforbindelser til anvendelse ved behandling af hyperaldosteronisme
BR0010693A (pt) Derivados azaindol para tratamento de depressão
RU94038256A (ru) Производные пиразолопиримидина, способ их получения, фармацевтические композиции на их основе
DE69834500D1 (de) Xanthinderivative zur behandlung von hirnischämie
IS6380A (is) Mótlyf viðtaka adenósíns og aðferðir til að búa þau til og nota

Legal Events

Date Code Title Description
FC2A Withdrawal, rejection or dismissal of laid open patent application