BE808377A - Coronary dilatory 2,6-diaminonebularine derivs - reaction of 2-halo adenosines and amine; agglomeration-inhibitory - Google Patents

Coronary dilatory 2,6-diaminonebularine derivs - reaction of 2-halo adenosines and amine; agglomeration-inhibitory

Info

Publication number
BE808377A
BE808377A BE138648A BE138648A BE808377A BE 808377 A BE808377 A BE 808377A BE 138648 A BE138648 A BE 138648A BE 138648 A BE138648 A BE 138648A BE 808377 A BE808377 A BE 808377A
Authority
BE
Belgium
Prior art keywords
agglomeration
inhibitory
diaminonebularine
adenosines
derivs
Prior art date
Application number
BE138648A
Other languages
French (fr)
Original Assignee
Takeda Chemical Industries 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 Takeda Chemical Industries Ltd filed Critical Takeda Chemical Industries Ltd
Publication of BE808377A publication Critical patent/BE808377A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/16Purine radicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/08Vasodilators for multiple indications
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hematology (AREA)
  • Biotechnology (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Biochemistry (AREA)
  • Diabetes (AREA)
  • Saccharide Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Cpds. of formula (I): where R = phenyl- or cyclohexyl, opt. substd. with lower alkyl, lower alkoxy or halogen; including acceptable salts of (I) are prepd. by reacting 2-haloadenosin or a cpd. (III): with a cpd. (II); R-Nh2 at 110-150 degrees C in inert solvent such as methylcellosolve or dioxan. In (III) A = a gp. which can form amino with ammonia such as halogen or -SOnR"; R" = H, alkyl or aralkyl; n = 0, 1 or 2; R' = H or acyl. (I) have high-and long-lasting dilatory activity on coronary vessels, and also have inhibitory activity on agglomeration of platelets in mammals.
BE138648A 1972-12-08 1973-12-07 Coronary dilatory 2,6-diaminonebularine derivs - reaction of 2-halo adenosines and amine; agglomeration-inhibitory BE808377A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12360272A JPS5549594B2 (en) 1972-12-08 1972-12-08

Publications (1)

Publication Number Publication Date
BE808377A true BE808377A (en) 1974-06-07

Family

ID=14864659

Family Applications (1)

Application Number Title Priority Date Filing Date
BE138648A BE808377A (en) 1972-12-08 1973-12-07 Coronary dilatory 2,6-diaminonebularine derivs - reaction of 2-halo adenosines and amine; agglomeration-inhibitory

Country Status (3)

Country Link
JP (1) JPS5549594B2 (en)
BE (1) BE808377A (en)
HK (1) HK15179A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5461195A (en) * 1977-10-21 1979-05-17 Takeda Chem Ind Ltd N2-substituted phenyl-2,6-diaminonebularin
JPH0477219U (en) * 1990-11-20 1992-07-06
GB0228723D0 (en) 2002-12-09 2003-01-15 Cambridge Biotechnology Ltd Treatment of pain
SG144146A1 (en) * 2004-03-05 2008-07-29 Cambridge Biotechnology Ltd Adenosine receptor agonists

Also Published As

Publication number Publication date
HK15179A (en) 1979-03-30
JPS5549594B2 (en) 1980-12-12
JPS4980096A (en) 1974-08-02

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