GB853232A - Improvements in or relating to coenzyme a - Google Patents

Improvements in or relating to coenzyme a

Info

Publication number
GB853232A
GB853232A GB28079/57A GB2807957A GB853232A GB 853232 A GB853232 A GB 853232A GB 28079/57 A GB28079/57 A GB 28079/57A GB 2807957 A GB2807957 A GB 2807957A GB 853232 A GB853232 A GB 853232A
Authority
GB
United Kingdom
Prior art keywords
metal salt
coenzyme
aqueous solution
reaction
calcium
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
Application number
GB28079/57A
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.)
MICHAEL ROBILLIART
Original Assignee
MICHAEL ROBILLIART
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 MICHAEL ROBILLIART filed Critical MICHAEL ROBILLIART
Publication of GB853232A publication Critical patent/GB853232A/en
Expired legal-status Critical Current

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
    • C07H19/20Purine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

A stable metal salt reaction product of coenzyme A is obtained by reacting coenzyme A with a water-soluble non-deliquescent metal salt in aqueous solution and then lyophilizing the reaction mixture. The metal salt is suitably a metal salt of a divalent acid and may be a salt of an organic acid or of a mineral acid such as hydrochloric acid. It is preferably a divalent metal salt of a dibasic organic acid. Specified salts are the salts of calcium, copper (cupric), magnesium, cadmium, nickel (nickelous), cobalt (cobaltous), iron (ferrous) and manganese with gluconic, benzoic, citric, acetic, formic, lactic, succinic, tartaric, hydrochloric, sulphuric, and nitric acids in so far as such salts are watersoluble and non-deliquescent. The reaction is preferably carried out by mixing the two reactants in aqueous solution at room temperature and then lyophilizing the solution thus obtained. The product after lyophilization is enzymatically stable and has the same spectrophotometric and chromatographic characteristics as pure coenzyme A stabilized by cold. In aqueous solution the product decomposes by hydrolysis to give coenzyme A. A stoichiometric excess of the metal salt may be used in the reaction. Examples are given in which coenzyme A is reacted with calcium gluconate, calcium benzoate, and calcium citrate respectively in aqueous solution. The solution is then filled into ampoules which are placed in a refrigerator and frozen to-70 DEG C. in 15 minutes. The mixture is then evaporated in vacuo over 10 hours with progressive increase of temperature to about 20 DEG C. and the ampoules are finally filled with nitrogen and sealed.
GB28079/57A 1956-09-05 1957-09-05 Improvements in or relating to coenzyme a Expired GB853232A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US853232XA 1956-09-05 1956-09-05

Publications (1)

Publication Number Publication Date
GB853232A true GB853232A (en) 1960-11-02

Family

ID=22190834

Family Applications (1)

Application Number Title Priority Date Filing Date
GB28079/57A Expired GB853232A (en) 1956-09-05 1957-09-05 Improvements in or relating to coenzyme a

Country Status (1)

Country Link
GB (1) GB853232A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5712258A (en) * 1995-03-23 1998-01-27 The Trustees Of The University Of Pennsylvania Inotropic ADP and ATP analogues and their pharmaceutical compositions
US7348315B2 (en) 1995-03-23 2008-03-25 The University Of Connecticut Methods of treating heart failure with modified ATP, ADP and AMP compounds

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5712258A (en) * 1995-03-23 1998-01-27 The Trustees Of The University Of Pennsylvania Inotropic ADP and ATP analogues and their pharmaceutical compositions
US6255292B1 (en) 1995-03-23 2001-07-03 The Trustees Of The University Of Pennsylvania Purine nucleotide analogues, pharmaceutical compositions thereof, and methods of improving cardiac functions
US7348315B2 (en) 1995-03-23 2008-03-25 The University Of Connecticut Methods of treating heart failure with modified ATP, ADP and AMP compounds

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