Literature DB >> 14077025

TAUTOMERISM AND PROTONATION OF GUANOSINE.

H T MILES, F B HOWARD, J FRAZIER.   

Abstract

Guanosine has been demonstrated, by infrared and nuclear magnetic resonance spectroscopy, to have a keto-amino structure in neutral aqueous solution and to undergo protonation at N(7) in acid solution.

Entities:  

Keywords:  NUCLEOSIDES; SPECTRUM ANALYSIS

Mesh:

Substances:

Year:  1963        PMID: 14077025     DOI: 10.1126/science.142.3598.1458

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  2 in total

1.  THE STRUCTURE OF THE THREE-STRANDED HELIX, POLY (A+2U).

Authors:  H T MILES
Journal:  Proc Natl Acad Sci U S A       Date:  1964-06       Impact factor: 11.205

2.  The nucleoside-copper (II) interaction and the tautomeric forms of the nucleosides.

Authors:  H Fritzsche; D Tresselt; C Zimmer
Journal:  Experientia       Date:  1971
  2 in total

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