Literature DB >> 18265

Determination of the preferred tautomeric form histamine by 13C nmr spectroscopy.

W F Reynolds, C W Tzeng.   

Abstract

The pH-dependent 13C chemical shifts for histamine indicate an approximate 4: 1 preference for the N-H tautomer of the imidazole ring, similar to that previously deduced for L-histidine. It is concluded that the 13C chemical shift method is a complimentary technique to the method of determining tautomer preference from pK values. Factors determining the tautomer preference in histamine and L-histidine are discussed.

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Year:  1977        PMID: 18265     DOI: 10.1139/o77-082

Source DB:  PubMed          Journal:  Can J Biochem        ISSN: 0008-4018


  3 in total

1.  pH-dependent random coil (1)H, (13)C, and (15)N chemical shifts of the ionizable amino acids: a guide for protein pK a measurements.

Authors:  Gerald Platzer; Mark Okon; Lawrence P McIntosh
Journal:  J Biomol NMR       Date:  2014-09-20       Impact factor: 2.835

2.  Organotin-protein interactions. Binding of triethyltin bromide to cat haemoglobin.

Authors:  K R Siebenlist; F Taketa
Journal:  Biochem J       Date:  1986-01-15       Impact factor: 3.857

3.  The Incorporation of Labile Protons into Multidimensional NMR Analyses: Glycan Structures Revisited.

Authors:  Mihajlo Novakovic; Marcos D Battistel; Hugo F Azurmendi; Maria-Grazia Concilio; Darón I Freedberg; Lucio Frydman
Journal:  J Am Chem Soc       Date:  2021-06-04       Impact factor: 15.419

  3 in total

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