Literature DB >> 2753934

Reaction of o-phthalaldehyde with amino acids and glutathione. Application to high-performance liquid chromatography determination.

G Morineau1, M Azoulay, F Frappier.   

Abstract

Experimental conditions were found for the preparation of stable fluorescent adducts of o-phthalaldehyde with glutathione and its metabolites: glutamine, glutamic and aspartic acids, gamma-glutamylglutamine and gamma-glutamylglutamylglutamine. The structure of the glutathione isoindole derivative obtained was confirmed by NMR studies. The procedure was applied to reversed-phase high-performance liquid chromatographic separation of the previous compounds. The method was extended to glutathione and "total glutathione" determinations.

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Year:  1989        PMID: 2753934     DOI: 10.1016/s0021-9673(01)93965-2

Source DB:  PubMed          Journal:  J Chromatogr


  3 in total

1.  Sulfur K-edge x-ray absorption spectroscopy: a spectroscopic tool to examine the redox state of S-containing metabolites in vivo.

Authors:  A Rompel; R M Cinco; M J Latimer; A E McDermott; R D Guiles; A Quintanilha; R M Krauss; K Sauer; V K Yachandra; M P Klein
Journal:  Proc Natl Acad Sci U S A       Date:  1998-05-26       Impact factor: 11.205

2.  A three enzyme pathway for 2-amino-3-hydroxycyclopent-2-enone formation and incorporation in natural product biosynthesis.

Authors:  Wenjun Zhang; Megan L Bolla; Daniel Kahne; Christopher T Walsh
Journal:  J Am Chem Soc       Date:  2010-05-12       Impact factor: 15.419

3.  Biosynthesis of 2-amino-3-hydroxycyclopent-2-enone moiety of bafilomycin in Kitasatospora cheerisanensis KCTC2395.

Authors:  Nguyen Phan Kieu Hanh; Jae Yoon Hwang; Hye Ryeung Oh; Geum Jin Kim; Hyukjae Choi; Doo Hyun Nam
Journal:  J Microbiol       Date:  2018-07-25       Impact factor: 3.422

  3 in total

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