Literature DB >> 9080316

Assay for the (R)- and (S)-enantiomers of salsolinols in biological samples and foods with ion-pair high-performance liquid chromatography using beta-cyclodextrin as a chiral mobile phase additive.

Y Deng1, W Maruyama, M Kawai, P Dostert, H Yamamura, T Takahashi, M Naoi.   

Abstract

A chromatographic procedure was devised for the quantitative determination of the enantiomers of salsolinol and N-methylsalsolinol, which are biologically important alkaloids. The enantiomers of salsolinol and N-methylsalsolinol were completely separated using beta-cyclodextrin in a reversed-phase ion-pair system. The HPLC method was sensitive enough to detect the isoquinolines at a concentration less than 0.1 pmol per injection. The presence of (R)- and (S)-salsolinol was confirmed in fermented foods and beverages, while N-methylsalsolinol was not detected. On the other hand, the (R)-enantiomers of both salsolinol and N-methylsalsolinol were found to predominate in the human brain.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9080316     DOI: 10.1016/s0378-4347(96)00359-3

Source DB:  PubMed          Journal:  J Chromatogr B Biomed Sci Appl        ISSN: 1387-2273


  9 in total

1.  Occurrence and distribution of salsolinol-like compound, 1-acetyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline (ADTIQ) in parkinsonian brains.

Authors:  Yulin Deng; Yongqian Zhang; Yujuan Li; Shengyuan Xiao; Dewei Song; Hong Qing; Qin Li; Ali H Rajput
Journal:  J Neural Transm (Vienna)       Date:  2011-11-08       Impact factor: 3.575

2.  Chiral capillary electrophoresis-mass spectrometry of tetrahydroisoquinoline-derived neurotoxins: observation of complex stereoisomerism.

Authors:  Hao Wu; Baiqing Yuan; Yi-Ming Liu
Journal:  J Chromatogr A       Date:  2011-03-21       Impact factor: 4.759

Review 3.  A possible physiological role for cerebral tetrahydroisoquinolines.

Authors:  Jerzy Vetulani; Lucyna Antkiewicz-Michaluk; Irena Nalepa; Mario Sansone
Journal:  Neurotox Res       Date:  2003       Impact factor: 3.911

4.  Quantification of salsolinol enantiomers by stable isotope dilution liquid chromatography with tandem mass spectrometric detection.

Authors:  Min Cai; Yi-Ming Liu
Journal:  Rapid Commun Mass Spectrom       Date:  2008-12       Impact factor: 2.419

5.  Computational Modeling of Inclusion Complexes of β-Cyclodextrin with enantiomers of Salsolinol, N-Methyl-Salsolinol, and 1-Benzyl-Tetrahydroisoquinoline.

Authors:  Ming-Ju Huang; Zhe Quan; Yi-Ming Liu
Journal:  Int J Quantum Chem       Date:  2009       Impact factor: 2.444

6.  Salsolinol, an endogenous compound triggers a two-phase opposing action in the central nervous system.

Authors:  Edyta Możdżeń; Małgorzata Kajta; Agnieszka Wąsik; Tomasz Lenda; Lucyna Antkiewicz-Michaluk
Journal:  Neurotox Res       Date:  2014-12-24       Impact factor: 3.911

Review 7.  Salsolinol: an Unintelligible and Double-Faced Molecule-Lessons Learned from In Vivo and In Vitro Experiments.

Authors:  Magdalena Kurnik-Łucka; Pertti Panula; Andrzej Bugajski; Krzysztof Gil
Journal:  Neurotox Res       Date:  2017-10-23       Impact factor: 3.911

8.  Salsolinol-neurotoxic or Neuroprotective?

Authors:  Magdalena Kurnik-Łucka; Gniewomir Latacz; Adrian Martyniak; Andrzej Bugajski; Katarzyna Kieć-Kononowicz; Krzysztof Gil
Journal:  Neurotox Res       Date:  2019-11-15       Impact factor: 3.911

Review 9.  Brain sites of movement disorder: genetic and environmental agents in neurodevelopmental perturbations.

Authors:  T Palomo; R J Beninger; R M Kostrzewa; T Archer
Journal:  Neurotox Res       Date:  2003       Impact factor: 3.978

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.