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A Comprehensive LC/MS Analysis of Novel Cyclopentenedione Library.

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    0466008 - ÚCHP 2017 RIV NL eng J - Článek v odborném periodiku
    Papoušková, B. - Bernard, Martin - Ottenschlager, Jakub - Karban, Jindřich - Velíšek, Petr - Hrbáč, J. - Sýkora, Jan - Storch, Jan - Vacek, J.
    A Comprehensive LC/MS Analysis of Novel Cyclopentenedione Library.
    Journal of Pharmaceutical and Biomedical Analysis. Roč. 128, SEP 5 (2016), s. 342-351. ISSN 0731-7085
    Institucionální podpora: RVO:67985858
    Klíčová slova: bioactive cyclopentenediones * liquid chromatography * mass spectrometry
    Kód oboru RIV: CF - Fyzikální chemie a teoretická chemie
    Impakt faktor: 3.255, rok: 2016

    Here we focused on the design and synthesis of a library of novelized benzylidene CPD derivatives that were consequently characterized by ultra-high performance liquid chromatography (UHPLC) on-line connected with tandem mass spectrometry (MS/MS). The library design was based on a 2-benzylidene-4-cyclopentene-1,3-dione skeleton substituted with a variety of hydroxy, methoxy, halogen, linear aliphatic, heterocyclic and saccharide moieties, primarily modulating the skeleton's hydrophobicity. The prepared CPDs were effectively ionized by positive/negative atmospheric pressure photoionization (APPI) and atmospheric pressure chemical ionization (APCI). After careful optimization of the dopant composition and flow rate, positive-mode APPI proved to be more sensitive than APCI. In negative mode, both ionization techniques gave similar results. Further, a detailed MS fragmentation study was performed, confirming the structure of the compounds and enabling positional isomers of CPDs to be differentiated on the basis of their collision spectra analysis. Finally, an optimization of the composition of the mobile phase and reversed-phased separation mode were done, followed by a selection of the most suitable UHPLC stationary phases, i.e. C-18, C-8 and phenyl. The applicability of the method was evaluated by the inclusion of the other two substances in the study, i.e. monomeric and dimeric bioactive CPDs, compound TX-1123 and nostotrebin 6 with cytostatic and antimicrobial activities, respectively. The results presented here could be used in further investigations of the chromatographic retention and MS behavior of CPDs, which could be utilized for their isolation, detailed characterization and analysis in biological systems.
    Trvalý link: http://hdl.handle.net/11104/0264466
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