SCHRAM, Karl, Petra MIKETOVA, Jiří SLANINA, Otakar HUMPA and Eva TÁBORSKÁ. Mass spectrometry of 1,3- and 1,5-dicaffeoylquinic acids. Journal of Mass Spectrometry. John Wiley & Sons, Ltd., 2004, vol. 39, No 4, p. 384-395. ISSN 1076-5174.
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Basic information
Original name Mass spectrometry of 1,3- and 1,5-dicaffeoylquinic acids
Name in Czech Hmotnostní spektrometrie 1,3- and 1,5-dicaffeoylchinové kyseliny
Authors SCHRAM, Karl (840 United States of America), Petra MIKETOVA (724 Spain), Jiří SLANINA (203 Czech Republic, guarantor), Otakar HUMPA (203 Czech Republic) and Eva TÁBORSKÁ (203 Czech Republic).
Edition Journal of Mass Spectrometry, John Wiley & Sons, Ltd. 2004, 1076-5174.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10401 Organic chemistry
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 3.056
RIV identification code RIV/00216224:14110/04:00011442
Organization unit Faculty of Medicine
UT WoS 000220860200006
Keywords in English tandem mass spectrometry; natural products; dicaffeoylquinic acids; electrospray ionization
Tags dicaffeoylquinic acids, electrospray ionization, natural products, tandem mass spectrometry
Tags International impact, Reviewed
Changed by Changed by: Mgr. Jiří Slanina, Ph.D., učo 689. Changed: 20/6/2009 00:01.
Abstract
Samples of 1,3- (1) and 1,5-dicaffeoylquinic acid (2) and their hexaacetate derivatives were examined using positive and negative electrospray ionization mass spectrometry and tandem mass spectrometry. Differences in the various spectra allow the discrimination of each of the isomers. Specific losses in the spectra of 2 also permit the identification of the site of substitution of one of the caffeic acid moieties as being at the 5-position. The spectra of 3,5- (3) and 4,5-dicaffeoylquinic (4) acids and their hexaacetate derivatives were compared with those of 1 and 2 and their derivatives, and differences in ion abundances or the presence/absence of specific ions can be used to identify uniquely each of the compounds.
Abstract (in Czech)
Vzorky 1,3-dicaffeoylchinové kyseliny a 1,5-dicaffeoylchinové kyseliny a jejich hexaacetylderivátů byly studovány pomocí pozitivní a negativní hmotnostní spektrometrie spojené s ionizací elektrosprejem a tandemovou hmotnostní spektrometrii. Rozdíly v různých spektrech umožňují rozlišení každého izomeru.
Links
GA303/00/D062, research and development projectName: Biologická dostupnost a mechanismus antioxidačního účinku fenolických kyselin a lignanů
Investor: Czech Science Foundation, Bioavailability and mechanism of antioxidant activity of phenolic acids and lignans
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