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Precursors and formation of pyrithione and other pyridyl-containing sulfur compounds in drumstick onion, Allium stipitatum

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60077344%3A_____%2F11%3A00359831" target="_blank" >RIV/60077344:_____/11:00359831 - isvavai.cz</a>

  • Alternative codes found

    RIV/67985858:_____/11:00359831 RIV/60076658:12220/11:43881940

  • Result on the web

    <a href="http://dx.doi.org/10.1021/jf200704n" target="_blank" >http://dx.doi.org/10.1021/jf200704n</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/jf200704n" target="_blank" >10.1021/jf200704n</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Precursors and formation of pyrithione and other pyridyl-containing sulfur compounds in drumstick onion, Allium stipitatum

  • Original language description

    Two novel, cysteine derivatives were isolated from the bulbs of Allium stipitatum (Allium sub) and shown to be S-(2-pyridyl)cysteine N-oxide and S-(2-pyridyl) glutathione N-oxide. The former compound is the first example of a naturally occurring alliinase substrate that contains an N-oxide functionality instead of the S-oxide group. In addition, S-methylcysteine S-oxide (methiin) and S-methyl thiomethyl)cysteine 4-oxide (marasmin) were found in the bulbs. The alliinase-mediated formation of pyridyl-containing compounds following disruption of A. stipitatum bulbs was studied by a combination of HPLC-MS, HPLC-PDA, DART-MS, and NMR techniques. No pyridyl-containing thiosulfinates are present in homogenized bulbs. Instead, various pyridine N-oxides such asN-hydroxypyridine-2(1H)-thione (pyrithione), 2-(methyldithio)pyridine N-oxide, 2-(methylthio) methyldithio]pyridine N-oxide, di(2-pyridyl) disulfide N-oxide, and di(2-pyridyl) disulfide N,N0-dioxide are reported.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CE - Biochemistry

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/IAA400720706" target="_blank" >IAA400720706: Structure of silyl moieties through J(29Si-13C) couplings as determined by triple {1H, 13C}29Si NMR experiments</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2011

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Agricultural and Food Chemistry

  • ISSN

    0021-8561

  • e-ISSN

  • Volume of the periodical

    59

  • Issue of the periodical within the volume

    10

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    8

  • Pages from-to

    5763-5770

  • UT code for WoS article

    000290691300076

  • EID of the result in the Scopus database