ID Name Structure References (top 5) Molecular Target(s)


in 1 ingredients:

  • 15

  • Properties
    C4H9NO3S    151.19

    1:  Sausen PJ, Elfarra AA.
    Cysteine conjugate S-oxidase. Characterization of a novel enzymatic activity in rat hepatic and renal microsomes.
    J Biol Chem.    impact factor:   7.666
    1990;  265(11): 6139-45

    2:  Blanco J, Moore RA, Kabaleeswaran V, Viola RE.
    A structural basis for the mechanism of aspartate-beta-semialdehyde dehydrogenase from Vibrio cholerae.
    Protein Sci.    impact factor:   4.457
    2003;  12(1): 27-33

    3:  Sklan NM, Barnsley EA.
    The metabolism of S-methyl-L-cysteine.
    Biochem J.    impact factor:   4.349
    1968;  107(2): 217-23

    4:  Doney RC, Thompson JF.
    The reduction of S-methyl-L-cysteine sulfoxide and L-methionine sulfoxide in turnip and bean leaves.
    Biochim Biophys Acta.    impact factor:   2.59
    1966;  124(1): 39-49

    5:  Hofmann U, Eichelbaum M, Seefried S, Meese CO.
    Identification of thiodiglycolic acid, thiodiglycolic acid sulfoxide, and (3-carboxymethylthio)lactic acid as major human biotransformation products of S-carboxymethyl-L-cysteine.
    Drug Metab Dispos.    impact factor:   2.519
    1991;  19(1): 222-6

    Time used: 94 milliseconds.

    Webpage designed by Dr. Xueliang Fang, last updated on 3/10/2005