1 e methylene group with a nitrogenous base or sulfhydryl compound.

2 ins, polysaccharides, polyphenols, and total sulfhydryl compounds.

3 he ortho-hydroxylated derivatives with model sulfhydryl compounds.

4 tionally, replacing a single hydroxyl with a sulfhydryl (compound 23, IC50 = 5.8 microM) results in o

5 sediment were present as Ag(2)S (55%) and Ag-sulfhydryl compounds (27%).

6 idues that may be sites of glycosylation and sulfhydryl compound activation, respectively.

7 with an acid pH optimum that is activated by sulfhydryl compounds and preferentially hydrolyzes the m

8 t sensitive to reduction by externally added sulfhydryl compounds, but apparently reacted with intrac

9 ractions were determined by colorimetry, and sulfhydryl compounds by gas chromatography with sulfur c

10 s S-methylation of aromatic and heterocyclic sulfhydryl compounds, including anticancer and immunosup

11 e S-methylation of aromatic and heterocyclic sulfhydryl compounds, including medications such as merc

12 um was activated by thiocyanate, cyanate, or sulfhydryl compounds; inhibited by sulfite, bisulfite, o

13 elation with glutathione suggests that other sulfhydryl compounds may contribute to antiradical activ

14 les and could be suppressed by the synthetic sulfhydryl compounds, N-acetylcysteine and bucillamine.

15 articularly hydroxycinnamic acids, and total sulfhydryl compounds on antioxidant potential.

16 such as aniline and veratrylamine as well as sulfhydryl compounds such as l-cysteine and beta-mercapt

17 do react readily with biologically important sulfhydryl compounds to give products derived from eithe