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1 ediated by hTRPV1 was capsaicin > sanshool > allicin.
2 early identify the active compound in AGE as allicin.
3 and NMR verified the active HPLC fraction as allicin.
4 sulphide (DAS), diallyl trisulphide (DATS), allicin, 3-vinyl-4H-1,3-dithiin (3-VD), 2-vinyl-4H-1,2-d
5 a, capsaicin) = 3.5206 x 10(-16) mol/L, K(a, allicin) = 5.0227 x 10(-15) mol/L, K(a, sanshool) = 1.78
7 terminants of TRPV1 activation by capsaicin, allicin, acid, ammonia and voltage have been identified.
12 that produce organosulfur compounds, such as allicin and diallyl disulfide (DADS), which account for
15 of A. fistulosum contained 28.3-95.9 muL/mL allicin and exhibited significant antioxidant and antiba
18 that the activation constants by capsaicin, allicin and sanshool, the active components of chili pep
19 ther experiments, three inhibitors (lithium, allicin and sodium) of acetyl CoA synthetase (EC 6.2.1.1
22 um bromide) cell viability assay to identify allicin as the active anticancer compound in aqueous gar
23 capacity for tolerance to the thiosulfinate "allicin" based on the presence of an eleven-gene, plasmi
24 h AsFMO being an S-monooxygenase involved in allicin biosynthesis through direct formation of sulfeni
30 ity and functionality, and compounds such as allicin could lead to entirely new culinary techniques a
36 growth inhibition of Escherichia coli during allicin exposure coincides with a depletion of the gluta
37 hilic compounds such as acrolein (tear gas), allicin (garlic), and allyl isothiocyanate (AITC) (musta
39 d beta-carotene bleaching assays showed that allicin had an antiradical action mechanism, as well as
44 rgely inhibited by allicin treatment in vivo Allicin-induced protein modifications trigger protein ag
45 results indicate that the mode of action of allicin is a combination of a decrease of glutathione le
52 l isothiocyanate (AITC), cinnamaldehyde, and allicin, produce nociceptive sensation by directly activ
55 The alt gene cluster is sufficient to confer allicin tolerance and protects the glutathione pool duri
57 d candidate protein, is largely inhibited by allicin treatment in vivo Allicin-induced protein modifi
62 and reduced the number of binding sites for allicin, whereas the number of non-covalent binding site