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1 atments of the tea polyphenols EGCG, GCG and theaflavins.
2 involved in the inhibition by catechins and theaflavins.
3 of 14 tested polyphenols, tannic acid (TA), theaflavin-3'-gallate (TF2B) and theaflavin-3,3'-digalla
4 lyphenols, theaflavin, theaflavin-3-gallate, theaflavin-3'-gallate, and theaflavin-3,3'-digallate (TF
6 aflavin (TF-1), theaflavin-3-monogallate and theaflavin-3'-monogallate mixture (TF-2), and theaflavin
7 heaflavin-3'-monogallate mixture (TF-2), and theaflavin-3,3'-digallate (TF-3) are the major black tea
8 acid (TA), theaflavin-3'-gallate (TF2B) and theaflavin-3,3'-digallate (TF3) exhibited inhibitory eff
10 ith (-)-epigallocatechin-3-gallate (EGCG) or theaflavin-3,3'-digallate (TFdiG) (20 mM) for different
12 flavin-3-gallate, theaflavin-3'-gallate, and theaflavin-3,3'-digallate (TFdiG), were compared with re
13 3'-digallate (TFdiG), theaflavin-3'-gallate, theaflavin-3-gallate, and theaflavin inhibited PL with I
14 mers, and black tea polyphenols, theaflavin, theaflavin-3-gallate, theaflavin-3'-gallate, and theafla
18 that inhibited cell transformation, EGCG and theaflavins also inhibited AP-1-dependent transcriptiona
19 ls were exposed to varying concentrations of theaflavin and analyzed for tumor necrosis factor-alpha-
21 ack tea involves oxidation of catechins into theaflavins and other complex phenolics by endogenous en
23 ating that catechins in green tea as well as theaflavins and thearubigins from black tea are the subs
28 t to the active site, and galloyl-containing theaflavins are then predicted to perturb the protonatio
29 at certain green tea catechins and black tea theaflavins are very potent inhibitors (K(i) in the nano
30 ossible to determine the major catechins and theaflavins as well as some of the catechin metabolites.
37 dation process was directed towards a higher theaflavins content, which is considered an important qu
38 ermine the individual and total catechin and theaflavin contents by HPLC and the total antioxidant ca
39 ults show that the polyphenol (catechins and theaflavins) contents were significantly influenced by p
40 ent transfections demonstrated that EGCG and theaflavins could repress the transcriptional activities
43 flavin-3'-gallate, theaflavin-3-gallate, and theaflavin inhibited PL with IC50 of 1.9, 4.2, 3.0, and
44 ition of interleukin-8 transcription because theaflavin inhibited tumor necrosis factor-alpha-mediate
49 itory effects on AP-1 activation by EGCG and theaflavins may further explain the anti-tumor promotion
52 nd their epimers, and black tea polyphenols, theaflavin, theaflavin-3-gallate, theaflavin-3'-gallate,
53 ergo oxidative coupling for the formation of theaflavins, theasinensins and polyhydroxylated flavan-3
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