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1 in presence of flavan-3-ols, epicatechin and epigallocatechin.
2 oids were isolated (1-3): gallocatechin (1), epigallocatechin (2) and epigallocatechin-3-O-gallate (3
3 echin (EGC), epicatechin 3-gallate (ECG) and epigallocatechin 3-gallate (EGCG) and caffeine in 29 com
4 sly, we showed that the green tea polyphenol epigallocatechin 3-gallate (EGCG) inhibits growth of NF6
6 ted that the major green tea polyphenol, (-)-epigallocatechin 3-gallate (EGCG), exerts potent neuropr
7 abilities of apigenin, baicalein, curcumin, epigallocatechin 3-gallate (EGCG), genistein, quercetin,
9 e we show that the tea-derived flavanol, (-)-epigallocatechin 3-gallate [(2R,3R)-5,7-dihydroxy-2-(3,4
10 By using this system, the natural product epigallocatechin 3-gallate was found to block Wnt signal
11 In a limited phytonutrient screen, EGCG ((-)-epigallocatechin 3-gallate), the major phytochemical in
12 inistration of green tea extracts containing epigallocatechin 3-gallate, a potent DYRK1A inhibitor, t
14 epimer mixture of (+)-gallocatechin and (-)-epigallocatechin, 3,3'-di-O-methylellagic acid 4'-O-xylo
15 sly, we showed that the green tea polyphenol epigallocatechin-3 gallate (EGCG) inhibits growth and tr
16 ole of green tea polyphenols, the effects of epigallocatechin-3 gallate (EGCG) on Her-2/neu-overexpre
17 ype, the effects of the green tea polyphenol epigallocatechin-3 gallate (EGCG) on mammary tumor cells
18 ecursor N-acetyl-L-cysteine (NAC), curcumin, epigallocatechin-3 gallate (EGCG), and p38 inhibitor SB2
20 phanyl-3-butenyl isothiocyanates; G) and (-)-epigallocatechin-3-gallate (E) were investigated in colo
22 sms of the protection conferred by sugars to epigallocatechin-3-gallate (EGCG) against deterioration.
23 catechin, (-)-epigallocatechin (EGC) and (-)-epigallocatechin-3-gallate (EGCG) and butylated hydroxyt
24 s of two main constituents of green tea, (-)-epigallocatechin-3-gallate (EGCG) and caffeine, on intes
25 s known to modulate its aggregation, such as epigallocatechin-3-gallate (EGCG) and dopamine (DA).
28 Recent reports suggest green tea-derived (-)-epigallocatechin-3-gallate (EGCG) can attenuate neuronal
30 we have shown that green tea polyphenol (-)-epigallocatechin-3-gallate (EGCG) exerts a beneficial ro
35 (4-hydroxyphenyl) retinamide (4-HPR) and (-)-epigallocatechin-3-gallate (EGCG) in altering expression
37 y was undertaken to evaluate the efficacy of epigallocatechin-3-gallate (EGCG) in down-regulating Mcl
38 of epigenetic bioactive botanicals including epigallocatechin-3-gallate (EGCG) in green tea polypheno
40 owed that the bioactive green tea polyphenol epigallocatechin-3-gallate (EGCG) inhibits growth in sof
43 with anti-amyloid agents like the polyphenol epigallocatechin-3-gallate (EGCG) is emerging as an expe
48 fect of vanillin, resveratrol, curcumin, and epigallocatechin-3-gallate (EGCG) on the aggregation of
50 to scavenge H2O2 (400muM) and influence (-)-epigallocatechin-3-gallate (EGCG) oxidation (400muM) in
51 ract and its main polyphenol constituent (-)-epigallocatechin-3-gallate (EGCG) possess potent neuropr
53 Polyphenon E with a standardized dose of epigallocatechin-3-gallate (EGCG) was administered using
55 major effective component in green tea, (-)-epigallocatechin-3-gallate (EGCG)'s potential benefits t
56 major green tea polyphenols (catechins), (-)-epigallocatechin-3-gallate (EGCG), (-)-epigallocatechin,
57 resent study, we investigated the effects of epigallocatechin-3-gallate (EGCG), a bioactive green tea
60 d antioxidants included three phenolics: (-)-epigallocatechin-3-gallate (EGCG), a flavanoid polypheno
62 the present study, we examined the effect of epigallocatechin-3-gallate (EGCG), a green tea polypheno
63 on CLL B cells, and we studied the impact of epigallocatechin-3-gallate (EGCG), a known receptor tyro
70 nefits of green tea are mainly attributed to epigallocatechin-3-gallate (EGCG), a polyphenolic compou
71 as conducted to determine to what extent (-)-epigallocatechin-3-gallate (EGCG), a widely used dietary
73 rions, Sindbis virus, and the polyphenol (-)-epigallocatechin-3-gallate (EGCG), and has been implicat
74 ation (1-500 muM) of a model polyphenol, (-)-epigallocatechin-3-gallate (EGCG), and matrix pH (2-7) o
75 muscle for the major green tea catechin, (-)-epigallocatechin-3-gallate (EGCG), but effects were obse
76 effect of two small molecules, FK506 and (-)-epigallocatechin-3-gallate (EGCG), known to inhibit alph
77 ea extract (GTE) and its major catechin, (-)-epigallocatechin-3-gallate (EGCG), on collagen homeostas
78 larly its major polyphenolic constituent (-)-epigallocatechin-3-gallate (EGCG), possesses remarkable
79 bond-containing tea polyphenols, such as (-)-epigallocatechin-3-gallate (EGCG), potently and specific
80 yphenols (GTPP) and their active ingredient, epigallocatechin-3-gallate (EGCG), protects cells from s
81 eritoneal (i.p.) injection (20 mg/kg) of (-)-epigallocatechin-3-gallate (EGCG), the main polyphenolic
86 n previously that topical application of (-)-epigallocatechin-3-gallate (EGCG), the major polyphenol
87 e and animal model studies indicate that (-)-epigallocatechin-3-gallate (EGCG), the major polyphenol
95 ion by two dietary polyphenols, curcumin and epigallocatechin-3-gallate (EGCG), with that by the endo
98 d reactivities of the green tea extract, (-)-epigallocatechin-3-gallate [(2R,3R)-5,7-dihydroxy-2-(3,4
99 showed that 3-d supplementation of combined epigallocatechin-3-gallate and resveratrol (EGCG+RES) in
100 h tea polyphenols or the major tea component epigallocatechin-3-gallate blocked expression of the hyp
101 ergies for (-)-epicatechin-3-gallate and (-)-epigallocatechin-3-gallate for the binding site on BSA n
103 biologically active green tea catechin, (-)-epigallocatechin-3-gallate or (-)-EGCG, has been shown t
104 ) at pH 7.5 and 25 degrees C: catechins [(-)-epigallocatechin-3-gallate, (-)-epigallocatechin, (-)-ep
107 nts, such as the vitamin E analog trolox and epigallocatechin-3-gallate, enhanced hypoxia-induced cas
108 e candidate compounds: rifampicin, curcumin, epigallocatechin-3-gallate, myricetin, and scyllo-inosit
109 Studies from our laboratory have shown that epigallocatechin-3-gallate, the major polyphenol present
110 oxaldehyde, ferulic acid, vanillic acid, and epigallocatechin-3-gallate, were effective inhibitors of
113 ea polyphenol preparation containing 65% (-)-epigallocatechin-3-gallate] and caffeine on 4-(methylnit
116 The major constituent of green tea, (-)-epigallocatechin-3-O-gallate (EGCG), has been shown to h
117 polyphenols [catechin, epicatechin, and (-)-epigallocatechin-3-O-gallate (EGCG)] and bioflavonoids (
118 en tea catechin derivative, oligomerized (-)-epigallocatechin-3-O-gallate (OEGCG) as a carrier for or
119 ld) and caffeic (1.7-fold) acids, as well as epigallocatechin (63-fold), rutin (41-fold) and querceti
121 ratio, and by a polyphenolic profile poor in epigallocatechin and rich in catechin-rich tannins.
124 tes (OCRs) are faster with higher copper and epigallocatechin contents and with higher absorbance at
126 B, and lower levels of (-)-epicatechin, (-)-epigallocatechin (EGC) and (-)-epigallocatechin gallate
127 B, and lower levels of (-)-epicatechin, (-)-epigallocatechin (EGC) and (-)-epigallocatechin gallate
128 erties of (+)-catechin, (-)-epicatechin, (-)-epigallocatechin (EGC) and (-)-epigallocatechin-3-gallat
129 ffeine content followed by epicatechin (EC), epigallocatechin (EGC) and to some extent in other chemi
130 f specific catechins, including epicatechin, epigallocatechin (EGC), and 4'-O-methyl-epigallocatechin
131 ents, namely catechin (C), epicatechin (EC), epigallocatechin (EGC), epicatechin 3-gallate (ECG) and
134 s to an antioxidant activity (r>0.7111) were epigallocatechin, epicatechin and rutin; while epicatech
135 , (-)-epigallocatechin-3-gallate (EGCG), (-)-epigallocatechin, (-)-epicatechin-3-gallate, (-)-epicate
136 techins [(-)-epigallocatechin-3-gallate, (-)-epigallocatechin, (-)-epicatechin-3-gallate], flavones (
137 howed higher levels of catechins (especially epigallocatechin galate, epicatechin gallate, and epicat
138 The pH 4.5 induced higher decrease in (-)-epigallocatechin gallate (71% and 79%) and quercetin-3-g
139 , with (+)-catechin, (-)-epicatechin, or (-)-epigallocatechin gallate (EGCG) added as chain breakers.
141 that two of the polyphenols from green tea (epigallocatechin gallate (EGCG) and epicatechin gallate
143 us green tea constituents, in particular (-)-epigallocatechin gallate (EGCG) and other polyphenols wi
144 We show that the polyphenolic compounds epigallocatechin gallate (EGCG) and silibinin bind to sp
146 special, hitherto-unexplored property of (-)-epigallocatechin gallate (EGCG) as a chiral solvating ag
148 etermine whether an ingredient of green tea, epigallocatechin gallate (EGCG) could attenuate oxidativ
150 y-Arg-Pro-Pro-Gln-Gly and the polyphenol (-)-epigallocatechin gallate (EGCG) has been determined usin
152 The encapsulation of green tea catechin and epigallocatechin gallate (EGCG) in soy lecithin liposome
153 ons of the tea catechins epicatechin (EC) or epigallocatechin gallate (EGCG) inhibited formation of h
156 microscopy (AFM), that the commonly used (-)-epigallocatechin gallate (EGCG) is a much less efficient
158 ory have demonstrated that the GT polyphenol epigallocatechin gallate (EGCG) is capable of antagonizi
163 en tea extract (GTE) supplementation high in epigallocatechin gallate (EGCG) on blood lipids in healt
164 luence of the polyphenolic amyloid inhibitor epigallocatechin gallate (EGCG) on the aggregation pathw
165 pared to standard green tea shoot (GL) while epigallocatechin gallate (EGCG) recorded higher levels i
166 t higher levels of the catechins, especially epigallocatechin gallate (EGCG) were found in green teas
168 study was to examine whether the antioxidant epigallocatechin gallate (EGCG), a catechin-base flavono
169 aim of this study was to provide support for epigallocatechin gallate (EGCG), a component of green te
170 antly, we also identified in this study that epigallocatechin gallate (EGCG), a green tea-derived cat
172 cently demonstrated that the antioxidant (-)-epigallocatechin gallate (EGCG), a major component in gr
175 nhibitory effects of curcumin, caffeine, (-)-epigallocatechin gallate (EGCG), and tea in animal model
176 acid, caffeic acid, caffeine, curcumin, (-)-epigallocatechin gallate (EGCG), gallic acid, propyl gal
177 omponent of green tea extracts, catechin (-)-Epigallocatechin gallate (EGCg), has been reported to be
178 Indian medicine and the green tea flavonoid, epigallocatechin gallate (EGCG), is reported to have glu
182 this hypothesis, we evaluated the effect of epigallocatechin gallate (EGCG), the main antioxidant de
188 opically with caffeine (6.2 micromol) or (-)-epigallocatechin gallate (EGCG; 6.5 micromol) once a day
189 sed, and when treated with 20 micromol/L (-)-epigallocatechin gallate (green tea) was restored back t
191 hemolysis while (-)-epicatechin gallate, (-)-epigallocatechin gallate and (-)-epigallocatechin protec
192 also show that addition of the antioxidants epigallocatechin gallate and alpha-lipoic acid reduces p
194 control model beverages were incubated with epigallocatechin gallate and green tea extract at 62 or
196 lly relevant Abeta oligomers is inhibited by epigallocatechin gallate and increased by the A2V mutati
197 ment Abeta(25-35) by two amyloid inhibitors (epigallocatechin gallate and scyllo-inositol) that are c
201 0.3 muM, which was smaller than that of (-)-epigallocatechin gallate in Phase III clinical trials an
202 asured, confirming the major contribution of epigallocatechin gallate in the peroxyl radical scavengi
203 ls tested, TF-2 and, to a lesser degree, (-)-epigallocatechin gallate inhibited cyclooxygenase (Cox)-
204 ine levels that were dose dependent, whereas epigallocatechin gallate levels did not accumulate nor a
205 nhibition of Bcl-2 by the green tea compound epigallocatechin gallate results in an increase in [Ca(2
206 and lactate and the thermosensitive compound epigallocatechin gallate were recovered without signific
208 (125-1,000 ppm), including (+)-catechin, (-)-epigallocatechin gallate, and green tea extract were add
209 that the astringent- and bitter-tasting (-)-epigallocatechin gallate, bitter-tasting caffeine, and t
210 The experiments reveal that polyphenols (epigallocatechin gallate, bromophenol blue, and resverat
211 quillaja saponin and polyphenols (vanillin, epigallocatechin gallate, green tea extract, and protoca
212 ertain tea polyphenols, such as catechin and epigallocatechin gallate, have been used to augment the
215 We hypothesized that prostate tumor specific epigallocatechin-gallate (EGCg) functionalized radioacti
216 nt with Dyrk1A inhibitor, green tea flavonol epigallocatechin-gallate (EGCG), from gestation to adult
218 rahydrofolate (l-5-MTHF) in combination with epigallocatechin-gallate-enriched extract (EGCGe) and ep
220 Wines consuming SO2 efficiently consume more epigallocatechin, prodelphinidins and procyanidins.
221 allate, (-)-epigallocatechin gallate and (-)-epigallocatechin protected at lowest concentrations agai
224 other identified phenolic compounds, whereas epigallocatechin was the lowest for all investigated lea
226 hin, epigallocatechin (EGC), and 4'-O-methyl-epigallocatechin, were measured in urine specimens that
227 n particular, incubation of epicatechin with epigallocatechin with tyrosinase gave a high, stable the
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