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1 ochondria as the potential site of action of daidzin.
2 (DOPAL) which accumulate in the presence of daidzin.
3 s well, which accumulates in the presence of daidzin.
4 s and mediates the antidipsotropic effect of daidzin.
5 a series of synthetic structural analogs of daidzin.
6 bited by ALDH inhibitors chloral hydrate and daidzin.
10 finding that it is bacterially derived from daidzin, an isoflavone abundant in soy foods, led to the
14 +/-0.02 min(-1), 4.54+/-0.32 min, 60 min for daidzin and 0.16+/-0.02 min(-1), 2.28+/-0.11 min, 60 min
15 oked sample, while increased the contents of daidzin and daidzein and decreased the content of genist
17 lity of established models in explaining the daidzin and daidzein transformation to equol as a functi
19 mount (X3) on transformation of isoflavones (daidzin and daidzein) to equol in soymilk fermented with
20 ALDH-2 and MAO, we prepared 44 analogues of daidzin and determined their potencies for ALDH-2 and MA
21 ization mass spectrometry was used to detect daidzin and genistin after solid-phase extraction of the
22 on process significantly lowered contents of daidzin and genistin in 60min cooked sample, while incre
24 n, genistein, biochanin A, and two of which, daidzin and genistin, are glycosilated, in lentils and o
25 earity ranging from 0.1 to 5mg/L, except for daidzin and genistin, for which it ranged from 0.1 to 10
27 s possibility, we have studied the effect of daidzin and its analogs on 5-HT and DA metabolism in iso
30 rom the graded dose-response curves for pure daidzin and RP extract daidzin are 23 and 2.3 mg per ham
31 we synthesized more structural analogues of daidzin and tested and compared their antidipsotropic ac
33 gh 48 h for compounds such as medicarpin and daidzin; and a lesser delayed and protracted response st
34 ponse curves for pure daidzin and RP extract daidzin are 23 and 2.3 mg per hamster per day, respectiv
35 A resolution shows the isoflavone moiety of daidzin binding close to the aldehyde substrate-binding
36 nts for the fact we previously observed that daidzin can suppress ethanol intake of this species with
38 den hamsters was compared with that of crude daidzin contained in a methanol extract of Radix puerari
41 d ALDH-2 inhibition by structural analogs of daidzin established a link between these two activities
42 DH2 and compared them to the ALDH2 inhibitor daidzin for selectivity against five ALDH1/2 isoenzymes.
43 procedure generally increased the amount of daidzin, genistin and daidzein, but decreased that of ge
44 quadratic on the length, moisture and on the daidzin, genistin and genistein content; linear on the f
45 imultaneous quantification of 6 isoflavones (daidzin, genistin, daidzein, genistein, formononetin and
46 genistein, and glycitein), and 9 glucosides (daidzin, genistin, glycitin, acetyldaidzin, acetylgenist
47 stein), their corresponding glycoside forms (daidzin, glycitin and genistin), and acetyl and malonyl
48 .p.injection indicate that the crude extract daidzin has approximately 10 times greater bioavailabili
49 ion for both the specificity and affinity of daidzin (IC50 =80 nM) and the affinity of analogues with
53 t appears that the antidipsotropic action of daidzin is not mediated by 5-HT (or DA) but rather by it
54 take-suppressive (antidipsotropic) action of daidzin is not mediated by the monoamines but rather by
58 l product 7-O-glucosyl-4'-hydroxyisoflavone (daidzin), isolated from the kudzu vine ( Peruraria lobat
60 ive, are consistent with the hypothesis that daidzin may act via the mitochondrial MAO/ALDH pathway a
61 ween these two activities and suggested that daidzin may suppress ethanol intake by inhibiting ALDH-2
62 e suppression and raise the possibility that daidzin may, in fact, suppress ethanol intake of golden
64 spectrometry failed to detect even traces of daidzin or genistin in plasma collected 1, 2, and 8 h af
65 mg of one of the isoflavone beta-glycosides (daidzin or genistin) or 250 mL soymilk containing mainly
66 hamsters administered various doses of pure daidzin or RP extract by i.p.injection indicate that the
68 or pure and crude daidzin using bioavailable daidzin rather than administered dose gives a single cur
70 AC) formation by six structural analogues of daidzin suggested a potential link between these two act
75 the dose-response effects for pure and crude daidzin using bioavailable daidzin rather than administe
76 indicated that the suppression of the BAC by daidzin was due mainly to delay of stomach emptying.