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1 ) and citrus honey (caffeine, 2-oxindole and indole-3-carbinol).
2 ry protein (FLIP) were all down-regulated by indole-3-carbinol.
3 mpounds ascorbigen (13.0 mumol/100 g FW) and indole-3-carbinol (4.52 mumol/100g FW) with their higher
4 l diet experiments show that the reaction of indole-3-carbinol, a breakdown product of indol-3-ylmeth
7 ethane (DIM) is a major digestive product of indole-3-carbinol, a potential anticancer component of c
9 nts showed that oviposition was increased by indole-3-carbinol and decreased by indole-3-acetonitrile
11 toxin, quercetin, flavone, chlorogenic acid, indole-3-carbinol, and rutin) and three insecticides (di
12 S breakdown products (indole-3-acetonitrile, indole-3-carbinol, ascorbigen and 3,3'-diindolylmethane
14 production is induced by herbivory, such as indole-3-carbinol, function not only to repel herbivores
18 Current chemical and biological interest in indole-3-carbinol (I3C) and its metabolites has resulted
20 ic MDA-MB-231 human breast cancer cells with indole-3-carbinol (I3C) directly inhibited the extracell
24 We tested the chemopreventive efficacy of indole-3-carbinol (I3C), a constituent of Brassica veget
31 established the cellular mechanism by which indole-3-carbinol (I3C), a promising anticancer phytoche
34 ked whether the antiestrogenic phytochemical indole-3-carbinol (I3C), found in cruciferous vegetables
36 vide several classes of compounds, including Indole-3-carbinol (I3C), may have chemopreventive activi
37 tables provides phytochemicals, particularly indole-3-carbinol (I3C), which may be responsible for th
41 s (a) the efficacy of sulforaphane (SFN) and indole-3-carbinol (I3C)/3,3'-diindolylmethane (DIM) on b
42 e tested the ability of dietary AhR ligands (indole-3-carbinol [I3C] and 3,3'-diindolylmethane [DIM])
43 multaneous determination of sulforaphane and indole-3-carbinol in broccoli using UPLC-HRMS/MS is desc
44 ietary supplementation of the AHR pro-ligand indole-3-carbinol in newborn mice promotes resistance to
45 w that OSU-A9 was 100 times more potent than indole-3-carbinol in suppressing the viability of Hep3B,
46 ients that inhibit carcinogenesis, including indole-3-carbinol, indole-3-carboxaldehyde, ferulic acid
47 iety of indole-containing chemicals, such as indole-3-carbinol, indolo[3, 2-b]carbazole, and UV photo
50 actor-kappaB (NF-kappaB), we postulated that indole-3-carbinol must mediate its activity through NF-k
52 ased protein interaction studies showed that indole-3-carbinol perturbs the auxin-dependent interacti
56 ely, re-addition of the plant-derived ligand indole-3-carbinol rescued the barrier deficiency even in
57 n machinery was suggested, as application of indole-3-carbinol rescues auxin-induced root phenotypes.