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1 amic acids (rosmarinic acid, caffeic acid, p-coumaric acid).
2 ogenicacid, quercetin 3-O-glucuronide, and p-coumaric acid).
3 in)>hydroxycinnamic acids (ferulic, caffeic, coumaric acids).
4 sinol, and caffeic, ferulic, vanillic, and p-coumaric acid.
5 erbascoside, oleuropein, ferulic acid, and p-coumaric acid.
6 atechol was markedly more mineralized than p-coumaric acid.
7 tivity with phenylpropene acids, such as rho-coumaric acid.
8  mainly ferulic acid and a lower amount of p-coumaric acid.
9  cinnamate 4-hydroxylase (C4H) reaction to 4-coumaric acid.
10 ng in an elevated 4CL enzyme activity with 4-coumaric acid.
11 to synthesize high-value compounds such as p-coumaric acid.
12 ts like trans-ferulic acid, quercetin, and p-coumaric acid.
13 , including caffeic acid, cinnamic acid, and coumaric acid.
14 lly from phenylalanine, cinnamic acid, and p-coumaric acid.
15 TAL) activity, leading to the formation of p-coumaric acid.
16 asitic, when the algae senesce and release p-coumaric acid.
17 henolics, catechin, epicatechin, caffeic and coumaric acids.
18  had higher amounts of salicylic, gallic and coumaric acids.
19 lic acid, as well as insoluble ferulic and p-coumaric acids.
20  1.15mg/d, of rosmarinic acid 0.09mg/d, of p-coumaric acid 0.0068mg/d, of kaempferol 0.0034mg/d, of l
21 00 g), syringic acid (1.08-2.80 ug/100 g), p-coumaric acid (0.69-1.35 ug/100 g), and ferulic acid (0.
22 elevated concentrations of cell wall-bound p-coumaric acid (~15% to 24%) and reduced biomass sugar re
23 ied, the highest relative increase was for p-coumaric acid (171%).
24 two flavonoids, with the predominance of rho-coumaric acid (1998.80mug/100g).
25 hlorogenic acid, 15.8 (T. microcarpus) for p-coumaric acid, 20.3 (A. campestris) for ferulic acid, 56
26 cetin-3-O-glucoside (155.1-197.2 ug/L) and p-coumaric acid (29.5-30.7 ug/L) were the main quantified
27 oyl transferases (PtrHCT1 and PtrHCT6) and 4-coumaric acid 3-hydroxylase 3 (PtrC3H3).
28 iosynthetic pathways via a peroxidase-type p-coumaric acid 3-hydroxylase enzyme were discovered.
29 15 compounds in giant fennel extract, with p-coumaric acid, 3-hydroxybenzoic acid, sinapic acid, and
30 This bioactivity was linked to PCs such as p-coumaric acid, 4-hydroxybenzoic acid, 4-hydroxybenzaldeh
31  and included five caffeic acid (1-5), three coumaric acid (6-8), and two cinnamyl alcohol (9-10) der
32 em Zea mays increased lignin (~4% to 13%), p-coumaric acid (~8% to 52%) and ferulic acid (~13% to 38%
33  caffeic acid (691%) in soluble phenolics, p-coumaric acid (98%), and catechin (161%) in bound phenol
34 not in nectar but in pollen in the case of p-coumaric acid (a monomer of sporopollenin, the principal
35 ate of the methyl ester of deprotonated para-coumaric acid - a model chromophore for photoactive yell
36             RMI biosynthesis is induced by p-coumaric acid, a product of algal lignin degradation.
37 yrroline, chlorogenic acids, ferulic acid, p-coumaric acid, abscisic acid, and jasmonic acid.
38 pounds, catechin, epicatechin, caffeic acid, coumaric acid, acetaldehyde, total and reduced glutathio
39           Newly generated cinnamic acid from coumaric acid aglycone was detected in fermented plant m
40  fluorogenic assay in which 7-amido-4-methyl coumaric acid (AMC)-conjugated Rad21 mitotic cleavage si
41                                        The p-coumaric acid amounts of the seed oils heated at 180, 72
42 cides, the roseobacticides, in response to p-coumaric acid, an algal lignin breakdown product that is
43           For lignin precursors, including p-coumaric acid and caffeic acid, we found strong associat
44 enolic compounds and their derivatives (e.g. coumaric acid and catechin) and in the expression of phe
45  leaves (gallic acid and rutin) and roots (p-coumaric acid and cinnamic acid) were higher at 15 degre
46  the industrially-relevant phenylpropanoid p-Coumaric acid and demonstrate that these optimizations s
47 siae mutants tolerant to two aromatic acids, coumaric acid and ferulic acid.
48 lds of naringin, tangeretin, ferulic acid, p-coumaric acid and gallic acid increased, but the amount
49 rulic acid, caffeic acid, rosmarinic acid, p-coumaric acid and gallic acid were identified in fruit p
50 illic acid), a glycoside of vanillic acid, p-coumaric acid and its phenethyl ester as well as free an
51  while cellulose favours the liberation of p-coumaric acid and malvidin-3-O-glucoside.
52 c compounds: chlorogenic acid, caffeic acid, coumaric acid and protocatechuic acid, as well as the am
53 nt and inhibitory power, with pinoresinol, p-coumaric acid and quercetin making the greater contribut
54  acid, rutin, scopoletin, l-phenylalanine, 4-coumaric acid and quercetin-3-glucoside, among others me
55          This was clearly demonstrated for p-coumaric acid and resveratrol, which is associated with
56  first intake estimates of trans-anethole, p-coumaric acid and rosmarinic acid in human populations.
57 nsoluble phenolic compounds, ferulic acid, p-coumaric acid and sinapic acid are mainly in ester linka
58 wo CoA ligation paths in vivo: one through 4-coumaric acid and the other through caffeic acid.
59  acid, vanillic acid, syringic acid, trans-p-coumaric acid and veratric acid.
60  types, they were ferulic, syringic, trans-p-coumaric acids and quercetin.
61 g reduced only the contents of ferulic and p-coumaric acids and significantly increased the extractab
62 O-glucoside with one hydroxycinnamic acid (p-coumaric acid) and two O-methylated hydroxybenzoic acids
63 llic, trans-cinnamic, caffeic, ferulic and p-coumaric acids) and two methylxanthines (caffeine, theob
64 sified as either pro-oxidants (malic acid, p-coumaric acid, and caffeic acid, % prodelphinidins, proc
65  extracts mainly consisted of quinic acid, p-coumaric acid, and cirsiliol.
66 ringic acid, syringaldehyde, ferulic acid, p-coumaric acid, and coniferyl aldehyde at trace levels in
67 by cyanidin-3-galactoside-xyloside-glucoside-coumaric acid, and cyanidin-3-galactoside-xyloside-gluco
68 revealed gallic acid, trans-cinnamic acid, p-coumaric acid, and ferulic acid as the main compounds.
69 feic acid, chlorogenic acid, sinapic acid, p-coumaric acid, and ferulic acid) were detected.
70 id, 4-dihydroxybenzoic acid, ferulic acid, p-coumaric acid, and m-coumaric acid, were identified and
71 2 can be induced by 4-hydroxyacetophenone, p-coumaric acid, and phenol, whereas these same phenolic c
72 n, resveratrol, caffeic acid, gallic acid, p-coumaric acid, and vanillic acid in red wines.
73      After heat treatment, gallic acid and p-coumaric acid are the major increased soluble and insolu
74 1 mutant plants are deficient in ferulic and coumaric acid, aromatic compounds known to be attached t
75 ed artepillin-C, kaempferide, drupanin and p-coumaric acid as main compounds by LC-MS analysis.
76 exhibited higher chlorogenic, ellagic, and p-coumaric acids as well as TFC, RSA, and rutin.
77 ed that aerial parts rich in fumaric acid, p-coumaric acid, ascorbic acid and hyperoside while onion
78               Ferulic, caffeic, sinapic, and coumaric acids, belonging to the class of hydroxycinnami
79  aglycones from glycosylated flavonols and p-coumaric acid, but not caffeic acid from phenylamides.
80                       Motions of the trans-p-coumaric acid carbonyl group following the photoexcitati
81 ols involved in bone metabolism, including m-coumaric acid, catechin derivatives and courmaroyl tarta
82         Hydroxybenzoic acid, ferulic acid, p-coumaric acid, catechin, and epicatechin were the most a
83                               The released p-coumaric acid causes the bacteria to synthesize roseobac
84 the trans to cis photoisomerization of its p-coumaric acid chromophore.
85           The PLS showed that gallic acid, p-coumaric acid, chrysin, kaempferol, Fe, and Mn stimulate
86 olic compounds: gallic acid, sinapic acid, p-coumaric acid, cinnamic acid, trans-fereulic acid, syrin
87 rganic ligands, namely, caffeic acid (CA), p-coumaric acid (CMA), vanillin (VNL), and cinnamic acid (
88                          Downregulation of 4-coumaric acid:coenzyme A ligase (4CL) can reduce lignin
89                                            4-Coumaric acid:coenzyme A ligase (4CL) is involved in mon
90 )-rich lignins and high levels of esterified coumaric acid compared with those of dicotyledonous plan
91 ation of models with individual polyphenols: coumaric acid (COU), caffeic acid (CAF), CAT, epigalloca
92   Compounds such as p-hydroxybenzoic acid, p-coumaric acid, coumaroylaldaric acid and feruloylaldaric
93 s associated with such classification were p-coumaric acid, delphinidin-3-O-glucoside, caffeic acid,
94                     Higher contents of the p-coumaric acid derivatives L-5-oxoproline and d-galactose
95 olics were characterised including several p-coumaric acid derivatives which were newly detected.
96         The latter were relatively rich in p-coumaric acid derivatives.
97  and proved its activity toward monophenols (coumaric acid), diphenols (caffeic acid, protocatechuic
98  formed from the conversion of caffeic and p-coumaric acids during fermentation.
99 ed in the release of free HCAs, especially p-coumaric acid, during the yeast fermentation.
100                                            p-Coumaric acid exhibited the highest inhibitory effect on
101 coffee-related metabolites like cinnamic and coumaric acids, explaining observed variations due to th
102 CDRBE (protocatechuic acid, vanillic acid, p-coumaric acid, ferulic acid and sinapic acid) were ident
103 zoic acid, 4-hydroxybenzaldehyde; Group 2: p-coumaric acid, ferulic acid).
104  were tentatively identified in PCF (major p-coumaric acid, ferulic acid, and 4-hydroxybenzaldehyde)
105 bility of phenolic compounds (gallic acid, p-coumaric acid, ferulic acid, chlorogenic acid, catechin)
106       The major phenolics were detected as p-coumaric acid, ferulic acid, myricetin, luteolin and que
107 ic acid, rosmarinic acid, p-coumaric acid, m-coumaric acid, ferulic acid, protocatechuic acid, and va
108 rally present within wetland environments (p-coumaric acid, gallic acid, protocatechuic acid, p-hydro
109 pounds (caffeic acid, protocatechuic acid, p-coumaric acid, gentisic acid and syringic acid).
110 rization showed a significant reduction in p-coumaric acid, Glc, Man, and cellulose contents.
111 e (48.8%), 4-methoxycinnamic acid (36.4%), p-coumaric acid glucose ester (9.2%) and 1-O-beta-d-glucop
112                    4-Methoxycinnamic acid, p-coumaric acid glucose ester and 1-O-beta-d-glucopyranosy
113  (50.33 mg/g) and 3-p-Feruloylquinic acid, p-Coumaric acid glucoside and 4-p-Coumaroylquinic acid (31
114 olic acid derivatives (main compound being o-coumaric acid glucoside), quercetin glycosides, and anth
115 a-->8)-catechin dimer (procyanidin B1), IV.p-coumaric acid glycoside, VI.epicatechin-(4beta-->8)-epic
116 , naringin, and chlorogenic, salicylic and p-coumaric acid) has been quantified.
117 nosyl sinapate (5.6%), while caffeic acid, p-coumaric acid, hesperidin and naringenin were present in
118 s measured by the ability to transform the p-coumaric acid (HPLC-DAD).
119 y, anthocyanin content, cinnamic acid, and p-coumaric acid in caper berries.
120 m which found that ferulic acid in RBE and p-coumaric acid in CDRBE were active in enzymatic browning
121 ons and hydroxylates cinnamic acid to form 4-coumaric acid in phenylpropanoid metabolism.
122                     Newly, the presence of m-coumaric acid in red rices was detected.
123 e response of gallic, caffeic, ferulic and p-coumaric acids in 0.050 M acetate buffer pH 4.5 containi
124 etin, quercetin, galangin and particularly p-coumaric acid (in honeydew honey).
125 and lignin phenolic monomers--catechol and p-coumaric acid--in the presence and absence of agricultur
126  compounds such as 4-hydroxyacetophone and p-coumaric acid induced the vir of KU12, but not A6.
127                            CoA ligation of 4-coumaric acid is essential for the 3-hydroxylation of 4-
128     As a major component of pollen grains, p-coumaric acid is ubiquitous in the natural diet of honey
129 coumaroylquinic acid, 5-caffeoylquinic acid, coumaric acid, kaempferol-3-O-rutinoside, proanthocyanid
130 zoic acid, cinnamic acid, rosmarinic acid, p-coumaric acid, m-coumaric acid, ferulic acid, protocatec
131 hich indicates spermidines conjugated with p-coumaric acid may be bioavailable compounds with anti-in
132     The processing of oxidized mixtures of p-coumaric acid methyl ester (pcm) revealed a new antitumo
133 .55 mug/kg, with a predominant presence of p-coumaric acid methyl ester.
134 ile of spaghetti by addition gallic acid and coumaric acid-o-hexoside, and increasing 2-fold and arou
135 eruloylquinic acid, caffeic acid-O-hexoside, coumaric acid-O-hexoside, sinapic acid-O-hexoside, catec
136  shikimates-phenylpropanoids (shikimic and p-coumaric acids) on soil bacteria or Brachypodium seedlin
137  was prepared to enrich and determine both p-Coumaric acid (p-CA) and ferulic acid (FA) based on syri
138 BSG was in the order of ferulic acid (FA), p-coumaric acid (p-CA) derivatives, FA derivatives, p-CA,
139 ing vanillic acid (VA), ferulic acid (FA), p-coumaric acid (p-CA), p-hydroxybenzoic acid (HBA), proto
140 oxycinnamic acids ferulic acid (FA) and para-coumaric acid (p-CA).
141 s caffeic acid, gallic acid, ferulic acid, m-coumaric acid, p-hydroxybenzoic acid, protocatechuic aci
142 icular focus on the interaction between para-Coumaric acid (pCA) and nitrile-incorporated photoactive
143         Absorption of a blue photon by the p-coumaric acid (pCA) chromophore in pG, the initial state
144     In the electronic ground state, the para-coumaric acid (pCA) chromophore of PYP is negatively cha
145 ing trans-to-cis photoisomerization of its p-coumaric acid (pCA) chromophore over 10 decades of time.
146  (PYP) is affected by isomerization of its p-coumaric acid (pCA) chromophore.
147 oreceptor with photochemistry based on its p-coumaric acid (pCA) chromophore.
148 idin B1, rutin, gallic acid, caffeic acid, p-coumaric acid, pelargonidin-3-glucoside, cyanidin-3-gluc
149 uid extraction (LLE) for quantification of p-coumaric acid (pHCA) in the supernatant of genetically e
150 hat constituents found in honey, including p-coumaric acid, pinocembrin, and pinobanksin 5-methyl eth
151 s significant for hydroxytyrosol, tyrosol, p-coumaric acid, pinoresinol and peroxide value.
152 ed the Greek olive oils were the phenolics p-coumaric acid, pinoresinol, 1-acetoxypinoresinol, syring
153  malvidin, ferulic, syringic, sinapic, and p-coumaric acids present in gluten-free breads were effect
154 fractions of quercetin, protocatechuic and p-coumaric acids presented positive and significant correl
155 wn to significantly improve the secretion in coumaric acid production strains.
156  better understand biochemical steps after p-coumaric acid production, we cloned and characterized th
157 rease in phenolic acids like caffeic acid, p-coumaric acid, protocatechuic acid, quinic acid, and met
158 cross the samples and p-hydroxybenzoic and p-coumaric acids proved to be the main components.
159 e reaction between quercetin-glucoside and p-coumaric acid (Q-Glu-p-CouA).
160 cinnamic acid, 2,4-dihydroxycinnamic acid, p-coumaric acid, quercetin, trans-ferulic acid, trans,tran
161 uce p-coumaroyl-HSL by using environmental p-coumaric acid rather than fatty acids from cellular pool
162 innamic acids, caffeic, sinapic, ferulic and coumaric acids, respectively and 59.1mg/100g for ascorbi
163 , epicatechin, myricetin, quercetin, trans-p-coumaric acid, rutin, quercetin-3-glucoside, and naringe
164 y known phenolics, including caffeic acid, p-coumaric acid, rutin, scopoletin, N-trans-feruloyl tyram
165 ntration of ferulic acid, didymin, dihydro-p-coumaric acid, sesaminol and matairesinol isomers were f
166 ds were identified, comprising caffeic and p-coumaric acids, seventeen polymers of caffeic acid and e
167 ely parallel RNA sequencing) revealed that p-coumaric acid specifically up-regulates all classes of d
168 ydroxybenzoic acid, caffeoylshikimic acid, p-coumaric acid, syringic acid hexoside and diosmin throug
169 otal losses for gallic-acid, caffeic-acid, p-coumaric-acid, syringic-acid, hesperidin, pelargonidin-3
170 ant-bacterial interactions, such as auxin, o-coumaric acid, t-cinnamaic acid, as well as analogs that
171  catalyze the coenzyme A (CoA) ligation of 4-coumaric acid to 4-coumaroyl-CoA and caffeic acid to caf
172 unctional significance in that that adding p-coumaric acid to a diet of sucrose increases midgut meta
173 thesis in P. trichocarpa SDX; one converts p-coumaric acid to caffeic acid and the other converts p-c
174          Alternatively, 3-hydroxylation of 4-coumaric acid to caffeic acid may occur through an enzym
175 in complex mediated the 3-hydroxylation of 4-coumaric acid to caffeic acid.
176 lactic acid to its caffeoyl derivative and p-coumaric acid to caffeic acid.
177  ranged, in mug g(-1), from 3.16 +/- 0.27 (p-coumaric acid) to 3803 +/- 217 (rutin).
178            The photoisomerization of trans-p-coumaric acid (trans-CA) triggers a photocycle in photoa
179    Phenolic compounds, namely gallic acid, p-coumaric acid, trans-ferulic acid, caffeic acid, trans-r
180 ds identified in all four ber species were p-coumaric acid, vanillin and ferulic acids.
181 techin, chlorogenic acid, caffeic acid and p-coumaric acid varied among species and found the maximum
182 accessibility and Caco-2 cell transport of p-coumaric acid was 370% and 127%, respectively, while it
183 tion of diagnostic products confirmed that p-coumaric acid was associated with lignins.
184                                            p-Coumaric acid was not detected in basil, buckwheat and g
185                                       Free p-coumaric acid was released after digestion, and epitheli
186                               In addition, p-Coumaric acid was the dominant free phenolic acids, wher
187          Dihydrocoumaric acid sulphate and p-coumaric acid were identified as metabolites formed in e
188 h tartaric, sinapic and ferulic acids, and p-coumaric acid were the major phenolics found in the non-
189 nillic acid, quercetion-3-O-glucoside, and p-coumaric acid were the most relevant compounds for discr
190                       However, ferulic and p-coumaric acids were abundant in the bound fractions.
191 aline hydrolysis, and no bound ferulic and p-coumaric acids were detected.
192 acid and antioxidants as trans-ferulic and p-coumaric acids were found and quantified in the brewing
193 of their phenolic acids, where ferulic and p-coumaric acids were the most representative.
194 c acid, ferulic acid, p-coumaric acid, and m-coumaric acid, were identified and quantified using high
195 cid, caffeic acid, vanillin, ortho- and para-coumaric acids, were identified and quantified.
196 ces were ferulic, protocatechuic and trans-p-coumaric acids, while the major free phenolics in red ri
197  exchanging coenzyme A (CoA) esterified to p-coumaric acid with shikimic or quinic acid as intermedia
198 r bioaccessible phenolics were ferulic and p-coumaric acids with bioaccessibility ranging from 131 to
199  chromophores such as retinal within opsins, coumaric acid within photoactive yellow protein, or vita
200 lic acid, XIII.sinapic acid glycoside, XVI.p-coumaric acid, XVII.ferulic acid, XVIII.sinapic acid, XI

 
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