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1 ohexenone starting material was derived from quinic acid.
2 n be relieved by the nontoxic small molecule quinic acid.
3 oaches were used, both starting from the (-)-quinic acid.
4 transport of shikimic acid and formation of quinic acid.
5 feruloyl octopamine (1.2-5.2), 5-O-feruloyl quinic acid (0.1-7.5), cis-ChA (1.1-2.2), caffeoyl putre
7 are reduced by the sizable concentrations of quinic acid and 3-dehydroshikimic acid that are formed a
8 ed in a convergent manner, starting with (-)-quinic acid and the corresponding (20R)- and (20S)-25-hy
9 d in convergent syntheses, starting with (-)-quinic acid and the protected 25-hydroxy Grundmann keton
10 rom the chiral compound derived from the (-)-quinic acid and, alternatively, from the commercially av
11 -type procyanidins) as also hydroxycinnamoyl-quinic acids and phloretin derivatives were identified i
12 ds (caffeic acid, ferulic acid, 5-O-caffeoyl quinic acid, and 3,4-dimethoxycinnamic acid) and four la
13 delivery system showed prolonged release of quinic acid, and could be used as an active component in
15 HQTs, but exhibits HQT activity, preferring quinic acid as acyl acceptor, and could therefore functi
16 terified to p-coumaric acid with shikimic or quinic acid as intermediates in the biosynthesis of the
17 ed computational methods, was used to design quinic acid based libraries that were synthesized and ev
18 er in tomato, AtMYB12 activates the caffeoyl quinic acid biosynthetic pathway, in addition to the fla
20 rcetin 3-O-rutinoside, 50.7%) and 5-caffeoyl-quinic acid (chlorogenic acid, 17.5%) were detected as d
22 jor peaks in the juice belonged to coumaroyl-quinic acid, chlorogenic acid, procyanidin B2, and procy
27 These experiments indicate that formation of quinic acid during biosynthesis of shikimic acid results
30 idin F beginning from a single enantiomer of quinic acid has been developed and successfully implemen
33 Halide-free, oxidative decarboxylation of quinic acid in fermentation broth with stoichiometric qu
35 rogenic acid, the ester of caffeic acid with quinic acid, is one of the most abundant polyphenols in
36 oylquinic acid lactone (3-CQAL), 4- caffeoyl quinic acid lactone (4-CQAL), and 4-feruloylquinic acid
37 lic lactones 6, 7a, and 7b, derived from the quinic acid lactone, which were converted to the bicycli
39 ding block, oxidation of microbe-synthesized quinic acid provides an example of how the toxicity of a
40 l reaction network for the regulation of the quinic acid (qa) gene cluster of Neurospora crassa is pr
41 ng the shikimate pathway and intermediacy of quinic acid requires 18 enzyme-catalyzed steps and 1 che
45 c acid (CQA), the ester of caffeic acid with quinic acid supplied to human organisms mainly with coff
46 Starting from commercially available (-)-quinic acid, the enantioselective total syntheses of tri
52 ee diacyl esters of trans-cinnamic acids and quinic acid were identified by ultra-performance liquid
54 ts, including oxalic, succinic, shikimic and quinic acids, which interfere with the growth and virule
55 ns suitable for oxidative decarboxylation of quinic acid with catalytic amounts of metal oxidant were
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