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1 tively demethylates 4-methoxybenzoic acid to 4-hydroxybenzoic acid.
2 t not its analogs, 3-hydroxybenzoic acid and 4-hydroxybenzoic acid.
3 the Q biosynthetic intermediate 3-hexaprenyl-4-hydroxybenzoic acid.
4 alts, delivers high para selectivity to give 4-hydroxybenzoic acids.
5 initiated by the novel starter unit, 3-amino-4-hydroxybenzoic acid (3,4-AHBA), and a cyclized 5-amino
6 ferulic acid 4-O-beta-D-glucoside (FAG) and 4-hydroxybenzoic acid 4-O-beta-D-glucoside resisted hydr
8 arabens and their common hydrolysis product, 4-hydroxybenzoic acid (4-HB), as well as BADGE and its t
9 conomic analysis of four exemplar compounds (4-hydroxybenzoic acid [4-HBA], catechol, muconic acid, a
10 y was linked to PCs such as p-coumaric acid, 4-hydroxybenzoic acid, 4-hydroxybenzaldehyde, chlorogeni
11 ents with the pesticide carbofuran (Group 1: 4-hydroxybenzoic acid, 4-hydroxybenzaldehyde; Group 2: p
12 Previous work has suggested the ability of 4-hydroxybenzoic acid (4HBA) to bind to beta -casein fol
13 ic acid derivatives, salicylic acid (SA) and 4-hydroxybenzoic acid (4HBA), began to accumulate in phl
14 (84.10 mg/g), rosmarinic acid (56.01 mg/g), 4-hydroxybenzoic acid (52.05 mg/g) and myricetin (40.00
15 omposition compared with controls, exogenous 4-hydroxybenzoic acid addition promoted increased abunda
17 The overexpression of Coq8 and the use of 4-hydroxybenzoic acid analogues represent innovative too
18 substrates were examined, including 3-amino-4-hydroxybenzoic acid and AcCoA, revealing K m values of
21 ting metabolites: selective growth substrate 4-hydroxybenzoic acid and putative signaling/facilitator
22 the stoichiometry of chlorine reactions with 4-hydroxybenzoic acid and several intermediates indicate
24 para-aminobenzoic acid (pABA) in addition to 4-hydroxybenzoic acid as a precursor of coenzyme Q, a re
25 n Q biosynthesis and accumulate 3-hexaprenyl-4-hydroxybenzoic acid as the predominant intermediate.
26 Using phenolic model compounds, particularly 4-hydroxybenzoic acid, as models for structures in humic
27 of the asukamycin building blocks: a 3-amino-4-hydroxybenzoic acid core component, a cyclohexane ring
28 l and efficient preparation of (13)C-labeled 4-hydroxybenzoic acid derivatives, thereby opening oppor
30 syringic acid (SA), vanillic acid (VA), and 4-hydroxybenzoic acid (HBA), which are problematic ligno
31 c (syringic acid, SA; vanillic acid, VA; and 4-hydroxybenzoic acid, HBA) compounds as the substrate i
33 ormation to occur, the hydroxyl group of the 4-hydroxybenzoic acid must be replaced with an amino gro
34 ng and by far the most abundant gallic acid, 4-hydroxybenzoic acid, protocatechuic acid, naringin, er
35 enolic compounds (ferulic acid, gallic acid, 4-hydroxybenzoic acid, salicylic acid, ellagic acid, and
36 not inhibited by carbonyl reagents and that 4-hydroxybenzoic acid served as an alternate substrate,
38 aweed prey, Halimeda incrassata, by tracking 4-hydroxybenzoic acid to find vegetative prey and the de
39 ed as the parent parabens were degraded into 4-hydroxybenzoic acid via hydrolysis pathway by the SDFs
41 By efficiently producing another compound, 4-hydroxybenzoic acid, we also demonstrate that the appr
43 furfural, chlorogenic acids, caffeine, and 3,4-hydroxybenzoic acid, were more abundant in light to me
44 ococcus jannaschii occurs by the reaction of 4-hydroxybenzoic acid with phosphoribosyl pyrophosphate
46 phenolics (i.e., protocatechuic aldehyde and 4-hydroxybenzoic acid, with the latter exhibiting the hi