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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 initiated by the novel starter unit, 3-amino-4-hydroxybenzoic acid (3,4-AHBA), and a cyclized 5-amino
5                                              4-Hydroxybenzoic acid (4-HB) was the predominant paraben
6 arabens and their common hydrolysis product, 4-hydroxybenzoic acid (4-HB), as well as BADGE and its t
7 ic acid derivatives, salicylic acid (SA) and 4-hydroxybenzoic acid (4HBA), began to accumulate in phl
8 case with natural substrate and the 3-methyl-4-hydroxybenzoic acid analog.
9    The overexpression of Coq8 and the use of 4-hydroxybenzoic acid analogues represent innovative too
10  substrates were examined, including 3-amino-4-hydroxybenzoic acid and AcCoA, revealing K m values of
11  suitably selected molecular probes, such as 4-hydroxybenzoic acid and methylene blue.
12                  Aromatic compounds, such as 4-hydroxybenzoic acid and phenylalanine, as well as nucl
13 the stoichiometry of chlorine reactions with 4-hydroxybenzoic acid and several intermediates indicate
14               The erythrolic acids contain a 4-hydroxybenzoic acid appended with a modified terpene s
15 para-aminobenzoic acid (pABA) in addition to 4-hydroxybenzoic acid as a precursor of coenzyme Q, a re
16 n Q biosynthesis and accumulate 3-hexaprenyl-4-hydroxybenzoic acid as the predominant intermediate.
17 Using phenolic model compounds, particularly 4-hydroxybenzoic acid, as models for structures in humic
18 of the asukamycin building blocks: a 3-amino-4-hydroxybenzoic acid core component, a cyclohexane ring
19  syringic acid (SA), vanillic acid (VA), and 4-hydroxybenzoic acid (HBA), which are problematic ligno
20 c (syringic acid, SA; vanillic acid, VA; and 4-hydroxybenzoic acid, HBA) compounds as the substrate i
21            Recent work has demonstrated that 4-hydroxybenzoic acid is the in vivo precursor to the 1-
22 ormation to occur, the hydroxyl group of the 4-hydroxybenzoic acid must be replaced with an amino gro
23 ng and by far the most abundant gallic acid, 4-hydroxybenzoic acid, protocatechuic acid, naringin, er
24  not inhibited by carbonyl reagents and that 4-hydroxybenzoic acid served as an alternate substrate,
25      Finally, we used synthetic analogues of 4-hydroxybenzoic acid to bypass deficient biosynthetic s
26 aweed prey, Halimeda incrassata, by tracking 4-hydroxybenzoic acid to find vegetative prey and the de
27                        A *OH trapping agent, 4-hydroxybenzoic acid, was included either in the microd
28   By efficiently producing another compound, 4-hydroxybenzoic acid, we also demonstrate that the appr
29                             Benzoic acid and 4-hydroxybenzoic acid were manipulated with a heated Wol
30 ococcus jannaschii occurs by the reaction of 4-hydroxybenzoic acid with phosphoribosyl pyrophosphate
31                              The behavior of 4-hydroxybenzoic acid with respect to yields of dichloro

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