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1 action to be thermodynamically favorable for p-nitrophenol.
2  less to p-methoxyphenol removal compared to p-nitrophenol.
3 er nitroaromatics such as p-nitrotoluene and p-nitrophenol.
4  the hydrolysis product of para-oxon, namely p-nitrophenol.
5 y covalent attachment to the tyrosine mimic, p-nitrophenol.
6 y covalent attachment to the tyrosine mimic, p-nitrophenol.
7 acid phosphatases in viable cells to produce p-nitrophenol.
8 inium(III) chelates, GdNP-DO3A (1-methlyene-(p-NitroPhenol)-1,4,7,10-tetraazacycloDOdecane-4,7,10-tri
9 ,10-triAcet ate) and GdNP-DO3AM (1-methlyene(p-NitroPhenol)-1,4,7,10-tetraazacycloDOdecane-4,7,10-tri
10 ding L-triiodothyronine, thyroxine, estrone, p-nitrophenol, 2-naphthylamine, and 2-naphthol.
11 posite was used to catalyze the reduction of p-nitrophenol (4-NP) to p-aminophenol (4-AP) as a model
12 sideration here, namely the reduction of (i) p-nitrophenol and (ii) hexacyanoferrate (iii), both by b
13                TG1/pBS(Kan)T3MO produced 66% p-nitrophenol and 34% m-nitrophenol from nitrobenzene an
14 timated by immunoblot analysis, and rates of p-nitrophenol and chlorzoxazone hydroxylation were eleva
15                                     Rates of p-nitrophenol and chlorzoxazone hydroxylation were eleva
16 etermined toward two prototypical aglycones, p-nitrophenol and estrone, in intact and digitonin-treat
17 also converts bis-p-nitrophenyl phosphate to p-nitrophenol and inorganic phosphate via a processive t
18 l phosphate (pNPP) leads to the formation of p-nitrophenol and inorganic phosphate.
19 (*), while the dominant removal mechanism of p-nitrophenol and p-methoxyphenol was a function of the
20    At low anodic potentials (1.7-1.8 V/SHE), p-nitrophenol and p-methoxyphenol were removed primarily
21 he conversion of p-nitrophenylphosphate into p-nitrophenol and phosphate via beads carrying the immob
22 ulfates small phenols such as 1-naphthol and p-nitrophenol and thyroid hormones, including 3,3'-diiod
23 ergy docked configurations of chlorzoxazone, p-nitrophenol, and N-nitrosodimethylamine, high-affinity
24              His L91, Arg L96, and the bound p -nitrophenol are linked into a hydrogen-bonding networ
25 m temperature, among which the catalyst with p-nitrophenol as ligand shows the highest catalytic acti
26                                         With p-nitrophenol as substrate, the V(max)/K(m) determined f
27 e deviations in V(max)/K(m) with dopamine or p-nitrophenol as substrate.
28   For all cell types examined, absorbance of p-nitrophenol at 405 nm is directly proportional to the
29             The decreased COD adsorption for p-nitrophenol at higher anodic potentials was attributed
30 ta-Glycosidase activity was quantified using p-nitrophenol-beta-d-glucopyranoside and SIM isoflavone
31 mined with model glucuronide substrates like p-nitrophenol-beta-D-glucuronide (pNPG), the GUS ortholo
32  high catalytic activity in the reduction of p-nitrophenol by NaBH4 .
33             Ultrasensitive SERS detection of p-nitrophenol can be achieved when oxidation of surface-
34 gene cluster, which encodes the enzymes of a p-nitrophenol catabolic pathway from Arthrobacter sp. st
35                    It was concluded that the p-nitrophenol catabolic pathway in JS443 most likely beg
36 tochemical pathways for aqueous solutions of p-nitrophenol, chosen as a representative nitroaromatic
37 ysis by adding a suitable chemical stimulus (p-nitrophenol cocatalyst) switched the reactivity decide
38 ronmental systems: an atmospheric pollutant (p-nitrophenol), crude oil extracts, and groundwater.
39               Spectrophotometric assays with p-nitrophenol derivatives also demonstrated that McaP is
40 ((1)O(2)) that, in turn, readily reacts with p-nitrophenol enzymatically produced under alkaline cond
41 orresponding prodrug component consists of a p-nitrophenol ester linked to the 3' end of an 8-mer oli
42                         The rate constant of p-nitrophenol formation followed by stopped-flow spectro
43 ical method is based on the determination of p-nitrophenol formed in the course of enzyme-catalyzed h
44 a one step process involving displacement of p-nitrophenol from appropriately substituted ring openin
45 sequent liberation of a second equivalent of p-nitrophenol from the phosphorylated calixarene interme
46 the A107T variant produced >98% p-cresol and p-nitrophenol from toluene and nitrobenzene, respectivel
47 mple sugar acceptor N-acetylglucosamine-beta-p-nitrophenol (GlcNAcbeta-pNP) is not inhibited by conce
48                                   Similarly, p-nitrophenol glucuronide formation was unaffected by he
49 d during the P450-dependent hydroxylation of p-nitrophenol has been developed.
50 cients of benzene, anthracene, m-cresol, and p-nitrophenol in enhanced-fluidity liquid mixtures of et
51                           Glucuronidation of p-nitrophenol in intact microsomes was increased in part
52 e S(0)-state p-nitrophenolate anion recovers p-nitrophenol in its electronic ground state.
53 e show that this system efficiently releases p-nitrophenol in the presence of all three components an
54 portantly, we show that catalytic release of p-nitrophenol is sensitive to the presence of a single b
55           At pH 9.5, the rate enhancement of p-nitrophenol liberation from BNPP relative to backgroun
56 n using synthetic (4-methylumbelliferone- or p-nitrophenol-linked) alpha- or beta-mannosides as subst
57                                   NpdA2 is a p-nitrophenol monooxygenase belonging to the two-compone
58     Autodock was used to dock chlorzoxazone, p-nitrophenol, N-nitrosodimethylamine, acetominophen, ca
59 olvated Au(+) onto the surface of an aqueous p-nitrophenol/NaBH4 mixture.
60  the rate of reaction (e.g., E214G increases p-nitrophenol oxidation 15-fold) by controlling substrat
61 e phosphatase activity by 1.39 and 1.44 umol p-nitrophenol P (pNP) g(-1) h(-1), respectively.
62 eriments as a function of organic compounds (p-nitrophenol, p-benzoquinone, p-methoxyphenol, and oxal
63 earch investigated the removal mechanisms of p-nitrophenol, p-methoxyphenol, and p-benzoquinone at a
64  stain for mineralization, and enzyme assay (p-nitrophenol phosphate cleavage) for alkaline phosphata
65 sphotransferase or phosphatase activity with p-nitrophenol phosphate, inorganic pyrophosphate, or a r
66 activity approximately 3-5-fold using either p-nitrophenol phosphate, or tyrosine-phosphorylated myel
67 Legionella type II-dependent exoenzymes is a p-nitrophenol phosphorylcholine (p-NPPC) hydrolase whose
68 rete the hydrolytic enzymes metalloprotease, p-nitrophenol phosphorylcholine hydrolase, lipase, phosp
69 ctivities; i.e., protease, acid phosphatase, p-nitrophenol phosphorylcholine hydrolase, lipase, phosp
70 1A family for their ability to glucuronidate p-nitrophenol (pNP) and 4-methylumbelliferone (4-MU) rev
71 cinetobacter TF, PobR, to 'sense' a chemical p-nitrophenol (pNP) and measured the response via a fluo
72 luster in Escherichia coli allowed growth on p-nitrophenol (PNP) as sole carbon source.
73                    Based upon the release of p-nitrophenol (pNP) from p-nitrophenyl phosphate, acid p
74             At low substrate concentrations, p-nitrophenol (pNP) was rapidly turned over (47 min(-1))
75              Substrates used produced either p-nitrophenol (PNP), o-nitrophenol (ONP), or p-aminophen
76 itters, steroid hormones, acetaminophen, and p-nitrophenol (PNP).
77 cess was optimized for hydrolysis of MP into p-nitrophenol (PNP).
78  system was developed for the degradation of p-nitrophenol (PNP).
79 fects for several phosphorothioate esters of p-nitrophenol (pNPPT) and compared the results with data
80 with (1)npai* electronic character, the S(1) p-nitrophenol population decays on a time scale of ~12 p
81  with a hydrophobic pocket that encloses the p -nitrophenol product.
82  explain why nitroaromatic compounds such as p-nitrophenol resist photo-oxidative degradation in the
83 old faster product release rate constant for p-nitrophenol resulting from nitrobenzene oxidation.
84 ntaining NpdA2, an E. coli lysate transforms p-nitrophenol stoichiometrically to hydroquinone and hyd
85 ody, both with and without the bound product p -nitrophenol, strongly support and extend the structur
86 f M-form and P-form PSTs toward dopamine and p-nitrophenol, the Dopa/tyrosine sulfotransferase activi
87 ely begins with a two-step transformation of p-nitrophenol to hydroxy-1,4-benzoquinone, catalyzed by
88 nm Au nanoparticles towards the reduction of p-nitrophenol to p-aminophenol by sodium borohydride.
89 verall recovery of the S(0) state of aqueous p-nitrophenol via these competing pathways is close to 1
90 atalyze the hydrolysis of paraoxon to yellow p-nitrophenol, which further reduced the intrinsic AIE f