ライフサイエンスコーパス: p-nitrophenol

1 er nitroaromatics such as p-nitrotoluene and p-nitrophenol.

2 action to be thermodynamically favorable for p-nitrophenol.

3 less to p-methoxyphenol removal compared to 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 ulfates small phenols such as 1-naphthol and p-nitrophenol and thyroid hormones, including 3,3'-diiod

22 ergy docked configurations of chlorzoxazone, p-nitrophenol, and N-nitrosodimethylamine, high-affinity

23 His L91, Arg L96, and the bound p -nitrophenol are linked into a hydrogen-bonding networ

24 m temperature, among which the catalyst with p-nitrophenol as ligand shows the highest catalytic acti

25 With p-nitrophenol as substrate, the V(max)/K(m) determined f

26 e deviations in V(max)/K(m) with dopamine or p-nitrophenol as substrate.

27 For all cell types examined, absorbance of p-nitrophenol at 405 nm is directly proportional to the

28 The decreased COD adsorption for p-nitrophenol at higher anodic potentials was attributed

29 ta-Glycosidase activity was quantified using p-nitrophenol-beta-d-glucopyranoside and SIM isoflavone

30 high catalytic activity in the reduction of p-nitrophenol by NaBH4 .

31 Ultrasensitive SERS detection of p-nitrophenol can be achieved when oxidation of surface-

32 gene cluster, which encodes the enzymes of a p-nitrophenol catabolic pathway from Arthrobacter sp. st

33 It was concluded that the p-nitrophenol catabolic pathway in JS443 most likely beg

34 ysis by adding a suitable chemical stimulus (p-nitrophenol cocatalyst) switched the reactivity decide

35 ronmental systems: an atmospheric pollutant (p-nitrophenol), crude oil extracts, and groundwater.

36 Spectrophotometric assays with p-nitrophenol derivatives also demonstrated that McaP is

37 orresponding prodrug component consists of a p-nitrophenol ester linked to the 3' end of an 8-mer oli

38 The rate constant of p-nitrophenol formation followed by stopped-flow spectro

39 a one step process involving displacement of p-nitrophenol from appropriately substituted ring openin

40 sequent liberation of a second equivalent of p-nitrophenol from the phosphorylated calixarene interme

41 the A107T variant produced >98% p-cresol and p-nitrophenol from toluene and nitrobenzene, respectivel

42 mple sugar acceptor N-acetylglucosamine-beta-p-nitrophenol (GlcNAcbeta-pNP) is not inhibited by conce

43 Similarly, p-nitrophenol glucuronide formation was unaffected by he

44 d during the P450-dependent hydroxylation of p-nitrophenol has been developed.

45 cients of benzene, anthracene, m-cresol, and p-nitrophenol in enhanced-fluidity liquid mixtures of et

46 Glucuronidation of p-nitrophenol in intact microsomes was increased in part

47 e show that this system efficiently releases p-nitrophenol in the presence of all three components an

48 portantly, we show that catalytic release of p-nitrophenol is sensitive to the presence of a single b

49 At pH 9.5, the rate enhancement of p-nitrophenol liberation from BNPP relative to backgroun

50 n using synthetic (4-methylumbelliferone- or p-nitrophenol-linked) alpha- or beta-mannosides as subst

51 NpdA2 is a p-nitrophenol monooxygenase belonging to the two-compone

52 Autodock was used to dock chlorzoxazone, p-nitrophenol, N-nitrosodimethylamine, acetominophen, ca

53 olvated Au(+) onto the surface of an aqueous p-nitrophenol/NaBH4 mixture.

54 the rate of reaction (e.g., E214G increases p-nitrophenol oxidation 15-fold) by controlling substrat

55 eriments as a function of organic compounds (p-nitrophenol, p-benzoquinone, p-methoxyphenol, and oxal

56 earch investigated the removal mechanisms of p-nitrophenol, p-methoxyphenol, and p-benzoquinone at a

57 stain for mineralization, and enzyme assay (p-nitrophenol phosphate cleavage) for alkaline phosphata

58 sphotransferase or phosphatase activity with p-nitrophenol phosphate, inorganic pyrophosphate, or a r

59 activity approximately 3-5-fold using either p-nitrophenol phosphate, or tyrosine-phosphorylated myel

60 Legionella type II-dependent exoenzymes is a p-nitrophenol phosphorylcholine (p-NPPC) hydrolase whose

61 rete the hydrolytic enzymes metalloprotease, p-nitrophenol phosphorylcholine hydrolase, lipase, phosp

62 ctivities; i.e., protease, acid phosphatase, p-nitrophenol phosphorylcholine hydrolase, lipase, phosp

63 1A family for their ability to glucuronidate p-nitrophenol (pNP) and 4-methylumbelliferone (4-MU) rev

64 cinetobacter TF, PobR, to 'sense' a chemical p-nitrophenol (pNP) and measured the response via a fluo

65 luster in Escherichia coli allowed growth on p-nitrophenol (PNP) as sole carbon source.

66 Based upon the release of p-nitrophenol (pNP) from p-nitrophenyl phosphate, acid p

67 At low substrate concentrations, p-nitrophenol (pNP) was rapidly turned over (47 min(-1))

68 Substrates used produced either p-nitrophenol (PNP), o-nitrophenol (ONP), or p-aminophen

69 cess was optimized for hydrolysis of MP into p-nitrophenol (PNP).

70 itters, steroid hormones, acetaminophen, and p-nitrophenol (PNP).

71 fects for several phosphorothioate esters of p-nitrophenol (pNPPT) and compared the results with data

72 with a hydrophobic pocket that encloses the p -nitrophenol product.

73 old faster product release rate constant for p-nitrophenol resulting from nitrobenzene oxidation.

74 ntaining NpdA2, an E. coli lysate transforms p-nitrophenol stoichiometrically to hydroquinone and hyd

75 ody, both with and without the bound product p -nitrophenol, strongly support and extend the structur

76 f M-form and P-form PSTs toward dopamine and p-nitrophenol, the Dopa/tyrosine sulfotransferase activi

77 ely begins with a two-step transformation of p-nitrophenol to hydroxy-1,4-benzoquinone, catalyzed by

78 nm Au nanoparticles towards the reduction of p-nitrophenol to p-aminophenol by sodium borohydride.