ライフサイエンスコーパス: aminophenol

1 (pAPP) to produce a redox-active product, p-aminophenol.

2 a rearrangement of hydroxylaminobenzene to 2-aminophenol.

3 nophenols (monophenolase activity) but not o-aminophenols.

4 etween this enzyme and other dioxygenases, 2-aminophenol 1,6-dioxygenase has been purified by ethanol

5 used to distinguish the two conformers of 3-aminophenol (3AP) on the basis of differences in their e

6 e the reduction of p-nitrophenol (4-NP) to p-aminophenol (4-AP) as a model system.

7 onditions, the active form responsible for 4-aminophenol (4-AP) oxidase activity in both G4DFsc and 3

8 ncive reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) within 45 seconds though the hydrogen

9 e hydrolysis product of paracetamol, i.e., 4-aminophenol (4-AP), and two antibacterials, namely, cefa

10 c compounds, such as hydroquinone (HQ) and 4-aminophenol (4-AP), were detected amperometrically in fl

11 duced by ischemia reperfusion and N-acetyl-p-aminophenol (acetaminophen) administration.

12 3- or 4-Aminophenols afforded esters in high yields and selectiv

13 reocenters, from feedstock chemicals such as aminophenols, alpha,beta-unsaturated aldehydes, and alph

14 APAP or a nonhepatotoxic isomer, N-acetyl-m-aminophenol (AMAP).

15 itu from a readily accessible valine-derived aminophenol and a Z- or an E-gamma-substituted boronic a

16 use of a new composite consisting of poly 3-aminophenol and graphene oxide for solid-phase microextr

17 s synthesized by in-situ polymerization of 3-aminophenol and graphene oxide in weak alkaline media.

18 epared by a conproportionation of the parent aminophenol and iminoquinone compounds.

19 r rearrangement of hydroxylaminobenzene to 4-aminophenol and in the enzymatic hydroxymutation of chor

20 The Km values for 2-aminophenol and oxygen were 4.2 and 710 microM, respecti

21 is precursor show rearranged protonated o-/p-aminophenols and solvent water adducts (catechol, hydroq

22 mal glucuronidation of estradiol, estrone, 4-aminophenol, and 4-nitrophenol by 103, 187, 162, and 92%

23 On the other hand, the reaction of 2-aminophenols/anilines produced the corresponding benzazi

24 ver injury induced by overdose of N-acetyl-p-aminophenol (APAP) and defined three distinct MF subsets

25 Paracetamol (N-acetyl-p-aminophenol (APAP), otherwise known as acetaminophen) is

26 use hepatocytes, HyperIL6 reduced N-acetyl-p-aminophenol (APAP)-induced cell death independent of STA

27 detoxification of acetaminophen [N-acetyl-p-aminophenol (APAP)]-induced hepatotoxicity.

28 adical-scavenging solvent; and N-acetyl-para-aminophenol (APAP, or paracetamol), a hepatotoxic analge

29 Acetaminophen (N-acetyl-p-aminophenol [APAP]) hepatotoxicity is a process characte

30 Acetaminophen (N-acetyl-p-aminophenol [APAP]) is one of the leading causes of acut

31 injury caused by acetaminophen (acetyl-para-aminophenol [APAP]) is the main cause of acute liver fai

32 Acetaminophen (N-acetyl-p-aminophenol, APAP) and (13)C6-APAP were incubated with r

33 Acetaminophen (N-acetyl-para-aminophenol; APAP) overdose is the most common cause of

34 Acetaminophen (N-acetyl-p-aminophenol; APAP) toxicity is a common cause of liver d

35 meta-Aminophenols are formed by the action of DBU on 3-amino-

36 While the pyrroles and aminophenols are formed when the propargylic alkyne is t

37 e inhibition of laccase activity and using 4-aminophenol as redox mediator at pH 5.0, LACC/PB/GPE exh

38 eventing the escape of volatile materials, p-aminophenol, as opposed to phenol, is the major liquid p

39 by a readily accessible l-threonine-derived aminophenol-based boryl catalyst, affording the desired

40 tion of the structures of the small-molecule aminophenol-based catalysts.

41 x noninnocence and covalency in the vanadium-aminophenol bonding.

42 yde, catalyzed by a proton-activated, chiral aminophenol-boryl catalyst.

43 , p-aminophenyl phosphate was converted to p-aminophenol by AP, and the electroactive product was qua

44 in the biodegradation of nitrobenzene and 2-aminophenol by Pseudomonas pseudoalcaligenes JS45.

45 towards the reduction of p-nitrophenol to p-aminophenol by sodium borohydride.

46 2-Aminophenol can be selectively N-arylated with CuI, alth

47 formation of N-arylated products of 3- and 4-aminophenols can be obtained with BrettPhos precatalyst,

48 is derived in situ from a readily accessible aminophenol compound at ambient temperature, were comple

49 The aminophenol compound that is needed for the second catal

50 mediate with the nucleophiles indoline and 2-aminophenol correlate with an upfield shift of the subst

51 Q intermediates in the catalytic cycles of o-aminophenol dioxygenases.

52 Electroactive p-aminophenol, enzymatically generated at the bead-enzyme

53 A new colorimetric probe, based on aminophenol-extended naphthoquinone (APNQ), was synthesi

54 Here we report a benzoxazine-based m-aminophenol-formaldehyde resin (APFac) polymerized at am

55 d air-sensitivity of diversely substituted o-aminophenols from which they are generally prepared by c

56 Coupling of anilines to o-aminophenol groups derived from tyrosine residues is als

57 e difference being that the ortho adducts (o-aminophenol, hydroquinone) are formed in a higher ratio

58 f 495 new Fe(III) complexes synthesized from aminophenol, hydroxybenzaldehyde, and pyridine derivativ

59 escribed involving addition of anilines to o-aminophenols in the presence of sodium periodate.

60 prepared by oxidative cyclocondensation of 2-aminophenols, including the natural products exfoliazone

61 In contrast, 2-aminophenol is cleaved to 2-aminomuconic acid semialdehy

62 of the substrate p-aminophenyl phosphate top-aminophenol is detectable in less than 30 s using cyclic

63 Selective O-arylation of 3- and 4-aminophenols is achieved with copper-catalyzed methods e

64 in catalyzes the two-electron oxidation of 4-aminophenol (k(cat)/K(M) = 1,500 M(-1).min(-1)) to the c

65 The o-aminophenol kynurenine catabolites 3HK and 3-hydroxyanth

66 ino-3-hydroxyphenyl)ethan-1-one, which is an aminophenol lacking the amino acid moiety of 3-hydroxyky

67 nation of FeCl3 to the redox-active pyridine-aminophenol ligand NNO(H2) in the presence of base and u

68 Coordination of a redox-active pyridine aminophenol ligand to Ru(II) followed by aerobic oxidati

69 ecies supported by two redox-active N-phenyl aminophenol ligands was prepared.

70 A commercially available aminophenol may be used, and allyl boronates, which may

71 ine analogues have been prepared where the 4-aminophenol "metabolic alert" has been modified by repla

72 zine-like compound, which suggested that the aminophenol moiety in 3-hydroxykynurenine is essential f

73 affect the metal-binding properties of the o-aminophenol-N,N,O-triacetic acid (APTRA)-based fluoresce

74 neuroprotective cell-permeant Ca2+ buffer, 2-aminophenol-N,N,O-triacetic acid acetoxymethyl ester (AP

75 trochemical polymerization of the oxidized O-aminophenol (O-AP) film imprinted with FMDV serotype O o

76 t oxidant for the coupling of anilines and o-aminophenols on protein substrates.

77 2-Aminophenol only gave amides in high yields under both c

78 redox-active ligands containing catechol, o-aminophenol or o-phenylenediamine moieties show great po

79 etal complexes containing either catechol, o-aminophenol or o-phenylenediamine type ligands.

80 The oxidative coupling of o-aminophenols or catechols with aniline functional groups

81 The strategy uses o-aminophenols or o-catechols that are oxidized to active

82 yl group afford tetrasubstituted pyrroles, o-aminophenols, or 1,6-dihydropyridine carbaldehydes.

83 onverted p-aminophenyl phosphate (PAPP) to p-aminophenol (PAP(R)) in the presence of 2.5 mM Ru(NH(3))

84 nitrophenol (PNP), o-nitrophenol (ONP), or p-aminophenol (PAP) as products.

85 as used in this work to isolate and detect 4-aminophenol (PAP) in an acetaminophen sample spiked at t

86 s provided a detection limit of 31 muM for p-aminophenol (PAP) using Pt electrodes and was also used

87 catalyzed PAPG to an electroactive species p-aminophenol (PAP) which could be monitored on an electro

88 p-aminophenyl beta-D-galactopyranoside to p-aminophenol (PAP).

89 p-aminophenyl galactopyranoside (PAPG) to p-aminophenol (PAP).

90 nzocaine, procainamide and mesalazine, and 4-aminophenol - precursor to paracetamol (acetaminophen).

91 am amperometric detection of the liberated 4-aminophenol product Factors influencing the reaction, se

92 O- or N-arylated aminophenol products constitute a common structural moti

93 ctive for conversion of 4-nitrophenol into 4-aminophenol, providing an example of the potential oppor

94 The aryl substructures encompassed aminophenol, resorcinol, dihydroxy benzophenone, and toc

95 tors based on arylsuphonyl derivatives of an aminophenol ring linked to a pyridyl-based S1 binding gr

96 , respectively, toward electrodetection of 4-aminophenol than cuboctahedrons, providing a label-free

97 hown that enzymes in cell extracts convert 2-aminophenol to 2-aminomuconate in the presence of NAD+.

98 l immunosensor along with redox cycling of 4-aminophenol to 4-quinoneimine was improved to a great ex

99 dechlorination of 2-Cl- and 3-Cl-aniline to aminophenols to obtain insights into the impact of the s

100 ed by NspF, a mono-oxygenase that converts o-aminophenols to the corresponding nitroso product (hydro

101 selective O- and N-arylation of unprotected aminophenols using aryl halides.

102 atic conversion of hydroxylaminobenzene to 2-aminophenol was carried out in 18O-labeled water, the pr

103 Pd-catalyzed carbonylation of styrenes with aminophenols was realized, chemoselectively affording am

104 Amino-TFM (aTFM; 3-trifluoromethyl-4-aminophenol) was the only reductive metabolite identifie

105 p-Aminophenol, which is enzymatically generated by the imm

106 ivity in the reduction of 4-nitrophenol to 4-aminophenol, while Cu(12) displays very low activity.

107 um-catalyzed chemoselective carbonylation of aminophenols with iodoarenes was realized by changing li