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

10 3- or 4-Aminophenols afforded esters in high yields and selectiv

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

31 2-Aminophenol can be selectively N-arylated with CuI, alth

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

55 2-Aminophenol only gave amides in high yields under both c

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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