ライフサイエンスコーパス: nitrophenol

1 -1), and an industrial byproduct (4-methyl-2-nitrophenol).

2 -nitration occurs giving 2,4-di-tert-butyl-6-nitrophenol.

3 he hydrolysis product of para-oxon, namely p-nitrophenol.

4 covalent attachment to the tyrosine mimic, p-nitrophenol.

5 sted except nitrobenzene, which gives only m-nitrophenol.

6 covalent attachment to the tyrosine mimic, p-nitrophenol.

7 ol is the lack of hydrogen bond acidity of 2-nitrophenol.

8 sitivity to the inhibition by 2,6-dichloro-4-nitrophenol.

9 id phosphatases in viable cells to produce p-nitrophenol.

10 generation in degrading 4-nitrophenol and 2-nitrophenol.

11 ose and l-glutamic acid, ascorbic acid and o-nitrophenol.

12 mpare these spectra to gaseous and aqueous 2-nitrophenol.

13 gh catalytic activity towards reduction of 4-nitrophenol.

14 aseous, aqueous, and organic aerosol-bound 2-nitrophenol.

15 tion to be thermodynamically favorable for p-nitrophenol.

16 ess to p-methoxyphenol removal compared to p-nitrophenol.

17 n demonstrated with catalytic reduction of 4-nitrophenol.

18 catalytic activities for the reduction of 4-nitrophenol.

19 nitroaromatics such as p-nitrotoluene and p-nitrophenol.

20 olar power absorbed per molecule for several nitrophenols.

21 ium(III) chelates, GdNP-DO3A (1-methlyene-(p-NitroPhenol)-1,4,7,10-tetraazacycloDOdecane-4,7,10-triAc

22 0-triAcet ate) and GdNP-DO3AM (1-methlyene(p-NitroPhenol)-1,4,7,10-tetraazacycloDOdecane-4,7,10-triac

23 hree substitution photoproducts: 2-methoxy-5-nitrophenol (2), 2-chloro-4-nitrophenol (3), and 3-chlor

24 d(atz,ur) complex at 457nm by the 2-chloro-4-nitrophenol (2-CNP) which produced from the reaction of

25 The separation of 4-nitrophenol, 2,4-dinitrophenol, 2-methyl-4-nitrophenol,

26 ng L-triiodothyronine, thyroxine, estrone, p-nitrophenol, 2-naphthylamine, and 2-naphthol.

27 , a creatinine deiminase (CD) enzyme and a 2-nitrophenol (2NPh) titrating group.

28 cts: 2-methoxy-5-nitrophenol (2), 2-chloro-4-nitrophenol (3), and 3-chloro-4-methoxyphenol (4), in ch

29 echol are good substrates whereas 3-methyl-4-nitrophenol, 3-methyl-4-nitrocatechol, 4-nitrophenol, 3-

30 4-nitrophenol, 2,4-dinitrophenol, 2-methyl-4-nitrophenol, 3-methyl-4-nitrophenol, and 2-nitrophenol (

31 l-4-nitrophenol, 3-methyl-4-nitrocatechol, 4-nitrophenol, 3-nitrophenol, and 4-chlorocatechol were no

32 a-cresol yielded (21.2 +/- 1.4) % 3-methyl-2-nitrophenol (3M2NP), (22.8 +/- 1.8) % 3-methyl-4-nitroph

33 ophenol (3M2NP), (22.8 +/- 1.8) % 3-methyl-4-nitrophenol (3M4NP), (23.5 +/- 1.8) % 5-methyl-2-nitroph

34 y was tested using methylene blue (MB) and 4-nitrophenol (4-NP) as model pollutants under visible lig

35 icles (AuNPs) for the reduction process of 4-nitrophenol (4-NP) in the presence of sodium borohydride

36 I was investigated during the reduction of 4-nitrophenol (4-NP) in unbuffered pH systems.

37 rous web showed the enhancive reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) within 45 sec

38 site was used to catalyze the reduction of p-nitrophenol (4-NP) to p-aminophenol (4-AP) as a model sy

39 our probe molecules-chloramphenicol (CAP), 4-nitrophenol (4-NP), amoxicillin (AMX), and furazolidone

40 phenylboronic acid and in the reduction of 4-nitrophenol (4-NP).

41 of NO3 radicals with para-cresol, 4-methyl-2-nitrophenol (4M2NP) and HNO3 were identified as products

42 o-complexed with reduced FAD (FADH(-)) and 4-nitrophenol (4NP) (HadA(WT)-FADH(-)-4NP) was solved at 2

43 ophenol (3M4NP), (23.5 +/- 1.8) % 5-methyl-2-nitrophenol (5M2NP), (4.2 +/- 0.7) % MQUIN and (72.3 +/-

44 with NO3 yielded (11.5 +/- 0.8) % 6-methyl-2-nitrophenol (6M2NP), (4.4 +/- 0.3) % methyl-1,4-benzoqui

45 e), pesticides (metolachlor metabolite and 4-nitrophenol), a UV filter (benzophenone-1), and an indus

46 he effective photocatalytic destruction of 4-nitrophenol, a dangerous organic pollutant, are synthesi

47 addition, both enzymes were active toward 4-nitrophenol, a preferred substrate for CYP2E1.

48 We also discuss how different nitrophenol absorption profiles alter important atmosphe

49 2-Nitrophenol adsorbed on mineral and chloride aerosol sub

50 We also measured the UV-vis spectra of 2-nitrophenol adsorbed on several aerosol substrates repre

51 oxy)propionic acid, 3-phenoxybenozic acid, 4-nitrophenol, alachlor, atrazine, azoxystrobin, chlorpyri

52 to bind neutral guests, such as phenol and 4-nitrophenol, albeit weakly.

53 ), which cannot form an isocyanate, releases nitrophenol almost as rapidly (kobs = 0.028 min-1).

54 henols result in the same spectra of ionized nitrophenols alone, indicating no possibility for the fo

55 deration here, namely the reduction of (i) p-nitrophenol and (ii) hexacyanoferrate (iii), both by bor

56 ized mobility and dissociation constant of 2-nitrophenol and 2,4,6-trichlorophenol from ITP experimen

57 demonstrate detection of chemical toxins (2-nitrophenol and 2,4,6-trichlorophenol) in tap water, wit

58 acid methyl thioester, and the more acidic 4-nitrophenol and 2-chloro-4-nitrophenol which mimic elect

59 n rates of nitrite and HONO (most notably, 4-nitrophenol and 2-methyl-4-nitrophenol) could significan

60 ygen species (ROS) generation in degrading 4-nitrophenol and 2-nitrophenol.

61 TG1/pBS(Kan)T3MO produced 66% p-nitrophenol and 34% m-nitrophenol from nitrobenzene and

62 Oxidation of 4-nitrophenol and 4-nitrocatechol was observed for both de

63 Besides carboxylic acids, 4-nitrophenol and 4-nitrocatechol were identified as furth

64 ohexylimidazole), toward different proton (4-nitrophenol and [DMF.H(+)](CF3SO3(-))) (DMF = dimethyl-f

65 mated by immunoblot analysis, and rates of p-nitrophenol and chlorzoxazone hydroxylation were elevate

66 Rates of p-nitrophenol and chlorzoxazone hydroxylation were elevate

67 wo analytes of interest for ITMS analysis: o-nitrophenol and ephedrine.

68 ermined toward two prototypical aglycones, p-nitrophenol and estrone, in intact and digitonin-treated

69 Rates of 4-nitrophenol and formaldehyde production from the O-demet

70 so converts bis-p-nitrophenyl phosphate to p-nitrophenol and inorganic phosphate via a processive two

71 phosphate (pNPP) leads to the formation of p-nitrophenol and inorganic phosphate.

72 ), while the dominant removal mechanism of p-nitrophenol and p-methoxyphenol was a function of the an

73 At low anodic potentials (1.7-1.8 V/SHE), p-nitrophenol and p-methoxyphenol were removed primarily b

74 conversion of p-nitrophenylphosphate into p-nitrophenol and phosphate via beads carrying the immobil

75 g H-bond base-pairing interactions between 4-nitrophenol and phosphine oxide side chains.

76 he separations of substituted phenols (i.e., nitrophenol and resorcinol) and a few important pharmace

77 s there was a poor relationship between para-nitrophenol and SN-38 glucuronidation (r = 0.08; P = 0.7

78 lays a larger first hyperpolarizability than nitrophenol and the beta tensor of the two entities migh

79 roxylation of 4-nitrophenylboronic acid to 4-nitrophenol and the following hydride reduction with NaB

80 fates small phenols such as 1-naphthol and p-nitrophenol and thyroid hormones, including 3,3'-diiodot

81 us interpretation of the interaction between nitrophenols and one of the basic organic drugs.

82 Nitrophenols and related compounds were especially impor

83 trolled by applying TFM (3-trifluoromethyl-4-nitrophenol) and niclosamide to streams infested with th

84 iscous films (10(-5)-10(-4) in the case of 4-nitrophenol) and overall reaction yields up to 0.3 in so

85 rophenol, 2-methyl-4-nitrophenol, 3-methyl-4-nitrophenol, and 2-nitrophenol (these are the dominant N

86 , 3-methyl-4-nitrocatechol, 4-nitrophenol, 3-nitrophenol, and 4-chlorocatechol were not.

87 mol) and one-pot reactions of formic acid, 2-nitrophenol, and aldehydes into benzoxazoles in near qua

88 (PFP), hexafluoroisopropyl alcohol (HFP), 4-nitrophenol, and N-hydroxyphthalimide.

89 gy docked configurations of chlorzoxazone, p-nitrophenol, and N-nitrosodimethylamine, high-affinity s

90 itrile, including protonated nitrogen bases, nitrophenols, anilines, and diamines, as well as cobalt

91 olar compounds, phenol, 4-chlorophenol and 4-nitrophenol are extracted under headspace SPME condition

92 His L91, Arg L96, and the bound p -nitrophenol are linked into a hydrogen-bonding network b

93 Nitrophenols are well-known absorbers of near-UV/blue ra

94 he results highlight that NAC, in particular nitrophenols, are important light absorption contributor

95 The location of the nitrophenol aromatic substitutions was found to be criti

96 in-DNA intermediate) and generates free para-nitrophenol as a product.

97 temperature, among which the catalyst with p-nitrophenol as ligand shows the highest catalytic activi

98 hen exposed to benzene, phenol, xylene and 4-nitrophenol as negative controls, thereby demonstrating

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

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

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

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

103 effect, we have designed and synthesized two nitrophenol-based boronic acid reporter compounds that c

104 -Glycosidase activity was quantified using p-nitrophenol-beta-d-glucopyranoside and SIM isoflavone ex

105 ned with model glucuronide substrates like p-nitrophenol-beta-D-glucuronide (pNPG), the GUS orthologs

106 values for 4-methyl-7-hydroxycoumarin and 4-nitrophenol between on-line and off-line glucuronidation

107 rent kinetic isotope effects (AKIEs) of four nitrophenol-biodegrading microorganisms (Bacillus sphare

108 of estradiol, estrone, 4-aminophenol, and 4-nitrophenol by 103, 187, 162, and 92%, respectively (at

109 igh catalytic activity in the reduction of p-nitrophenol by NaBH4 .

110 ity than cubes toward reduction of 2-amino-5-nitrophenol by NaBH4 at 30 degrees C, but both particle

111 trated phenol (NP) compounds in ambient air (nitrophenol C6H5NO3, methylnitrophenol C7H7NO3, nitrocat

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

113 Irradiated nitrophenols can produce nitrite and nitrous acid (HONO)

114 C [(2S,3S)-trans-3-phenyl-2-oxiranylmethyl 4-nitrophenol carbonate], suggesting that Cif may be reduc

115 ne cluster, which encodes the enzymes of a p-nitrophenol catabolic pathway from Arthrobacter sp. stra

116 It was concluded that the p-nitrophenol catabolic pathway in JS443 most likely begin

117 chemical pathways for aqueous solutions of p-nitrophenol, chosen as a representative nitroaromatic co

118 is by adding a suitable chemical stimulus (p-nitrophenol cocatalyst) switched the reactivity decidedl

119 Various nitrophenol compounds also were modified in this reactio

120 sitizers and suggest that NS-123 and similar nitrophenol compounds may be effective in antiglioma mod

121 ory stress, that is, after immunization with nitrophenol-conjugated chicken gamma-globulin in alum.

122 (most notably, 4-nitrophenol and 2-methyl-4-nitrophenol) could significantly contribute to the occur

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

124 s pentachlorophenol (PCP) and 2,6-dichloro-4-nitrophenol (DCNP) were used to modulate DNA adduct and

125 tide vinyl sulfone Z-L3VS and a 125I-labeled nitrophenol derivative (125I-NIP-L3VS) covalently modify

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

127 1)O(2)) that, in turn, readily reacts with p-nitrophenol enzymatically produced under alkaline condit

128 responding prodrug component consists of a p-nitrophenol ester linked to the 3' end of an 8-mer oligo

129 The lipophilicity of the nitrophenols, expressed as a water-solvent partition coe

130 The rate constant of p-nitrophenol formation followed by stopped-flow spectroph

131 N activity was assessed by quantification of nitrophenol formation, and total antioxidant capacity (T

132 al method is based on the determination of p-nitrophenol formed in the course of enzyme-catalyzed hyd

133 one step process involving displacement of p-nitrophenol from appropriately substituted ring opening

134 ontaining polymers extracted up to >99% of 4-nitrophenol from aqueous solution, and the solvent-extra

135 an)T3MO produced 66% p-nitrophenol and 34% m-nitrophenol from nitrobenzene and 100% p-methoxyphenol f

136 formed 75% m-cresol from toluene and 100% m-nitrophenol from nitrobenzene; thus, for the first time

137 acetyl galactosaminidase would also liberate nitrophenol from the above substrates.

138 result of acid-catalyzed dissociation of the nitrophenol from the lanthanide.

139 quent liberation of a second equivalent of p-nitrophenol from the phosphorylated calixarene intermedi

140 ion is readily monitored by the release of 4-nitrophenol from the polymer using UV-vis spectrophotome

141 e A107T variant produced >98% p-cresol and p-nitrophenol from toluene and nitrobenzene, respectively,

142 Nitrophenols from both methyl chavicol and toluene photo

143 The nitrophenols giving the highest photoproduction rates of

144 le sugar acceptor N-acetylglucosamine-beta-p-nitrophenol (GlcNAcbeta-pNP) is not inhibited by concent

145 Similarly, p-nitrophenol glucuronide formation was unaffected by hepa

146 The nitrophenol group in Gd(NP-DO3AM) does not dissociate fr

147 A template with three 4-nitrophenol H-bond donor recognition units was used with

148 FF and APRIL were created and immunized with nitrophenol hapten-conjugated keyhole limpet hemocyanin

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

150 n of 5-nitro-benzisoxazole forming 2-cyano-4-nitrophenol has long served as a design platform of enzy

151 Nitrophenols have been identified in a variety of phases

152 ents of benzene, anthracene, m-cresol, and p-nitrophenol in enhanced-fluidity liquid mixtures of etha

153 ent avobenzone and the industrial chemical 4-nitrophenol in follicular and seminal fluids suggests th

154 Glucuronidation of p-nitrophenol in intact microsomes was increased in partia

155 S(0)-state p-nitrophenolate anion recovers p-nitrophenol in its electronic ground state.

156 s found to be critically important, with the nitrophenol in the photo-oxidation of 4-methyl catechol

157 show that this system efficiently releases p-nitrophenol in the presence of all three components and

158 2,6-Dichloro-4-nitrophenol inhibits phenolsulfotransferases, but not hy

159 be catalytically active for conversion of 4-nitrophenol into 4-aminophenol, providing an example of

160 H optimum for the standard assay substrate 4-nitrophenol is at pH 5.5; upon oxidation, the optimum ch

161 rtantly, we show that catalytic release of p-nitrophenol is sensitive to the presence of a single bas

162 lipophilicity of 2-nitrophenol over 3- and 4-nitrophenol is the lack of hydrogen bond acidity of 2-ni

163 decomposes rapidly in buffer with release of nitrophenol (kobs = 0.13 min-1); under the same conditio

164 V/K)bridge]; and at the nitrogen atom in the nitrophenol leaving group [15(V/K)].

165 V/K)bridge], and at the nitrogen atom in the nitrophenol leaving group [15(V/K)].

166 V/K)bridge], and at the nitrogen atom in the nitrophenol leaving group [15(V/K)].

167 hat, after enzymatic reduction and loss of a nitrophenol leaving group, a reactive iminium species wa

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

169 using synthetic (4-methylumbelliferone- or p-nitrophenol-linked) alpha- or beta-mannosides as substra

170 nd agglutination was inhibited by mannan and nitrophenol-modified sugar derivatives, but not by simpl

171 ects several nitroaromatic compounds such as nitrophenols, mononitroaniline, and dinitrotoluene with

172 NpdA2 is a p-nitrophenol monooxygenase belonging to the two-component

173 tigated the C and N isotope fractionation of nitrophenol monooxygenation to complement the characteri

174 Autodock was used to dock chlorzoxazone, p-nitrophenol, N-nitrosodimethylamine, acetominophen, caff

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

176 endritic cells was followed using the hapten nitrophenol (NP) conjugated to rat Ig carrier.

177 cric acid (PA), 2,4-dinitrophenol (DNP), and nitrophenol (NP), via the fluorescence quenching mechani

178 ising a ligand of CD22 linked to an antigen (nitrophenol; NP) can use a monoclonal anti-NP IgM as a d

179 report a novel system to analyze atmospheric nitrophenols (NPs).

180 4-6 ppm upfield from the aglycone 2-fluoro-4-nitrophenol (OFPNP).

181 used produced either p-nitrophenol (PNP), o-nitrophenol (ONP), or p-aminophenol (PAP) as products.

182 led to catalyze the sulfate conjugation of 4-nitrophenol or 17beta-estradiol, prototypic substrates f

183 elative standard deviation, in the case of 3-nitrophenol or bromothymol blue, respectively.

184 nt zone containing the acid-base indicator 3-nitrophenol or bromothymol blue.

185 oxic priority pollutants including hazardous nitrophenols, organophosphates, and polychlorinated aren

186 r factor in the increased lipophilicity of 2-nitrophenol over 3- and 4-nitrophenol is the lack of hyd

187 he rate of reaction (e.g., E214G increases p-nitrophenol oxidation 15-fold) by controlling substrate

188 ares some properties with previously studied nitrophenol oxygenases.

189 phosphatase activity by 1.39 and 1.44 umol p-nitrophenol P (pNP) g(-1) h(-1), respectively.

190 ried for the sensitive determination of para-nitrophenol (p-NP) through the electrochemical method.

191 iments as a function of organic compounds (p-nitrophenol, p-benzoquinone, p-methoxyphenol, and oxalic

192 rch investigated the removal mechanisms of p-nitrophenol, p-methoxyphenol, and p-benzoquinone at a po

193 tain for mineralization, and enzyme assay (p-nitrophenol phosphate cleavage) for alkaline phosphatase

194 hotransferase or phosphatase activity with p-nitrophenol phosphate, inorganic pyrophosphate, or a ran

195 tivity approximately 3-5-fold using either p-nitrophenol phosphate, or tyrosine-phosphorylated myelin

196 Ymt also used bis(para-nitrophenol) phosphate as a substrate.

197 motifs reduced the turnover rate of bis(para-nitrophenol) phosphate by a factor of 10(4) and phosphol

198 gionella type II-dependent exoenzymes is a p-nitrophenol phosphorylcholine (p-NPPC) hydrolase whose a

199 te the hydrolytic enzymes metalloprotease, p-nitrophenol phosphorylcholine hydrolase, lipase, phospho

200 ivities; i.e., protease, acid phosphatase, p-nitrophenol phosphorylcholine hydrolase, lipase, phospho

201 nitrophenyl-beta-alanine nor the 2-methoxy-5-nitrophenol photolysis side product activates, inhibits,

202 mprehensive study of the interaction between nitrophenols (pi-acceptors) and amiodarone (AM) was perf

203 family for their ability to glucuronidate p-nitrophenol (pNP) and 4-methylumbelliferone (4-MU) revea

204 netobacter TF, PobR, to 'sense' a chemical p-nitrophenol (pNP) and measured the response via a fluore

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

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

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

208 Substrates used produced either p-nitrophenol (PNP), o-nitrophenol (ONP), or p-aminophenol

209 ss was optimized for hydrolysis of MP into p-nitrophenol (PNP).

210 ters, steroid hormones, acetaminophen, and p-nitrophenol (PNP).

211 ystem was developed for the degradation of p-nitrophenol (PNP).

212 cts for several phosphorothioate esters of p-nitrophenol (pNPPT) and compared the results with data f

213 th (1)npai* electronic character, the S(1) p-nitrophenol population decays on a time scale of ~12 ps.

214 ocess is particularly important for the para-nitrophenols, possibly because their less sterically hin

215 the indoleninium-substituent entity and the nitrophenol (present in the protonated open form, b(+))

216 th a hydrophobic pocket that encloses the p -nitrophenol product.

217 with either three phosphine oxide or three 4-nitrophenol recognition units to form the noncovalent ba

218 monstrated in a recyclable manner by using 4-nitrophenol reduction as a probe reaction.

219 ibility of Au25 (SG)18 is evaluated by the 4-nitrophenol reduction reaction.

220 alladium- or silver-nanoparticle-catalyzed 4-nitrophenol reduction, and 3) gold-nanoparticle-catalyze

221 This nitrophenol release probably involves cyclization to an

222 ermined to be 0.79 mM and 31.1 micromol para-nitrophenol released/min/mg with p-nitrophenyl-beta-D-ma

223 xplain why nitroaromatic compounds such as p-nitrophenol resist photo-oxidative degradation in the en

224 ctra of possible interactions between AM and nitrophenols result in the same spectra of ionized nitro

225 d faster product release rate constant for p-nitrophenol resulting from nitrobenzene oxidation.

226 s activity against the glycosides of phenol, nitrophenols, serine, and threonine.

227 hemical fate of 4NC, and presumably of other nitrophenols, should depend on whether they undergo phot

228 Substituted nitrophenols showed an exponential decay, with the nitro

229 ionation was neither masked substantially by nitrophenol speciation nor transport across cell membran

230 aining NpdA2, an E. coli lysate transforms p-nitrophenol stoichiometrically to hydroquinone and hydro

231 , both with and without the bound product p -nitrophenol, strongly support and extend the structural

232 cterized their kinetic activity against para-nitrophenol substrates esterified with consecutively lon

233 chemoenzymatic methods for synthesizing para-nitrophenol-tagged alpha2-3- and alpha2-6-linked sialyl

234 The lampricides 3-trifluoromethyl-4-nitrophenol (TFM) and 2',5-dichloro-4'-nitrosalicylanili

235 further used to quantify 3-trifluoromethyl-4-nitrophenol (TFM) reductive metabolism.

236 erant native species, to 3-trifluoromethyl-4-nitrophenol (TFM), a pesticide commonly used in sea lamp

237 The lampricide, 3-trifluoromethyl-4-nitrophenol (TFM), is a primary component to sea lamprey

238 ntrol with the pesticide 3-trifluoromethyl-4-nitrophenol (TFM).

239 M-form and P-form PSTs toward dopamine and p-nitrophenol, the Dopa/tyrosine sulfotransferase activiti

240 4-nitrophenol, 3-methyl-4-nitrophenol, and 2-nitrophenol (these are the dominant NPs, typically in th

241 1) shows high activity in the reduction of 4-nitrophenol to 4-aminophenol, while Cu(12) displays very

242 y begins with a two-step transformation of p-nitrophenol to hydroxy-1,4-benzoquinone, catalyzed by Np

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

244 me P450s CYP3A1 and CYP2B1/2, testosterone/4-nitrophenol uridine diphosphate glucuronosyltransferase

245 me, the investigation of both pyridine and 4-nitrophenol vapor adsorption isotherms at very low conce

246 within 1 s of exposure) and ultrasensitive 4-nitrophenol vapor detection (at a sub-ppb level) were su

247 rall recovery of the S(0) state of aqueous p-nitrophenol via these competing pathways is close to 100

248 Only when 4-nitrophenol was biodegraded by Pseudomonas sp. 1A did is

249 idation of 4-methyl-7-hydroxy coumarin and 4-nitrophenol were determined using the CE method and by o

250 phthalene, 2,4-dichloronicotinic acid, and 4-nitrophenol were similar to or higher than those of urin

251 -DFT as well as geometry optimization of the nitrophenols were calculated with the B3LYP functional,

252 the more acidic 4-nitrophenol and 2-chloro-4-nitrophenol which mimic electronically excited cofactor

253 alyze the hydrolysis of paraoxon to yellow p-nitrophenol, which further reduced the intrinsic AIE flu

254 nction achieved an 86% degradation rate of 4-nitrophenol, while the MoS(2)/Bi(2)O(3)/CdS composite ex

255 evaluated with respect to the reduction of 4-nitrophenol with NaBH4.