ライフサイエンスコーパス: peroxide

1 rtant for V. cholerae resistance to hydrogen peroxide.

2 dative stress, finally convert into hydrogen peroxide.

3 one and reduces molecular oxygen to hydrogen peroxide.

4 regulated production of apoplastic hydrogen peroxide.

5 ns catalyst for oxygen reduction to hydrogen peroxide.

6 urement of the enzymatic by-product hydrogen peroxide.

7 en without generating superoxide or hydrogen peroxide.

8 lower limit of detection of 368 nM hydrogen peroxide.

9 ducing the generation of superoxide/hydrogen peroxide.

10 li treated with a sublethal dose of hydrogen peroxide.

11 o controllably produce bactericidal hydrogen peroxide.

12 n metastatic disease is mediated by hydrogen peroxide.

13 -) anion radical in the presence of hydrogen peroxide.

14 member, catalyzes the production of hydrogen peroxide.

15 nuous on-site production of neutral hydrogen peroxide.

16 id-catalyzed skeletal rearrangement of these peroxides.

17 ioxidant stabilizer, thus more prone to form peroxides.

18 from ferroptosis by eliminating phospholipid peroxides.

19 c acid and CO(2) upon reaction with hydrogen peroxide (150 mM).

20 ectability was down to picomoles of hydrogen peroxide (4 pmol for CL and 210 pmol for amperometry) an

21 ts from iron-dependent accumulation of lipid peroxide(5,6).

22 the formation of callose papillae, hydrogen peroxide accumulation and the Salicylic acid (SA) - depe

23 and produce reactive radicals from hydrogen peroxide activation have been extensively studied in ord

24 The use of hydrogen peroxide altered AQP3 and NOTCH1 expression, and the use

25 ion of harmful byproducts including hydrogen peroxide, ammonia, and reactive aldehydes.

26 Hydrogen peroxide and 1,4-dioxane degradations were maximized nea

27 On the other hand, the reaction of hydrogen peroxide and ammonium thiocyanate followed by one-pot ad

28 ts were repeated in the presence of hydrogen peroxide and AMP-PNP, an ATP analog and competitive inhi

29 travital biosensor imaging showed that wound peroxide and arachidonic acid converged on half-millimet

30 reduction of superoxide radicals to hydrogen peroxide and are important in the protection against oxi

31 edded peroxidasin was supplied with hydrogen peroxide and bromide.

32 The reactivity of hydrogen peroxide and catalytic hydroiodic acid toward 3,6-dimeth

33 cessfully used for colorimetric detection of peroxide and glucose in medical diagnostics.

34 active oxygen species - superoxide, hydrogen peroxide and hydroxyl radicals - have long been suspecte

35 forward mechanism for generation of hydrogen peroxide and induction of metabolic stress through enhan

36 two solid oxygen fertilizers (SOFs, calcium peroxide and magnesium peroxide) to reduce N(2)O product

37 NAD(+)-depleting genotoxins such as hydrogen peroxide and methylmethane sulfonate.

38 zyme that can effectively breakdown hydrogen peroxide and minimize the downstream reactive oxygen spe

39 on of superoxide free radicals into hydrogen peroxide and oxygen, is known to be among the slowest fo

40 xidative stress parameters such as, hydrogen peroxide and reactive substances were significantly elev

41 ects of oxidation on calmodulin (CaM), using peroxide and the Met to Gln oximimetic mutations.

42 The reactive oxygen species hydrogen peroxide and the polyunsaturated fatty acid arachidonic

43 e TGF-beta1-dependent production of hydrogen peroxide and the presence of myeloperoxidase (MPO) deriv

44 s the influences of indigenous milk hydrogen peroxide and thiocyanate.

45 of cydD renders cells resistant to hydrogen peroxide and to aminoglycoside antibiotics.

46 al Organization for EPA and DHA Omega-3s for peroxide and/or p-anisidine value suggesting a compromis

47 However, peroxide and/or p-anisidine value were only suitable for

48 g singlet oxygen, superoxide anion, hydrogen peroxide, and hydroxyl radicals, to afford superb antitu

49 nlight, ultraviolet light, ethanol, hydrogen peroxide, and hypochlorite attain 99.9% reduction.

50 (ROS) quenchers, the generation of hydrogen peroxide, and increased levels of intracellular oxidativ

51 2,6,6-tetramethylpiperidine-1-oxyl, hydrogen peroxide, and ozone.

52 ns, breakdown of radical chains and hydrogen peroxide, and scavenging of reactive oxygen species.

53 ant electrophiles peroxynitrite and hydrogen peroxide, and with the probe monobromobimane, were studi

54 g effect through cell populations in a lipid peroxide- and iron-dependent manner.

55 Using the approach, we confirm peroxide- and thioredoxin-related quaternary transitions

56 misynthetic artemisinins and other bioactive peroxides are best known for their powerful antimalarial

57 eveloped in an aqueous medium using hydrogen peroxide as a benign oxidant and ammonium thiocyanate as

58 ids was achieved employing the di-tert-butyl peroxide as a source of free radicals and a dehydrogenat

59 tional groups and relies on the dual role of peroxide as nucleophile and oxidant through an orchestra

60 antiomeric excess (up to 99%) using hydrogen peroxide as oxidant and a Bronsted acid additive under m

61 of sulfonylcyclopropanes using a bis(silyl) peroxide as the electrophilic oxygen source.

62 The use of inexpensive tert-butyl hydrogen peroxide as the oxidant to promote the desired selective

63 ing earth-abundant cobalt salts and hydrogen peroxide as the oxidant.

64 and tertiary alkyl sources, and aryl diacyl peroxides as the arylating source.

65 de (TBHP) as the methyl source, alkyl diacyl peroxides as the primary alkyl source, alkyl peresters a

66 as performed under electrogenerated hydrogen peroxide at a constant voltage of - 0.6 V vs Hg/HgSO(4)

67 ct of modifying okara with alkaline hydrogen peroxide at different H(2)O(2) concentrations and treatm

68 hane oxidation by in situ generated hydrogen peroxide at mild temperature (70 degrees C).

69 anode and usually the reduction of oxygen or peroxide at the cathode.

70 e to symmetry breaking by producing hydrogen peroxide at the egg's future posterior pole.

71 Multistaged discharge constructing lithium peroxide-based heterostructure with band discontinuities

72 tro and provides protection against hydrogen peroxide, bleach, and ciprofloxacin.

73 Bromelain, ficin-based, and carbamide peroxide bleaching gels showed a similar color change (p

74 ecifically, the mechanism relies on anionic, peroxide-bound intermediates.

75 r corresponding tetrahydropyrans lacking the peroxide bridge, to ascertain if this group is a key pha

76 d are more stable than those containing only peroxide bridges.

77 applied arachidonic acid and skin-permeable peroxide by micropipette perfusion to unwounded zebrafis

78 nerate superoxide anion radical and hydrogen peroxide by ozone-treated fruit was significantly lower

79 d specifically by the generation of hydrogen peroxide by the VL domain of the light chain.

80 onstrated that reactive oxygen (eg, hydrogen peroxide) can activate host cell signaling pathways that

81 dical anion (superoxide dismutase), hydrogen peroxide (catalase), hydroxyl radicals (mannitol) and si

82 In the presence of hydrogen peroxide, Cd-MsrB formed reversible intra- and intermole

83 erved that the oil has low acidity, value of peroxide, chlorophyll, carotenoids, beta-carotene and hi

84 Here, a ferric heme peroxide complex, [(F(8))Fe(III)-(O(2)(2-))](-) (P) (F(8

85 TMB is linearly associated with the hydrogen peroxide concentration.

86 The exhaled breath condensate hydrogen peroxide concentrations trended toward higher values in

87 Horseradish peroxidase (HRP) and hydrogen peroxide concentrations were directly measured, while gl

88 ng of catechol oxidation byproduct, hydrogen peroxide, confirmed that catechol was oxidized as a resu

89 g groups (n = 10): Group 1, 20 wt% carbamide peroxide (control); group 2, 1% papain-based whitening;

90 The reactivities of nonnative organic peroxide cosubstrates effectively exclude the possibilit

91 te: povidone-iodine, chlorhexidine, hydrogen peroxide, cyclodextrin, Citrox, cetylpyridinium chloride

92 d as well as endogenously generated hydrogen peroxide decreases spermathecal contractility by inhibit

93 neurons to control the induction of hydrogen peroxide defenses in the organism.

94 s expression of catalases and other hydrogen peroxide defenses.

95 exhibit complex kinetic behavior, requiring peroxide-dependent activation and undergoing suicide ina

96 compared to traditional redox techniques for peroxide detection.

97 rgy-dissipating ion channels, while hydrogen peroxide distributes oxidative stress to sensitize the n

98 um-oxygen batteries cycle by forming lithium peroxide during discharge and oxidizing it during rechar

99 t O(2) and associated generation of hydrogen peroxide during the regeneration step drive the oxidatio

100 pose that it is unlikely that SpAhpD removes peroxides either directly or via AhpC, and that SpAhpD c

101 reduced browning, superoxide anion, hydrogen peroxide, electrolyte leakage and malondialdehyde conten

102 Hydrogen peroxide emission was modestly higher in the ischemic mu

103 nts, supplementation with exogenous hydrogen peroxide enhanced E. coli growth through AppBCX-mediated

104 tions of xenon with recently discovered iron peroxide FeO(2), forming robust xenon-iron oxides Xe(2)F

105 ication of adenosine, dopamine, and hydrogen peroxide fluctuations occurring >10 min from the initial

106 Here we introduce Ferroptosis Inducing Peroxide for Chemoproteomics-1 (FIPC-1), a reactivity-ba

107 o measure exhaled breath condensate hydrogen peroxide for monitoring oxidative stress in asthma.

108 imitate peroxidase, which scavenges hydrogen peroxide for the mitigation of potential cytotoxicity.

109 Because peroxide formation is induced by a strong electric field

110 l potential to be used in the development of peroxide-free tooth whitening gels.

111 nematode's food source, can deplete hydrogen peroxide from the local environment and thereby protect

112 The hydrogen peroxide generated by XO catalysed oxidation of hypoxant

113 Hydrogen peroxide generated in the medium contributed to the cyto

114 roneal nerve induced increased mitochondrial peroxide generation, measured in permeabilised AT fibers

115 In conclusion, the peroxide group proved not to be crucial for the antileis

116 reactive oxygen species (ROS), with hydrogen peroxide (H(2) O(2) ) as the most abundant form that occ

117 Hydrogen peroxide (H(2) O(2) ) is ubiquitous in cells and at the

118 Hydrogen peroxide (H(2) O(2) ) mediates the biology of wound heal

119 l presence of glutathione (GSH) and hydrogen peroxide (H(2) O(2) ) with high specificity on a basis o

120 tive material, such reactions yield hydrogen peroxide (H(2) O(2) ), a reactive side-product, which ma

121 ning cetylpridinium chloride (CPC), hydrogen peroxide (H(2) O(2) ), sodium bicarbonate, and antioxida

122 how that eCO(2) triggers apoplastic hydrogen peroxide (H(2) O(2) )-dependent auxin production in toma

123 port on the development of a unique hydrogen peroxide (H(2) O(2) )-sensing motif and its capacity for

124 The UV/hydrogen peroxide (H(2)O(2)) advanced oxidation process (AOP) fre

125 crobial membranes were treated with hydrogen peroxide (H(2)O(2)) and sodium hypochlorite (NaOCl, liqu

126 Two species, hydrogen peroxide (H(2)O(2)) and the superoxide anion radical (O(

127 though hydroxyl radical ((*)OH) and hydrogen peroxide (H(2)O(2)) are regarded as major oxidants assoc

128 gical redox reactions, I identified hydrogen peroxide (H(2)O(2)) as a normal constituent of aerobic l

129 We continuously monitored hydrogen peroxide (H(2)O(2)) from household non-bleach surface cl

130 itrate stabilized AgNPs by O(2) and hydrogen peroxide (H(2)O(2)) in the dark and in irradiated Suwann

131 Hydrogen peroxide (H(2)O(2)) is a major reactive oxygen species i

132 Hydrogen peroxide (H(2)O(2)) is a reactive oxygen species (ROS) t

133 The reaction with hydrogen peroxide (H(2)O(2)) is considered to be the main cloud o

134 vel supply or in situ generation of hydrogen peroxide (H(2)O(2)) is essential for the stability of un

135 reproduction.SIGNIFICANCE STATEMENT Hydrogen peroxide (H(2)O(2)) is often studied in a pathological c

136 .S.A, 116, 19294-19298 (2019)] that hydrogen peroxide (H(2)O(2)) is spontaneously produced in microme

137 mumT mutant is no more sensitive to hydrogen peroxide (H(2)O(2)) killing than wild-type A. baumannii

138 Mechanistically, excessive hydrogen peroxide (H(2)O(2)) originated from monoamine oxidase B

139 Hydrogen peroxide (H(2)O(2)) plays an important role physiologica

140 Streptococcus parasanguinis, a hydrogen peroxide (H(2)O(2)) producing oral commensal, has antimi

141 ochondrial respiratory capacity and hydrogen peroxide (H(2)O(2)) production than aSAT (p < 0.05).

142 pathways resulting in promotion of hydrogen peroxide (H(2)O(2)) production.

143 nt electrocatalytic activity toward hydrogen peroxide (H(2)O(2)) reduction.

144 red for aerobic respiration but for hydrogen peroxide (H(2)O(2)) respiration using cytochrome c perox

145 ducing antioxidant power (FRAP) and hydrogen peroxide (H(2)O(2)) scavenging assays, showed that GG ex

146 ions (Fe(3+)) reducing power; (iv) hydrogen peroxide (H(2)O(2)) scavenging.

147 transporter of water, glycerol and hydrogen peroxide (H(2)O(2)) that is expressed in various epithel

148 Here, we used hydrogen peroxide (H(2)O(2)) to induce oxidative stress in E. gra

149 cale electrocatalytic production of hydrogen peroxide (H(2)O(2)) using a rotating ring-disk electrode

150 ous oxidation of dissolved SO(2) by hydrogen peroxide (H(2)O(2)) using pH-buffered, submicrometer, de

151 Epithelial production of hydrogen peroxide (H(2)O(2)) was analyzed in murine colonic epith

152 ion of virus-mediated generation of hydrogen peroxide (H(2)O(2)) we developed a model of intranasal s

153 them, mainly polyphenols, generated hydrogen peroxide (H(2)O(2)) when added to Dulbecco's modified Ea

154 idised glucose to gluconic acid and hydrogen peroxide (H(2)O(2)) while the chitin-AcOH decomposed the

155 ike behavior for the degradation of hydrogen peroxide (H(2)O(2)) with a K(m) of about 13 mM and speci

156 ion in HeLa cells after exposure to hydrogen peroxide (H(2)O(2)), a reagent commonly used to introduc

157 After reacting with hydrogen peroxide (H(2)O(2)), sickle-cell hemoglobin (HbS, betaE6

158 n honey: sugars, gluconic acid, and hydrogen peroxide (H(2)O(2)), which result from the enzymatic con

159 ethionine residues are sensitive to hydrogen peroxide (H(2)O(2))-mediated oxidation in vitro and in l

160 being exposed to a strong oxidant, hydrogen peroxide (H(2)O(2)).

161 onstruct an enzymatic biosensor for hydrogen peroxide (H(2)O(2)).

162 ter incubation with the pro-oxidant hydrogen peroxide (H(2)O(2)).

163 ecies biofilms via the secretion of hydrogen peroxide (H(2)O(2)).

164 plete reduction of oxygen (O(2)) to hydrogen peroxide (H(2)O(2)).

165 also thought to generate cytosolic hydrogen peroxide (H(2)O(2)).

166 te toward sustainable production of hydrogen peroxide (H(2)O(2)).

167 stimulates the rapid production of hydrogen peroxide (H(2)O(2)).(1)(,)(2) This then acts as an activ

168 uperoxide ([Formula: see text]) and hydrogen peroxide (H(2)O(2)); however, the precise mechanisms are

169 Hydrogen peroxide (H2O2) promotes a range of phenotypes depending

170 Hence, the unification of an isoxazoline and peroxide heterocycles could be a potential direction to

171 tate or arginine for the rate enhancement of peroxide heterolysis.

172 BIC) was produced with taurolidine, hydrogen peroxide, human serum, potassium iodide and doxorubicin/

173 evaluated exhaled breath condensate hydrogen peroxide in 60 patients (ages 20-83; 30 healthy patients

174 e sterilization efficacy of gaseous hydrogen peroxide in aseptic filling machines.

175 o measure exhaled breath condensate hydrogen peroxide in asthma patients and healthy participants.

176 talase control to scavenge residual hydrogen peroxide in calibrant solutions provided analytically se

177 ilizers in mineral soil (98-99%) and calcium peroxide in organic soil (25%) successfully reduced N(2)

178 ce assay and a device for measuring hydrogen peroxide in the exhaled breath condensate of asthma pati

179 can determine dynamic alteration of hydrogen peroxide in tumor, can evaluate the effectiveness of che

180 e oxygen generation from endogenous hydrogen peroxide in tumors.

181 nization of free aliphatic acids, the use of peroxides in C-H activation reactions directed by weakly

182 Rather, the accumulation of lipid peroxides in NKAP-deficient T cells was observed.

183 converted into three-dimensional polycyclic peroxides in the presence of H(2)O(2) under acid catalys

184 he finding that elevation of ROS by hydrogen peroxide increased Src phosphorylation, while ROS reduct

185 ased on Ca(2+) imaging, we isolated hydrogen-peroxide-induced Ca(2+) increases (hpca) mutants in Arab

186 icrovascular endothelial cells from hydrogen peroxide-induced cell death, as well as preservation of

187 on conserved defenses to prevent and repair peroxide-induced damage, but whether similar defenses mi

188 that cyclin C represses a subset of hydrogen peroxide-induced genes under normal conditions but is in

189 mutant had increased sensitivity to hydrogen peroxide-induced stress, was inhibited in its ability to

190 superoxide, which then recombines to form a peroxide intermediate.

191 react with both ferric superoxide and ferric peroxide intermediates formed during O(2) reduction thro

192 metals, ultraviolet radiation, or preformed peroxide intermediates, which has prevented the developm

193 e to effectively convert endogenous hydrogen peroxide into oxygen and then elevate the production of

194 bacterium can withstand endogenous hydrogen peroxide is incompletely understood.

195 the bactericidal effects of LTP and hydrogen peroxide is necessary but not sufficient for antibacteri

196 udy examines whether an increase in hydrogen peroxide is sustained posttreatment and potential mechan

197 plains why formation of the most stable tris-peroxide is the least kinetically viable and is not obse

198 Hydrogen peroxide is the preeminent chemical weapon that organism

199 Notably, tert-butyl hydrogen peroxide is used as the sole oxidant for these reactions

200 of Fe(2+)-PyC3A to Fe(3+)-PyC3A by hydrogen peroxide is very rapid, and we capitalized on this behav

201 ad and showed a trend toward higher hydrogen peroxide levels (mean 172.8 vs 115.9 nM; p = 0.25), and

202 cytoplasmic, but not mitochondrial, hydrogen peroxide levels were reduced in LPS-treated mCAT BMDMs.

203 the activities of thiol-based peroxidases in peroxide-mediated redox signaling processes.

204 ibit cytoprotective effects against hydrogen peroxide-mediated toxicity in H9c2 cells and cardioprote

205 hese data suggest that dysregulated hydrogen peroxide metabolism is a common mechanism by which high-

206 lly, we hybridized the cryogels with calcium peroxide microparticles to controllably produce bacteric

207 ing mechanism in which ROS, such as hydrogen peroxide, modulate AMPAR transport by modifying activity

208 nd to the introduction of one, two, or three peroxide moieties.

209 l-derived 2-methyl-2-tetrahydropyranyl alkyl peroxides (MTHPs) in tetrahydrofuran at 0 degrees C to g

210 dation is traditionally initiated by organic peroxides, N-acyloxyamines are now preferred due to thei

211 is study examines the sorption of the uranyl peroxide nanocluster [UO(2)(O(2))(OH)](60)(60-) (U(60))

212 scavenging capacity for superoxide, hydrogen peroxide, nitric oxide and DPPH (1,1-diphenyl-2-picrylhy

213 r show that continuous formation of hydrogen peroxide occurs in the presence of Cu(II), SRFA, and Cl(

214 NMR analysis of CaM oxidation by peroxide offers further insights into the susceptibility

215 d in the unprecedented detection of hydrogen peroxide on a temporal level not previously seen in resp

216 tible to the microbicidal effect of hydrogen peroxide or human beta-defensin-3.

217 arrangement of the carbenoid, with a rhodium peroxide or peroxy radical species generated upon the ac

218 ions often need an expensive oxidant such as peroxides or other species to drive such reactions.

219 cluding yeast, lactic acid bacteria, enzyme, peroxide, ozone, UV light and cold plasma.

220 namel roughness were caused by the carbamide peroxide (p < 0.05).

221 Free fatty acid, peroxide, p-anisidine, and total oxidation values were m

222 onstrate that boronate oxidation by hydrogen peroxide, peroxymonocarbonate, hypochlorite, or peroxyni

223 ough the synthesis of a nanotube-like uranyl peroxide phosphate (NUPP), Na(12) [(UO(2) )(mu-O(2) )(HP

224 Laser-induced hydrogen peroxide photolysis generates hydroxyl radicals that rea

225 Hydrogen peroxide plays a key role in honey antibacterial activit

226 In the case of the four uranyl peroxide POMs studied, clusters with hydroxide bridges h

227 of HCO(3) (-)/CO(2) was due to HCO(4) (-), a peroxide present in equilibrated solutions of H(2)O(2) a

228 stored mitochondrial superoxide and hydrogen peroxide production and inactivated HIF (hypoxia-inducib

229 and its selectivity for water over hydrogen peroxide production is important for these technologies.

230 of degradation was correlated with hydrogen peroxide production.

231 cally, as the thermodynamic stability of the peroxide products increases along this reaction cascade,

232 his frustration is relieved in the tricyclic peroxide products, where strongly stabilizing anomeric n

233 Peroxide promoted chemotaxis to arachidonic acid without

234 on of oxidative substrates, such as hydrogen peroxide, provide mechanisms to control spatiotemporal d

235 a stable dimer under treatment with hydrogen peroxide, recently recognized as a signaling molecule in

236 ~20-fold, making it the most efficient amine-peroxide redox initiator to date.

237 y as a reliable detection scheme of hydrogen peroxide related enzymatic bioassays for ultrasensitive

238 as demonstrated by detection of the hydrogen peroxide released from HeLa cells stimulated with N-Form

239 , to test causality for the role of hydrogen peroxide, reversed the P-AscH(-)-induced increases in DU

240 They serve as peroxide scavengers, sensors, signal transducers, and ch

241 n of pyruvate, however, does have remarkable peroxide scavenging effects, considering minimal peroxid

242 y as well as increased motility and hydrogen peroxide sensitivity compared to the wild-type.

243 autoagglutination, quorum sensing, hydrogen peroxide sensitivity, and chicken colonization in C. jej

244 in our understanding of the nature hydrogen peroxide sensors and the role of thiol-dependent signali

245 Here, peroxides serve the dual role of oxidants as well as alk

246 to superoxide, which, after dismutation into peroxide, serves as the substrate for the generation of

247 was unaffected by the level of superoxide or peroxide, showing that molecular oxygen itself is the cu

248 Following peroxide stress, cyclin C promoter occupancy increased f

249 isualized and quantitative detection towards peroxides, such as 2,2,6,6-tetramethylpiperidine-1-oxyl,

250 h led to a significant reduction in hydrogen peroxide, superoxide anion and malondealdehyde contents

251 ronmentally friendly tertiary butyl hydrogen peroxide (TBHP)-mediated rearrangement of aryl/alkyliden

252 patients also trended toward higher hydrogen peroxide than healthy participants (mean 172.8 vs 115.5

253 eumoniae generates large amounts of hydrogen peroxide that can accumulate to millimolar concentration

254 short-term increase in the flux of hydrogen peroxide that is preferentially cytotoxic to cancer cell

255 ](2+) suggest the intermediacy of an organic peroxide that, upon protonation, converts back into the

256 We observed that in the presence of hydrogen peroxide, the enzyme generates (1)O(2) and that this is

257 active sites, while confining the generated peroxide there to enhance its reaction probability.

258 aspartate and arginine in the heterolysis of peroxide to form the catalytic intermediate compound I (

259 (MPO), a heme protein that converts hydrogen peroxide to hypochlorous acid (HOCl), compared with sens

260 e), nitric oxide, oxidized GSH, and hydrogen peroxide to post-translationally modify and inhibit the

261 ize 3,3,5,5-tetramethylbenzidine by hydrogen peroxide to yield a blue product.

262 lizers (SOFs, calcium peroxide and magnesium peroxide) to reduce N(2)O production in mineral and orga

263 Alkaline hydrogen peroxide treatment altered the color, chemical compositi

264 iation, oxygen plasma and vaporized hydrogen peroxide treatments, measured with EGA and HPC.

265 ce, which allows separation of mono- and bis-peroxide tricyclic products, also explains why formation

266 hesis in cancer and are generated from lipid peroxides underlying the non-caspase-dependent form of c

267 Reduction of the peroxide unit of the 3-sila-1,2,4-trioxepane yields six-

268 lpiperidin-1-yl)oxyl hydroxylamine while the peroxide, unlike the superoxide, proved capable of defor

269 ond cleavage, reductive C-O bond cleavage in peroxides using the Pd catalyst and H(2) is described, w

270 (bleomycin, doxorubicin, topotecan, hydrogen peroxide, UV, photosensitized reactions) and fragmentati

271 ry essential oil and ferulago extract showed peroxide value (2.29 and 2.80 meq O(2)/kg oil), anisidin

272 ay in (i), and the effect of this rinsing on peroxide value (PV) or TBA-reactive substances (TBARS) d

273 action, total volatile base nitrogen (TVBN), peroxide value (PV), malondialdehyde (MDA), and bacteria

274 le showed lower total volatile base content, peroxide value and thiobarbituric acid reactive substanc

275 The peroxide value changed in the range of 4.5-5.3 and 6.7-1

276 PGSS-drying yielded particles with a maximum peroxide value of 2.5 meq O(2)/kg oil after 28 days of s

277 The peroxide value of SPH emulsion increased after the first

278 and stability parameters of oil (acid value, peroxide value, anisidine value and thiobarbituric acid

279 Free fatty acids and peroxide value, as indicators of enzymes activity, impli

280 Peroxide value, formation of volatile oxidation products

281 Peroxide value, malondialdehyde, 2,4-heptadienal and 2,4

282 The increase of free fatty acid, peroxide value, p-anisidine value, K(232) and K(268) at

283 oxidant activity of raw sesame seeds and the peroxide value, p-anisidine, fatty acids, and tocopherol

284 arameters including droplet size, viscosity, peroxide value, volatile compounds, and sensory properti

285 atments with adverse impact of sonication on peroxide value.

286 esults for free fatty acid (R(2) = 0.97) and peroxide values (R(2) = 0.87).

287 PL did not increase the peroxide values above the usual levels reported in dry-c

288 We found high correlations among peroxide values, K(232), K(270), and storage time.

289 Peroxide values, sensory analysis and volatile profile w

290 and tocopherol content, and p-anisidine and peroxide values, whereas it reduced b* and L* values, mo

291 We evaluated the efficacy of hydrogen peroxide vapor (HPV) to inactivate MS2 and Phi6 bacterio

292 Low concentration hydrogen peroxide vapor (LCHP; 25 ppm) was effective against both

293 ile; thus, analysis of particle-phase (hydro)peroxides via F-TD may not be appropriate.

294 ensitive electrochemical sensing of hydrogen peroxide was carried out at -100 mV vs Ag|AgCl; the resu

295 peroxides as well as silyl, benzyl, and acyl peroxides were successfully prepared with good yields an

296 ectronic frustration of H(2)O(2), the parent peroxide, where the lone pairs of oxygen are not involve

297 ctive oxygen species (ROS), such as hydrogen peroxide, which are known modulators of calcium signalin

298 eroxidase, leading to production of hydrogen peroxide, which is measured with an optimized luminol su

299 duct, whether it exists as a superoxide or a peroxide, which thus merits consideration in discussions

300 induce iron-dependent accumulation of lipid peroxides within tumor cells by transferring myeloperoxi