ライフサイエンスコーパス: singlet oxygen

1 their endoperoxides 1-O2 upon oxidation with singlet oxygen.

2 ak1), that lacks the acclimation response to singlet oxygen.

3 ed cells, its effects were less dependent on singlet oxygen.

4 themselves photosensitize the production of singlet oxygen.

5 ments as the possible origins or targets for singlet oxygen.

6 ecular orbital energies, and reactivity with singlet oxygen.

7 ed-state control for truly local delivery of singlet oxygen.

8 capacity to both scavenge ABTS(+) and quench singlet oxygen.

9 n of cells was dependent on the formation of singlet oxygen.

10 TO is essentially inert to visible light and singlet oxygen.

11 n was predominantly due to the production of singlet oxygen.

12 ternal conversion, intersystem crossing, and singlet oxygen.

13 cavenged hydroxyl radicals and GSE scavenged singlet oxygen.

14 excellent sensitizers for the generation of singlet oxygen.

15 peroxide reacting with the Tyr radical or by singlet oxygen.

16 te so it can act as an effective quencher of singlet oxygen.

17 n, emphasizing the role of non-H2O2 ROS like singlet oxygen.

18 tes in vivo and preventing the production of singlet oxygen.

19 hotodynamic damage through the generation of singlet oxygen.

20 affords the parent anthracenes by release of singlet oxygen.

21 ed species, as evidenced by the formation of singlet oxygen.

22 lly useful 13 mus excited state and produces singlet oxygen.

23 ed to minimize blinking and sensitization of singlet oxygen.

24 ed on the basis of virus susceptibilities to singlet oxygen.

25 rrier is developed for efficiently producing singlet oxygen ((1) O2 ) and inducing hypoxia to promote

26 be activated by photoirradiation, producing singlet oxygen ((1) O2 ) and inducing hypoxia to promote

27 A biocompatible fluorescent nanoprobe for singlet oxygen ((1) O2 ) detection in biological systems

28 s been developed that enables tumor-specific singlet oxygen ((1) O2 ) generation for cancer therapy,

29 photosensitizer that specifically generates singlet oxygen ((1) O2 ) in mitochondria under white lig

30 hat can reversibly control the generation of singlet oxygen ((1) O2 ) is of great interest for photod

31 Moreover, FR pretreatment resulted in singlet oxygen ((1) O2 ) production and a rapid inhibiti

32 , with two representatives exhibiting strong singlet oxygen ((1) O2 ) quenching (HCP2, HCP3) and anot

33 The ene reaction between singlet oxygen ((1)O(2)) and simple alkenes has been rep

34 Soon after the release of singlet oxygen ((1)O(2)) in chloroplasts of the flu muta

35 Enhanced levels of singlet oxygen ((1)O(2)) in chloroplasts trigger program

36 Singlet oxygen ((1)O(2)) is a reactive oxygen species th

37 onal response to the reactive oxygen species singlet oxygen ((1)O(2)) is mediated by ChrR, a zinc met

38 s undertaken on Lake Superior to investigate singlet oxygen ((1)O(2)) photoproduction.

39 y based on the generation of highly reactive singlet oxygen ((1)O(2)) through interactions of photose

40 the first line of defense of plants against singlet oxygen ((1)O(2)) toxicity because of their capac

41 in the dark but prone to rapid oxidation by singlet oxygen ((1)O(2)) under irradiated conditions.

42 ynylpentacenes by using chemically generated singlet oxygen ((1)O(2)) without irradiation and identif

43 is dependent on light and the generation of singlet oxygen ((1)O(2)), similar to the mechanistic par

44 linking reactions that require production of singlet oxygen ((1)O(2)), whose half-life is extended by

45 ophage MS2 to UV254, simulated sunlight, and singlet oxygen ((1)O2) and analyzed the oligomer reactio

46 COOH-MWCNTs generated singlet oxygen ((1)O2) and hydroxyl radical ((*)OH) unde

47 s (RIs), including hydroxyl radical ((*)OH), singlet oxygen ((1)O2) and superoxide radical anion (O2(

48 onic nanostructure platform with a source of singlet oxygen ((1)O2) at a well-defined distance from t

49 anic matter (DOM) were present as a mixture, singlet oxygen ((1)O2) generation concentrations were 1.

50 This technique utilises singlet oxygen ((1)O2) generation via a laser excited ph

51 This Review describes singlet oxygen ((1)O2) in the organic synthesis of targe

52 Distinct ROS signaling pathways initiated by singlet oxygen ((1)O2) or superoxide and hydrogen peroxi

53 eparation, and characterization of a dormant singlet oxygen ((1)O2) photosensitizer that is activated

54 e-containing NDIs (i.e., 11) behaved as both singlet oxygen ((1)O2) photosensitizers and fluorescent

55 Singlet oxygen ((1)O2) plays an important role in the in

56 ype of particle, Rose Bengal as an efficient singlet oxygen ((1)O2) producer was covalently bound to

57 ffort to generate a molecule capable of both singlet oxygen ((1)O2) production and ligand exchange up

58 g to significantly enhanced fluorescence and singlet oxygen ((1)O2) production upon laser irradiation

59 In contrast, singlet oxygen ((1)O2) quantum yields increased, which i

60 Singlet oxygen ((1)O2) reaction kinetics of individual p

61 e investigation of a directed intramolecular singlet oxygen ((1)O2) transfer.

62 in the dark but prone to rapid oxidation by singlet oxygen ((1)O2) under irradiated conditions and t

63 s to novel photosensitizers that can produce singlet oxygen ((1)O2) upon photoirradiation.

64 xcited triplet state formation and therefore singlet oxygen ((1)O2) yield.

65 In contrast, the intramolecular transfer of singlet oxygen ((1)O2), a reactive and short-lived oxyge

66 ranscriptional response of this bacterium to singlet oxygen ((1)O2), a reactive oxygen species genera

67 tates of dissolved organic matter ((3)DOM*), singlet oxygen ((1)O2), and the hydroxyl radical ((*)OH)

68 riplet dissolved organic matter ((3)DOM) and singlet oxygen ((1)O2), contributes to the degradation o

69 bance and fluorescence) and the formation of singlet oxygen ((1)O2), DOM triplet excited states ((3)D

70 triplet states by molecular oxygen produces singlet oxygen ((1)O2), which reacts with the anthracene

71 Studies of the singlet oxygen ((1)O2)-overproducing flu and chlorina1 (

72 rt half-life and limited diffusion radius of singlet oxygen ((1)O2).

73 reactive oxygen species (ROS), predominantly singlet oxygen ((1)O2).

74 s in the lipid bilayer via the production of singlet oxygen ((1)O2).

75 ter ((3)DOM*), hydroxyl radical (HO(*)), and singlet oxygen ((1)O2).

76 queous reactions with hydroxyl radical (OH), singlet oxygen ((1)O2*), and excited triplet states ((3)

77 ntribution of reactive oxygen species (e.g., singlet oxygen, (1)O2) in dissolved organic matter-sensi

78 found not to be introduced by moisture or by singlet oxygen [(18)((1)O2 (1)Deltag)] produced thermall

79 nsitizers in aquatic environments, producing singlet oxygen (1O2) alongside other photochemically pro

80 te OM (3OM*) and apparent quantum yields for singlet oxygen (1O2) were measured for both whole water

81 lly produced reactive intermediates, such as singlet oxygen (1O2).

82 produced from DOM photochemistry, including singlet oxygen, 1O2.

83 we show that photodegradation occurs through singlet oxygen, a highly reactive form of dissolved oxyg

84 Here we describe a mutant, singlet oxygen acclimation knocked-out 1 (sak1), that la

85 nes from the substrates, and thus, secondary singlet oxygen addition was observed to give hydroperoxy

86 les us to draw conclusions about the role of singlet oxygen and (1)O2 carriers in photodynamic therap

87 f these processes involve a reaction between singlet oxygen and a given amino acid in a protein.

88 n about rate constants for reactions between singlet oxygen and amino acids when the latter are in a

89 identified by proximity-based labeling using singlet oxygen and by an adapted version of TRICEPS-base

90 Reaction with singlet oxygen and direct photolysis are secondary proce

91 they undergo clean cycloreversion, releasing singlet oxygen and emitting light.

92 otoprotects cyanobacteria cells by quenching singlet oxygen and excess excitation energy.

93 f these studies implicate reaction with both singlet oxygen and excited state triplet NOM.

94 The singlet oxygen and fluorescence quantum yields of these

95 and' activated photosensitizer that produces singlet oxygen and fluorescence when activated with near

96 c acid and monogalactosyldiacylglycerol from singlet oxygen and from hydroxyl radical.

97 wastewater treatment wetland) that generated singlet oxygen and hydroxyl radical.

98 The PapaMBlue produced higher amounts of singlet oxygen and hydroxyl radicals than free MB, possi

99 e DAA2 shows inertness toward reactions with singlet oxygen and OH(-) ions during photo- and electroc

100 cid is a potent antioxidant and scavenger of singlet oxygen and other radicals in humans.

101 m of this cross-linking, which involves both singlet oxygen and radical generation, can occur very ef

102 ss of a fiber optic technique for generating singlet oxygen and releasing the pheophorbide photosensi

103 ivation probably leads to elevated levels of singlet oxygen and severe oxidative stress, which ultima

104 d PSII charge recombination rates, producing singlet oxygen and subsequent photodamage.

105 ase of nitric oxide (NO) in combination with singlet oxygen and superoxide radicals (O2(*-)) as react

106 itizers that can both induce cell death (via singlet oxygen) and monitor it (via caspase detection).

107 olvement in the bonding mechanism of oxygen, singlet oxygen, and association of RB with stromal colla

108 a source of highly oxidative species such as singlet oxygen, and atomic oxygen.

109 rucidal agents (heat, UV, hypochlorous acid, singlet oxygen, and chlorine dioxide).

110 l involving the cleavage of aminoacrylate by singlet oxygen, and demonstrated its application to visi

111 virus functions to achieve inactivation: UV, singlet oxygen, and hypochlorous acid treatments general

112 dicals, hydroxyl radicals, superoxide anion, singlet oxygen, and peroxynitrite were determined by usi

113 ions of carbonate radical, hydroxyl radical, singlet oxygen, and triplet-excited state DOM were measu

114 was slower in a high concentration of ozone, singlet oxygen appeared to be a parallel oxidant for uns

115 y, acute water stress showed accumulation of singlet oxygen as determined by fluorescence of Singlet

116 ed-triplet-state quenchers and scavengers of singlet oxygen as well as ground-state oxygen.

117 We produced singlet oxygen at a point near the oil-water interface o

118 bubbles (1.4 mm diameter, 90 muL) containing singlet oxygen at levels toxic to bacteria and fungus.

119 ned to probe the "ene" reaction mechanism of singlet oxygen at the air-water interface.

120 A core gene set of 118 genes, common to singlet oxygen, biotic and abiotic stresses was defined

121 Thus, singlet oxygen bubble toxicity was inversely proportiona

122 ygenated solutions, it was reasoned that the singlet oxygen bubbles inactivate Escherichia coli and A

123 Loss-of-function mbs mutants produce singlet oxygen but are unable to fully respond to it at

124 at the photogeneration of 2 does not involve singlet oxygen but rather likely occurs via a free-radic

125 hoester)s that allow efficient scavenging of singlet oxygen, but do not react with molecular oxygen i

126 The efficient generation of singlet oxygen by the photosensitizer is observed when t

127 Collectively, the results show that singlet oxygen can be produced by multiple stress pathwa

128 und that light irradiation of HerGa produces singlet oxygen, causing mitochondrial damage and cytochr

129 ug of PTX by conjugating photosensitizer via singlet oxygen-cleavable aminoacrylate linker.

130 plastoquinone pool and reduced production of singlet oxygen compared with control strains.

131 photoprotection is related to a decrease of singlet oxygen concentration due to OCP action.

132 , solar irradiance, water matrix absorbance, singlet oxygen concentration, and the virus-specific app

133 zeranol family decay at neutral pH, although singlet oxygen contributes modestly in more alkaline wat

134 As singlet oxygen decays rapidly to triplet oxygen, the bub

135 We find that miniSOG oxidizes ADPA by both singlet oxygen-dependent and -independent processes.

136 ity (MBS), that is required for induction of singlet oxygen-dependent gene expression and, upon oxida

137 and correlated with increased levels of the singlet oxygen-derived carotenoid beta-cyclocitral, a re

138 The singlet oxygen device offers intriguing possibilities fo

139 nd recombination leading to the formation of singlet oxygen diminishes.

140 shows significantly enhanced absorption and singlet oxygen efficiency relative to that of the accept

141 Singlet oxygen emerges through the fiber tip with 669-nm

142 ted by light, X-ray and microwave to produce singlet oxygen for cancer treatment.

143 for photothermal therapy (PTT), and light to singlet oxygen for photodynamic therapy (PDT).

144 ption, fluorescence, and ability to generate singlet oxygen), for their uptake into Colo-26 cells in

145 bic acid ((2E,4E)-hexa-2,4-dienoic acid) and singlet oxygen formation to quantify the triplet states

146 ll triplet species before they can sensitize singlet oxygen formation.

147 tion to triplet states, which photosensitize singlet oxygen formation.

148 e mechanism was established by generation of singlet oxygen from the excited maleimides.

149 a soluble protein, it is able to quench the singlet oxygen generated in the thylakoid membranes.

150 ight (>470 nm) leads to full recovery of the singlet oxygen generating ability of the porphyrin sensi

151 Applying the singlet oxygen-generating electron microscopy probe mini

152 Thanks to a favorable combination of singlet oxygen generation and cellular uptake properties

153 The nanosystem also inhibits extracellular singlet oxygen generation by Ce6, leading to fewer side

154 Singlet oxygen generation is not observed when the diary

155 Compared to porphyrin FRET donor constructs, singlet oxygen generation was unquenched prior to caspas

156 Photostability and singlet oxygen generation were investigated under pulsed

157 tersystem crossing to the triplet state, and singlet oxygen generation, as assayed by transient absor

158 tically boost NIR photon utility and enhance singlet oxygen generation.

159 let yields estimated from quantum yields for singlet oxygen generation.

160 ucing minimal fluorescence and no measurable singlet oxygen generation.

161 eling, photooxidation of a ligand-conjugated singlet oxygen generator is coupled to chemical labeling

162 Studies in which A2E was incubated with a singlet oxygen generator yielded results consistent with

163 As proof-of-concept, we expressed the 'singlet oxygen generator' miniSOG as a fusion with the S

164 cally encoded photosensitizer, miniSOG (mini singlet oxygen generator).

165 ency of ROS generation by His-mSOG, the mini singlet oxygen generator, miniSOG, fused to a histone.

166 We used a genetically encoded singlet oxygen generator, miniSOG, to conduct chromophor

167 hymidine and 2,4-dithiothymine are efficient singlet oxygen generators, with singlet oxygen quantum y

168 her fluorescent proteins reported to date as singlet oxygen generators.

169 ovides an assessment of the contributions of singlet oxygen, hydroxyl radical, hydrogen peroxide, and

170 her extending the lifetime while sensitizing singlet oxygen in an aerated solution.

171 ic methods that allow us to directly examine singlet oxygen in mammalian cells.

172 The results imply that the role of singlet oxygen in plant stress regulation and response i

173 nt protein of 106 amino acids that generates singlet oxygen in quantum yield upon blue-light illumina

174 selectively photoactivate the production of singlet oxygen in ROS stressed vs regular cells was succ

175 TP can also efficiently function to generate singlet oxygen in situ (PhiDelta approximately 20 %) and

176 fact that beta-carotene efficiently quenches singlet oxygen in solution-phase systems is invariably i

177 en Sensor Green detected rapid production of singlet oxygen in the Arabidopsis (Arabidopsis thaliana)

178 fluorescence decay and reduced production of singlet oxygen, indicating upgraded photoprotection.

179 nses of detoxification genes are part of the singlet oxygen-induced acclimation process in C. reinhar

180 RES can be formed after singlet oxygen-induced lipid peroxidation, indicating th

181 lorophyllide and transcripts associated with singlet oxygen-induced stress.

182 ce the intracellular volume element in which singlet-oxygen-initiated perturbation of the cell occurs

183 In a second mechanism, singlet oxygen interacts directly with E. coli that accu

184 Singlet oxygen is a highly toxic and inevitable byproduc

185 e noninvasive control over the generation of singlet oxygen is demonstrated in a bicomponent system c

186 Singlet oxygen is formed from the hydroxido ligands and

187 In the presence of red light and oxygen, singlet oxygen is formed on the superhydrophobic surface

188 Singlet oxygen is formed when these triplet states inter

189 At room temperature and neutral pH value, singlet oxygen is generated by PCN-222/MOF-545 using an

190 The reason is that photoexcited singlet oxygen is highly reactive, so the photoactive mo

191 The controlled generation of singlet oxygen is of great interest owing to its potenti

192 Singlet oxygen is produced at the probe tip surface whic

193 tection against photooxidative stress due to singlet oxygen is provided by carotenoid molecules, whic

194 t inside and outside of the bubble such that singlet oxygen is solvated and diffuses through the aque

195 Such photodynamic production of singlet oxygen is thought to be involved in stress signa

196 The production of singlet oxygen is typically associated with inefficient

197 (1)O(2) (singlet oxygen) is a reactive O(2) species produced from

198 nd responds to the presence of intracellular singlet oxygen, its behavior in this arguably complicate

199 fic apparent second-order rate constant with singlet oxygen (k2).

200 Furthermore, we show the influence of singlet oxygen lifetime and diffusion coefficient (D) on

201 The singlet oxygen lifetime determines its diffusion distanc

202 Singlet oxygen lifetimes, solvent deuteration, and the e

203 We used (1)O(2) luminescence (or singlet oxygen luminescence (SOL)) as a gold-standard me

204 resonance spectroscopy and the induction of singlet oxygen marker genes.

205 -mediated cell death where the generation of singlet oxygen may play a role.

206 Photoconversion likely involves singlet-oxygen mediated photochemical cleavage, yielding

207 ecrease the susceptibility of the dye toward singlet oxygen-mediated degradation.

208 he signal transduction and activation of the singlet oxygen-mediated response, a mutant selection was

209 acid can have significant ramifications for singlet-oxygen-mediated events that perturb cell functio

210 agen, that bonding requires oxygen, and that singlet oxygen mediates protein crosslinking.

211 Singlet oxygen, O(2)(a(1)Delta(g)), plays a key role in

212 tive damage occurs through the generation of singlet oxygen operating as a cell death inducer.

213 properties, to the ability to photogenerate singlet oxygen, or to act as photoacoustic imaging agent

214 rmation of a stable radical species, and the singlet oxygen photoproduction are responsible for the s

215 A Type-II (singlet oxygen) photosensitized mechanism is suggested f

216 Arabidopsis, due to differentially localized singlet oxygen photosensitizers.

217 Singlet oxygen plays a role in cellular stress either by

218 This widely used commercial singlet oxygen probe was covalently linked to a polyacry

219 The singlet oxygen produced by PCN-222/MOF-545 selectively o

220 mydomonas reinhardtii cells to low levels of singlet oxygen, produced either by photoreactive chemica

221 We now demonstrate that intracellular singlet oxygen, produced in a photosensitized process, i

222 t 1 (sor1) mutant, which is more tolerant to singlet oxygen-producing chemicals and shows a constitut

223 ae to subsequent exposure to normally lethal singlet oxygen-producing conditions.

224 ive role of CP29 phosphorylation in reducing singlet oxygen production and enhancing excess energy di

225 wavelengths in the visible spectrum leads to singlet oxygen production and photooxidation of A2E.

226 s for cancer treatment should both have good singlet oxygen production capability and be excitable by

227 phyrin-triphenylamine hybrids with excellent singlet oxygen production capacities and good two-photon

228 revealed moderate to high quantum yields of singlet oxygen production depending on the solvent appli

229 centration, tissue oxygen concentration, and singlet oxygen production in real-time may allow for ada

230 which mainly depends on a very high yield of singlet oxygen production in the surroundings of the bac

231 a conjugated porphyrin dimer photosensitizes singlet oxygen production is shown to depend on the exci

232 ed excitation profile and exceptionally high singlet oxygen production under both visible light and i

233 Structural modifications induced by singlet-oxygen production within the chromophore pocket

234 High singlet oxygen quantum yield in water at longer waveleng

235 diated killing of pathogens with outstanding singlet oxygen quantum yield PhiDelta of >97%.

236 ined by an O(2) saturation kinetics study of singlet oxygen quantum yields (Phi(1O2)) in buffered D(2

237 n moiety are also conserved, with comparable singlet oxygen quantum yields found to the free chlorin.

238 re efficient singlet oxygen generators, with singlet oxygen quantum yields of 0.42 +/- 0.02 and 0.46

239 e quantum yields between 0.078 and 0.20, and singlet oxygen quantum yields ranging 0.58-0.69.

240 e molecules in combination with vitamin C as singlet oxygen quencher significantly improved survival

241 as progerin induction was suppressed by the singlet oxygen quencher sodium azide, and as mRNA expres

242 nal domain of OCP is not more efficient as a singlet oxygen quencher than a protein without carotenoi

243 onstrated that, in vitro, OCP is a very good singlet oxygen quencher.

244 ective functions as an energy quencher and a singlet oxygen quencher.

245 aracterized, and they proved to be very good singlet oxygen quenchers.

246 3221 and Alr4783) were shown to be very good singlet oxygen quenchers.

247 Singlet oxygen quenching, reducing power and ferrous ion

248 as proof for a long-term protection against singlet oxygen quenching, with comparable efficiencies o

249 chls while optimizing the triplet energy for singlet oxygen quenching.

250 yptophan residue, that the rate constant for singlet oxygen reaction with tryptophan depends signific

251 The singlet oxygen reactivities and regioselectivities of th

252 th short peptides, it has been proposed that singlet oxygen reacts with the histidyl imidazole ring t

253 photoinhibition of PSI and increased rate of singlet oxygen release from isolated PSI light-harvestin

254 This selection led to the isolation of the singlet oxygen resistant 1 (sor1) mutant, which is more

255 Second, singlet oxygen returns the reduced catalyst to the Cr(II

256 anges in RNA abundance during acclimation to singlet oxygen revealed that SAK1 is a key regulator of

257 h by acute water stress was inhibited by the singlet oxygen scavenger histidine and was accompanied b

258 Cell death could be inhibited by the singlet oxygen scavenger histidine in treatments with AO

259 nteract with reactive oxygen species through singlet oxygen scavenging, electron transfer, hydrogen a

260 ion, whereas only LHCBM1 is also involved in singlet oxygen scavenging.

261 Singlet oxygen sensitized photodynamic therapy (PDT) rel

262 acid, in the presence of O(2), light, and a singlet oxygen sensitizer ([Ru(bpy)(3)](2+) or Rose Beng

263 nary ammonium salts as alkylating agents and singlet oxygen sensitizers.

264 elated commercially available product called Singlet Oxygen Sensor Green (SOSG).

265 the dark, the singlet oxygen-specific probe Singlet Oxygen Sensor Green detected rapid production of

266 Subcellular localization of Singlet Oxygen Sensor Green fluorescence showed its accu

267 ny of the limitations of the molecular probe Singlet Oxygen Sensor Green((R)) (SOSG).

268 glet oxygen as determined by fluorescence of Singlet Oxygen Sensor Green, by electron paramagnetic re

269 ped a genetic screen for early components of singlet oxygen signaling.

270 in oxygenated solvents efficiently generates singlet oxygen similar to the parent benzophenone.

271 biotic and abiotic stresses in the dark, the singlet oxygen-specific probe Singlet Oxygen Sensor Gree

272 ii is capable of acclimating specifically to singlet oxygen stress, but the retrograde signaling path

273 DX1.2 is strongly induced by heat as well as singlet oxygen stress, concomitant with an enhancement o

274 g sustained NPQ in LHCII, thereby preventing singlet oxygen stress.

275 ygen species (ROS) to be released, including singlet oxygen, superoxide anion radicals, and hydrogen

276 id A to leucosceptroids C, K, O, and P using singlet oxygen supports the hypothesis that leucosceptro

277 are effective antioxidants, which can quench singlet oxygen, suppress lipid peroxidation, and prevent

278 oxacin was associated with the generation of singlet oxygen that caused extensive protein oxidation.

279 none result in the formation of the reactive singlet oxygen that reacts with alkenes to form endopero

280 Oil oxidation was initiated by singlet oxygen that was produced by chlorophylls irradia

281 Singlet oxygen, the lowest excited state of molecular ox

282 id to artemisinin using a chemical source of singlet oxygen, thus avoiding the need for specialized p

283 tic tip delivered pheophorbide molecules and singlet oxygen to discrete locations.

284 n range of up to several tens of nanometres: singlet oxygen triplet energy transfer.

285 Such mechanisms involve singlet oxygen, ubiquitination, the 26S proteasome, and

286 ur results show that aged-T-Lite SF produced singlet oxygen under low intensity long wave UV and form

287 ron microscopy due to its ability to produce singlet oxygen upon light irradiation.

288 e first PTX prodrug that can be activated by singlet oxygen using tissue penetrable and clinically us

289 kly fluorescent compounds rapidly react with singlet oxygen via a pi2 + pi4 cycloaddition to irrevers

290 cient photosensitizers for the generation of singlet oxygen via photoinduced energy transfer processe

291 Singlet oxygen was also detected in fructose and glucose

292 A relatively high level of singlet oxygen was detected.

293 Low reactivity of DMABN with singlet oxygen was found (second-order rate constant <2

294 Singlet oxygen was identified as the major cause of lipi

295 diation of the released sensitizer generates singlet oxygen, which accelerates the release of more se

296 duct formed from reaction of tryptophan with singlet oxygen, which can be produced under high light s

297 Ultraviolet and blue light generates singlet oxygen, which oxidizes and activates the ion cha

298 ciably inhibit or accelerate the reaction of singlet oxygen with a given amino acid can have signific

299 sitizer molecules upon a [2 + 2] addition of singlet oxygen with the ethene spacer and scission of a

300 nated silica surface occurs by a reaction of singlet oxygen with the vinyl ether bond linker with sci