ライフサイエンスコーパス: singlet oxygen

1 ting cells from the reactive oxygen species, singlet oxygen.

2 ysically quench and/or chemically react with singlet oxygen.

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

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

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

6 hotodynamic damage through the generation of singlet oxygen.

7 affords the parent anthracenes by release of singlet oxygen.

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

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

10 ed to minimize blinking and sensitization of singlet oxygen.

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

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

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

14 themselves photosensitize the production of singlet oxygen.

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

16 ecular orbital energies, and reactivity with singlet oxygen.

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

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

19 toxic after the bacteria are pretreated with singlet oxygen.

20 dark toxicity effects following exposure to singlet oxygen.

21 ions on the generation and reactivity toward singlet oxygen.

22 must thus be designed for stability against singlet oxygen.

23 de a (Ppa) could be controllably released by singlet oxygen ((1) O(2) ) generated by light irradiatio

24 ptides nanolayer converts the H(2) O(2) into singlet oxygen ((1) O(2) ) in a sustained manner for neu

25 (fc2) that conditionally accumulates the ROS singlet oxygen ((1) O(2) ) leading to chloroplast degrad

26 (SPNpd) that not only efficiently generates singlet oxygen ((1) O(2) ) under NIR photoirradiation bu

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

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

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

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

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

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

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

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

35 les and react with dissolved O(2) to produce singlet oxygen ((1)O(2)(*)).

36 was observed in parallel with an increase in singlet oxygen ((1)O(2)) and fluorescence quantum yields

37 Singlet oxygen ((1)O(2)) and triplet chromophoric dissol

38 pro-nanoenzyme not only generates cytotoxic singlet oxygen ((1)O(2)) for photodynamic therapy (PDT),

39 Singlet oxygen ((1)O(2)) generation quantum yields from

40 The importance of singlet oxygen ((1)O(2)) in the environmental and biomed

41 Singlet oxygen ((1)O(2)) is a biologically relevant reac

42 mic substance isolates and whole waters with singlet oxygen ((1)O(2)) phosphorescence and determined

43 The singlet oxygen ((1)O(2)) photosensitizing propensity of

44 sulting in a significant alteration of their singlet oxygen ((1)O(2)) production.

45 DOM properties and triplet DOM ((3)DOM) and singlet oxygen ((1)O(2)) quantum yields, contradictory e

46 first step involves the formation of primary singlet oxygen ((1)O(2)) through the complex interaction

47 aromatic precursors were found to sensitize singlet oxygen ((1)O(2)), an arguably underappreciated a

48 tates of dissolved organic matter ((3)DOM*), singlet oxygen ((1)O(2)), and hydroxyl radicals ((*)OH),

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

50 Singlet oxygen ((1)O(2)), the major reactive oxygen spec

51 oxin, is readily oxidized upon reaction with singlet oxygen ((1)O(2)).

52 enetically-encodable light-induced source of singlet oxygen ((1)O(2)).

53 pyrrole moieties can undergo reactions with singlet oxygen ((1)O(2)).

54 udies, they seem susceptible to oxidation by singlet oxygen ((1)O(2)); therefore, we designed and syn

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

80 n kinetics and localized oxidation caused by singlet oxygen, (1)O(2), a major photochemically derived

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

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

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

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

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

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

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

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

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

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

91 Reaction with singlet oxygen and direct photolysis are secondary proce

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

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

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

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

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

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

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

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

100 ctions between the photosensitizer-generated singlet oxygen and substrate molecules remain elusive at

101 eration of reactive oxygen species including singlet oxygen and superoxide ion through both type 1 an

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

103 led to increased light absorption and lower singlet oxygen and triplet-state quantum yields and stea

104 elease via photodynamic (photooxygenation by singlet oxygen) and photothermal effects.

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

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

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

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

109 peroxide (H(2)O(2)), hypochlorous acid, and singlet oxygen are generated.

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

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

112 phospho-(1'-rac-glycerol) (POPG) mediated by singlet oxygen at the air-water interface of levitated w

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

114 se reactions are likely hydroxyl radical and singlet oxygen based on the use of selective quenchers.

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

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

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

118 As sustained generation of secondary singlet oxygen by the tumor cells is activated at the si

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

120 Singlet oxygen can severely damage biological tissue, wh

121 rug based on combretastatin A-4 (CA4) with a singlet oxygen-cleavable aminoacrylate linker, and a bio

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

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

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

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

126 ors, photouncaging, photodynamic therapy, or singlet-oxygen detection.

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

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

129 Herein, we show that use of the singlet oxygen ene reaction, combined with [2 + 2] cyclo

130 several protobruceol natural products using singlet oxygen ene reactions.

131 ong triplet lifetime ensures high-efficiency singlet oxygen evolution according to homogeneous photo-

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

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

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

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

136 h were tested for their ability to sensitize singlet oxygen formation, were found to do so efficientl

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

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

139 ysical properties, such as quantum yields of singlet-oxygen formation, decomposition, and fluorescenc

140 In PDT-induced hypoxia, providing singlet oxygen from stored chemical energy may enhance t

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

142 cenes toward O(2) and the thermal release of singlet oxygen from the respective endoperoxides.

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

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

145 cancerous tissue and design pH-controllable singlet oxygen-generating boron-dipyrromethene (BODIPY)

146 The resulting pH-controlled singlet oxygen-generating dyes with pK(a) values in the

147 Enhanced singlet oxygen generation and antiproliferative activiti

148 d)] and evaluated this system with regard to singlet oxygen generation and antiproliferative activity

149 bystander effect-like spreading of secondary singlet oxygen generation and catalase inactivation with

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

151 With PDT, Ce6-SCs demonstrate high singlet oxygen generation and produce a significant dela

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

153 hancement, as well as a 1.9-fold increase in singlet oxygen generation efficiency over free rose beng

154 ydroxyl radical generation from Hf(12) SBUs, singlet oxygen generation from DBB-Ir ligands, and super

155 ved the antagonistic effect by a decrease in singlet oxygen generation from the photosensitizer when

156 diseased tissues, the photoinduced cycle of singlet oxygen generation has always been considered to

157 Singlet oxygen generation is not observed when the diary

158 ed in conjunction with photosensitizers (for singlet oxygen generation or dye-sensitized solar cells)

159 restoration of the fluorescence emission and singlet oxygen generation upon removal of the DNBS group

160 Photostability and singlet oxygen generation were investigated under pulsed

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

162 avor triplet-state formation as required for singlet oxygen generation, iodine substituents were intr

163 s-A(2)B(2) porphyrins showed decent in vitro singlet oxygen generation, which was supported by the in

164 ucing minimal fluorescence and no measurable singlet oxygen generation.

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

166 class of photoactive material for efficient singlet-oxygen generation with potential photodynamic th

167 idone-tetraphenylethylene (DPPTPE) with high singlet-oxygen-generation ability both in dichloromethan

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

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

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

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

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

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

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

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

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

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

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

179 d with antibodies, and then reacted with the singlet oxygen in the presence of specific antigens and

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

181 rs, the environmental half-life of DA due to singlet oxygen-induced transformations is between 5 and

182 Singlet oxygen is a highly toxic and inevitable byproduc

183 Singlet oxygen is a versatile reagent for the selective

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

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

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

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

188 The singlet oxygen is produced through quenching of an optic

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

190 esponse of tumor cells to generate secondary singlet oxygen is the essential motor for their self-des

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

192 The production of singlet oxygen is typically associated with inefficient

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

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

195 ism called singlet oxygen priming (SOP), the singlet oxygen leads to hydroperoxides then to peroxyl r

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

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

198 Singlet oxygen may be endogenously produced, among vario

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

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

201 Development of a visible light-induced and singlet oxygen-mediated green protocol has been accompli

202 al motor for their self-destruction, after a singlet oxygen-mediated triggering process by CAP or PAM

203 irectly created through energy transfer from singlet oxygen molecules ((1)O(2)).

204 photosensitizer that can generate cytotoxic singlet oxygen molecules upon activation by X-rays.

205 ch involves the participation of the species singlet oxygen (O(2)((1)Delta(g))).

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

207 Airborne singlet oxygen obtained from photosensitization of tripl

208 hyrazines revealed that it is independent of singlet oxygen, occurring mainly via photoinduced electr

209 The total quenching rate constant (k(T)) of singlet oxygen of the alkene surfactant was measured to

210 sensitized manner and then thermally release singlet oxygen on demand on the other hand.

211 e design of highly effective sensitizers for singlet oxygen on one hand and the realization of materi

212 andwich-format immunoassay, the PPs produced singlet oxygen once sensitized by 680 nm diode lasers, a

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

214 y photo-oxidize DNA without the mediation of singlet oxygen or other reactive oxygen species, phototo

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

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

217 Arabidopsis, due to differentially localized singlet oxygen photosensitizers.

218 Singlet oxygen plays a role in cellular stress either by

219 Singlet oxygen precursors were efficiently isolated, whi

220 Through a new mechanism called singlet oxygen priming (SOP), the singlet oxygen leads t

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

222 Importantly, one round of singlet oxygen produced a persistent secondary wave of m

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

224 Singlet oxygen produced from triplet excited chlorophyll

225 The singlet oxygen produced not only induced a significant p

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

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

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

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

230 article size, morphology, surface charge and singlet oxygen production during ultrasound exposure.

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

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

233 ight irradiation, Ti-TBP not only sensitizes singlet oxygen production, but also transfers electrons

234 etween MS2 and DOM sites with locally higher singlet oxygen production.

235 (50)(dark)/IC(50)(light) ratio of ~368 and a singlet oxygen quantum yield of about 20%.

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

237 Mg(II) porphyrazines (MgPzs) having similar singlet oxygen quantum yields and side groups with diffe

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

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

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

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

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

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

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

245 3221 and Alr4783) were shown to be very good singlet oxygen quenchers.

246 ulfur quantum dots ("lumidots") show similar singlet oxygen quenching rate constants, based on the mo

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 The singlet oxygen reactivities and regioselectivities of th

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

251 Singlet oxygen resulting from peroxymonosulfate self-dec

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

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

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

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

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

257 Singlet oxygen sensitized photodynamic therapy (PDT) rel

258 However, the latter serves as an effective singlet oxygen sensitizer, as demonstrated in the prefer

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

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

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

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

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

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

265 for physical and chemical studies involving singlet oxygen, single-walled carbon nanotubes, and othe

266 (catalase), hydroxyl radicals (mannitol) and singlet oxygen (sodium azide) and carbon-centered radica

267 s, upon the laser irradiation, the generated singlet oxygen species are consumed by WONPs, in turn le

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

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

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

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

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

273 s various reactive oxygen species, including singlet oxygen, superoxide anion, hydrogen peroxide, and

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

275 e mediator is markedly more reactive towards singlet oxygen than the oxidized form, from which we der

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

277 ox mediators are predominantly decomposed by singlet oxygen that forms during cycling.

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

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

280 d then elevate the production of tumor-toxic singlet oxygen to significantly enhance PDT.

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

282 truction is mainly caused by highly reactive singlet oxygen (Type II reaction).

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

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

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

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

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

288 Singlet oxygen was also detected in fructose and glucose

289 ) counterparts, and drives the generation of singlet oxygen was designed.

290 A relatively high level of singlet oxygen was detected.

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

292 Singlet oxygen was involved in aBL inactivation of N. go

293 The ability of phenalenones to generate singlet oxygen was then harnessed in three photooxygenat

294 t illumination, the photosensitizer produces singlet oxygen which oxidizes phenolic compounds present

295 This imprint is mediated by primary singlet oxygen, which is mainly generated through the in

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

297 We investigated the chemistry of singlet oxygen with a cadmium-sulfur cluster, (Me(4)N)(2

298 henalenone molecular structure in generating singlet oxygen with high yields.

299 Ph)(10)] is indeed a very strong quencher of singlet oxygen with total rate constants for (1)O(2) rem

300 composition, and fluorescence or affinity to singlet oxygen, within 2-3 orders of magnitude.