ライフサイエンスコーパス: hydroxyl

1 estrogenic side chain of endoxifen or a free hydroxyl.

2 the regioselectivity observed is greater for hydroxyl.

3 tively weak nucleophilicity of the primer 3'-hydroxyl.

4 ociated with removal of the C2-methyl and C3-hydroxyl.

5 s hydrogen bond acceptor sites to the serine hydroxyl.

6 ucosamine (O-GlcNAc) to serine and threonine hydroxyls.

7 ch Ag atom bonded with two or three terminal hydroxyls.

8 allic complexes with compounds with adjacent hydroxyls.

9 uracy), but differ in the number of terminal hydroxyls.

10 tion of RNA by selective acylation of the 2'-hydroxyl (2'-OH) group has emerged as a powerful alterna

11 egion of the CHIKV genome using selective 2'-hydroxyl acylation analysed by primer extension (SHAPE)

12 2'-Hydroxyl acylation analyzed by primer extension (SHAPE)

13 Here, we apply selective 2'-hydroxyl acylation analyzed by primer extension (SHAPE)

14 Using biophysical analyses and Selective 2' Hydroxyl Acylation analyzed by Primer Extension (SHAPE)

15 ere experimentally supported by selective 2'-hydroxyl acylation analyzed by primer extension (SHAPE).

16 mutational profiling (DMS-MaP), selective 2'-hydroxyl acylation analyzed by primer extension and muta

17 ation of high-resolution SHAPE (selective 2'-hydroxyl acylation analyzed by primer extension) structu

18 ium site by interacting with the O3' and O4' hydroxyls alongside additional specific interactions of

19 ilicity and abundant exchangeable protons of hydroxyl, amine, and amide anchored on the surface, we r

20 to the ortho- or para-positions of phenolic hydroxyl/amino groups and the C2-position of the indole

21 -phenyl-N-tert-butyl nitrone (PBN) bearing a hydroxyl, an acetate, or an acetamide substituent on the

22 verse alkyl, alkenyl, aryl, alkynyl, fluoro, hydroxyl and amino groups at the beta position of the pa

23 They possess hydroxyl and ester groups for further functionalization

24 The pendant polar hydroxyl and non-polar butyrate groups between amides al

25 gen bonded THC/VEA complex linked by the THC hydroxyl and VEA carbonyl groups.

26 tes sandwiched by two pyrene linkers and the hydroxyls and water molecules on the Zr(6) nodes, which

27 ite) and 4' (4`-hydroxymidazolam metabolite) hydroxyl, and the 1' and 4' glucuronide metabolites were

28 d sequence at the 3' end is not required, 2' hydroxyls are, paralleling requirements for Prp43p bioch

29 egio-isomers synthesized, those carrying the hydroxyl at the 7- and 9-positions presented growth inhi

30 often utilized to provide hydrophilicity and hydroxyl-based hydrogen bonds in self-assembling glycope

31 h both the backbone amide and the side-chain hydroxyl (bidentate interaction) to promote binding by s

32 3alpha5alpha-P or pregnanolone reduced to a hydroxyl, binding affinity is reduced by 1,000-fold, whe

33 h overlap with the stretch absorption of the hydroxyl bond.

34 Hydroxyl-by-fluorine substitution has proven its merits

35 l origins, five groups (i.e., amine, phenol, hydroxyl, carboxyl, and carbonyl) are found to be the do

36 kers with common functional groups (phenolic hydroxyl/carboxyl/primary amine).

37 ting group (ie, catechol, hydroxamate, alpha-hydroxyl-carboxylate, or mixed types).

38 In addition, alpha-hydroxyl carboxylates are probably more easily oxidized

39 The flexibility of the hydroxyl carboxylic acid catalyst leads to significant d

40 he mechanism of the asymmetric BINOL-derived hydroxyl carboxylic acid catalyzed allylboration of benz

41 As, employing 2-enoyl-CoA hydratase (ECH), 3-hydroxyl-CoA dehydrogenase (HAD), and 3-ketothiolase (KT

42 eguide sensor was able to identify different hydroxyl compounds, such as water, methanol, and ethanol

43 most chemical modifications at predicted 2'-hydroxyl contact positions, whereas editing activity in

44 o group distributions of database compounds, hydroxyl-containing metabolites were severely underdetec

45 ntinental-marine mixed air had more abundant hydroxyl dicarboxylic acids (OHDCA), with anthropogenic

46 report a unique method for preparing diaryl hydroxyl dicarboxylic acids in a diastereospecific manne

47 this prediction and demonstrate that this 5'-hydroxyl dinucleotide hydrolase (HDH) activity for DXO i

48 ion of either the Mo-O5 (carboxyl) or Mo-O7 (hydroxyl) distance that switches the Mo-homocitrate liga

49 PVP with well-defined aldehyde and hydroxyl end groups lead to the formation of Ag nanocube

50 ilability of multiple functional groups like hydroxyl, ester, or lactone in the resultant products ex

51 The abundant terminal hydroxyls existed on nanosized gamma-Al(2)O(3) can lead

52 led to the discovery of fatty acid esters of hydroxyl fatty acids (FAHFAs), which are naturally occur

53 he alkyoxy group on silicon with a substrate hydroxyl followed by activation of a nearby carbonyl by

54 aride selectivity and identify the essential hydroxyls for interaction.

55 pecies protonation states remain unaffected, hydroxyl-for-bisulfide ligand substitution is avoided, a

56 der twisting of beta3 because its side chain hydroxyl forms a hydrogen bond with Thr-498.

57 eport on ultracold collision dynamics of the hydroxyl free-radical OH with Sr atoms leading to quench

58 Activation of the hydroxyl function with thionyl chloride in the presence

59 A linear pre-polymer containing hydroxyl functional group was produced, which could be s

60 maticity decrease rejection, that methyl and hydroxyl functional groups increase rejection, and that

61 the orthogonality between the azide and the hydroxyl functional groups, the former was next selectiv

62 nes or azides onto the terephthalic phenolic hydroxyl functionalities, which are situated at opposite

63 ross atmospheric species having carbonyl and hydroxyl functionalities.

64 ordinated formate ligands (HCO(2)(-)) by 1,2-hydroxyl-functionalized l-glycerate (l-gly, l-HOCH(2)(HO

65 We report that a hydroxyl-functionalized, cuboctahedral Rh(II)-based MOP

66 atalyzes the hydrolysis of RNAs bearing a 5'-hydroxyl group (5'-OH RNA).

67 mportant to inhibit alpha-amylase, while the hydroxyl group (OH) at C3 of the C-ring was related to i

68 ofiles depending on the configuration of the hydroxyl group and size of the P1' group.

69 The first set all have a C-3 hydroxyl group and the second has a carboxymethoxy ether

70 We observed that menthol uses its hydroxyl group as a hand to specifically grab with R842,

71 lmitic acids, consisting of isomers with the hydroxyl group at different positions, were identified i

72 For example, a hydroxyl group at the 12-position and facing the hydroph

73 ) derived by systematically exchanging every hydroxyl group by a fluorine atom, we developed a strate

74 the MD simulation indicate that a ribose 2'-hydroxyl group destabilizes the pai-pai stacking of the

75 at were modified only by removal of a single hydroxyl group from the terminal ribose.

76 ered azaenediyne, while the substrate with a hydroxyl group gave only traces of the desired 10-member

77 nylcyclobutane precursor bearing an appended hydroxyl group herein.

78 by the tight-bonding of active centers with hydroxyl group intermediate, while the Mg atom coordinat

79 , we firstly investigated how the additional hydroxyl group of NE could affect the properties of the

80 e (k(1), rho = 0.65), and the pK(a)'s of the hydroxyl group of the carbinolamide (rho = 0.23) are rep

81 ned that PDI inhibition relied on the A ring hydroxyl group of the chalcone scaffold and cLogP increa

82 etween the oxygen of the directing group and hydroxyl group of the ligating acetic acid is crucial fo

83 e also establish that methylation of the C-3 hydroxyl group of the terminal alpha-l-Rha is achieved b

84 a methyltransferase that methylates the C-2 hydroxyl group of the terminal alpha-l-rhamnose (Rha) un

85 that differentiate BAs is the presence of a hydroxyl group on C12 of the steroid ring.

86 Methylation of miRNAs at the 2'-hydroxyl group on the ribose at 3'-end (2'-O-methylation

87 ated by a second tetrahedral Al atom and its hydroxyl group protons in zeolite HZSM-5 is clearly reso

88 ation transfer (CEST) property of the labile hydroxyl group protons on maltitol (malCEST).

89 addition and demonstrate engineering of the hydroxyl group stereoselectivity.

90 Most notable is a trans-acting gamma/delta' hydroxyl group that 99% of other AAA+ proteins lack.

91 ng from the integrase active site the DNA 3'-hydroxyl group that is required for strand transfer acti

92 In the absence of the hydroxyl group the O(2) reduction proceeds via an electr

93 modate coplanar intermediates once the first hydroxyl group was introduced into the substrate.

94 differs from dopamine only for an additional hydroxyl group was not investigated at all in biosensing

95 l hydrophilic environments near the reactive hydroxyl group which stabilize both the proton and chlor

96 talyzes regiospecific methylation at the C-7 hydroxyl group, (ii) TnmH exhibits broad substrate promi

97 During proton transfer to a basic support hydroxyl group, electron density is distributed through

98 ' effectiveness depends on the presence of a hydroxyl group, the chain length (four carbons), and the

99 noside-CK but containing a single additional hydroxyl group, was also inactive at P2X7.

100 Furthermore, the hydroxyl group-containing cellulose fibers help connect

101 artially localized on the protonated support hydroxyl group.

102 all-trans trienes separated by a stereogenic hydroxyl group.

103 followed by the allyl group and next by the hydroxyl group.

104 the stereogenic center bearing the secondary hydroxyl group.

105 the resulting primer strand lacks a terminal hydroxyl group.

106 of (+)strand DNA with either a phosphate or hydroxyl group; and (iv) the 5' end of the DP-rcDNA (-)s

107 Engaging multiple hydroxyl groups along the molecular backbone of CNC, we

108 udy, we examined whether the distribution of hydroxyl groups among flavones could influence their pot

109 dentification and differentiation of surface hydroxyl groups and (sub-)surface oxygen species.

110 Carrageenan, which has a large number of hydroxyl groups and is fully negatively charged, is a ne

111 strategy enables direct introduction of key hydroxyl groups and rapid construction of key bonds and

112 r the lipase activity can be replaced by the hydroxyl groups at the GO surface.

113 is a promising technique for the analysis of hydroxyl groups because of its unique characterization c

114 hat at least two framework Al(IV) sites with hydroxyl groups can exist in acidic zeolite catalysts in

115 In contrast to the broad potential of hydroxyl groups for molecular recognition is their excep

116 Removal of either C1" or C3" hydroxyl groups from ADPR resulted in loss of agonist ac

117 oscopy offers unique advantages in measuring hydroxyl groups in a single spectrum with high signal re

118 tion and the nature of glycosylations on the hydroxyl groups in C-13 and C-19 of steviol.

119 its for chemically mapping the importance of hydroxyl groups in carbohydrate-receptor interactions.

120 ive functionalization of seemingly identical hydroxyl groups in carbohydrates remains a long-standing

121 Our data demonstrate the existence of free hydroxyl groups in cutin and provide insight into how th

122 support the notion that the aminomethyl and hydroxyl groups in the capping group of Suprastat establ

123 ing hydrogen and chelating bonds with excess hydroxyl groups in the hydrogel.

124 blueberry pectin increased as the number of hydroxyl groups increased on anthocyanins.

125 ure, which, after ion exchange, contain only hydroxyl groups inside.

126 The role of the hydroxyl groups is to anchor the clathrate-like water th

127 plication templates, while lagging strand 3'-hydroxyl groups may prime endonuclease-independent L1 re

128 hat catalyze the addition of GalNAc onto the hydroxyl groups of serines or threonines in protein subs

129 roteins within multicellular eukaryotes have hydroxyl groups of specific serine and threonine residue

130 o the hydrogen-bonding interactions with the hydroxyl groups of the end station.

131 In addition, a compound with all hydroxyl groups of the terminal ribose blocked as its 1"

132 oscopy analysis confirms the presence of the hydroxyl groups on the INFGN surface, which acts as the

133 activity, as is the position of a number of hydroxyl groups on the triterpenoid scaffold.

134 in a single aspect of the orientation of the hydroxyl groups or harbor subtle chemical modifications.

135 ueous solution, we proved the need for eight hydroxyl groups per carborane.

136 emonstrate the importance of the location of hydroxyl groups relative to the hydrophobic face of the

137 hydrogen-bond networks, the contribution of hydroxyl groups to affinity can reach several orders of

138 d GPL modifications, ranging from acyl chain hydroxyl groups to novel headgroup structures.

139 d stereoselective alkylation of carbohydrate hydroxyl groups via Rh(II)-catalyzed insertion of metal

140 insertion step, which prefers insertion into hydroxyl groups with an adjacent axial substituent.

141 to that in Y-SiO(2) but which lacks adjacent hydroxyl groups, and are 7 times more active than the ac

142 kenes, esters, ketones, acetals, unprotected hydroxyl groups, and phosphines) have been demonstrated

143 er aliphatics, free acid end-groups and free hydroxyl groups, differentiating between those derived f

144 vatives, depending on the positioning of the hydroxyl groups, induce various conformations of the est

145 -hydroxy-2-propyl)benzene, which has distant hydroxyl groups, is able to catalyze nucleophilic fluori

146 PEG2000 was bound to adenosine on the 3',4' hydroxyl groups, stimulated cAMP increases and these inc

147 ocols and does not require the protection of hydroxyl groups, thus allowing the facile synthesis of a

148 e during interactions with water and surface hydroxyl groups, which can be used as fingerprints for t

149 ties, when the glycan moieties contain axial hydroxyl groups.

150 to be chemically bound to compounds with cis-hydroxyl groups.

151 phery that is functionalized by sulfonic and hydroxyl groups.

152 oups including keto, ester, amino, halo, and hydroxyl groups.

153 s a carboxyl head group and GMS has two free hydroxyl groups.

154 be analyzed in four-channel CIL LC-MS where hydroxyls (H), amines and phenols (A), carboxyls (C), an

155 (-)/ONOOH), as well as peroxynitrite-derived hydroxyl (HO(*)) and carbonate anion (CO(3) (*-)) radica

156 positioned to recognize 5hmC through a thiol-hydroxyl hydrogen bond.

157 oroacetamide, to substitute the exchangeable hydroxyl-hydrogens with trifluoroacetate derivatives tha

158 of SO(2) by the two main isomers of isoprene hydroxyl hydroperoxide (ISOPOOH), the primary low-NO(x)

159 ut affecting TIPS protection of the phenolic hydroxyl in beta-tyrosine and N-Boc protection in lysine

160 hemistries as molecular hydrogen (H(2) ) and hydroxyl ions (OH(-) ) are produced and reduced carbon c

161 he pH was increased due to the production of hydroxyl ions at the cathode.

162 The generation of protons and hydroxyl ions at the electrodes facilitated a neutraliza

163 The accumulation of hydroxyl ions near the cathode increased the local solut

164 ibits early E(2)-induced apoptosis if a free hydroxyl is present.

165 gues with diazirine moieties replacing the 3-hydroxyl (KK148 and KK150) bind to all three sites, but

166 4)](5-) complexes are favored, stabilized by hydroxyl ligands and charge balancing calcium ions in th

167 of simple functionalities such as carbonyl, hydroxyl, methyl, or methoxyl groups is known to cause d

168 (2) labeling showed that the oxygens of both hydroxyl moieties originate from molecular oxygen rather

169 o tyrosine differs only by the presence of a hydroxyl moiety in the latter, but this results in an up

170 The hydroxyl moiety of Y2018 thus serves as a "brake" that s

171 on promoted an increase in the inhibition of hydroxyl, nitric oxide and alpha-amylase, as well as a d

172 al base abstracting a proton from the D-ring hydroxyl of 17-HOPC-CoA and Tyr-344 as the general acid

173 fined complex, where the axially oriented C2-hydroxyl of a mannose residue points toward the Ser41 of

174 Surprisingly, methylation of the 7-hydroxyl of CDCA led to a further dramatic increase in p

175 alpha-KDOp-(2 -> partially O-acetylated at 3-hydroxyl of GlcNAc.

176 ylation proceeded exclusively on the primary hydroxyl of tyrosol, thus forming rhamnosylated derivati

177 uences of amino-acid attachment at 2'- or 3'-hydroxyls of the terminal ribose in oligoribonucleotides

178 Surface-bounded species, such as hydroxyl (OH(*) , *=surface site) on the exposed PtNi PF

179 ified by the catalytic roles of the adsorbed hydroxyl (OH(ad))-water-alkali metal cation (AM(+)) addu

180 We predict hydroxyl (OH) and chlorine (Cl) radical production durin

181 ensive picture connecting the chemistries of hydroxyl (OH) and hydroperoxy radicals, oxidized nitroge

182 Carboxylic (COOH), carbonyl (C=O), and hydroxyl (OH) groups were enumerated by esterification,

183 environment, namely, CH(3)Cl degradation by hydroxyl ((.)OH) and chlorine ((.)Cl) radicals in the tr

184 eiki extract identified oleuropein aglycone, hydroxyl oleuropein aglycone, and oleuropein as key comp

185 atives act as antiestrogens with a free para-hydroxyl on the phenyl ring that contains an antiestroge

186 t Ag atom is mainly anchored by the terminal hydroxyls on (100) surface, forming a staple-like local

187 Herein, we reveal that the terminal hydroxyls on gamma-Al(2)O(3) are responsible for anchori

188 The presence of ligands belonging to alpha-hydroxyl or carbonyl carboxylates, such as tartrate, mal

189 Analysis of DPO analogs showed that a hydroxyl or carbonyl group at the 2'-position is critica

190 (18)O(2) and (16)O(2) demonstrated that both hydroxyl oxygens originate from a single molecule of O(2

191 is a pentagonal assembly of 25 Zr-oxy/peroxo/hydroxyl polyhedra and is the largest Zr/Hf cluster topo

192 Hydroxyl polymer doping thus offers a pathway for effici

193 tive sulphation at different and/or multiple hydroxyl positions.

194 psulation of DHA in the pH dependant polymer hydroxyl-propyl-methyl-cellulose-acetate-succinate (HPMC

195 In combination with the orthogonal hydroxyl protecting groups levulinic (Lev) ester, thexyl

196 ed analyte ions highlights the importance of hydroxyl proton mobilization in this low proton mobility

197 Phenol contains an exchangeable hydroxyl proton resonant at 4.8 ppm from the resonance f

198 and displayed the highest similarity to the hydroxyl pyruvate reductase isoform 2 in Arabidopsis tha

199 ral unique structural features of this plant hydroxyl pyruvate reductase.

200 Although hydroxyl radical ((*)OH) and hydrogen peroxide (H(2)O(2)

201 ng and wastewater relies on ozone (O(3)) and hydroxyl radical ((*)OH) as oxidants.

202 The hydroxyl radical ((*)OH) scavenging capacity is a useful

203 rocess (AOP) frequently employed to generate hydroxyl radical ((*)OH) to treat reverse osmosis permea

204 orus chemistry, and its association with the hydroxyl radical ((.) OH) to yield metaphosphorous acid

205 the well understood mechanism through which hydroxyl radical (.OH) produced by nitrate and nitrite p

206 Chemical oxidation with hydroxyl radical (HO(*)) and sulfate radical (SO(4)(*-))

207 Hydroxyl radical (HO(.) ) has long been believed to reac

208 for an autoxidation mechanism, initiated by hydroxyl radical (OH) addition to C=C bonds and propagat

209 The hydroxyl radical (OH) fuels tropospheric ozone productio

210 The formation of hydroxyl radical (OH) induced by air was found in all 18

211 studied, wherein the primary species is the hydroxyl radical (OH).

212 ) is produced by the formal dehydration of a hydroxyl radical adduct of dG as well as by deprotonatio

213 s activated water molecules to form covalent hydroxyl radical adducts at nearby residues, which were

214 The steady-state concentrations of hydroxyl radical and chlorine radical decrease by 38-100

215 ities involved in these reactions are likely hydroxyl radical and singlet oxygen based on the use of

216 plest dioxophosphorane HPO(2) and an elusive hydroxyl radical complex (HRC) of (.) PO form.

217 tial distribution of radicals, we found that hydroxyl radical concentration was strongly dependent on

218 Here we report the results of a hydroxyl radical footprinting analysis of the zinc-selec

219 Here hydroxyl radical footprinting coupled with mass spectrom

220 The hydroxyl radical footprinting method, fast photochemical

221 orbic acid depletion (denoted as OP(AA)) and hydroxyl radical formation (denoted as OP(*OH)) from bot

222 proceeds through 1,5-H atom abstraction by a hydroxyl radical generated with iron.

223 nt than those in tobacco TPM with respect to hydroxyl radical generation yield per unit EPFR.

224 jor photolytic source of the highly reactive hydroxyl radical in air.

225 showed high DPPH scavenging capacity and low hydroxyl radical inhibition.

226 trary to frequent reports in the literature, hydroxyl radical is not a key species participating in e

227 FPOP uses hydroxyl radical labeling to probe the surface-accessibl

228 Using time-resolved X-ray-mediated in situ hydroxyl radical labeling, we probed real-time solvent a

229 ficantly increases the signal quality of the hydroxyl radical modification products and the dose-resp

230 ties of platinum nanoparticles combined with hydroxyl radical probes produced at the particle surface

231 SAR and hydroxyl radical probing identified aptamer structural e

232 in doxorubicin uptake, temperature increase, hydroxyl radical production and nuclear membrane modific

233 ionally important for nucleosome binding and hydroxyl radical protection.

234 Hydroxyl radical protein footprinting (HRPF) is a powerf

235 hemical oxidation of proteins (IV-FPOP) is a hydroxyl radical protein footprinting method used to stu

236 bed sunlight was affected by the presence of hydroxyl radical scavengers, indicating the likely invol

237 ing ability (DRSA), reducing power (RP), and hydroxyl radical scavenging ability (HRSA) assays to tes

238 h in-vitro assays namely, DPPH(*), ABTS(*+), hydroxyl radical scavenging ability, reducing activity,

239 s requires high flux density to overcome the hydroxyl radical scavenging reactions produced by the bu

240 d reactive conformation and guides a derived hydroxyl radical toward formation of a copper-oxyl inter

241 venging activity of the extracts against the hydroxyl radical was also measured.

242 onlinear chemistry coupling isoprene and the hydroxyl radical, OH-its primary sink(10-13).

243 iologically relevant radicals, including the hydroxyl radical, peroxyl radicals, the trioxidocarbonat

244 s and protected the oxidative DNA damage and hydroxyl radical-induced protein fragmentation.

245 comparable 1,1-diphenyl-2-picrylhydrazyl and hydroxyl radical-scavenging activities in most cases.

246 ioxide, which forms when nitrite reacts with hydroxyl radical.

247 SEC-SAXS, SHAPE and hydroxyl-radical cleavage establish that PCBP2 stabilize

248 ighest reducing power (absorbance 0.366) and hydroxyl-radical-scavenging activity (91%) at 15 mg/mL;

249 ter ((3)DOM*), singlet oxygen ((1)O(2)), and hydroxyl radicals ((*)OH), for surface waters collected

250 reaction for production of highly efficient hydroxyl radicals (*OH) and consequently suppressing the

251 (GAC) (O(3)/GAC) to promote the formation of hydroxyl radicals (.OH) was evaluated at 1.0 mg O(3)/mg

252 ne (epsilon(C) = -3.6 to -4.6 per mille) and hydroxyl radicals (epsilon(C) = 0.0 to -1.2 per mille).

253 de dismutase), hydrogen peroxide (catalase), hydroxyl radicals (mannitol) and singlet oxygen (sodium

254 ir-water interface from two potent oxidizers hydroxyl radicals (OH) and singlet delta oxygen (SDO).

255 ers, and HONO photolysis was used to produce hydroxyl radicals (OH) in the perturbed chamber.

256 Hydroxyl radicals (OH) play a central role in the inters

257 es of BCA and LA due to reactions with O(3), hydroxyl radicals (OH), and due to photolysis were calcu

258 photolysis of nitrous acid (HONO) generates hydroxyl radicals (OH), and since OH is fast reacting, i

259 The source of water (H(2)O) and hydroxyl radicals (OH), identified on the lunar surface,

260 species - superoxide, hydrogen peroxide and hydroxyl radicals - have long been suspected of constrai

261 echanism is principally related to attack by hydroxyl radicals and ozone.

262 Our mechanistic investigations reveal that hydroxyl radicals are unreactive toward HFPO-DA, while e

263 ic pollutants with oxidants such as ozone or hydroxyl radicals by compound-specific stable isotope an

264 alytic system with the most effective use of hydroxyl radicals in oxidation treatment scenarios.

265 iron and copper) versus direct scavenging of hydroxyl radicals on the effect of chitosan.

266 duced hydrogen peroxide photolysis generates hydroxyl radicals that react with solvent-accessible sid

267 contribution of the reactions with ozone or hydroxyl radicals to overall transformation.

268 mical oxidation of proteins (FPOP), utilizes hydroxyl radicals to oxidatively modify solvent accessib

269 her concentrations of oxides of nitrogen and hydroxyl radicals, is more efficient in terms of O(3) an

270 We find that isoprene 'scavenges' hydroxyl radicals, preventing their reaction with monote

271 en, superoxide anion, hydrogen peroxide, and hydroxyl radicals, to afford superb antitumor efficacy o

272 f photochemically generated oxidants such as hydroxyl radicals, ultimately leading to an enhanced atm

273 ly absorbed X-rays and efficiently generated hydroxyl radicals, which enhanced the radiotherapy effec

274 of processes whose photochemistry generates hydroxyl radicals.

275 onstants for reactions of the compounds with hydroxyl radicals.

276 y binds to nucleosomes and protects DNA from hydroxyl radicals.

277 ue to its catalytic role in the formation of hydroxyl radicals.

278 sibly, cell expansion via H(2) O(2) -derived hydroxyl radicals.

279 of solvent-exposed amino acid side chains by hydroxyl radicals.

280 binding protein that protects chromatin from hydroxyl radicals.

281 ration of superoxide, hydrogen peroxide, and hydroxyl radicals.

282 o its critical role as a nighttime source of hydroxyl radicals.

283 esults demonstrate that a histidine-enhanced hydroxyl reactivity can contribute to protease inhibitio

284 Here, we have investigated the role of hydroxyl reactivity in a protease inhibitor by comparing

285 inhibition at pH 5, indicating that A2ML1's hydroxyl reactivity is not an adaption to its acidic epi

286 l, demonstrating that His-1084 increases the hydroxyl reactivity of A2ML1's thiol ester.

287 ment components C3 and C4B have an increased hydroxyl reactivity that is conveyed by a conserved hist

288 s a monomeric protease inhibitor but has the hydroxyl reactivity-conveying histidine residue.

289 ormed by a serine or threonine residue whose hydroxyl side chain H-bonds to an over-coordinated carbo

290 The adsorbed hydroxyl species blocked O-O bond cleavage that would de

291 to demonstrate that the presence of surface hydroxyl species by co-electrolysis of CO(2) with low co

292 urated sphingomyelins (C34:1, C36:1, C42:3), hydroxyl-sphingomyelins (C34:1, C38:3), and a hexosylcer

293 glycine, but only WT A2ML1 reacted with the hydroxyl substrate glycerol, demonstrating that His-1084

294 ymerizations are well controlled and produce hydroxyl telechelic PPC with predictable molar masses an

295 lammatory and antioxidant drug conjugated to hydroxyl terminated generation-4 PAMAM dendrimer (D-Sino

296 propylene is then converted into alpha,omega-hydroxyl-terminated polypropylene and used as a macroini

297 their stability when they are attached to a hydroxyl-terminated surface.

298 Mutation of this hydroxyl to a methyl group impedes clamp binding and ope

299 osition using an innocent ligand (acetate or hydroxyl) to prepare dual-action and triple-action prodr

300 n of the peak frequency and shape of the MOF hydroxyl vibration below 0.1 GPa.