ライフサイエンスコーパス: catechol

1 ounds gave better activities than trolox and catechol.

2 al intermediates, such as protocatechuate or catechol.

3 of reaching a limit of detection of 0.01 nM catechol.

4 light and during the photodecay of adsorbed catechol.

5 discs were supplied with exogenously applied catechol.

6 talytic efficiency (3.3x10(6)) with 4-methyl catechol.

7 2.57 DeltaA420nm/minx10(-1), determined with catechol.

8 intermediates including protocatechuate and catechol.

9 y for chlorogenic acid, 4-methylcatechol and catechol.

10 surface-functionalized with mussel-inspired catechols.

11 including 2,4-pyridinedicarboxylic acid and catechols.

12 that deliver either meta- or para-methylated catechols.

13 .0 ppmv O3(g) with microdroplets containing [catechol] = 1-150 muM.

14 d light on the prevalence of subfamily I.2.C catechol 2,3-dioxygenases in petroleum hydrocarbon conta

15 mRNA transcripts of subfamily I.2.C catechol 2,3-dioxygenases were detected in considerable

16 4-(Pentafluorosulfanyl)catechol, 2-amino-4-(pentafluorosulfanyl)phenol, and 2-a

17 Optimal temperatures were 40 degrees C for catechol, 25 degrees C for 4-methylcatechol and 20 degre

18 lution containing gallic acid (GA), 4-methyl-catechol (4-MC), in which the concentration of the pheno

19 This work shows how catechol, a molecular probe of the oxygenated aromatic h

20 rganocatalyst 1-Bcat-2-PPh2-C6H4 ((1); cat = catechol) acts as an ambiphilic metal-free system for th

21 Sensitivities of these rigid catechol agonists to the effects of the serine mutations

22 control unit for the detection of oxygen and catechol analytes, which are central to medical and envi

23 Dioxygenation of nitrobenzene to catechol and 2-nitrotoluene to 3-methylcatechol showed l

24 The optimal pH values were 5.5 for catechol and 4-methylcatechol and 5.0 for chlorogenic ac

25 n electrophoretic separation of dopamine and catechol and a micellar electrokinetic chromatography se

26 icity of DOPAL and demonstrate that both the catechol and aldehyde are required to potently inhibit T

27 3-dihydroxybenzoylglycine (H3L), which bears catechol and carboxyl functionalities in tandem, on to t

28 lic compounds including phenol, bisphenol A, catechol and cresols is reported.

29 eview describes the crosslinking pathways of catechol and derivatives in both natural and synthetic s

30 Experiments with the model compound catechol and further hydroxylated benzenes were performe

31 alyzed the sulfonation of benzo[a]pyrene-7,8-catechol and generated two isomeric benzo[a]pyrene-7,8-c

32 The detection limits of catechol and glucose were 1.0 x 10(-5) and 5.0 x 10(-6)

33 The reactions of Fe(III) with catechol and guaiacol produced significant changes in th

34 mechanism were shown to include oxidation of catechol and guaiacol to hydroxy- and methoxy-quinones.

35 Here, dark reaction of Fe(III) with catechol and guaiacol was investigated in an aqueous sol

36 the phenolic compounds tested: 0.03 muM for catechol and guaiacol; 0.14 muM for pyrogallol and 0.21

37 and benzoic acids as well as phenols such as catechol and its derivatives from the action of colonic

38 s-bacterial iron chelators-consist of paired catechol and lysine functionalities, thereby providing a

39 portionation leading to equimolar amounts of catechol and o-quinone products.

40 typical humus and lignin phenolic monomers--catechol and p-coumaric acid--in the presence and absenc

41 Catechol and phenol, which were persistent biotransforma

42 products that did not transform further were catechol and phenol.

43 Catechol and sodium data were compared by using a longit

44 rtant 0.1-1 muM range and in the presence of catechol and such dopamine precursors and metabolites as

45 he laccase-catalyzed domino reaction between catechols and 6-substituted 1,2,3,4-tetrahydro-4-oxo-2-t

46 Recently, catechols and amines-two functionalities that account fo

47 acids, dye molecules, amino acids, alcohols, catechols and nitrogen containing compounds on single cr

48 lating functional groups (i.e., hydroxamate, catechol, and mixed type).

49 side (vitisin B), pyranomalvidin-3-glucoside-catechol, and pyranomalvidin-3-glucoside-epicatechin] us

50 logical diols such as fructose, glucose, and catechol, and the thiosemicarbazide-functionalized nopol

51 The use of catechols, and more specifically of dopamine, as a speci

52 at incorporated carboxylic acid side chains, catechols, and sequences derived from phage display sele

53 tween dietary fava beans, plasma and urinary catechols, and urinary sodium excretion in 13 healthy vo

54 ored complexes by the known reaction between catechol- and pyrogallol-containing anthocyanins and alu

55 However, variable [catechol] and [O3(g)] can affect the ratio of the primar

56 ors describing the concentration of adsorbed catechol are very similar suggesting that light does not

57 f the 5-Cl substitution of compound 1 on the catechol aryl ring system led to a new analogue compound

58 able sensor platform and electrocatalyst for catechol as probe in aptasensor.

59 ydrogen peroxide as the enzyme substrate and catechol as redox mediator was employed to monitor the a

60 e inactivation in between 2.0</=pH>10, using catechol as substrate.

61 ruit guaiacol emission, which suggested that catechol availability might limit guaiacol production.

62 in 2, Bet v 1 is capable of binding iron via catechol-based siderophores.

63 These catechol-bearing dendrons provide a fast and efficient m

64 s alpha-pinene and limonene and the aromatic catechol (benzene-1,2-diol).

65 d cations from the mineral surface, allowing catechol binding to underlying oxides.

66 The catechol biosensor exhibited wide sensing linear range f

67 lytical performances were investigated for a catechol biosensor, based on the PEDOT-rGO-Fe2O3-PPO com

68 Most notably, 1 reacts with catechol borane to afford the unprecedented hydroborylen

69 ght, increases the concentration of adsorbed catechol by a factor of 3 over 60 min relative to dry co

70 ruction to the electrocatalytic oxidation of catechol by Ag@Pt-GRs after binding to the surface of el

71 mation via the one-electron oxidation of the catechol by approximately 400 mV (9 kcal mol(-1)).

72 -7,8-dione was reduced to benzo[a]pyrene-7,8-catechol by dithiothreitol under anaerobic conditions an

73 We investigated whether sulfonation of PAH catechols by human sulfotransferases (SULT) could interc

74 nitroaromatic compounds to the corresponding catechols by two enzymes, namely, nitrobenzene and 2-nit

75 d semiquinone radical after the oxidation of catechol (CA) can donate an H-atom to generate quinone,

76 Petrobactin, a mixed catechol-carboxylate siderophore, is required for full v

77 in a molecule reduces adhesion, and (3) the catechol-cation synergy is greatest when both functional

78 brication of laccase biosensor to detect the catechol (CC) using laccase immobilized on graphene-cell

79 crosslinking and parameters that affect the catechol chemistry in detail.

80 for further investigation of the complicated catechol chemistry.

81 Here, we report that redox cycling with this catechol-chitosan redox capacitor can amplify electroche

82 Aniline-modified DNA was coupled to catechol-coated electrodes that were oxidized to o-quino

83 The Mo-catechol complex (2a) was found to react within minutes

84 By binding to ferric catechol complexes, SCN can sequester iron, a growth-lim

85 In this work, a polymer-catechol conjugate containing a superhydrophilic nonfoul

86 The corresponding bis-catechol conjugate, 42, has excellent activity against G

87 e poor pharmacokinetic profiles intrinsic to catechol-containing molecules and to elevate the agonist

88 Importantly, catechol-containing thienopyrimidinones also inhibit HIV

89 hanging the reaction time and the underlying catechol content, the final DNA surface coverage could b

90 y incorporating sacrificial, reversible iron-catechol cross-links into a dry, loosely cross-linked ep

91 The novel boronate-catechol crosslinked nanocarrier platform demonstrated i

92 Catechol crosslinked protein networks, such as sclerotiz

93 We discuss existing pathways of catechol crosslinking and parameters that affect the cat

94 e oligonucleotide generated by two oxidants, catechol/Cu(2+)/NADPH and Fenton's reagent, were located

95 45, and 248 were most frequently oxidized by catechol/Cu(2+)/NADPH with relative oxidation of 5.6, 7.

96 However, under an O2 environment, catechol degradation decreased when SCT was <1 mug/mg bu

97 matite coating on a silica surface inhibited catechol degradation in N2, especially at low catechol l

98 The introduction of O2 into the catechol degradation system substantially decreased the

99 the chain-breaking antioxidant properties of catechol derivatives in a rational and predictable fashi

100 cluding several hydroquinone, resorcinol and catechol derivatives, either chlorinated or not.

101 e phenols, such as p-hydroxybenzoic acid and catechol, derived from the catabolism of gallotannins, e

102 Importantly, we demonstrate that catechol-derived oxidants can be quantified in human neu

103 of catecholics is a big concern, because the catechol-derived semiquinone radical after the oxidation

104 The catechol-derived SOM absorbed light in the ultraviolet (

105 tivity of Ag@Pt-GRs towards the oxidation of catechol, determination of TNF-alpha antigen was based o

106 Members of the catechol diether class are highly potent non-nucleoside

107 Earlier analogues of the catechol diether compound series have picomolar activity

108 binding modes and future optimization of the catechol diether series.

109 resolution are reported for two complexes of catechol diethers with HIV-1 reverse transcriptase.

110 series of very potent nanomolar to picomolar catechol diethers.

111 ds I and II, which are members of a class of catechol diethers.

112 ere separated and identified by LC-ESI-MS as catechol-diglycine adduct that undergoes polymerization

113 nolic compounds in E. polonica, initiated by catechol dioxygenase action, are important to the infect

114 f the pIPP2 derivatives to S. coelicolor and catechol dioxygenase assays demonstrated that all four c

115 s were identified in E. polonica that encode catechol dioxygenases carrying out these reactions.

116 wth peptide (OGP) domain and surface-binding catechol domains were obtained through solid phase synth

117 criminates nine diol-containing bioanalytes--catechol, dopamine, fructose, glucose, glucose-1-phospha

118 eract with quinones (electron acceptors) and catechols (electron donors), producing pH-dependent PL q

119 n the enzyme-catalyzed para-carboxylation of catechols, employing 3,4-dihydroxybenzoic acid decarboxy

120 ridium-catalysed tyrosinase-like approach to catechols, employing an oxyacetamide-directed C-H hydrox

121 he presence of competitive concentrations of catechol, epinephrine, norepinephrine, 3,4-dihydroxy-phe

122 Initial (11)B NMR spectroscopy of the H3BO3-catechol equilibria reveals a large pressure-driven exch

123 ic content of HBMe was 206.81 +/- 1.11 mg of catechol equivalents/g extract.

124 fections, including roles for metabolites of catechol estrogen and oxysterols of parasite origin as i

125 ese helminth infections, including roles for catechol estrogen- and oxysterol-metabolites of parasite

126 Uptake and photoreactivity of catechol-Fe complexes are investigated at the gas/solid

127 enhances the initial photodecay kinetics of catechol-Fe complexes at 30% RH by a factor of 10 relati

128 om 3.5 to 7.5) and substrate concentrations (catechol from 0 to 0.5M).

129 detect minute amounts of urushiol, the toxic catechol from poison oak, poison ivy, and poison sumac,

130 Metalation of the catechol functionality residing in the MOFs resulted in

131 s study, copolyampholytes, which combine the catechol functionality with amphiphilic and ionic featur

132 to the Dopa (3,4-dihydroxyphenylalanine) or catechol functionality, which continues to raise concern

133 ssel-inspired wet adhesion typically entails catechol functionalization of polymers and/or polyelectr

134 Despite the success in developing catechol-functionalized materials, the crosslinking chem

135 by means of mussel-inspired metal-chelating catechol-functionalized polymer networks, biological sel

136 micking the natural proteins using synthetic catechol-functionalized polymers.

137 The advantage of silyl protection for catechol-functionalized polysiloxanes is demonstrated an

138 After premixing a catechol-functionalized weak polyanion with a polycation

139 activity with pyrogallol, 3-methylcatechol, catechol, gallic acid, and protocatechuic acid.

140 e-activity relationship study shows that the catechol group in 7,8-dihdyroxyflavone, a selective smal

141 The absence of the catechol group on apigenin drastically decreased arginas

142 les enter plant cells, conjugate enediol and catechol group-rich flavonoids in situ, and exit plant c

143 ions of flavonoids is the methylation of the catechol group.

144 Molecular dynamics simulations confirm that catechol groups anchor to a variety of mineral surfaces

145 Redox active catechol groups in melanins permit efficient and reversi

146 ated with polydopamine (PDA), whose reducing catechol groups subsequently immobilized silver ions in

147 ith molecules bearing enediol and especially catechol groups.

148 (2H(+)/2e(-)), i.e., the first 1H(+)/1e(-) (catechol--> phenoxyl radical) and the second 1H(+)/1e(-)

149 The role of antiradical moieties (catechol, guaiacyl and carboxyl group) and molecular con

150 o-/p-aminophenols and solvent water adducts (catechol, hydroquinone) and ammonium ion.

151 he distance between the amino group and each catechol hydroxyl.

152 ss bees, and we report the identification of catechol in Brazilian honey samples for the first time.

153 sulfotransferases (SULT) could intercept the catechol in human lung cells.

154 The interest of catechol in SECM as a sensitive redox mediator is exempl

155 r(II) core, which hydroxylates tyrosine to a catechol in the first committed step of melanin biosynth

156 ) increasing the ratio of cationic amines to catechols in a molecule reduces adhesion, and (3) the ca

157 Biosensor response is characterized towards catechol, in terms of graphene oxide concentration, numb

158 mutants and can be used to prepare alkylated catechols, including ethyl vanillin.

159 The aptamer competes with a catechol iron-siderophore, the natural ligand of mLcn2.

160 Under certain conditions, catechol is degraded up to 65.6% to oxalic acid referrin

161 derstanding of the crosslinking mechanism of catechols is of vital importance.

162 zed materials, the crosslinking chemistry of catechols is still a subject of debate.

163 for the substrate-binding, thus phenols and catechols, lacking a p-hydroxyl group, do not bind to Pc

164 reduction of silver ions in the presence of catechol, leading to the in situ deposition of silver pa

165 These lines also showed a trend toward lower catechol levels.

166 nd have implications for the design of rigid catechol ligands.

167 atechol degradation in N2, especially at low catechol loadings on solid particles (SCT).

168 The adjacent catechol-lysine placement provides a "one-two punch," wh

169 hlorophenol, 2-chlorophenol, salicylic acid, catechol, maleic acid, oxalate, and urea), the DeltaEE o

170 led underwater by the formation of extensive catechol-mediated interfacial hydrogen bonds.

171 as a broad substrate range; and an inducible catechol meta-cleavage pathway gene cluster adoXEGKLIJC.

172 4-hydroxy-estradiol (4-OH-E2), a predominant catechol metabolite of E2, caused transformation of norm

173 KEY POINTS: The catechol metabolites of 17beta-oestradiol (E2 beta), 2-h

174 ines ionoprinting techniques with reversible catechol-metal ion coordination chemistry found in musse

175 inelandii is due to an interference with the catechol-metalophores assisted uptake of Mo.

176 ated by hydrogen bonding between interfacial catechol moieties, and consolidated by the recruitment o

177 udes a second order in both boronic acid and catechol moieties, and inverse second order in MeOH conc

178 s of carvedilol, including the carbazole and catechol moieties, as well as the linker chain containin

179 h the slow autoxidation and cross-linking of catechol moieties.

180 groups and in particular the presence of the catechol moiety remains the most significant features in

181 f the phenolic group to give an intermediate catechol moiety that is subsequently O-alkylated.

182 with one of the oxygen atoms of taxifolin's catechol moiety, and finally, further oxidation to form

183 icating 2H(+)/2e(-) processes as inherent to catechol moiety.

184 eacting different ratios of C3-symmetric DBA catechol monomers with C2-symmetric pyrene-2,7-diboronic

185 drolytic products of more stable substrates (catechol monophosphate, ascorbic 2-phosphate and hydroqu

186 e ligand 4,5-bis(pyridine-2-carboxamido)-1,2-catechol ((N,O)LH4) with Mn(III) affords the chain compo

187 echol-O-methyltransferase (COMT), regulating catechol neurotransmitter catabolism.

188 e more rapid than any reported activity with catechol neurotransmitters.

189 trophenol in the photo-oxidation of 4-methyl catechol not partitioning into the aerosol phase until i

190 ically the S-adenosyl-l-methionine pocket of catechol O-methyl transferase allowed the identification

191 Catechol O-methyl transferase belongs to the diverse fam

192 Catechol O-methyltransferase (COMT) inhibitors are an es

193 Catechol O-methyltransferase (COMT) is the enzyme respon

194 e involves three enzymes: monoamine oxidase, catechol O-methyltransferase, and sulfotransferase.

195 y of properties is observed between GNMT and catechol O-methyltransferase, despite significant differ

196 e modified by variation in the gene encoding catechol O-methyltransferase.

197 nd generated two isomeric benzo[a]pyrene-7,8-catechol O-monosulfate products that were identified by

198 conclusion, redox-active ligands containing catechol, o-aminophenol or o-phenylenediamine moieties s

199 ocusses on metal complexes containing either catechol, o-aminophenol or o-phenylenediamine type ligan

200 abolomic signature of two models of disease, catechol-O-methyl transferase (COMT(-/-)) and endothelia

201 nt non-linear interaction between two genes--catechol-O-methyl transferase (COMT) and dysbindin (dys;

202 rily regulate prefrontal dopamine clearance--catechol-O-methyl transferase (COMT) and two isoforms of

203 pone and entacapone are potent inhibitors of catechol-O-methyl transferase (COMT) for the treatment o

204 Specifically, using the brain penetrant catechol-O-methyl transferase (COMT) inhibitor tolcapone

205 demonstrated that copy number elevations of catechol-O-methyl-transferase (COMT) or Tbx1, two genes

206 abolites suggest that enzymatic catalysis by catechol-O-methyl-transferase (COMT) predominates over D

207 undant expression of the DA catalytic enzyme catechol-O-methyl-transferase (COMT), but negligible exp

208 i) to determine whether polymorphisms in the catechol-O-methyltransferase (COMT) gene affect the rela

209 The Val158Met polymorphism of the catechol-O-methyltransferase (COMT) gene is an important

210 functional polymorphism (Val(158)Met) in the catechol-O-methyltransferase (COMT) gene is associated w

211 The catechol-O-methyltransferase (COMT) gene is located in t

212 Functional genetic variants in the catechol-O-methyltransferase (COMT) gene result in a dif

213 In particular, the catechol-O-methyltransferase (COMT) gene, located on chr

214 a functional polymorphism (Val158Met) in the catechol-O-methyltransferase (COMT) gene, whose protein

215 r (OPRM1), multidrug resistance (ABCB1), and catechol-o-methyltransferase (COMT) genes are associated

216 or placebo (n = 537) and were stratified by catechol-O-methyltransferase (COMT) genotype activity (h

217 The Val158Met polymorphism of human catechol-o-methyltransferase (COMT) is one of the most w

218 Catechol-O-methyltransferase (COMT) metabolizes dopamine

219 Catechol-O-methyltransferase (COMT) modulates dopamine l

220 Additionally, catechol-O-methyltransferase (COMT) polymorphism has bee

221 our-hour urinary hydroxytyrosol and HVAL and catechol-O-methyltransferase (COMT) rs4680 genotypes wer

222 Catechol-O-methyltransferase (COMT), an important therap

223 he DAT1 VNTR and functional polymorphisms in catechol-O-methyltransferase (COMT), DRD2, and DRD4 were

224 Enzymatic methyl transfer, catalyzed by catechol-O-methyltransferase (COMT), is investigated usi

225 is amplified by allelic variants in a gene, catechol-O-methyltransferase (COMT), regulating catechol

226 (OPRD1), cannabinoid receptor 1 (CNR1), and catechol-o-methyltransferase (COMT), was strongly associ

227 ion of a fungal tyrosinase and the mammalian catechol-O-methyltransferase (COMT), which can effect th

228 s and quercetin strongly inhibit human liver catechol-O-methyltransferase (COMT)-mediated O-methylati

229 ent in humans is the Val/Met polymorphism in catechol-O-methyltransferase (COMT).

230 n the expression of tyrosine hydroxylase and catechol-O-methyltransferase (COMT).

231 he rs4680 single-nucleotide polymorphism for catechol-O-methyltransferase (COMT).

232 In genetically modified mice with reduced catechol-O-methyltransferase activity there was selectiv

233 ently reported isotope-effect variations for catechol-O-methyltransferase and its mutant structures.

234 in which we administered the brain penetrant catechol-O-methyltransferase inhibitor tolcapone or plac

235 a novel, once-daily, potent third-generation catechol-O-methyltransferase inhibitor.

236 g several other medications, such as MAOBIs, catechol-O-methyltransferase inhibitors, or dopamine ago

237 e-derivatives like 3-iodothyronamine (T1AM), catechol-O-methyltransferase products like 3-methoxytyra

238 receptor, ATP-binding cassette subfamily B, catechol-O-methyltransferase, and cytochrome 2D6 current

239 a proof-of-concept, we study three enzymes (catechol-O-methyltransferase, glucose-6-phosphate dehydr

240 The cleavage of catechol occurs at the 1,2 carbon-carbon bond at the air

241 CTOMT1) with homology to a Nicotiana tabacum catechol OMT.

242 Cyclic voltammetric studies of catechol on the enzyme modified electrode revealed highe

243 that is fabricated by grafting redox-active catechols onto a chitosan film.

244 determining the effect of AA and EDTA on the catechol or galloyl iron binding ability of pure phenoli

245 icals via double processes by involvement of catechol or guaiacyl moiety.

246 and tyramine), the enzyme is classified as a catechol oxidase.

247 Tyrosinases and catechol oxidases belong to the family of polyphenol oxi

248 suggest that the physiological role of plant catechol oxidases were previously underestimated, as the

249 and oxidation of phenolic compounds, whereas catechol oxidases were so far defined to lack the hydrox

250 oup, together with the MOM-protection in the catechol part of the tetrahydroisoquinoline ring system,

251 r chemical analogues, such as ascorbic acid, catechol, phenethylamine, tyrosine, epinephrine, and nor

252 Catechols play an important role in many natural systems

253 i(II)) were successfully incorporated into a catechol porous organic polymer (POP) and characterized

254 nant CTOMT1 enzyme preferentially methylated catechol, producing guaiacol.

255 The resulting catechol pyrazolinones act as potent TbrPDEB1 inhibitors

256 This work shows how catechol, pyrogallol, 3-methylcatechol, 4-methylcatechol

257 This biosensor was successfully applied to catechol quantification in spiked water samples.

258 tion of OPD at higher rates than pyrogallol, catechol, quercetin and 2,2'-azino-bis(3-ethylbenzothiaz

259 peting the classic disproportionation-driven catechol-quinone coupling and suggest that this hitherto

260 an form over a wide range of boronic acid-to-catechol ratios, thus producing frameworks with composit

261 DA and other catechols readily oxidize into highly reactive o-quinone

262 rting with simple phenol derivatives such as catechol, resorcinol, and hydroquinone.

263 oefficient of 0.995 and 0.996 for phenol and catechol, respectively.

264 Marine mussels use catechol-rich interfacial mussel foot proteins (mfps) as

265 s favourably influenced by the presence of a catechol (ring-B) and enol (ring C) function.

266 ached to the aromatic ring as a monoether of catechol S-(-)-6 and subsequently subjected to oxidative

267 es increases, while under Mo-limitation only catechol siderophore production is increased, with the s

268 orporating a conjugated enyne as an atypical catechol-simulating moiety were synthesized in enantiome

269 A competitive monofunctional catechol slows COF-5 formation but does not redissolve a

270 Compounds lacking the catechol structure had a decreasing order of H-atom and

271 The catechol structure improved both hydrogen and electron d

272 din-3-glucoside (Pet-3-glc), both carrying a catechol substituted B-ring.

273 s strategy identified 3',4'-dihydroxyphenyl (catechol) substituted thienopyrimidinones with submicrom

274 chrome P450 enzyme (CYP84A4) to generate the catechol-substituted substrate for an extradiol ring-cle

275 s capable of directly carboxylating aromatic catechol substrates under ambient conditions.

276 The strategy uses o-aminophenols or o-catechols that are oxidized to active coupling species i

277 a series of physiologic unconjugated urinary catechols that were able to function as SCN ligands of w

278 atalyses the aerobic oxidation of phenols to catechols through the binuclear copper centres.

279 ydrogen bond that impairs the ability of the catechol to engage the receptor.

280 tion reactions between arylboronic acids and catechol to give boronate esters are the most favored th

281 ation to form phenols and polyphenols (e.g., catechol) typically identified in the complex mixture of

282 in the hydrogen-bonding network upon gaseous catechol uptake are observed in the dark and light and d

283 rovides a convenient route to (18)O-labelled catechols using (18)O-labelled acetic acid.

284 does not significantly enhance the uptake of catechol vapor on FeCl3.

285 ghly boronic acid-deficient to networks with catechol voids.

286 as of 1.74mM; for pyranomalvidin-3-glucoside-catechol was 1.17mM and for pyranomalvidin-3-glucoside-e

287 Determination of catechol was carried out successfully by Differential Pu

288 Catechol was chosen as a simple model for organics in ae

289 Catechol was the most readily oxidized substrate followe

290 .46 mM and 0.98 U/ml/min, respectively, when catechol was used as substrate.

291 , protocatechuic acid, 4-methylcatechol, and catechol) were computationally studied using density fun

292 ounds, methyl chavicol, toluene and 4-methyl catechol, were investigated at the European Photoreactor

293 nts demonstrated the highest affinity toward catechol, whereas PPO from BABA-elicited lettuce showed

294 hich shows fast electron transfer on Pt, and catechol, which exhibits fast electron transfer on Au.

295 ed at different rates, with the exception of catechol, which resulted in irreversible inhibition.

296 nspired themes for wet adhesion by combining catechol with hydrophobic and electrostatic functional g

297 The oxidative coupling of o-aminophenols or catechols with aniline functional groups is chemoselecti

298 chieves one-step, redox-neutral synthesis of catechols with diverse substituent groups under mild con

299 lied to the synthesis of different important catechols with fluorescent property and bioactivity from

300 gin siderophore system, but can also use the catechol xenosiderophore enterobactin via the BfeA outer