ライフサイエンスコーパス: carbonylation

1 eactions (Sonogashira, Suzuki, and reductive carbonylation).

2 th annelation, while the reverse is true for carbonylation.

3 tissue lipid aldehyde production and protein carbonylation.

4 philicity increases upon both annelation and carbonylation.

5 be more influential on the extent of protein carbonylation.

6 omplex attenuated ouabain-stimulated protein carbonylation.

7 eptibility to mitochondrial membrane protein carbonylation.

8 col involves Michael addition and subsequent carbonylation.

9 se secondary structure, oligomerization, and carbonylation.

10 ein amino acids in a reaction termed protein carbonylation.

11 es that do not undergo simple ring-expansion carbonylation.

12 resent alternative reactants to enable (11)C-carbonylation.

13 es reactive oxygen species-dependent protein carbonylation.

14 ed by tandem intramolecular Heck cyclization/carbonylation.

15 l as its ability to suppress ROS and protein carbonylation.

16 A high raffinose level increases ROS and carbonylation.

17 o a Bronsted acid site in the 8MR to undergo carbonylation.

18 cies present in the MOR side pockets undergo carbonylation.

19 uction yields (100 t/y) compared to methanol carbonylation (0.26 pound/kg, 261 pound/t) and ethane di

20 ts activation), malonyl-CoA content, protein carbonylation (a marker of oxidative stress), plasma adi

21 e protocol was set up using Paraquat-induced carbonylation, a model that induces protein aggregation

22 Protein carbonylation, a sensitive marker of hemoglobin neurotox

23 n IP; this correlated with decreased protein carbonylation, a surrogate marker for oxidative stress.

24 proceeds via carbonylation-carbocyclization-carbonylation-alkynylation involving sequential insertio

25 oxidation, total carbonylation, and specific carbonylation (alpha-amino adipic and gamma-glutamic sem

26 days, and protein oxidation was evaluated as carbonylation (alpha-amino adipic and gamma-glutamic sem

27 d cysteine residues, referred to as "protein carbonylation." Although not widely appreciated, reactiv

28 ines via a sequential one-pot multicomponent carbonylation/amination reaction has been developed.

29 Levels of protein carbonylation, amount of glutathione stores, and lipid p

30 t synthesize CL, exhibited increased protein carbonylation, an indicator of reactive oxygen species (

31 uropathies, we predicted that an increase in carbonylation and aggregation of PMP22 may be associated

32 rkers of proteostasis stress such as protein carbonylation and aggregation.

33 s exhibited significant elevation in protein carbonylation and alterations in protein conformation.

34 tes, complex I protein and activity, protein carbonylation and ATP levels were all fully protected in

35 xin-mediated reductive signaling to regulate carbonylation and decarbonylation mechanisms.

36 We confirmed the carbonylation and degradation of MyBPC using HL-1 cardio

37 The carbonylation and degradation of MyBPC were time- and dr

38 We confirmed carbonylation and degradation of this protein under oxid

39 m to industrial chemical processes: methanol carbonylation and ethane direct oxidation.

40 n the generation of reactive oxygen species, carbonylation and glutathionylation of cellular proteins

41 ction of reactive oxygen species, along with carbonylation and glutathionylation of the cellular prot

42 plants, as evidenced from decreased protein carbonylation and hydrogen peroxide accumulation.

43 The use of compatible epoxide carbonylation and lactone polymerization catalysts allow

44 sed with OA treatment as measured by protein carbonylation and lipid peroxidation.

45 ptophan and thiols depletion, higher protein carbonylation and more intense formation of protein cros

46 n p38K are associated with increased protein carbonylation and Nrf2-dependent transcription, while ad

47 tions, and (iv) one-flask palladium-mediated carbonylation and ring closure to form the imide.

48 es (UF) for the extent of protein oxidation (carbonylation and Schiff base formation) and their senso

49 We propose that carbonylation and subsequent degradation of annexin A1 m

50 ical examples, such as alcohol oxidation and carbonylation and the asymmetric reduction of ketones.

51 lucose) for their ability to promote protein carbonylation and tryptophan depletion in myofibrillar p

52 and exhibit decreased mitochondrial protein carbonylation and UCP2-dependent reduction in intracellu

53 e and selective for both epoxide and lactone carbonylation, and by the identification of a solvent th

54 drial respiration, tissue nitration, protein carbonylation, and contractile function in the heart dur

55 ding lysine, arginine, proline and threonine carbonylation, and cysteine oxidation.

56 ocyclization, ring cleavage, hydrogen shift, carbonylation, and decarbonylation contributed to CBZ tr

57 higher levels of lipid peroxidation, protein carbonylation, and DNA oxidative damage even at a young

58 ctive aldehyde 4-hydroxynonenal (HNE) caused carbonylation, and HNE-glutathione adducts were detected

59 hase-2 expression, tissue nitration, protein carbonylation, and mitochondrial morphology and function

60 gnals related to lipid peroxidation, protein carbonylation, and nitration in WAT and liver.

61 dinitrogen loss became competitive with N(2) carbonylation, and significant quantities of the zircono

62 tion was evaluated as thiol oxidation, total carbonylation, and specific carbonylation (alpha-amino a

63 D1 pI 6.0 isoform is oxidatively modified by carbonylation, and the pI 5.0 isoform is selectively acc

64 The rates of both epoxide and lactone carbonylation are independent of carbon monoxide pressur

65 -induced oxidative damage to DNA and protein carbonylation are involved in the observed toxicity of H

66 This process and further carbonylation are slow compared to isomerizing methoxyca

67 These data identify carbonylation as a novel mechanism that contributes to S

68 In the biotechnology industry, oxidative carbonylation as a post-translational modification of pr

69 We focused on protein carbonylation as an indicator of severe oxidative damage

70 hat DJ-1 protein is irreversibly oxidized by carbonylation as well as by methionine oxidation to meth

71 lular H(2)O(2) levels as measured by protein carbonylation assays and fluorescence-activated cell sca

72 Carbonylation at the alpha-position with respect to the

73 rphyrins, and lipid peroxidation and protein carbonylation blockers/inhibitors (edaravone and lazaroi

74 of vemurafenib and UVA caused little protein carbonylation but were nevertheless inhibitory to nucleo

75 2) C-H activation (i.e., ortho acylation) or carbonylation by activation of the carbonyl group (i.e.,

76 etailed mechanistic investigation of epoxide carbonylation by the catalyst [(salph)Al(THF)2]+ [Co(CO)

77 The insertion cascade proceeds via carbonylation-carbocyclization-carbonylation-alkynylatio

78 rsed the effects of IPC on postischemic Rpt5 carbonylation, cardiac function, morphology and morphome

79 step by PdI(2)/KI-catalyzed direct oxidative carbonylation, carried out in alcoholic media under rela

80 ted by effective activation to a homogeneous carbonylation catalyst [(dtbpx)PdH(L)](+) by addition of

81 rs also demonstrated the practicality of the carbonylation catalyst for complex molecule synthesis as

82 active and selective porphyrin-based epoxide carbonylation catalyst, [(OEP)Cr(THF)2][Co(CO)4] (1; OEP

83 Furthermore, carbonylation, CoA binding, and methyl transfer can all

84 owed to react under PdI2-catalyzed oxidative carbonylation conditions, depending on the nature of the

85 Carbonylation converts [H1H](0) into [1(CO)](0).

86 s of 8-oxo-dG-modified DNA and total protein carbonylation corresponded to cardioprotective activity.

87 ted 2-aminoquinazolin-4(1H)-ones by a domino carbonylation/cyclization process.

88 A Pd-catalyzed and ligand-free carbonylation/cycloaddition/decarboxylation cascade synt

89 er forms contained higher degrees of damage (carbonylation, deamidation) and far less IE.

90 allmarks of oxidative stress such as protein carbonylation, decreased aconitase activity, and lower l

91 ns that are susceptible to substoichiometric carbonylation during oxidative stress.

92 alkylation, halogenation, carboxylation, and carbonylation), each representing a distinct handle for

93 ibited severe lipid peroxidation and protein carbonylation, for oxidative stress damage at the cellul

94 eductive N-O bond cleavage of 40 followed by carbonylation gave cyclic urea 47 in which inversion of

95 ntial and non-overlapping, such that epoxide carbonylation goes to completion before any of the inter

96 Both annelation and carbonylation have been found to decrease the stability

97 Increased (P<0.05) carbonylation in a 53-kDa band following I/R was diminis

98 pression of GSTA4 and the role(s) of protein carbonylation in adipocyte function.

99 th increased DJ-1 oxidative modification and carbonylation in FECDi as compared with HCECi.

100 was employed to identify specific targets of carbonylation in GSTA4-silenced or overexpressing 3T3-L1

101 dot blot method for quantitation of protein carbonylation in homogenates or purified proteins.

102 f sensitivity allowed measurement of protein carbonylation in individual Drosophila.

103 novel DNPH-based method to quantify protein carbonylation in muscle and meat.

104 Protein carbonylation in response to ligand-receptor interaction

105 cies formation and a higher level of protein carbonylation in response to RSV infection.

106 istinct advantage over traditional reductive carbonylation in that no carbon monoxide, pressurized ga

107 506 pretreatments markedly increased protein carbonylation in the myocardium despite elevated mangane

108 To address the role of protein carbonylation in the pathogenesis of mitochondrial dysfu

109 Ethanol sensitivity and increased protein carbonylation in the taz1Delta mutant but not in crd1Del

110 show significantly lower protein oxidation (carbonylation) in Mexican free-tailed bats (Tadarida bra

111 Cu-MOR and Cu-ZSM-5 are oxidation active but carbonylation inactive.

112 red adipocytes resulted in increased protein carbonylation, increased mitochondrial ROS, dysfunctiona

113 late stationary phase, mitochondrial protein carbonylation increases in all strains, particularly in

114 earlier reported transition-metal-catalyzed carbonylations involved either toxic carbon monoxide (CO

115 These results suggest that protein carbonylation is a post-translational modification invol

116 Elevated protein carbonylation is accompanied by diminished complex I act

117 from aryl chlorides via palladium-catalyzed carbonylation is described using atmospheric pressure of

118 n donor solvent, whereas the rate of lactone carbonylation is first-order in lactone and inversely de

119 he stages differ in that the rate of epoxide carbonylation is independent of substrate concentration

120 The effect of carbonylation is more pronounced than annelation toward

121 However, the effect of carbonylation is more pronounced than annelation toward

122 es to succinic anhydrides via one-pot double carbonylation is reported.

123 Ouabain-stimulated protein carbonylation is reversed after removal of ouabain, and

124 Carbonylation is the covalent, non-reversible modificati

125 Protein carbonylation is the most commonly used measure of oxida

126 es and subsequent direct palladium-catalyzed carbonylation/lactonization provide an efficient route t

127 s a target for oxidant-induced PTMs, such as carbonylation, leading to impaired function during epile

128 ich significantly correlated with fibrinogen carbonylation level (r(2)=0.33, P<0.0001), residual beta

129 new procedure reflected an increased protein carbonylation level measuring overall two to fourfold mo

130 Moreover, mitochondrial protein carbonylation levels in sod1, sod2, and sod1sod2 mutants

131 ring striatal aconitase activity and protein carbonylation levels.

132 on step corresponds to subsequent side chain carbonylation, likely at Lys72/73.

133 ia/reoxygenation hypersomnolence but also to carbonylation, lipid peroxidation injury, and the proinf

134 ylis-Hillman reactions, conjugate additions, carbonylations, methylations, silylations, and brominati

135 Taken together, the data indicate that carbonylation modification of the Na/K-ATPase alpha1 sub

136 ular enolate alkylation, an effective Stille carbonylation/Nazarov cyclization sequence, and a high-r

137 ere, numerous proteins are carbonylated, and carbonylation occurs in both collecting ducts and thin l

138 tannylacrylate is prepared by stereospecific carbonylation of (E)-1,2-difluorovinyl iodide followed b

139 When the carbonylation of 1,2-epoxybutane (EB) to beta-valerolact

140 Palladium-catalyzed carbonylation of 2,4-enyne carbonates in an alcohol and

141 were selectively obtained when the oxidative carbonylation of 2-alkynylbenzamides, bearing a terminal

142 Thus, oxidative carbonylation of 2-ethynylbenzamides, bearing a terminal

143 2061) was developed via palladium-catalyzed carbonylation of 2-iodo-5-methoxyaniline (4) with thiazo

144 licon-tethered acrylate; an efficient Stille carbonylation of a sterically encumbered vinyl triflate;

145 Monoselective gamma-C-H olefination and carbonylation of aliphatic acids has been accomplished b

146 nent reaction based on a palladium-catalyzed carbonylation of alpha-chloroketones in the presence of

147 yzed protocol for the oxidative cross double carbonylation of amines and alcohols.

148 On the other hand, the oxidative carbonylation of amines occurs with alpha-bromomethyl su

149 They promote the catalytic carbonylation of amines under relatively mild conditions

150 Palladium-catalyzed chemoselective carbonylation of aminophenols with iodoarenes was realiz

151 ed that 4-HNE treatment of cells resulted in carbonylation of AMPKalpha/beta, which was not observed

152 The cascade process involves carbonylation of an aryl iodide/Michael acceptor to give

153 (-) catalyst for a late-stage regioselective carbonylation of an enantiomerically pure cis-epoxide to

154 in posterior eyecups of mutant mice, whereas carbonylation of an RPE-specific protein was observed in

155 Carbonylation of annexin A1 by endothelin-1 was followed

156 The direct carbonylation of aromatic sp(2) and unactivated sp(3) C-

157 A method for the Pd-catalyzed carbonylation of aryl bromides has been developed using

158 conducting the palladium-catalyzed reductive carbonylation of aryl iodides and bromides using 9-methy

159 ation has been found to facilitate the rapid carbonylation of aryl iodides into acid chlorides via re

160 omplished using a palladium-catalyzed double carbonylation of aryl iodides with near stoichiometric c

161 loride synthesis via the palladium-catalyzed carbonylation of aryl iodides.

162 general protocol for the palladium-catalyzed carbonylation of aryl tosylates and mesylates to form es

163 tially useful alternative to metal-catalyzed carbonylation of aryl triflates.

164 Pd(0)-mediated (11)C-carbonylation of aryl(mesityl)iodonium salts followed by

165 herein two catalysts for the regioselective carbonylation of cis-disubstituted epoxides.

166 t of oxidative modification, we assessed the carbonylation of cytosolic proteins in phagocytic neutro

167 Unprecedented insight into the carbonylation of dimethyl ether over Mordenite is provid

168 Altogether, carbonylation of disubstituted epoxides is established a

169 The carbonylation of each particular protein was quantified

170 bstrate scope has been demonstrated allowing carbonylation of electron-rich, electron-poor, and heter

171 Regarding the carbonylation of epoxides to beta-lactones, catalyst 1 e

172 e derived from beta-lactones prepared by the carbonylation of epoxides.

173 e stress markers (P<0.001) and with a marked carbonylation of fibrinogen (P<0.001), whose secondary s

174 areful control of reaction conditions in the carbonylation of glycidyl esters, the exclusive producti

175 owever, an effective catalyst for the direct carbonylation of methane to acetic acid, which might ena

176 vehicle for the low-temperature vapor-phase carbonylation of methanol by insertion of CO into the O-

177 ive site in supported gold catalysts for the carbonylation of methanol has been identified as dimers/

178 istic study of the electrochemical oxidative carbonylation of methanol with CO for the synthesis of d

179 rocesses, such as the Cativa process for the carbonylation of methanol.

180 Several examples on Pd-catalysed carbonylation of methyl C(sp(3))-H bonds with gaseous CO

181 Carbonylation of MyBPC showed significant functional imp

182 myosin light chain-2 slow and troponin T and carbonylation of myosin heavy chains.

183 and PP2, which correlated with a decline in carbonylation of PP2.

184 Catechin (200ppm) reduced significantly carbonylation of protein spots identified as glycogen ph

185 High urea or NaCl also greatly increases carbonylation of proteins in mIMCD3 cells.

186 d evoked Ca(2+) release from the SR, reduced carbonylation of RyR2s, and increased binding of [(3)H]r

187 GSTA4-silenced adipocytes displayed elevated carbonylation of several key mitochondrial proteins incl

188 Hip to be square: Direct carbonylation of solutions of the heptaphosphide trianio

189 igand-controlled regioselective Pd-catalyzed carbonylation of styrenes with aminophenols was realized

190 This work reports oxidative N-dealkylation/carbonylation of tertiary amines to tertiary amides by u

191 Carbonylation of the hafnocene dinitrogen complex, [Me(2

192 HepG2 cells with 4-HNE resulted in increased carbonylation of the lipid phosphatase known as "phospha

193 Carbonylation of the majority of proteins occurred trans

194 close proximity to the active site of CI and carbonylation of the residue is predicted to induce subs

195 ysis of target proteins revealed significant carbonylation of the S100A9 subunit of calprotectin, a t

196 N-C bond formation was also accomplished by carbonylation of the silylated product, yielding an unpr

197 Two-electron reductive carbonylation of the uranium(VI) nitride [U(Tren(TIPS))(

198 by hydrogenation and C-H bond activation, as carbonylation of the zirconocene and hafnocene dinitroge

199 and selectivity of Rh(III) in the oxidative carbonylation of toluene to toluic acid.

200 atalysts are reported for the regioselective carbonylation of trans-disubstituted epoxides to cis-bet

201 Furthermore, ouabain stimulated direct carbonylation of two amino acid residues in the actuator

202 The palladium-catalyzed carbonylation of urea derivatives with aryl iodides and

203 tive Pd/C-catalyzed oxidative N-dealkylation/carbonylation of various aliphatic as well as cyclic ter

204 substrates and represent the first catalytic carbonylations of alkyl bromides with carbon monoxide.

205 Catalytic carbonylations of organohalides are important C-C bond f

206 Carbonylations of unactivated alkyl halides remain a cha

207 s to identify the site and extent of protein carbonylation on a proteome-wide scale has expanded our

208 methanol synthesis, and subsequent methanol carbonylation on homogeneous catalysts.

209 iples, understanding the impact of oxidative carbonylation on product quality of protein pharmaceutic

210 tates extended characterization of oxidative carbonylation on recombinant monoclonal antibodies and p

211 to investigate the effect of annelation and carbonylation on the electronic and ligand properties of

212 The effect of annelation and carbonylation on the electronic and ligating properties

213 The effect of annulation and carbonylation on the electronic and ligating properties

214 istent with the low or undetectable rates of carbonylation on zeolites without 8-MR channels (H-BEA,

215 both species, the dose-response for protein carbonylation parallels that for fecundity reduction, ma

216 ant activity towards lipid oxidation and the carbonylation pathway at different concentrations under

217 The carbonylation pathway involves the oxidative deamination

218 n, quercetin and gallic acid) on the protein carbonylation pathway occurred during the oxidation of m

219 This reaction contrasts sharply to the carbonylation pathway well known for homogeneously catal

220 single electron transfer to enable a radical carbonylation pathway.

221 These results suggest that protein carbonylation plays a major instigating role in cytokine

222 de, among others, Friedel-Crafts alkylation, carbonylation, polymerization, cyclization, olefin metat

223 The generality of the C-H carbonylation process is aided by the action of xantphos

224 tes were subjected to the Fe(CO)(5)-mediated carbonylation process under a CO atmosphere, leading to

225 through the development of C-H amination and carbonylation processes, leading to the synthesis of azi

226 fonyl azides employing a palladium-catalyzed carbonylation protocol has been developed.

227 An efficient Pd-catalyzed carbonylation protocol is described for the coupling of

228 DME carbonylation rates are proportional to the number of O-

229 This elementary step controls catalytic carbonylation rates of dimethyl ether (DME) to methyl ac

230 s 3, bearing alkyl or aryl substituents, the carbonylation reaction led to a mixture of Boc-protected

231 An oxidative carbonylation reaction that generates acid chloride func

232 A Pd-catalyzed oxidative ortho-carbonylation reaction using ketone directing groups to

233 Remarkably, the aforementioned carbonylation reaction was found to be thermally reversi

234 The carbonylation reaction, known to occur predominantly in

235 g states and rate-determining steps for each carbonylation reaction.

236 hen D2O is introduced in the feed during the carbonylation reaction.

237 Carbonylation reactions constitute important methodologi

238 mackerel (Scomber scombrus) mince to undergo carbonylation reactions during chilled storage, and the

239 Carbonylation reactions have been widely used in organic

240 In particular, palladium-catalyzed carbonylation reactions have found broad application in

241 sformation proceeds via two tandem catalytic carbonylation reactions mediated by Pd(P(t)Bu3)2 and pro

242 Palladium(II)-catalyzed C-H carbonylation reactions of methylene C-H bonds in second

243 tion complexes as stoichiometric reagents in carbonylation reactions with (11)CO to produce structura

244 thway well known for homogeneously catalyzed carbonylation reactions, such as the synthesis of acetic

245 cules via various transition-metal-catalyzed carbonylation reactions.

246 ated using Cu-MOR by coupling oxidation with carbonylation reactions.

247 ive CO detection based on palladium-mediated carbonylation reactivity.

248 mulated Na/K-ATPase.c-Src signaling, protein carbonylation, redistribution of Na/K-ATPase and sodium/

249 However, methylene C(sp(3))-H carbonylation remains a great challenge, largely due to

250 Carbonylation results in thioester formation via a reduc

251 in adipose tissue leads to increased protein carbonylation, ROS production, and mitochondrial dysfunc

252 Hence, reductive carbonylations run with (13)COgen provide a facile acces

253 Overall, our findings indicate that MyBPC carbonylation serves as a critical determinant of cardio

254 cipitation studies indicated that the 53-kDa carbonylation signal was of proteasomal origin.

255 thoxy species from the oxidation site to the carbonylation site.

256 However, comprehensive identification of carbonylation sites has so far remained a very difficult

257 Here we mapped protein carbonylation sites in raw milk and different brands of

258 The number of carbonylation sites increased with the harsher processin

259 roach were demonstrated by identification of carbonylation sites on both unstressed and oxidized anti

260 he first time the identification of specific carbonylation sites on recombinant monoclonal antibodies

261 demonstrated by identification of 14 common carbonylation sites on three highly similar IgG1s.

262 oach, which enabled direct identification of carbonylation sites without any fractionation or affinit

263 Overall, 53 unique carbonylated peptides (37 carbonylation sites, 15 proteins) were identified.

264 IR spectroscopy, which reveals that the two carbonylation stages are sequential and non-overlapping,

265 ntally benign process, [Pd]-catalyzed direct carbonylation starting from simple and commercially avai

266 tions of sea buckthorn fruits also inhibited carbonylation stimulated by H2O2/Fe.

267 Carbonylation/sulfur-release/CO-removal cycles can be re

268 We applied a gas-phase carbonylation technique previously tested on short-lived

269 is far more resistant to IR-induced protein carbonylation than is the much more radiosensitive nemat

270 imal-source were more susceptible to protein carbonylation than soy proteins and globular were more s

271 and suffer more DNA damage and more protein carbonylation than the parent.

272 also be transformed through direct oxidative carbonylation to acetic acid, which is commercially obta

273 tured CI identified specific metal catalyzed carbonylation to Arg76 within the 75 kDa subunit concomi

274 reaction occurs in tandem through an initial carbonylation to generate an aroyl halide, which undergo

275 lcohols undergo W(CO)(6)-catalyzed oxidative carbonylation to the corresponding hydroxyalkylureas wit

276 ile synthetic intermediates that can undergo carbonylation to yield acyl anion equivalents.

277 ls and led to a disproportionate decrease in carbonylation turnover rates (per total H+).

278 rotein that showed a significant increase in carbonylation under Dox-induced cardiotoxic conditions i

279 Compared to higher olefins, ethylene carbonylation under identical conditions is much faster,

280 These experiments identified protein carbonylation upon exposure of cells to sub-lethal conce

281 n a rapid and selective fashion by catalytic carbonylation using [(OEP)Cr(THF)2][Co(CO)4].

282 g amino amides employing oxidative catalytic carbonylation using W(CO)(6) as the catalyst, I(2) as th

283 Protein carbonylation was 65% higher in hearts of hypoxic rats c

284 Carbonylation was dependent on NADPH oxidase and myelope

285 Mitochondrial-specific carbonylation was increased acutely (48 h) and chronical

286 A 4-fold increase in protein carbonylation was measured within 15 min of initiating p

287 ctedly, the oxidative DNA damage and protein carbonylation was more severe in the DeltatrxC mutant th

288 Considerable carbonylation was observed in the digestive tract, espec

289 ce an increase in protein post-translational carbonylation was observed.

290 Protein carbonylation was significantly increased in T24 cells t

291 Oxidant stress (i.e., carbonylation) was detected within 8 hrs of CLP and pers

292 Because aldehydes are important mediators of carbonylation, we explored the immunomodulatory properti

293 tochondrial density, ATP content and protein carbonylation were measured in cardiac muscle.

294 ass (i.e., cardiolipin content), and protein carbonylation, were assessed at various time points (8,

295 d loss of CcO activity and increased protein carbonylation, which was accompanied by a decline in the

296 The mechanism of epoxide double carbonylation with 1 was investigated by in situ IR spec

297 clopride, for the dopamine D2/D3 receptor by carbonylation with excellent radiochemical purity and yi

298 N-(o-bromoaryl)amides by palladium-catalyzed carbonylation with paraformaldehyde as the carbonyl sour

299 n, atgrxcp lines displayed increased protein carbonylation within chloroplasts.

300 es to delineate the physiochemical impact of carbonylation yielded channels with enhanced or reduced