ライフサイエンスコーパス: salicylate

1 -methyl-5-hepten-2-one, benzaldehyde, methyl salicylate).

2 mechanisms (cyclooxygenase-2 inhibitors and salicylates).

3 esidues that could potentially interact with salicylate.

4 in cetyltrimethylammonium bromide and sodium salicylate.

5 idue is required for efficient production of salicylate.

6 rob systems function together in response to salicylate.

7 were resistant to these metabolic effects of salicylate.

8 in the LA were also dramatically altered by salicylate.

9 disappeared upon treatment of seedlings with salicylate.

10 ly on a marked accumulation of jasmonate and salicylate.

11 tion was moderately increased in response to salicylate.

12 ter membrane porin expression in response to salicylate.

13 gnaling and that of jasmonate, ethylene, and salicylate.

14 dually manipulated by the prestin inhibitor, salicylate.

15 tin biosynthesis by converting chorismate to salicylate.

16 for the ionophore I with chloride as well as salicylate.

17 ivation by converting acetophenone to methyl salicylate.

18 rin and indomethacin and minimally by sodium salicylate.

19 hat contributes to the metabolic efficacy of salicylates.

20 e inhibition of protein synthesis induced by salicylates.

21 FVT of methyl salicylate-1-(13)C 7a revealed a deep-seated rearrangeme

22 uple hypothesis; however, the application of salicylate (10 mM), which inhibits electromotility, is n

23 in the AC, we used a micropipette to infuse salicylate (20 mul, 2.8 mM) into the amygdala.

24 arked increase in relative content of benzyl salicylate (43.30%) and a significant decrease in methyl

25 Salsalate (nonacetylated salicylate, 4500 mg/d), a compound that inhibits NF-kapp

26 Furthermore, high doses of aspirin or salicylate (5 mM), well above therapeutic plasma concent

27 -containing antibacterial agent, and 5-amino-salicylate (5-ASA), an anti-inflammatory agent.

28 sis (FVT) with Ar-matrix isolation of methyl salicylate (7), 2-phenylbenzo-1,3-dioxan-4-one (8), phth

29 rved labeling pattern in the isolated methyl salicylate 7a/7b and methyl cyclopentadienecarboxylates

30 Prior treatment with salicylate, a disrupter of the SSC, confirms the influen

31 Furthermore, we find that salicylate, a hormone involved in biotrophic defense tha

32 in opposite directions during treatment with salicylate, a known competitor of required chloride bind

33 Treatment with salicylate, a known inhibitor of NLC, reestablishes cont

34 Salicylate, a plant product, has been in medicinal use s

35 ed electrode was fabricated to detect methyl salicylate, a volatile organic compound released by path

36 against COX-2, with the exception of sodium salicylate (A549 cells).

37 g SA and methylsalicylate, as a reporter for salicylate accumulation in the apoplast of plant leaves.

38 on of salsalate or of aspirin at high doses, salicylate activates adenosine monophosphate-activated p

39 A single dose of salicylate added with LPS/IFNgamma inhibited NOS-2 expre

40 Salicylate administration (250 mg/kg) resulted in a sign

41 esence of both mutant proteins and synthetic salicylate analogues of Ent.

42 nd K44 significantly reduced binding to both salicylate and 2,4-dinitrophenol, while a mutation in re

43 e method for the rapid determination of five salicylate and benzophenone-type UV absorbing substances

44 pulations of nonlinear capacitance with both salicylate and chloride that an enhanced area motor mode

45 er, the movements were also diminished by Na salicylate and depended on the intracellular anion, prop

46 of the CD81-HCV interaction, namely, benzyl salicylate and fexofenadine, were shown to overlap the H

47 The results show that both salicylate and ibuprofen increase membrane disorder, as

48 nts sprayed with methyl jasmonate and methyl salicylate and in excised leaves supplied through cut pe

49 The nonselective COX inhibitors salicylate and indomethacin enhanced the expression of i

50 The salicylate and isochorismate synthase activities of MbtI

51 tions regarding the biosynthetic role of the salicylate and its potential impact on the mechanism of

52 (JA) biosynthesis genes and exogenous methyl salicylate and methyl jasmonate applications showed that

53 ble of detecting as low as ~80 ppb of methyl salicylate and naphthalene.

54 lyase activity resulting in the formation of salicylate and pyruvate as the reaction products.

55 so of its complex with the reaction products salicylate and pyruvate at 1.85 A and 2.1 A resolution,

56 raphic structures are reported for K42A with salicylate and pyruvate bound and for apo-I87T.

57 It is a bifunctional enzyme that forms salicylate and pyruvate from chorismate and water via th

58 PchB physiologically produces salicylate and pyruvate from isochorismate for ultimate

59 , we sought to unravel the interplay between salicylate and the fitness cost of MarA-mediated antibio

60 Activation of AMPK by salicylate and the thienopyridone A-769662 is critically

61 -methoxy-3-(1-methylpropyl)-pyrazine, methyl salicylate and tridecane.

62 We assessed the repellency of methyl salicylate and verbenone to two putative laurel wilt vec

63 tabolites and drug-like molecules, including salicylates and diclofenac, as MR1-binding ligands.

64 ively minor effects were observed with other salicylates and PJ34.

65 Two structural series included the salicylates and the N-phenylanthranilic acids, and addit

66 ast but not least, together with jasmonates, salicylate, and abscisic acid, ethylene is important in

67 nction increases the vulnerability to noise, salicylate, and aminoglycosides.

68 nas putida G7 cells were exposed to glucose, salicylate, and silver nanoparticles (AgNPs) and their m

69 rent salicylate-based drugs (aspirin, sodium salicylate, and sulfasalazine) on the development of ear

70 We examined the effects of sulfasalazine, salicylates, and the poly(ADP-ribose) polymerase-1 inhib

71 r the macrocycle 1, while 1 + SA(-) (SA(-) = salicylate anion) and 1 + HSO(4)(-) were the weakest one

72 ling network, jasmonate, ethylene, PAD4, and salicylate, are disabled, the hypersensitive response (H

73 convergent synthesis of this agent using the salicylate as a novel molecular switch for the chemosele

74 Using salicylate as an inducer of MarA, we found that a wide s

75 otential amperometry using hydrolyzed methyl salicylate as the analyte.

76 ated metabolites (5-hydroxy-L-tryptophan and salicylate) as activators of the aryl hydrocarbon recept

77 its voltage dependence and susceptibility to salicylate, as well as an associated chloride-sensitive

78 Intriguingly, salicylate/aspirin prevents the phosphorylation of AMPKa

79 aspirin to salicylate in humans and the high salicylate/aspirin ratios in serum, it is likely that th

80 We found that the HIPVs menthol and methyl salicylate at 1 and 10 nmol.ml(-1) improved many perform

81 We have reported previously that salicylate at 10(-5) M inhibited LPS/IFNgamma-induced CC

82 ations in residues shown as interacting with salicylate at SAL-A and SAL-B in the MarR-salicylate str

83 nfusion of a known ototoxic compound (sodium salicylate) at 50 nL/min for 20 min.

84 ents of the stress-associated phytohormones (salicylates, auxins, trans-jasmonic acid, and abscisic a

85 logues WN-2-WN-7 and the previously reported salicylate-based analogue WN-8 are described.

86 fects of oral consumption of three different salicylate-based drugs (aspirin, sodium salicylate, and

87 es in the retinal vasculature, and all three salicylate-based drugs inhibited this cell death and for

88 EFR-triggered immunity: the potentiation of salicylate-based immunity and the repression of a jasmon

89 es, to which plants respond accordingly with salicylate-based or jasmonate/ethylene-based defensive s

90 imulants, methyl salicylate (MeS) and benzyl salicylate (BeS) applied to and recovered from the hair

91 homologue MTH313 suggested the presence of a salicylate binding site buried at the interface between

92 e MarR-salicylate structure had no effect on salicylate binding, indicating that these sites were not

93 to test which amino acids were essential in salicylate binding, we examined the role of residues tha

94 Salicylate binds at the same site as the synthetic activ

95 genous applications of jasmonate upregulated salicylate biosynthesis genes and caused leaf damage in

96 af damage in wild-type plants but not in the salicylate biosynthesis mutant Salicylic acid induction-

97 only its downstream promoters in response to salicylate but also the marRAB promoter.

98 xide (DMSO), dimethylformamide (DMF), methyl salicylate, caffeine, l-leucine, l-histidine, loratadine

99 In this study, we find that salicylate can induce persister formation in Escherichia

100 of different MarA variants and suggests that salicylate can lead to selection against MarA-mediated r

101 motor model, including augmented deltaCsa by salicylate, can accurately account for our novel finding

102 teractions between ST1710 and three ligands, salicylate, carbonyl cyanide m-chlorophenylhydrazone (CC

103 sensitive to amphipathic compounds including salicylate, chlorpromazine (CPZ), and trinitrophenol (TN

104 gnaling pathways of jasmonate, ethylene, and salicylate (classic defense hormones) as well as a mutan

105 The ferric salicylate complexes display quasi-reversible reduction

106 dose resulting in clinically relevant serum salicylate concentrations ( approximately 1 mmol/L).

107 Plasma salicylate concentrations reached the midtherapeutic ran

108 On the other hand, the fatty acid salicylate conjugate 11 has been shown to have a unique

109 fatty acid niacin conjugates and fatty acid salicylate conjugates.

110 inomycin A is a member of a new class of bis-salicylate-containing polyene macrodiolides, which have

111 43.30%) and a significant decrease in methyl salicylate content in spring bamboo shoots were observed

112 nown to undergo a change from catecholate to salicylate coordination in acidic conditions, which is p

113 While Scn binding hinders salicylate coordination transformation, strong acidifica

114 py was applied to investigate the effects of salicylate, CPZ, and TNP on di-8-ANEPPS orientation in t

115 Although salicylate decreased topo IIalpha ATPase activity in a d

116 Among those tested, diflunisal, a salicylate derivative not previously identified to have

117 etophenone was reduced, while that to methyl salicylate did not change.

118 d a plant-derived repellent compound, methyl salicylate, differed between morphs or sexes.

119 es (DDDs) of MRP inhibitors (NSAIDs, PDE5-i, salicylates, dipyridamole) were collected.

120 Salicylate directly activates AMPK via the beta1 subunit

121 ntially accumulates in the membrane, whereas salicylate does not.

122 We hypothesized that salicylates downregulate 11beta-HSD1 expression, contrib

123 mproves glucose homeostasis and NAFLD is via salicylate-driven mitochondrial uncoupling.

124 g by possible withholding of antiplatelet or salicylate drugs before invasive dental treatment or by

125 rsons with prescriptions for antiplatelet or salicylate drugs before treatment.

126 tal concentration), followed by 2-ethylhexyl salicylate (EHS, ~29%), E- and Z-2-ethylhexyl 4-methoxyc

127 it locus (QTL) linked to higher fruit methyl salicylate emissions.

128 Now, with Ir catalysis and low-cost salicylate esters, alkene oxyacylation can be promoted b

129 ork provides a quantitative understanding of salicylate exposure on the fitness of different MarA var

130 Oral aspirin (as a representative of the salicylate family) inhibited diabetes-induced increase i

131 catecholate [Fe(III)(Ent)](3)(-) to the tris-salicylate [Fe(III)(H(3)Ent)](0) upon protonation, the c

132 Birch reduction of the SEM ether of methyl salicylate followed by oxidation of the intermediate eno

133 -deficient mice and C57Bl/6 mice with sodium salicylate for 4 weeks.

134 hloride over major lipophilic anions such as salicylate ( [Formula: see text] ) and thiocyanate ( [Fo

135 y competent intermediate in the synthesis of salicylate from chorismate.

136 NSAIDs containing benzoate or salicylate groups were identified as having the highest

137 Methyl salicylate has been identified as one of the most import

138 Salsalate, a nonacetylated prodrug of salicylate, has been shown to decrease blood glucose con

139 While salicylates have potential disease-preventative activity

140 tory drug aspirin and its metabolite, sodium salicylate, have profound effects on cellular protein sy

141 s of SA through the transgenic expression of salicylate hydroxylase (NahG) in both stably transformed

142 ased electrochemical biosensor consisting of salicylate hydroxylase and tyrosinase enzymes immobilize

143 er a mutation in EDS1 or the presence of the salicylate hydroxylase gene, NahG.

144 xpression of a C(2)H(4) biosynthesis gene in salicylate hydroxylase tobacco plants implicated transcr

145 Introduction of the Naphthalene/salicylate hydroxylase transgene, which suppresses SA ac

146 Challenging salicylate hydroxylase-expressing tobacco lines and tiss

147 ld-type levels by expressing nahG, bacterial salicylate hydroxylase.

148 high-affinity BSA and HSA binding sites for salicylate, ibuprofen and picosulfate by using these sen

149 Recent trials show salicylates improve glycemic control in type 2 diabetes,

150 In C57Bl/6 DIO mice, salicylate improved glucose tolerance and downregulated

151 olds during and after middle ear infusion of salicylate in artificial perilymph (AP), applied near th

152 based on the rapid metabolism of aspirin to salicylate in humans and the high salicylate/aspirin rat

153 te, both of which are rapidly broken down to salicylate in vivo.

154 -2 responded to both acetophenone and methyl salicylate in vivo.

155 the potential benefit of aspirin and natural salicylates in cancer prevention.

156 a useful new tool to non-destructively assay salicylates in situ and to map their spatial distributio

157 l for methyl salicylate synthesis and methyl salicylate, in turn, likely has an important role in con

158 Salicylates, in doses administrated in our experiments,

159 ally produces bioluminescence in response to salicylates including SA and methylsalicylate, as a repo

160 h 5-aminoimidazole-4-carboxamide riboside or salicylate increased nNOS S1412 phosphorylation and was

161 hese AMPK-independent effects, we found that salicylate increases oligomycin-insensitive respiration

162 d in the presence of a high concentration of salicylate indicated two possible salicylate sites, SAL-

163 We show here that salicylates induce phosphorylation of the alpha-subunit

164 Salicylate induced a significant increase of the gap-det

165 Aspirin and its major metabolite sodium salicylate induced apoptosis and decreased colon cancer

166 Exposure to salicylate induced smooth movement with few acceleration

167 To determine if salicylate-induced changes restricted to the LA would re

168 t mounted normal local resistance and methyl salicylate-induced defense responses, suggesting that mo

169 Our findings reveal that salicylate-induced oxidative stress can lead to persiste

170 Salicylate-induced ROS cause a decrease in the membrane

171 These results suggest that salicylate-induced temporal processing deficits may be d

172 nd 20 kHz (frequencies near the pitch of the salicylate-induced tinnitus in the rat).

173 c stress via the locus coeruleus; [3] sodium salicylate induces an acute excitotoxicity by potentiati

174 In addition, salicylate induction upregulates two antibiotic target g

175 resholds were elevated reversibly during the salicylate infusion.

176 short-term diabetes (2-4 months), all three salicylates inhibited the diabetes-induced loss of neuro

177 All three salicylates inhibited the diabetes-induced translocation

178 lfasalazine (also as a representative of the salicylates) inhibited the diabetes-induced upregulation

179 We propose that salicylate inhibits C/EBPbeta binding at 4 h and C-Rel b

180 e have now determined the mechanism by which salicylate inhibits topo II.

181 otopic shift in the amygdala and infusion of salicylate into the amygdala can profoundly enhance soun

182 chorismate for ultimate incorporation of the salicylate into the siderophore pyochelin.

183 Salicylate is also able to stimulate brown adipose tissu

184 Salicylate is an inducer of MarA that can be found in th

185 Our results demonstrate that salicylate is unable to intercalate DNA, and does not pr

186 y activate micF transcription in response to salicylate, leading to reduced OmpF expression.

187 lysis revealed that growth of S. aureus with salicylate leads to the induction of genes involved with

188 cell death through modulating jasmonate and salicylate levels.

189 tion of plant volatiles, particularly methyl salicylate, making bean plants, Vicia faba, repellent to

190 We propose that aspirin/salicylate may augment metformin's hepatic action to sup

191 tein (ACP) domain of MbtB to form covalently salicylated MbtB-ACP.

192 noncompetitive manner, this was secondary to salicylate-mediated inhibition of DNA cleavage.

193 findings provide a definitive mechanism for salicylate-mediated inhibition of topo IIalpha and provi

194 Salicylate-mediated signaling has been implicated in oth

195 aluated using two chemical simulants, methyl salicylate (MeS) and benzyl salicylate (BeS) applied to

196 omponents elicited varying responses; Methyl salicylate (MeSA) elicited the highest positive chemotax

197 resistance (SAR) in tobacco; SABP2's methyl salicylate (MeSA) esterase activity is required in healt

198 netic backgrounds, we showed that the methyl salicylate (MeSA) esterase activity of salicylic acid-bi

199 SABP2 is a methyl salicylate (MeSA) esterase that has high affinity for SA

200 The first such signal identified was methyl salicylate (MeSA) in tobacco (Nicotiana tabacum).

201 Methyl salicylate (MeSA) is a volatile plant secondary metaboli

202 id (GABA), methyl jasmonate (MeJA) or methyl salicylate (MeSA) on antioxidant systems and sensory qua

203 yleborus volvulus was not repelled by methyl salicylate (MeSA) or verbenone in laboratory assays, whi

204 posure to methyl jasmonate (MeJA) and methyl salicylate (MeSA) vapours at 10 and 100micromoll(-1) was

205 h five GLVs: methyl jasmonate (MeJa), methyl salicylate (MeSa), cis-3-hexenyl acetate (HxAc), cis-3-h

206 ancer activity of aspirin is also due to the salicylate metabolite.

207 f jasmonate, but ethylene (ET) responses and salicylate modulate the resistance of hub1 mutants to ne

208 hid-induced VOCs (ethanone, limonene, methyl salicylate, myrcene, ocimene) triggered resistance in re

209 voltages and obtaining ion peaks for methyl salicylate, naphthalene, benzene, and 2-butanone.

210 Recent studies found that salicylate not only affects outer hair cell motility in

211 To identify the physiological effects of salicylate on central auditory system function, the infe

212 tartle reflex was used to measure effects of salicylate on gap detection acuity.

213 ivity that displaces pyruvate to form either salicylate or anthranilate.

214 g guinea pig cochleas from apex to base with salicylate or KCl solutions that reduced outer-hair-cell

215 tor (indomethacin), selective COX-1 (valeryl salicylate), or selective COX-2 (SC-236) inhibitors into

216 nduced by wounding, methyl jasmonate, methyl salicylate, or ethephon, synthetic GmSubPep peptide, whe

217 In mutants deficient in jasmonate, salicylate, or ethylene signaling, APR mRNA levels were

218 ey are induced by their respective inducers: salicylate, paraquat, and decanoate.

219 ants deficient in the jasmonate/ethylene and salicylate pathways, and in wild-type plants by treatmen

220 ertechnetate, etc.) or organic anions (e.g., salicylate, pharmaceuticals, and their metabolites, whic

221 c acid induction-deficient2, indicating that salicylate plays a crucial role in PCD downstream of jas

222 result supports other findings that suggest salicylate primarily influences electromotiliy and OHC n

223 One of these is salicylate, probably the oldest medicinal agent known to

224 The salicylate prodrug salsalate has been shown to improve m

225 of SlyA bound to the small molecule effector salicylate (Protein Data Bank code 3DEU), reveal that, u

226 ponse to inducible substrate concentrations (salicylate) ranging from 250 to 5000 ppb.

227 ity of the cyclic amide through ring strain, salicylates reduce the electrophilicity of the aryl este

228 Both resveratrol and salicylate reduced the formation of tetraploid or higher

229 o regulate cross-talk between jasmonate- and salicylate-regulated disease response pathways.

230 is associated with reduced expression of the salicylate-regulated PR-1 gene.

231 sensor can be used to reliably detect methyl salicylate released by unhealthy plants.

232 ither resveratrol or aspirin, the prodrug of salicylate, repressed the accumulation of tetraploid int

233 Surprisingly, comparison of salicylate's effects using purified human topo IIalpha a

234 K1, EIN2, and HUB1 but not genes involved in salicylate (SA) functions.

235 Salicylate (SA, 2-hydroxybenzoate) is a phytohormone bes

236 nate, ethylene, phytoalexin-deficient 4, and salicylate sectors, which together govern up to 80% of t

237 n topo IIalpha and topo IIbeta revealed that salicylate selectively inhibits the alpha isoform.

238 Thus, salicylates selectively trigger an endoplasmic reticulum

239 Salicylate significantly reduced deposition of G7 cells

240 tration of salicylate indicated two possible salicylate sites, SAL-A and SAL-B.

241 rent compound, such as pterin-SMX and methyl salicylate-SMX conjugates.

242 Surprisingly, salicylate somewhat activates transcription of rob, whil

243 potential interference from anions including salicylate, sorbate, citrate, phosphate, acetate and chl

244 th salicylate at SAL-A and SAL-B in the MarR-salicylate structure had no effect on salicylate binding

245 The presence of CCCP and salicylate suppressed ST1710-ST1 interaction, indicating

246 Mg(2+)-dependent Mycobacterium tuberculosis salicylate synthase (MbtI) is a key enzyme involved in t

247 ase (ADCS), isochorismate synthase (IS), and salicylate synthase (SS) are structurally homologous cho

248 other chorismate-utilizing enzymes, such as salicylate synthase and anthranilate synthase.

249 kinetic mechanisms of the isochorismate and salicylate synthase enzymes of siderophore biosynthesis.

250 e isochorismate synthase enzymes but not the salicylate synthase enzymes.

251 The bifunctional salicylate synthase MbtI catalyzes the first step of myc

252 The salicylate synthase, Irp9, from Yersinia enterocolitica

253 indicate that SlSAMT is critical for methyl salicylate synthesis and methyl salicylate, in turn, lik

254 The C-4 salicylate takes the place of the more common C-4 dimeth

255 e first crystal structure of the MbtI-Mg(2+)-salicylate ternary complex.

256 ed significantly greater responses to methyl salicylate than to acetophenone.

257 ketones, chlorinated hydrocarbons and methyl salicylate that forms ions in both polarities.

258 efore and after treating rats with a dose of salicylate that induces tinnitus and hyperacusis-like be

259 Salsalate is a prodrug of salicylate that lowers blood glucose in patients with ty

260 tems with two AMPK activators, metformin and salicylate (the active form of aspirin).

261 The effects of aspirin, salicylate (the natural deacetylated form of aspirin), a

262 tabolites in SAR signaling, including methyl salicylate, the abietane diterpenoid dehydroabietinal, t

263 We previously identified salicylate, the primary metabolite of aspirin, as a nove

264 In AMPK knockout mice, effects of salicylate to increase fat utilization and to lower plas

265 ic acid binding protein 2) hydrolyzes methyl salicylate to salicylic acid.

266 Local delivery of salicylate to the amygdala significantly increased the a

267 a GDSL family acyltransferase that transfers salicylate to the C-4 hydroxyl of a tetracycline interme

268 ation, antiinflammatory strategies including salicylate treatment and genetic suppression of myeloid

269 s assessment of Clin, which increases during salicylate treatment as motors are locked in the expande

270 gether, these results indicate that systemic salicylate treatment can induce hyperactivity and tonoto

271 Although salicylate treatment did not trigger activation of inosi

272 tinomycin D treatment blocked, and high dose salicylate treatment inhibited by 80%, TNFalpha-induced

273 ession in subcutaneous adipose, and in vitro salicylate treatment reduced adipocyte 11beta-HSD1 expre

274 sidues that bind intracellular chloride, and salicylate treatment which prevents chloride binding, ha

275 recruit to aboveground herbivory and methyl salicylate treatment, that larval D. speciosa are relati

276 of intracellular chloride and was blocked by salicylate treatment.

277 cy surpasses the reductions of NLC caused by salicylate treatments that are known to abolish cochlear

278 Methyl salicylate undergoes hydrolysis to form methanol, which

279 Salicylate unexpectedly increased the amplitude of the l

280 Treating plants with salicylate upregulated the DAD genes and downregulated O

281 opo II (alpha and beta), we examined whether salicylate was isoform selective.

282 Conversion of acetophenone to methyl salicylate was observed in the medium of CYP1a2-expressi

283 rticular, the interference from chloride and salicylate was reduced by 2 and 6 orders of magnitude, r

284 lementation of chemically defined media with salicylate was required for equibactin production.

285 etween AERD and control subjects, and sodium salicylate was without effect.

286 menting abilities of chloroquine and quinine salicylate were assessed in a human skin equivalent mode

287 ionone, hotrienol, methylpyrazine and methyl salicylate were major volatile constituents in all the e

288 yperglycemic and antiinflammatory effects of salicylates were not connected to the pathogenesis of in

289 Over a hundred years ago, high doses of salicylates were shown to lower glucose levels in diabet

290 Using the well known ototoxicant, salicylate, which competes with the putative anion bindi

291 au acetylation is inhibited by salsalate and salicylate, which enhance tau turnover and reduce tau le

292 ed in the presence of the aspirin-derivative salicylate, which impaired activation of NF-kappaB p65 i

293 onds to phenolic compounds, including sodium salicylate, which inhibit its activity.

294 t ambient temperature comprise 12.30% methyl salicylate, which provides protection against insect att

295 plex to the hsp70 loci in cells treated with salicylate, which triggers chromatin remodeling at these

296 Bandits Wintergreen was dominated by methyl salicylate, while Marlboro Spice consists of a more comp

297 s also seen with equimolar concentrations of salicylate, while selective Cox inhibitors did not inhib

298 MP-activated protein kinase (AMPK) including salicylate, whose chemopreventive action has been establ

299 s pH value the enzyme converts chorismate to salicylate without the accumulation of isochorismate in

300 The synthesis of salicylate WN-8 is accomplished through the union of fra