ライフサイエンスコーパス: limonene

1 on (2-methyl 2-pentene), and one terpene (DL-limonene).

2 nol-benzaldehyde, octanol-octanal, and [+/-]-limonene).

3 soprene, beta-pinene, alpha-terpineol, and d-limonene.

4 les formed by ozonolysis of alpha-pinene and limonene.

5 hat of 4-OPA, were also reduced in line with limonene.

6 M for the maximum extraction of naringin and limonene.

7 l products such as alpha-pinene, menthol and limonene.

8 1, has been accomplished starting from S-(-)-limonene.

9 ulsed delivery of iso-amyl acetate (IAA) and limonene.

10 llylic isomer 3S-linalyl diphosphate, to (-)-limonene.

11 erted geranyl diphosphate to the monoterpene limonene.

12 of (+)-alpha-pinene, (+)-camphene, and (+/-)-limonene.

13 er indoor relevant organic compounds such as limonene.

14 lternatives, including the renewable solvent limonene.

15 on of isoprene, B-pinene, a-terpineol, and d-limonene.

16 of two common monoterpenes, alpha-pinene and limonene.

17 nd readily available starting material R-(+)-limonene.

18 was also successfully synthesized from S-(-)-limonene.

19 ow volatility compared to that of SOA from d-limonene.

20 nthesis of stolonidiol starting from (R)-(+)-limonene.

21 s in filled hydrogels reduces the release of limonene.

22 ction of a commercially valuable isoprenoid, limonene.

23 nditions did not change the configuration of limonene.

24 t found in the ozonolysis of cyclohexene and limonene.

25 arnesene, (-)-alpha-pinene, beta-pinene, and limonene.

26 of alpha-pinene (0.020 +/- 0.0050 nmol/mug), limonene (0.0059 +/- 0.0010 nmol/mug), and beta-caryophy

27 Other terpene compounds such as limonene (0.11-3.58 mg/kg), terpinolene (0.00-1.61 mg/kg

28 pounds responsible for aroma perception were limonene, 1,8-cineole, terpinen-4-ol, estragole and tran

29 ely high resistance; still, no production of limonene-1,2-diol and a loss of activity of the biocatal

30 bioconversion process of S-(-)-limonene into limonene-1,2-diol with the already established biotransf

31 d as an aerobic system that was catalysed by limonene-1,2-epoxide hydrolase, had an intracellular nat

32 than 1,000-fold, as well as the monoterpene limonene 10-30 fold, and seems equally suited to generat

33 ve of which were identified as alpha-pinene, limonene, 2-methoxy-3-(1-methylpropyl)-pyrazine, methyl

34 ized using chemical standards (benzaldehyde, limonene, 2-nonanone, and ethyl octanoate).

35 ) at 30 degrees C were 4.5 and 3.5x10(6) for limonene, 2.2 and 9.0x10(5) for linalool and 39 and 1.0x

36 39.05%), whereas dill oil contained mostly d-limonene (21.11%) and a-phellandrene (22.68%).

37 39.05%), whereas dill oil contained mostly d-limonene (21.11%) and alpha-phellandrene (22.68%).

38 nferred by two regiospecific cytochrome P450 limonene-3- and limonene-6-hydroxylases.

39 cDNAs encoding the limonene-3-hydroxylase from peppermint and the limonene-

40 y and catalytic efficiency of the peppermint limonene-3-hydroxylase.

41 he tamarinds were mainly caused by linalool, limonene, 4-hydroxy-2,5-dimethyl-3(2H)-furanone, nonanal

42 s showed decreasing amounts of monoterpenes (limonene, 4-terpineol, terpinolene, citronellol, alpha-t

43 = 3 with Mg2+ as cofactor), the monoterpenes limonene (48%), terpinolene (15%), and myrcene (15%) are

44 %), menthol (24.3%), trans-menthone (9.23%), limonene (5.84%), menthofuran (4.44%) and isomenthol (3.

45 monene-3-hydroxylase from peppermint and the limonene-6-hydroxylase from spearmint have been isolated

46 ed within secretory cell leucoplasts, (-)-4S-limonene-6-hydroxylase labeling was associated with glan

47 of a single residue (F363I) in the spearmint limonene-6-hydroxylase led to complete conversion to the

48 ynthase, spearmint (Mentha spicata) (-)-(4S)-limonene-6-hydroxylase, peppermint (-)-trans-isopiperite

49 ochemistry and facial stereochemistry of the limonene-6-hydroxylase- (CYP71D18-) mediated hydroxylati

50 egiospecific cytochrome P450 limonene-3- and limonene-6-hydroxylases.

51 Citrus essential oils, abundant in limonene (74.4-33.7 %), exhibited great antioxidant acti

52 of male and female diabetic zebrafish, using limonene - a natural product which has shown several pro

53 The optimized strain produced 6.7 mg/L of limonene, a 2.3-fold improvement in productivity.

54 Limonene, a common fragrance constituent, dominates the

55 derived from ozone-initiated chemistry with limonene, a commonly occurring indoor terpene.

56 beta-myrcene, an acyclic monoterpene, and d-limonene, a cyclic monoterpene, were investigated to ass

57 We additionally show that d-limonene, a dietary monoterpene known to induce ROS, is

58 Among 44 identified VOCs, d-limonene, a terpene comprising 76 %-92 % of the total, r

59 ntiomeric analyses revealed an excess of (-)-limonene, (-)-a-pinene, and (+)-linalool for all cultiva

60 cumulate terpenes in peel oil glands, with d-limonene accounting for approximately 97% of the total v

61 nce is related to the working pressure drop: limonene allows one to work with high centrifugal fields

62 zone with a biogenic precursor (beta-pinene, limonene, alpha-pinene) in a flow tube reactor.

63 Limonene, alpha-pinene, 3-carene, dihydromyrcenol, geran

64 The ability of methyl-isoeugenol, limonene, alpha-pinene, isovaleric acid, and isosafrole

65 exanal, 3-carene, alpha-terpinene, p-cymene, limonene, alpha-terpinolene and ethyl octanoate, were ta

66 ntiomeric analyses revealed an excess of (-)-limonene, (-)-alpha-pinene, and (+)-linalool for all cul

67 Following hydroxylation of limonene, an apparently similar dehydrogenase oxidizes (

68 re of monoterpene (C10) olefins in which (-)-limonene and (-)-alpha- and (-)-beta-pinene are prominen

69 -)-beta-pinene are prominent components; (-)-limonene and (-)-pinene synthase activities are also ind

70 ples of chiral molecules, namely (R) and (S) Limonene and (R) and (S) Carvone, were tested and severa

71 The presence of (S)-limonene and (R)-carvone as the unique enantiomeric form

72 omers of chiral analytes, including those of limonene and 1-phenylethanol.

73 Knockout rice plants deficient in D-limonene and alpha-pinene synthesis lost their appeal to

74 soluble SOA generated from two monoterpenes, limonene and alpha-pinene, and two different oxidants, o

75 ly was related to the compounds (E)-anetole, limonene and beta-pinene, citronellol, and eugenol, resp

76 d from reactions with the y-terpinene isomer limonene and by analogy to reactions catalyzed by relate

77 tely 1% of two chiral monoterpene molecules, limonene and camphor, are irradiated by a circularly pol

78 on of natural sources of pure enantiomers of limonene and carvone, is performed by using on-line coup

79 agent, substantially lower concentrations of limonene and formaldehyde were observed.

80 A dark reaction was observed between limonene and HOCl/Cl(2) leading to gas-phase reaction pr

81 I (-) data for SOAs produced by oxidation of limonene and isoprene and compared them online to O/C me

82 of eugenol, carvacrol, thymol, alpha-pinene, limonene and linalool was determined.

83 lar cleaning agents emitted terpenes, mainly limonene and linalool.

84 tivity patterns evoked by the enantiomers of limonene and of terpinen-4-ol were not statistically dif

85 ) was produced from 0.5 ppm mixing ratios of limonene and ozone in a 5 m(3) Teflon chamber.

86 Monoterpenes such as d-limonene and perillyl alcohol derived from orange peels

87 extraction of bioactive compounds such as d-limonene and polyunsaturated fatty acids due to the abse

88 including the monoterpenes alpha-pinene and limonene and the aromatic catechol (benzene-1,2-diol).

89 uice were observed due to the degradation of limonene and the formation of alpha-terpineol, an off-fl

90 Limonene and trans-caryophyllene were two terpenes deter

91 positive chemotaxis (70-80%), alpha-pinene, limonene and tridecane were intermediate (54-60%), and 2

92 In the presence of 26 ppb limonene and under atmospherically relevant UV-visible i

93 omarkers of exposure and dimethyl disulfide, limonene, and 2-ethyl-1-hexanol as biomarkers of disease

94 made of beta-ionone, (+/-)-citronellal, (+)-limonene, and flavone dissolved in DMSO-d6/GL-d8 (5:5, v

95 alpha-terpineol, an oxygenated derivative of limonene, and found that the reaction products and kinet

96 yloctanoic acid, 3-methylindole (skatole), d-limonene, and indole.

97 OCs (i.e., alpha,beta-pinene, Delta3-carene, limonene, and isoprene) supporting the results from the

98 uced through the ozonolysis of alpha-pinene, limonene, and ocimene.

99 hanced with 15% dimethylsulfoxide (DMSO), 1% limonene, and rosemary oil.

100 rpenes camphene, alpha- and beta-pinene, and limonene, and the sesquiterpene compounds alpha- and bet

101 Limonene, andaliman major volatiles, was lost considerab

102 On the whole, beta-myrcene and d-limonene appear to undergo oxidation by OH largely indep

103 ated hydroxylation of the monoterpene olefin limonene are determined by the absolute configuration of

104 econdary organic aerosol (SOA) produced from limonene are known to form brown carbon (BrC) with a dis

105 e (3-methyl butane nitrile) and temperature (limonene) are identified through a multi-trait analysis.

106 ata, confocal microscopy, and the release of limonene as assessed by solid-phase microextraction usin

107 lso allowed identifying geranylacetone and d-limonene as potential biomarkers to classify tomatoes ac

108 -phase humic acid as the photosensitizer and limonene as the VOC.

109 In this research, the encapsulation of d-limonene, as an aromatic component with several distinct

110 Oxidation of (R)-limonene at 25 degrees C occurred at the C-1,2-cyclic al

111 ze the regiospecific hydroxylation of (-)-4S-limonene at C3 or C6 exclusively.

112 c aerosol (SOA) formation from ozonolysis of limonene at total aerosol mass loadings ranging from 3.2

113 phenyl acetaldehyde, 3-methylbutyric acid, d-limonene, B-linalool, menthol, and estragole; these incl

114 pinene, beta-pinene, beta-myrcene, 3-carene, limonene, beta-caryophyllene, and alpha-humulene) in hum

115 rich in monoterpenes, including 1,8-cineole, limonene, beta-myrcene, alpha- and beta-pinene, sabinene

116 ffer in three floral terpenoid volatiles - d-limonene, beta-myrcene, and E-beta-ocimene - that are at

117 frequency of appearance for alpha-pinene, d-limonene, beta-pinene in both types of milk.

118 lic burden, revealing bottlenecks that limit limonene bioproduction.

119 Abies grandis was expressed to optimize the limonene biosynthetic pathway.

120 volatiles and specific monoterpenes, mainly limonene, but also linalool and alpha-terpineol was enha

121 terise the bioconversion of R-(+)- and S-(-)-limonene by cellular detoxification using ultra-structur

122 ion; no flavour complexes were reported with limonene by itself but were observed when added in binar

123 sized by the direct reaction of sulfur and d-limonene, by-products of the petroleum and citrus indust

124 thases of conifers, [(-)-pinene (C(10)), (-)-limonene (C(10)), (E)-alpha-bisabolene (C(15)), delta-se

125 Linalool, Geranyl acetate, Limonene, Camphor, Geraniol, and other while leaves are

126 LBL also repressed limonene catabolism and triggered phenylpropanoid deriva

127 e hexanal (green), acetoin (buttery, green), limonene (citrus), 2-hexanol (green, pungent) and 1-octe

128 ver, the magnitude of alterations depends on limonene concentration, model membrane composition and,

129 iments were conducted at realistic ozone and limonene concentrations in a 240 m(3) chamber configured

130 mass yield of 40% relative to the amount of limonene consumed.

131 nverse correlation between the increase in d-limonene content and the decrease in the defense respons

132 Surface and encapsulated limonene content was determined by measurement of the ab

133 The surface limonene content was significant, especially for gellan

134 s, the KCl gels had the greater encapsulated limonene content.

135 isperse polyurea microcapsules (PUMC) with a limonene core.

136 linalyl diphosphate, as shown previously for limonene cyclase.

137 doubled in these KCl gels, the encapsulated limonene decreased.

138 c monoterpenes (alpha-pinene, beta-pinene, D-limonene, Delta(3)-carene) monitored with the ASGDI quad

139 The 24% higher limonene density is a difference with heptane that has m

140 as chiral P(V)-building blocks, based on the limonene-derived oxathiaphospholane sulfide, were synthe

141 ylation is presented herein by using simple, limonene-derived reagent systems.

142 The strongest fluorescence for the limonene-derived SOA was observed for lambdaexcitation =

143 PX) as well as a range of novel, substituted limonene dimers.

144 The d-limonene (DL), a bioactive ingredient in citrus peels, i

145 presence of airborne odorants (amyl acetate, limonene, earthworm wash vapor, fish water vapor, earthw

146 Specifically deuterated limonene enantiomers were prepared to investigate the ne

147 nditions, the maximum amount of naringin and limonene extracted were found to be 8.955, 2.122 mg/g fr

148 r than 2 g/L geraniol from prenol as well as limonene, farnesol, diaponeurosporene, and lycopene.

149 a second-order degradation kinetics, whereas limonene followed a first-order kinetics.

150 he diastereoselective bifunctionalization of limonene, followed by effective elimination leading to t

151 sulted in maximum extraction of naringin and limonene from kinnow pomace and pulp residue and showed

152 nable materials synthesis process in which d-Limonene functions simultaneously both as a solvent for

153 ujene, camphene, sabinene, delta-3-carene, d-limonene, gamma-terpinene, camphor, beta-citronellene, a

154 g lemon essential oil incorporated terpenes (limonene, gamma-terpinene, p-cymene and alpha-citral) to

155 Limonene, geranial, a-pinene, sabinene, B-myrcene, (E)-2

156 t variations in major essential oils, namely limonene, germacrene D, and beta-myrcene, between system

157 Limonene has a strong tendency to form secondary organic

158 tive kinetic mechanism, indicating that (4R)-limonene has sufficient freedom of motion within the act

159 Limonene has the capability to be a "green" alternative

160 from elemental sulfur, gamma-terpinene, and limonene in 61% yield.

161 sient AMFs" from ozonolysis of pulse-emitted limonene in a ventilated chamber, for 18 experiments at

162 Degradation of trans-cinnamaldehyde and limonene in cucumber was evaluated under laboratory and

163 The encapsulation of limonene in freeze-dried gellan systems was investigated

164 In this study, reactions of HOCl/Cl(2) with limonene in the gas phase and on indoor relevant surface

165 eta-pinene, myrcene, delta3-carene, ocimene, limonene) in seawater and air during three cruises in th

166 It was found that limonene incorporates into lipid monolayers causing thei

167 ence of strong volatility and evaporation of limonene increasing with temperature.

168 ready established biotransformation of R-(+)-limonene into alpha-terpineol using the same biocatalyst

169 compared the bioconversion process of S-(-)-limonene into limonene-1,2-diol with the already establi

170 Limonene is a biorenewable cycloterpene solvent coming f

171 ay scattering indicate that applying (R)-(+)-limonene is able to greatly promote the molecular order

172 evaporation is dependent on whether SOA from limonene is formed before or during the formation of SOA

173 (-)-(4S)-Limonene is hydroxylated at the C6 allylic position to g

174 (4S)-Limonene is oxygenated with almost complete stereospecif

175 Moreover, the influence of limonene is stronger at lower temperatures and, in the l

176 growth from direct reactions of (3)IC* with limonene, isoprene, alpha-pinene, beta-pinene, and tolue

177 that photosensitized production of SOA from limonene, isoprene, alpha-pinene, beta-pinene, and tolue

178 Lower-value compounds, including limonene, latex, and PHB, require at least an order-of-m

179 prices and applications, including <$10/kg (limonene, latex, and polyhydroxybutyrate [PHB]), $10 to

180 The oxygenation of (4R)-limonene leading to the formation of (+/-)-trans-carveol

181 In nature, d-limonene levels increase in orange fruit once the seeds

182 0muM JA increased the linalool, eugenol, and limonene levels, while 1muM JA caused the highest increa

183 Limonene, linalool and citral are common non-phenolic te

184 esults indicate that antioxidant behavior of limonene, linalool and citral occurs by co-oxidation wit

185 Eucalyptol, limonene, linalool, thymol, parthenolide, andrographolid

186 oduction of various monoterpenes such as (-)-limonene, (-)-linalool, (-)-alpha-pinene/beta-pinene or

187 etramethylpyrazine (TetraMP), myrcene (Myr), limonene (LM), ethylphenyl acetate (EpHAc) and 2-phenyle

188 antioxidant actions of thymoquinone (TQ) and limonene (LMN) were investigated by giving 1 ml of 10mg

189 n be used as an appropriate stabilizer for d-limonene-loaded emulsions and a food grade delivery carr

190 l aging of SOA produced by the ozonolysis of limonene (LSOA) in the presence of gaseous ammonia.

191 ganic aerosol produced through ozonolysis of limonene (LSOA).

192 or the detection of trans-cinnamaldehyde and limonene metabolites.

193 The polar and apolar phases of the limonene/methanol/water 10/9/1 v/v have -0.025 g/cm(3) d

194 The limonene/methanol/water and heptane/methanol/water phase

195 the five major aphid-induced VOCs (ethanone, limonene, methyl salicylate, myrcene, ocimene) triggered

196 The double bonds of the limonene molecule allows for possible pi-pi interactions

197 cineole cassette' monoterpenes 1,8-cineole, limonene, myrcene, beta-pinene, alpha-pinene, sabinene a

198 nsistent with allelic variation at two loci, LIMONENE-MYRCENE SYNTHASE (LMS) and OCIMENE SYNTHASE (OS

199 this, we probe the possibility that SOA from limonene+NO3 and beta-pinene+NO3 reactions is highly vis

200 The SOA yields from limonene+NO3 are approximately constant ( approximately

201 mally dilute the oxidation products from the limonene+NO3 reaction at 25 degrees C and observe neglig

202 Herein the influence of limonene on artificial membranes was studied to verify t

203 h volatile organic compounds (VOCs), such as limonene, one of the most abundant compounds found in in

204 In this study, we studied the reaction of limonene, one of the most common indoor volatile organic

205 i-MJ either promotes the bioformation of (+)-limonene or inhibits that of (-)-limonene to a greater e

206 carvone, but not between the enantiomers of limonene or terpinen-4-ol, in an olfactory habituation t

207 tection of recombination products of IC with limonene or with itself, in bulk and flow tube experimen

208 xposed to either caproic acid, butyric acid, limonene, or purified air and the spatial distribution o

209 uce either the monoterpenes alpha-pinene and limonene, or the sesquiterpene 7-epizingiberene, with th

210 In contrast, (-)-limonene oxidation favors the scission of the carbon ske

211 NH(4)Cl and H(2)O(2), gave unreacted cis-(+)-limonene oxide and diastereoenriched mixtures of the sec

212 of the commercially available cis/trans-(+)-limonene oxide mixture by ring opening with primary phos

213 ylic acid, ethyl ester, isopentyl ethanoate, limonene oxide, (E)-2-pentenal, tetradecane, and gamma-e

214 Synthesized from trans-limonene oxide, this reagent class displays an unexpecte

215 of BrC material produced by the reaction of limonene + ozone SOA with ammonia vapor (aged LIM/O3 SOA

216 fractions of alpha-pinene, d-limonene (R-(+)-limonene), p-cymene, and camphene (a terpene not present

217 s observed in alpha-pinene where growth of d-limonene, p-cymene, and camphene has been observed in tr

218 ta-pinene and alpha-pinene, with growth of d-limonene, p-cymene, and camphene, in nickel-plated carbo

219 ave -0.025 g/cm(3) density difference (lower limonene phase) compared to +0.132 g/cm(3) with heptane

220 The system is stable for the production of limonene, pinene and sabinene, and can operate continuou

221 The binding of mercury(II) to the sulfur-limonene polysulfide resulted in a color change.

222 enzyme fidelity analysis [percentage of (-)-limonene produced] indicated which residues are most lik

223 us limon were expressed in cyanobacteria for limonene production.

224 /hour biomass productivity and 0.2 mg/L/hour limonene productivity over a sustained period in photobi

225 ith the remaining exocyclic bond of oxidized limonene products in the SOA phase.

226 ease in the defense response suggests that d-limonene promotes infection by microorganisms that are l

227 For example, oxidation of (+)-limonene promotes the formation of alkoxy radicals, whic

228 while the mole fractions of alpha-pinene, d-limonene (R-(+)-limonene), p-cymene, and camphene (a ter

229 C-MS) chirality analysis showed that (R)-(+)-limonene, (R)-(-)-linalool, (S)-(-)-alpha-terpineol and

230 Knowing the AER and initial ozone-limonene ratio is crucial to predict indoor transient SO

231 decreasing AERs and increasing initial ozone-limonene ratios, which together likely promoted more ozo

232 hange rates (AER) with varying initial ozone-limonene ratios.

233 Furthermore, highly oxygenated limonene reaction products were detected, clearly explai

234 ne/terpenoid surface reactions), for ozone/D-limonene reactions on stainless steel.

235 as-phase reaction products of HOCl/Cl(2) and limonene readily adsorb on both SiO(2) and TiO(2).

236 IAA and limonene reproducibly activated different subsets of rec

237 centrations of carvone, (-) citronellal, and limonene, respectively.

238 (alpha-pinene, beta-pinene, Delta-3-carene, limonene, sabinene, and beta-caryophyllene), were invest

239 tones are closely related to the monoterpene-limonene secondary biotransformation and menthofuran has

240 omposed of ammonium sulfate (AS) and either: limonene secondary organic carbon (LSOC), alpha, 4-dihyd

241 perilla ketone, B-dehydro-elsholtzia ketone, limonene, shisofuran, farnesene (Z, E, alpha), B-caryoph

242 alpha-pinene, gamma-terpinene, p-cymene and limonene showed significant variations with drying trial

243 le pi-pi interactions with solutes rendering limonene slightly more polar than heptane giving small d

244 sis of two structural monoterpene isomers: D-limonene SOA (LSOA) and alpha-pinene SOA (PSOA).

245 -dicarbonyl structural motif present in many limonene SOA compounds.

246 ilarity was attributed to high solubility of limonene SOA in water.

247 ated, and aged at <5%, 50 and 90% RH, and on limonene SOA particles at <5% and 90% RH.

248 demonstrated by reacting 2-MP with 4-OPA or limonene SOA, both of which produced BrC with absorption

249 capable of browning by the same mechanism as limonene SOA.

250 Monoterpenes such as (R)-(+)-limonene stimulated both glucose uptake (17.4%) and lipo

251 predict that indoor spaces in which ozone/D-limonene surface reactions would likely lead to meaningf

252 Crystal structural data for (4S)-limonene synthase [(4S)-LS] of spearmint (Mentha spicata

253 n be inferred by homology modeling of (-)-4S-limonene synthase based on the three-dimensional structu

254 duction of limonene was two-fold higher with limonene synthase from M. spicata than that from C. limo

255 The crystal structure of (4S)-limonene synthase from Mentha spic ata, a metal ion-depe

256 eport, we showed that down-regulation of a d-limonene synthase gene alters monoterpene levels in oran

257 (-)-4S-Limonene synthase preprotein from spearmint bears a long

258 e deduced amino acid sequences indicated the limonene synthase to be 637 residues in length (73.5 kDa

259 The monoterpene cyclase limonene synthase transforms geranyl diphosphate to a mo

260 transgenic expression of a gene encoding (+)-limonene synthase was used to accumulate elevated levels

261 ry showed that these sequences encoded a (-)-limonene synthase, a myrcene synthase, and a (-)-pinene

262 Developmental immunoblotting of limonene synthase, which catalyzes the committed step of

263 acterized genes, specifically CsTPS14CT [(-)-limonene synthase] and CsTPS15CT (beta-myrcene synthase)

264 Limonene synthases from the plants Mentha spicata and Ci

265 of an allylic diphosphate ester bond, as in limonene synthases, or protonation of a terminal olefin

266 This precludes the use of this limonene system with hydrodynamic CCC columns that need

267 The quantified eucalyptol and d-limonene terpenes - found in the P. dulcis extract - hav

268 Furthermore, beta-myrcene, d-limonene, terpinolene, and alpha-pinene are often report

269 Gellan gels encapsulated greater amounts of limonene than solutions.

270 is procedure is used to isolate the peak for limonene, the largest peak in the analytical-ion chromat

271 ated products formed from the degradation of limonene, the most ubiquitous terpenoid species in the i

272 dehyde ranged from 2.02 to 2.49 h, while for limonene this value ranged from 0.49 to 6.17 h.

273 tion of (+)-limonene or inhibits that of (-)-limonene to a greater extent than the other three MJ ste

274 ng the concentration of CSNPs and ratio of d-limonene to Pickering emulsion, viscosity of Pickering e

275 s (0.43, 0.25, and 0.07% w/v) and ratio of d-limonene to Pickering emulsions (5, 15, and 25%).

276 , supporting efficient conversion of (S)-(-)-limonene to the menthol precursor trans-isopiperitenol.

277 how endogenous metabolites change following limonene treatment.

278 we show that the developed sensor can detect limonene, undecanal, and geraniol vapors, and differenti

279 Among tentatively identified metabolites, limonene, undecane, and 2,7-dimethyl-undecane, significa

280 of two biogenic compounds (alpha-pinene and limonene), under different environmental conditions in a

281 Limonene undergoes a regioselective Pd(II)-catalyzed C(s

282 ruits revealed that the down-regulation of d-limonene up-regulated genes involved in the innate immun

283 he chemistry of peroxy radicals derived from limonene upon addition of oxygen explains the formation

284 rat mammary carcinomas treated with dietary limonene using a newly developed method termed subtracti

285 ne and camphene, or two alkene moieties like limonene, valencene, and beta-caryophyllene is among the

286 In addition, limonene was able to reverse the elevated expression of

287 Limonene was added at two different concentrations (1 an

288 However, when the concentration of limonene was doubled in these KCl gels, the encapsulated

289 The SOA mass using 15 ppb limonene was strongly dependent on O(3) concentrations a

290 Production of limonene was two-fold higher with limonene synthase from

291 d-glucitol, d-galactitol, d-mannitol, and d-limonene were incorporated as plasticizers.

292 as used to accumulate elevated levels of (+)-limonene, which allows oil derived from transgenic plant

293 ynechococcus elongatus UTEX 2973, to produce limonene, which increases cyanobacterial cell surface hy

294 ion of ozone reactions with surface-sorbed D-limonene, which is common indoors.

295 comparator group, except for coconut oil and limonene, which were found in 1 patient each.

296 s scent arises from the volatile monoterpene limonene, whose cyclic nature can be viewed as a miniatu

297 This is the first study of the oxidation of limonene with HOCl and Cl(2), and it illustrates the pot

298 ted that the major volatile compound was the limonene with relative percentage of 3.1, 7.5 and 10.8,

299 o identify major products of the reaction of limonene with the triplet state of IC by direct (+/-)ESI

300 arveol as the only product, whereas (+)-(4R)-limonene yields multiple hydroxylation products with (+)

301 Citronellal, limonene, (Z)-B-ocimene, (E)-B-ocimene, B-citronellol, s