ライフサイエンスコーパス: monoterpene

1 volatile classes (e.g. green leaf volatiles, monoterpenes).

2 eristic blend including the cineole cassette monoterpenes.

3 s derived from the oxidation of isoprene and monoterpenes.

4 ibitors of protein prenylation or by further monoterpenes.

5 , a surrogate for organic vapors formed from monoterpenes.

6 erpene synthases, forming cyclic and acyclic monoterpenes.

7 S showed a peculiar composition of irregular monoterpenes.

8 , which were mostly hydrocarbons and alcohol monoterpenes.

9 w molecular weight isoprenoids, particularly monoterpenes.

10 yll cycle pigments, beta-carotene and stored monoterpenes.

11 ormation of significant amounts of irregular monoterpenes.

12 , exert substantial control over flux toward monoterpenes.

13 e pigments and enhanced emission of volatile monoterpenes.

14 hod to improve physicochemical properties of monoterpenes.

15 oral scent comprising the' cineole cassette' monoterpenes 1,8-cineole, limonene, myrcene, beta-pinene

16 termediate, iridoid synthase uses the linear monoterpene 10-oxogeranial as substrate and probably cou

17 ompounds (13.2%), sesquiterpenes (13.0%) and monoterpenes (10.9%).

18 ks', leading to 5-carbon isoprene, 10-carbon monoterpenes, 15-carbon sesquiterpenes and 20-carbon dit

19 omprising ketones (27), sesquiterpenes (26), monoterpenes (19), aliphatic esters (19), higher alcohol

20 rs, 6 monoterpene hydrocarbons, 2 oxygenated monoterpenes, 20 sesquiterpene hydrocarbons, 7 oxygenate

21 ng the potent antimicrobial and insecticidal monoterpene 3-carene.

22 The monoterpene (+)-3-carene is associated with resistance o

23 )-phorbol in only 19 steps from the abundant monoterpene (+)-3-carene.

24 e-induced defense responses, suggesting that monoterpenes act in parallel with SA The volatile emissi

25 The acyclic monoterpene alcohol linalool is one of the most frequent

26 hich has a completely different composition, monoterpenes alcohols being the most abundant.

27 Considerably larger amounts of monoterpenes, aliphatic alcohols and benzene derivatives

28 provides the tetracyclic core of many indole monoterpene alkaloids in only three steps from commercia

29 r specifically influence accumulation of the monoterpene alpha-thujene (IL1-3 and IL1-4) were identif

30 dopsis thaliana to a mixture of the bicyclic monoterpenes alpha-pinene and beta-pinene induced defens

31 of volatile organic compounds, including the monoterpenes alpha-pinene and limonene and the aromatic

32 These produce either the monoterpenes alpha-pinene and limonene, or the sesquiter

33 port novel in situ speciated observations of monoterpenes (alpha- and beta-pinene, myrcene, delta3-ca

34 of SOA and ON from the NO3 oxidation of two monoterpenes (alpha-pinene and beta-pinene) and investig

35 2) perturbations impact the oxidation of two monoterpenes, alpha-and beta-pinene.

36 y OA (SOA) markers derived from isoprene and monoterpenes also exhibited higher concentrations in con

37 e small subunit (MpGPS.SSU) on production of monoterpene and geranylgeranyl diphosphate (GGPP) divers

38 Among the monoterpene and sesquiterpene and diterpene synthases, s

39 d in reduced trichome formation and impaired monoterpene and sesquiterpene production.

40 d in diverged plants and nine rather unusual monoterpene and sesquiterpene synthase-like genes.

41 cted SmMTPSLs were determined to function as monoterpene and sesquiterpene synthases.

42 s of magnitude higher than that observed for monoterpene and sesquiterpene synthases.

43 sed defenses, which include insect-inducible monoterpene and sesquiterpene volatiles.

44 Some also exhibited monoterpene and/or diterpene synthase activities.

45 acetyl-CoA to several commercially important monoterpenes and achieve up to 125-fold increase over cy

46 c plants, there was no increase in the major monoterpenes and diterpene acids of the resin and no cha

47 nthases (TPSs) that specify the synthesis of monoterpenes and diterpenes from cis-prenyl diphosphates

48 on of several aroma compounds and especially monoterpenes and esters.

49 Gamma-irradiation generally decreased monoterpenes and increased oxygenated compounds, but the

50 Oxidation products of monoterpenes and isoprene have a major influence on the

51 from O3 and OH radical oxidation of several monoterpenes and isoprene in a series of laboratory expe

52 and 69% efficient, respectively, in removing monoterpenes and isoprene.

53 A major fraction of monoterpenes and norisoprenoids in young wines is conjug

54 rganic compounds (BVOCs), consisting of five monoterpenes and one sesquiterpene (alpha-pinene, beta-p

55 The hydrocarbon monoterpenes and oxygenated volatiles emitted from calli

56 ers of the acyclic polyhalogenated Plocamium monoterpenes and permitted the evaluation of their selec

57 es involved in the biosynthesis of the major monoterpenes and sesquiterpenes routinely assayed by can

58 Most of the products formed were typical monoterpenes and sesquiterpenes that have been previousl

59 Bay leaves, with their abundant monoterpenes and sesquiterpenes, are used to impart flav

60 nging to chemical classes such as the simple monoterpenes and sesquiterpenes, iridoid monoterpenes, c

61 r trans-farnesyl diphosphate (C15), to yield monoterpenes and sesquiterpenes, respectively.

62 Terpene synthases, which synthesize monoterpenes and sesquiterpenes, which comprise much of

63 ce resulted from reduced levels of repellant monoterpenes and sesquiterpenes.

64 ferences in odor impressions from the parent monoterpenes and their derivatives in most cases; howeve

65 ass spectrometry to detect and quantify five monoterpenes and two sesquiterpenes in the low parts-per

66 cated among fluxes (respiration and volatile monoterpenes) and biomass C pools (total biomass, nonstr

67 diurnal and seasonal variation in isoprene, monoterpene, and methanol fluxes from a temperate forest

68 -LIT successfully quantified isoprene, total monoterpenes, and isomeric isoprene oxidation products m

69 xyl radicals, preventing their reaction with monoterpenes, and the resulting isoprene peroxy radicals

70 ally important compounds including isoprene, monoterpenes, and very recently, dimethyl sulfide.

71 major constituents in 10-fold lemon oil were monoterpenes ( approximately 35%), sesquiterpenes ( appr

72 addition to their function in plant defense, monoterpenes are also used as flavors, fragrances and me

73 Monoterpenes are important for plant survival and useful

74 Monoterpenes are non-polar secondary metabolites widely

75 Different monoterpenes are produced in our system by changing the

76 acterized, stable gas cylinder standards for monoterpenes at the nmol/mol level was previously tested

77 However, the mole fraction of the key monoterpene beta-pinene decreased, while the mole fracti

78 enes identified and semi-quantified were the monoterpenes beta-pinene, alpha-pinene, alpha-thujene, c

79 hexanol, cis-3-hexenol, trans-2-hexenol) and monoterpenes (beta-myrcene, cis-beta-ocimene and trans-b

80 ioenergetic processes determine flux through monoterpene biosynthesis in GTs.

81 ranylgeranyl reductase1 mutants with reduced monoterpene biosynthesis were SAR-defective but mounted

82 ux from carotenoid formation towards GPP and monoterpene biosynthesis.

83 A new model is proposed in which the monoterpene blocks an MEP pathway-dependent protein gera

84 mechanistic view of the biosynthesis of the monoterpene bornyl diphosphate (BPP) from geranyl diphos

85 ion in amount, diversity, and composition of monoterpenes, but no effects on sesquiterpenes.

86 The monoterpenes camphene, alpha- and beta-pinene, and limon

87 Two phenolic monoterpenes (carvacrol and thymol) display allosteric a

88 h organic components similar to isoprene and monoterpene chamber studies, also resulting in nonacid c

89 s similar to those observed for isoprene and monoterpene chamber studies, but in biogenic aerosols tr

90 lts indicate that nighttime ON formed by NO3+monoterpene chemistry can serve as either permanent or t

91 of indoor SOA formation due to indoor ozone-monoterpene chemistry.

92 us enzyme, which synthesizes the "irregular" monoterpenes chrysanthemyl diphosphate (CPP), lavandulyl

93 ly (1) is shown to catalytically cyclize the monoterpene citronellal and two homologues.

94 nes responsible for the biosynthesis of both monoterpene classes, it is unclear why regular monoterpe

95 nic compounds, arising from the oxidation of monoterpenes, cluster directly with single sulfuric acid

96 es required for the indole and seco-iridoid (monoterpene) components identified transcriptional cross

97 ed the pharmacological effects of a group of monoterpene compounds on recombinant 5-HT3Rs expressed i

98 Tukey's test revealed that monoterpenes content is a reliable indicator of fruit ma

99 ishmanicidal assay-guided isolation, two new monoterpene coumarins, minutin A and minutin B, were pur

100 ple monoterpenes and sesquiterpenes, iridoid monoterpenes, cyanogenic glycosides, benzoic acid deriva

101 In contrast to all known monoterpene cyclases, which use geranyl diphosphate as s

102 on, produces hundreds of biologically active monoterpene-derived indole alkaloid (MIA) metabolites an

103 Isoprene and monoterpene-derived organosulfates and oligomers were id

104 By comparison, the UV absorption of the monoterpene-derived SOMs was negligible.

105 Each of the isoprene- and monoterpenes-derived groups exhibited a strong diel tren

106 noterpene classes, it is unclear why regular monoterpenes dominate the oil.

107 Monoterpenes dominated the emission profile with emissio

108 ential whilst acyclic unsaturated oxygenated monoterpenes (e.g. linalool) may act as pro-oxidants in

109 Measured soil and litter monoterpene emission rates were compared with modeled ca

110 Results suggest surface soil and litter monoterpene emissions could range from 12 to 136% of can

111 Taking into account compound specific monoterpene emissions has a moderate effect on the model

112 simulation, we estimate total global marine monoterpene emissions of 0.16 Tg C yr(-1), similar to a

113 -producing mutant plants associated SAR with monoterpene emissions.

114 Over Boreal regions, monoterpenes emitted from the forest are the main precur

115 terranean ecosystems are dominated by strong monoterpene emitters, as shown by the new BEFs.

116 Monoterpenes, exhibited low 2,2-diphenyl-2-picrylhydrazy

117 e also report that GTs with high flux toward monoterpenes express, at very high levels, genes coding

118 ne (D5-siloxane) for personal care products, monoterpenes for fragrances, p-dichlorobenzene for insec

119 ils are constituted predominantly of regular monoterpenes, for example linalool, 1,8-cineole, and cam

120 SSU led to a more than threefold increase in monoterpene formation in tomato fruits relative to the p

121 Novel syntheses of monoterpene fragments used to construct the target molec

122 The family of polyhalogenated monoterpenes from Plocamium counts over a hundred known

123 ity methodology, together with a synthesised monoterpene glucoside.

124 By understanding monoterpene glycoconjugation in wine grapes, scientists

125 Overall monoterpene glycoconjugation patterns may align with und

126 udy investigated the sensory significance of monoterpene glycosides during tasting, by retronasal per

127 Monoterpene glycosides were isolated from Gewurztraminer

128 n constituents in single-fold lemon oil were monoterpenes (>90%), whereas the major constituents in 1

129 terpene in tobacco but only trace amounts of monoterpenes have been detected.

130 (+)-alpha-Pinene is a monoterpene hydrocarbon that is widely distributed in th

131 , analysed by GC and GC-MS, was dominated by monoterpene hydrocarbons (50.0%) responsible for the pep

132 ompounds were organised in different groups: monoterpene hydrocarbons and monoterpene oxygen-containi

133 metabolites, mainly comprising 18 esters, 6 monoterpene hydrocarbons, 2 oxygenated monoterpenes, 20

134 he drying method, including the loss of most monoterpene hydrocarbons, as compared with fresh samples

135 whereas calendula aroma was predominated by monoterpene hydrocarbons.

136 yi, Ukrainiandes one is mainly consisted by monoterpene hydrocarbons.

137 ing strategies have been explored to produce monoterpene in tobacco but only trace amounts of monoter

138 method was successfully applied to determine monoterpenes in 27 berry samples of different varieties

139 for the potential of long-term stability of monoterpenes in a gas mixture.

140 the mole fraction trends, assess the role of monoterpenes in atmospheric chemistry, and relate measur

141 light mass spectrometry for determination of monoterpenes in fresh berries was developed.

142 Monoterpenes in hop essential oil and corn, sesquiterpen

143 es responsible for the production of regular monoterpenes in lavenders are now known, enzymes (includ

144 mass and the overall mass yield derived from monoterpenes in mixtures of atmospheric vapours.

145 recognize the diverse influences exerted by monoterpenes in the atmosphere, including roles in parti

146 iomeric and non-enantiomeric distribution of monoterpenes in the headspace of Juniperus communis L. a

147 S)) catalyzing the biosynthesis of irregular monoterpenes in these plants have not been described.

148 ively low abundance of LPP-derived irregular monoterpenes in this plant.

149 However, they also contain irregular monoterpenes including lavandulol and lavandulyl acetate

150 cularly those of section Alatae, are rich in monoterpenes, including 1,8-cineole, limonene, beta-myrc

151 Transgenic tomato fruits produced monoterpenes, including geraniol, geranial, neral, citro

152 produce essential oils consisting mainly of monoterpenes, including the potent antimicrobial and ins

153 t wine with the biocatalyst for 20days, free monoterpenes increased significantly (from 1119 to 2132m

154 Camptothecin is a monoterpene indole alkaloid (MIA) used to produce semisy

155 the strict requirement of class II CPRs for monoterpene indole alkaloid biosynthesis with a minimal

156 erivatives, identification of bottlenecks in monoterpene indole alkaloid biosynthesis, and discovery

157 ast common biosynthetic intermediate for all monoterpene indole alkaloid enzymatic pathways.

158 ated tryptophan, which is then shuttled into monoterpene indole alkaloid metabolism to yield chlorina

159 Saccharomyces cerevisiae host from 14 known monoterpene indole alkaloid pathway genes, along with an

160 nthesis of arborisidine, a caged pentacyclic monoterpene indole alkaloid, has been accomplished in bo

161 The pharmaceutically valuable monoterpene indole alkaloids (MIAs) in Catharanthus rose

162 at synthesizes more than a hundred different monoterpene indole alkaloids (MIAs).

163 The monoterpene indole alkaloids are a large group of plant-

164 Monoterpene indole alkaloids comprise a diverse family o

165 pathways are involved in the biosynthesis of monoterpene indole alkaloids either through multiple iso

166 racyclic skeleton of the apparicine class of monoterpene indole alkaloids in only four steps in 80% o

167 There are approximately 3,000 monoterpene indole alkaloids produced by thousands of pl

168 ry root culture eliminates all production of monoterpene indole alkaloids, a class of natural product

169 Monoterpene indole alkaloids, a class of specialized met

170 hesis of 8-hydroxygeraniol, the precursor of monoterpene indole alkaloids, and cannabigerolic acid, t

171 rived compounds, focusing on monoterpenoids, monoterpene indole alkaloids, and cannabinoids.

172 ing plant natural products--specifically the monoterpene indole alkaloids, the benzylisoquinoline alk

173 In our quest to discover new monoterpene indole alkaloids, we demonstrate the utility

174 ying the role of CPRs in the biosynthesis of monoterpene indole alkaloids, we provide compelling evid

175 the C20-quaternary stereocenters of multiple monoterpene indole alkaloids.

176 tural products, including approximately 3000 monoterpene indole alkaloids.

177 Some monoterpenes inhibited alpha-amylase and alpha-glucosida

178 roach we model the tail-to-head formation of monoterpenes inside a resorcin[4]arene-based capsule (ca

179 nyl diphosphate (GPP), the precursor of most monoterpenes, is synthesized in plastids from dimethylal

180 owever, our results demonstrate that the two monoterpene isomers produce unique suites of oxidation p

181 generated from ozonolysis of two structural monoterpene isomers: D-limonene SOA (LSOA) and alpha-pin

182 additionally show that d-limonene, a dietary monoterpene known to induce ROS, is capable of overcomin

183 ds, including various phenolic glycosides, a monoterpene lactone, a spermine derivative, and fatty ac

184 Autoxidation of monoterpenes leads to rapid formation of Highly Oxygenat

185 ulation of a d-limonene synthase gene alters monoterpene levels in orange antisense (AS) fruits, lead

186 sule I, and we explain why additional stable monoterpenes, like camphene, are not observed.

187 sparkling wines showed decreasing amounts of monoterpenes (limonene, 4-terpineol, terpinolene, citron

188 ence of water-soluble SOA generated from two monoterpenes, limonene and alpha-pinene, and two differe

189 These lactones are closely related to the monoterpene-limonene secondary biotransformation and men

190 An initial route employing the linear monoterpene linalool generated a lower oxidation state g

191 germacrene-D and (E)-beta-caryophyllene, the monoterpenes linalool and alpha-pinene, and the homoterp

192 the emission of total volatiles and specific monoterpenes, mainly limonene, but also linalool and alp

193 Monoterpenes, major constituents of essential oils, are

194 Taken together, the selected monoterpenes may not confer strong protection against fr

195 s (GPP versus NPP) by Li3CARS indicates that monoterpene metabolism may be controlled in part through

196 hus, this study aims to use (-)-borneol as a monoterpene model to prepare inclusion complexes between

197 rs containing approximately 1% of two chiral monoterpene molecules, limonene and camphor, are irradia

198 Results for 4 of the 11 monoterpenes, monitored versus an internal standard of b

199 The emissions of total monoterpenes (MTs) were dominating (96-98% of total VOCs

200 Instead, ASM olfactory responses to the monoterpene nerol were predominated by the activity of C

201 s, the overall development patterns of total monoterpenes, norisoprenoids and sesquiterpenes were sim

202 s, most of volatiles were found in the skin (monoterpenes, norisoprenoids, aldehydes, and C6 alcohols

203 The impact of this monoterpene on the production of capsidiol in Nicotiana

204 We found no evidence of sexual dimorphism in monoterpene or sesquiterpene profiles.

205 brochaites accessions that synthesize either monoterpenes or sesquiterpenes was performed to identify

206 Cs do not correlate with levels of isoprene, monoterpenes, or dimethyl sulfide.

207 Monoterpene oxidation products enhance atmospheric new p

208 By contrast to monoterpene oxidation, in which extremely low volatility

209 secondary organic aerosol (SOA) derived from monoterpene oxidation.

210 nic compounds following SO2 perturbations of monoterpene oxidation; whether these are the result of p

211 fferent groups: monoterpene hydrocarbons and monoterpene oxygen-containing compounds (oxides, alcohol

212 mber of molecular formulas matching those of monoterpene ozonolysis SOA were observed; they include o

213 Our data suggest that monoterpenes, particularly pinenes, promote SAR, acting

214 mol (2-isopropyl-5-methylphenol) is the main monoterpene phenol occurring in essential oils isolated

215 termine the origin of the 'cineole cassette' monoterpene phenotype other potential parent species of

216 gene to show that it produces sabinene, the monoterpene precursor of alpha-thujone.

217 he biosynthetic pathway of preakuammicine, a monoterpene precursor of the anti-cancer agent vinblasti

218 ), converted geranyl diphosphate (the linear monoterpene precursor) primarily to 1,8-cineole with K (

219 nent or temporary NOx sinks depending on the monoterpene precursor.

220 ion of the major essential oil constituents (monoterpenes, prenylated coumarins, and polymethoxylated

221 for the experimentally observed kinetics of monoterpene product formation and product distribution u

222 ate the importance of NAC TFs in controlling monoterpene production and other traits in ripening frui

223 ion in N. benthamiana and the improvement of monoterpene production in transgenic tobacco plants.

224 mpared to understand the regulation of fruit monoterpene production.

225 resulted in increased levels of ZIS-derived monoterpene products compared to fruits expressing ZIS a

226 e peroxy radicals scavenge highly oxygenated monoterpene products.

227 of plasticity, capable of producing multiple monoterpene products.

228 utively emitting isoprene (Populus nigra) or monoterpenes (Quercus ilex), or that do not emit isopren

229 Oceanic concentrations of the individual monoterpenes ranged from below the detection limit of <1

230 g that model mechanisms that treat all NO3 + monoterpene reactions equally will lead to errors in pre

231 ude a representation of organic aerosol from monoterpene reactions with nitrate radicals (the primary

232 Defense traits, including constitutive monoterpenes, resin ducts and wood density, were higher

233 A formation via nitrate radical oxidation of monoterpenes, resulting in the formation of condensable

234 Av molecule shows that deletion of the outer monoterpene results in a 62% reduction in permeability,

235 ced by the position of a methyl group on the monoterpene ring.

236 )-mesembranol (2) has been achieved from the monoterpene (S)-(-)-perillyl alcohol.

237 erpenes that uses the commercially available monoterpene (S)-carvone as a C-ring synthon, which is in

238 ide evidence that OeISY likely generates the monoterpene scaffold of oleuropein in olive fruits.

239 od-2 leaves accumulate only trace levels of monoterpenes, sesquiterpenes, and flavonoids.

240 selectivity of particular target compounds, monoterpenes, sesquiterpenes, and oxygenated terpenes in

241 Monoterpenes, sesquiterpenes, hydrocarbons, cannabinoids

242 Of these, monoterpenes showed the most significant increase.

243 gradually increased during ripening, whereas monoterpenes significantly decreased.

244 ting that the mass contribution of dimers to monoterpene SOA has been significantly overestimated in

245 nd facilitation of anthropogenic sulfate for monoterpenes SOA.

246 ivity of the fractions was due to oxygenated monoterpenes, specifically alpha-terpineol and cis-sabin

247 .SSU could enhance the production of various monoterpenes such as (-)-limonene, (-)-linalool, (-)-alp

248 Monoterpenes such as (R)-(+)-limonene stimulated both gl

249 ies for human health, mainly attributable to monoterpenes such as thymol and carvacrol.

250 e major components of volatile fraction were monoterpenes, such as eucalyptol, linalool and p-cymene.

251 Measurements of key monoterpenes suggest atmospheric mole fractions ranging

252 specific, methyl jasmonate (MeJA)-responsive monoterpene synthase (Li3CARS) from Lavandula x intermed

253 t has been shown to possess both sesqui- and monoterpene synthase activities resulted in increased le

254 ible for 1,8-cineole biosynthesis, the first monoterpene synthase discovered in fungi.

255 gene was created by a duplication event of a monoterpene synthase followed by a localized gene conver

256 All previously isolated 'cineole cassette'-monoterpene synthase genes are multi product enzymes tha

257 The monoterpene synthase genes in the cluster likely evolved

258 method would allow the identification of new monoterpene synthase genes using transient expression in

259 omated pipeline for the screening of diverse monoterpene synthase libraries, employing robotic liquid

260 A monoterpene synthase producing the set of 'cineole casse

261 oded by three of these complementary DNAs: a monoterpene synthase that belongs to the TPS-b clade cat

262 dization to map the expression of a putative monoterpene synthase to the epithelium of glands and use

263 ray structure of the unique "head-to-middle" monoterpene synthase, lavandulyl diphosphate synthase (L

264 ng this a hemiterpene synthase rather than a monoterpene synthase.

265 two that were functionally characterized as monoterpene synthases and three that preferred farnesyl

266 Genes encoding monoterpene synthases are also prevalent, and they fall

267 The isoprene synthase is cytosolic; six monoterpene synthases are plastidic, and four are cytoso

268 to two P450s that were coexpressed with two monoterpene synthases in flowers and were thus predicted

269 ae), thus indicating gene diversification of monoterpene synthases in section Alatae.

270 ion of alternative product profiles of these monoterpene synthases of conifer defense against insects

271 e nature of the branched reaction mechanism, monoterpene synthases often produce multiple products wh

272 hase falls into the TPS-d1 group (gymnosperm monoterpene synthases) and is most closely related to li

273 ne synthase, 10 exclusively or predominantly monoterpene synthases, 17 sesquiterpene synthases and si

274 The enzymes of clade III mainly act as monoterpene synthases, forming cyclic and acyclic monote

275 d biosynthesis and others with activities as monoterpene synthases.

276 S-b subfamily that typically contains mostly monoterpene synthases.

277 at the produced GPP can be used by plastidic monoterpene synthases.

278 DXS in Nicotiana benthamiana leaves elevated monoterpene synthesis by AaTPS1 more than 100-fold, indi

279 ases the cytosolic pool of GPP available for monoterpene synthesis in this compartment via GPP export

280 accumulating higher concentrations of toxic monoterpenes than whitebark pine, where they co-occur.

281 7 enzymes for the conversion of glucose into monoterpenes that generates both NAD(P)H and ATP in a mo

282 prise a large family of distinctive bicyclic monoterpenes that possess a wide range of pharmacologica

283 ay leads from several biogenic VOCs, such as monoterpenes, to the formation of large amounts of extre

284 artemisinin, non-amorphadiene sesquiterpene, monoterpene, triterpene, 2-C-methyl-D-erythritol 4-phosp

285 ng 22 sesquiterpenes (e.g., artemisinin), 26 monoterpenes, two triterpenes, one diterpene and 38 othe

286 umulation of AcTPS1 transcript, protein, and monoterpene volatiles in this species.

287 The oil with higher amounts of irregular monoterpenes was the most effective.

288 MS) analysis revealed that oxygen-containing monoterpenes was the principal group of compounds identi

289 A series of twelve monoterpenes were assessed in the present study.

290 btusifolia emitted solely 1,8-cineole and no monoterpenes were found in floral scents of N. petunoide

291 stingly, similar enantiomeric preferences of monoterpenes were obtained between needles and berries o

292 Monoterpenes which represent 'freshness', e.g. beta-pine

293 ial oil is composed of regular and irregular monoterpenes, which are derived from linear precursors g

294 m EOs composition is dominated by oxygenated monoterpenes, while I. crithmosmall yi, Ukrainiandes one

295 ha-pinene as the precursor because it is the monoterpene with the most well characterized SOA chemist

296 eously the characteristic 'cineole cassette' monoterpenes with 1,8-cineole as the dominant volatile p

297 ioning of organic nitrates from isoprene and monoterpenes with a focus on the Southeast United States

298 vious studies, no clear relationships of the monoterpenes with biological variables were found.

299 derivatives, borneol (up to 10.9%), bicyclic monoterpenes with pinane skeleton (pinocarvone up to 10.

300 Large variations in chiral distribution of monoterpenes within the same plant species and between t