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1 3-ol, 6-methyl-5-hepten-2-one, benzaldehyde, methyl salicylate).
2  OR activation by converting acetophenone to methyl salicylate.
3 dly metabolized to SA O-beta-D-glucoside and methyl salicylate.
4 onomer is mainly responsible for protonating methyl salicylate.
5 dimethyl methylphosphonate and 40 ppt(v) for methyl salicylate.
6 n air of the chemical warfare agent simulant methyl salicylate (1.24 ppb) and for nitrobenzene (629 p
7                                       FVT of methyl salicylate-1-(13)C 7a revealed a deep-seated rear
8                                              Methyl salicylate, 2-heptanol, 2-nonanol, and heptanone
9 hermolysis (FVT) with Ar-matrix isolation of methyl salicylate (7), 2-phenylbenzo-1,3-dioxan-4-one (8
10 he observed labeling pattern in the isolated methyl salicylate 7a/7b and methyl cyclopentadienecarbox
11  modified electrode was fabricated to detect methyl salicylate, a volatile organic compound released
12 act plants sprayed with methyl jasmonate and methyl salicylate and in excised leaves supplied through
13  conducted field experiments in Hungary with methyl salicylate and known attractants for Chrysoperla
14 c acid (JA) biosynthesis genes and exogenous methyl salicylate and methyl jasmonate applications show
15 as capable of detecting as low as ~80 ppb of methyl salicylate and naphthalene.
16 nene, 2-methoxy-3-(1-methylpropyl)-pyrazine, methyl salicylate and tridecane.
17                We assessed the repellency of methyl salicylate and verbenone to two putative laurel w
18 v) for 1 s of averaging for various ketones, methyl salicylate, and chlorinated hydrocarbons.
19  given for chemical warfare agent simulants, methyl salicylate, and dimethyl methyl phosphonate (DMMP
20                Exogenous applications of MJ, methyl salicylate, and ethylene were used to assess indu
21 s of salicylaldehyde, o-hydroxyacetophenone, methyl salicylate, and methyl N-methyl- or N-phenylanthr
22 est that the responses of green lacewings to methyl salicylate are context-dependent, and the ecologi
23 on of the alpha-chlorophenylacetate ester of methyl salicylate as demonstrated by a trapping experime
24 stant potential amperometry using hydrolyzed methyl salicylate as the analyte.
25 that SABP2 has strong esterase activity with methyl salicylate as the substrate, and that SA is a pot
26          We found that the HIPVs menthol and methyl salicylate at 1 and 10 nmol.ml(-1) improved many
27 rla carnea species complex were attracted to methyl salicylate, but to a much lesser extent compared
28 l sulfoxide (DMSO), dimethylformamide (DMF), methyl salicylate, caffeine, l-leucine, l-histidine, lor
29 rmone analogues such as methyl jasmonate and methyl salicylate can trigger defense responses in plant
30                      MJ and ethylene but not methyl salicylate caused enhanced phenolic synthesis in
31 ylate (43.30%) and a significant decrease in methyl salicylate content in spring bamboo shoots were o
32                           On the other hand, methyl salicylate did not attract Chrysopa formosa.
33 2 to acetophenone was reduced, while that to methyl salicylate did not change.
34 peas and a plant-derived repellent compound, methyl salicylate, differed between morphs or sexes.
35 ive trait locus (QTL) linked to higher fruit methyl salicylate emissions.
36          Birch reduction of the SEM ether of methyl salicylate followed by oxidation of the intermedi
37 nd 2, the approach was first to react either methyl salicylate (for 1) or phenyl salicylate (for 2) w
38                                              Methyl salicylate has been identified as one of the most
39                                              Methyl salicylate in air gives a recognizable mass spect
40  MOR161-2 responded to both acetophenone and methyl salicylate in vivo.
41 critical for methyl salicylate synthesis and methyl salicylate, in turn, likely has an important role
42 ormance of the technique is established with methyl salicylate, including a limit of quantification o
43 ed attraction of natural enemies to the HIPV methyl salicylate, including green lacewings.
44 tive but mounted normal local resistance and methyl salicylate-induced defense responses, suggesting
45                   The limit of detection for methyl salicylate, introduced as the pure vapor, is esti
46  production of plant volatiles, particularly methyl salicylate, making bean plants, Vicia faba, repel
47  was evaluated using two chemical simulants, methyl salicylate (MeS) and benzyl salicylate (BeS) appl
48                               Two simulants, methyl salicylate (MeS) with vegetable oil and benzyl sa
49 ophysiological responses in female antennae: methyl salicylate (MeSA) and delta-decalactone.
50 idual components elicited varying responses; Methyl salicylate (MeSA) elicited the highest positive c
51 cquired resistance (SAR) in tobacco; SABP2's methyl salicylate (MeSA) esterase activity is required i
52 rent genetic backgrounds, we showed that the methyl salicylate (MeSA) esterase activity of salicylic
53                                   SABP2 is a methyl salicylate (MeSA) esterase that has high affinity
54         The first such signal identified was methyl salicylate (MeSA) in tobacco (Nicotiana tabacum).
55                                              Methyl salicylate (MeSA) is a plant metabolite that indu
56                                              Methyl salicylate (MeSA) is a volatile plant secondary m
57 yric acid (GABA), methyl jasmonate (MeJA) or methyl salicylate (MeSA) on antioxidant systems and sens
58       Xyleborus volvulus was not repelled by methyl salicylate (MeSA) or verbenone in laboratory assa
59      Exposure to methyl jasmonate (MeJA) and methyl salicylate (MeSA) vapours at 10 and 100micromoll(
60 O2* with five GLVs: methyl jasmonate (MeJa), methyl salicylate (MeSa), cis-3-hexenyl acetate (HxAc),
61 ndogenously produced and exogenously applied methyl salicylate (MeSA).
62 compounds and hormone derivatives, including methyl salicylate (MeSA).
63                          Here we reveal that methyl-salicylate (MeSA), salicylic acid-binding protein
64 ajor aphid-induced VOCs (ethanone, limonene, methyl salicylate, myrcene, ocimene) triggered resistanc
65 ectrode voltages and obtaining ion peaks for methyl salicylate, naphthalene, benzene, and 2-butanone.
66 s not induced by wounding, methyl jasmonate, methyl salicylate, or ethephon, synthetic GmSubPep pepti
67 c ArM with a novel peptide ligand carrying a methyl salicylate palladium complex.
68                                              Methyl salicylate palladium LLEYLKR peptide (2-Pd) succe
69 sed biosensor can be used to reliably detect methyl salicylate released by unhealthy plants.
70               When presented in combination, methyl salicylate showed a synergistic effect, confirmin
71  the parent compound, such as pterin-SMX and methyl salicylate-SMX conjugates.
72  eucalyptol, hexetidine, menthol, triclosan, methyl salicylate, sodium fluoride and povidone, against
73 results indicate that SlSAMT is critical for methyl salicylate synthesis and methyl salicylate, in tu
74 exhibited significantly greater responses to methyl salicylate than to acetophenone.
75 ferent ketones, chlorinated hydrocarbons and methyl salicylate that forms ions in both polarities.
76 mall metabolites in SAR signaling, including methyl salicylate, the abietane diterpenoid dehydroabiet
77 salicylic acid binding protein 2) hydrolyzes methyl salicylate to salicylic acid.
78 peciosa recruit to aboveground herbivory and methyl salicylate treatment, that larval D. speciosa are
79                                              Methyl salicylate undergoes hydrolysis to form methanol,
80 ers from tert-butyl N-sulfinyl carbamate and methyl salicylate via in situ formation of sulfonimidoyl
81                Conversion of acetophenone to methyl salicylate was observed in the medium of CYP1a2-e
82 , beta-ionone, hotrienol, methylpyrazine and methyl salicylate were major volatile constituents in al
83 plant hormone salicylic acid (SA) to produce methyl salicylate, which acts as a plant-to-plant commun
84 hoots at ambient temperature comprise 12.30% methyl salicylate, which provides protection against ins
85 f Skoal Bandits Wintergreen was dominated by methyl salicylate, while Marlboro Spice consists of a mo