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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 n air of the chemical warfare agent simulant methyl salicylate (1.24 ppb) and for nitrobenzene (629 p
6                                       FVT of methyl salicylate-1-(13)C 7a revealed a deep-seated rear
7 hermolysis (FVT) with Ar-matrix isolation of methyl salicylate (7), 2-phenylbenzo-1,3-dioxan-4-one (8
8 he observed labeling pattern in the isolated methyl salicylate 7a/7b and methyl cyclopentadienecarbox
9  modified electrode was fabricated to detect methyl salicylate, a volatile organic compound released
10 act plants sprayed with methyl jasmonate and methyl salicylate and in excised leaves supplied through
11 c acid (JA) biosynthesis genes and exogenous methyl salicylate and methyl jasmonate applications show
12 nene, 2-methoxy-3-(1-methylpropyl)-pyrazine, methyl salicylate and tridecane.
13  given for chemical warfare agent simulants, methyl salicylate, and dimethyl methyl phosphonate (DMMP
14                Exogenous applications of MJ, methyl salicylate, and ethylene were used to assess indu
15 s of salicylaldehyde, o-hydroxyacetophenone, methyl salicylate, and methyl N-methyl- or N-phenylanthr
16 on of the alpha-chlorophenylacetate ester of methyl salicylate as demonstrated by a trapping experime
17 stant potential amperometry using hydrolyzed methyl salicylate as the analyte.
18 that SABP2 has strong esterase activity with methyl salicylate as the substrate, and that SA is a pot
19          We found that the HIPVs menthol and methyl salicylate at 1 and 10 nmol.ml(-1) improved many
20 l sulfoxide (DMSO), dimethylformamide (DMF), methyl salicylate, caffeine, l-leucine, l-histidine, lor
21 rmone analogues such as methyl jasmonate and methyl salicylate can trigger defense responses in plant
22                      MJ and ethylene but not methyl salicylate caused enhanced phenolic synthesis in
23 ylate (43.30%) and a significant decrease in methyl salicylate content in spring bamboo shoots were o
24 2 to acetophenone was reduced, while that to methyl salicylate did not change.
25 peas and a plant-derived repellent compound, methyl salicylate, differed between morphs or sexes.
26 ive trait locus (QTL) linked to higher fruit methyl salicylate emissions.
27          Birch reduction of the SEM ether of methyl salicylate followed by oxidation of the intermedi
28 nd 2, the approach was first to react either methyl salicylate (for 1) or phenyl salicylate (for 2) w
29                                              Methyl salicylate has been identified as one of the most
30                                              Methyl salicylate in air gives a recognizable mass spect
31  MOR161-2 responded to both acetophenone and methyl salicylate in vivo.
32 critical for methyl salicylate synthesis and methyl salicylate, in turn, likely has an important role
33 ormance of the technique is established with methyl salicylate, including a limit of quantification o
34 tive but mounted normal local resistance and methyl salicylate-induced defense responses, suggesting
35                   The limit of detection for methyl salicylate, introduced as the pure vapor, is esti
36  production of plant volatiles, particularly methyl salicylate, making bean plants, Vicia faba, repel
37 idual components elicited varying responses; Methyl salicylate (MeSA) elicited the highest positive c
38 cquired resistance (SAR) in tobacco; SABP2's methyl salicylate (MeSA) esterase activity is required i
39 rent genetic backgrounds, we showed that the methyl salicylate (MeSA) esterase activity of salicylic
40                                   SABP2 is a methyl salicylate (MeSA) esterase that has high affinity
41         The first such signal identified was methyl salicylate (MeSA) in tobacco (Nicotiana tabacum).
42                                              Methyl salicylate (MeSA) is a volatile plant secondary m
43      Exposure to methyl jasmonate (MeJA) and methyl salicylate (MeSA) vapours at 10 and 100micromoll(
44 O2* with five GLVs: methyl jasmonate (MeJa), methyl salicylate (MeSa), cis-3-hexenyl acetate (HxAc),
45 ajor aphid-induced VOCs (ethanone, limonene, methyl salicylate, myrcene, ocimene) triggered resistanc
46 s not induced by wounding, methyl jasmonate, methyl salicylate, or ethephon, synthetic GmSubPep pepti
47 sed biosensor can be used to reliably detect methyl salicylate released by unhealthy plants.
48 results indicate that SlSAMT is critical for methyl salicylate synthesis and methyl salicylate, in tu
49 exhibited significantly greater responses to methyl salicylate than to acetophenone.
50 mall metabolites in SAR signaling, including methyl salicylate, the abietane diterpenoid dehydroabiet
51 salicylic acid binding protein 2) hydrolyzes methyl salicylate to salicylic acid.
52 peciosa recruit to aboveground herbivory and methyl salicylate treatment, that larval D. speciosa are
53                                              Methyl salicylate undergoes hydrolysis to form methanol,
54                Conversion of acetophenone to methyl salicylate was observed in the medium of CYP1a2-e
55 , beta-ionone, hotrienol, methylpyrazine and methyl salicylate were major volatile constituents in al
56 hoots at ambient temperature comprise 12.30% methyl salicylate, which provides protection against ins

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