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1 ced by formalin, acetic acid, capsaicin, and cinnamaldehyde.
2 mmatory capacity was primarily attributed to cinnamaldehyde.
3 aldehydes, a hindered aromatic aldehyde, and cinnamaldehyde.
4 ctrophilic compounds such as mustard oil and cinnamaldehyde.
5 ingredients such as allyl isothiocyanate and cinnamaldehyde.
6 ctively prevented by higher release of trans-cinnamaldehyde.
7  in a chemospecific anti-aldol reaction with cinnamaldehyde.
8 duct of decarboxylation from such compounds, cinnamaldehydes.
9  for by elevated levels of benzaldehydes and cinnamaldehydes.
10               Four treatments (control, 0.1% cinnamaldehyde, 0.75% calcium chloride and combination o
11 0.31 mg GAE/g), TFC (0.50 +/- 0.01 mg QE/g), cinnamaldehyde (19.33 +/- 0.002 mg/g), eugenol (10.57 +/
12                       Films containing trans-cinnamaldehyde (2-10%) showed high antifungal efficacy a
13 bes that contain 2-nitro- (1-3) and 4-fluoro-cinnamaldehyde (4-6) and applied them to the anion recog
14 ve 4-chloro-N-methyl-N-nitrosoaniline (76%), cinnamaldehyde (55%), 3-phenyl-5-hydroxyisoxazoline (26%
15 ensitive, lung-specific neurons responded to cinnamaldehyde, a TRPA1 agonist, with increases in intra
16  of 1,2,4-trimethoxybenzene, indole, and (E)-cinnamaldehyde, all blossom components, is highly attrac
17  products [e.g., allyl isothiocyanate (ITC), cinnamaldehyde, allicin, and gingerol].
18                  TRPA1 activators, including cinnamaldehyde, allyl isothiocyanate (AITC), and 4-hydro
19                                          The cinnamaldehyde alone and a combination of cinnamaldehyde
20                                              Cinnamaldehyde also induced TRPA1-like inward currents (
21 included octanal, octanoic acid, octanol and cinnamaldehyde among others (all at 30microM).
22              Similarly, the oxidation of the cinnamaldehyde analogue occurs at an even higher potenti
23 75% calcium chloride and combination of 0.1% cinnamaldehyde and 0.75% calcium chloride) were used to
24 lcohol dehydrogenase subfamily that includes cinnamaldehyde and benzaldehyde dehydrogenases.
25 he cinnamaldehyde alone and a combination of cinnamaldehyde and calcium chloride treatments yielded b
26 nds with demonstrated halogenation pathways (cinnamaldehyde and citric acid) across guar gels with va
27 and evaluated in the DA reaction between (E)-cinnamaldehyde and cyclopentadiene.
28 , little to mild toxicity was seen for trans-cinnamaldehyde and eugenol, respectively, while carvacro
29                         Degradation of trans-cinnamaldehyde and limonene in cucumber was evaluated un
30 wn modes) allowed for the detection of trans-cinnamaldehyde and limonene metabolites.
31  3-phenylpropionate, methyl 2-phenylacetate, cinnamaldehyde and methyl cinnamate were produced during
32 tal irritants and pungent chemicals, such as cinnamaldehyde and mustard oil.
33 ty problems with the lipophilic vanillin and cinnamaldehyde and neutralizing their volatility, produc
34 king interactions between the phenyl ring of cinnamaldehyde and phenylated SAMs allowed tuning of rea
35 ontrolling the liquid phase hydrogenation of cinnamaldehyde and related benzylic aldehydes over Pt na
36  criteria for the subsurface halogenation of cinnamaldehyde and the broad capacity for THM formation
37  The TRPA1 agonists allyl isothiocyanate and cinnamaldehyde and the TRPV4 agonist GSK1016790A caused
38              Three nanoemulsions of eugenol, cinnamaldehyde and their mixture were fabricated and tes
39 tion of the alpha,beta-unsaturated aldehyde (cinnamaldehyde) and the catalyst.
40 h three reference substrates ketoisophorone, cinnamaldehyde, and (S)-carvone.
41 rent structures, including carvone, eugenol, cinnamaldehyde, and acetophenone.
42 emicals such as allyl isothiocyanate (AITC), cinnamaldehyde, and allicin, produce nociceptive sensati
43 amon have a higher concentration of eugenol, cinnamaldehyde, and antioxidant capacity, as well as a l
44 ing nonenolizable aliphatic aldehydes, trans-cinnamaldehyde, and beta-substituted styrenes were also
45 alpha-ionone, ethyl 2-methylbutanoate, trans-cinnamaldehyde, and eugenol.
46 ymethylfurfural, anisaldehyde, benzaldehyde, cinnamaldehyde, and phenylaldehyde are commonly generate
47 rovided good encapsulation and protection of cinnamaldehyde, and the controlled release of cinnamalde
48                                          The cinnamaldehyde- and crotonaldehyde-derived phosphonates
49 reboxetine from commercially available trans-cinnamaldehyde are described.
50 (hydroxycinnamoyl-SCoAs) to cinnamaldehydes; cinnamaldehydes are then reduced to cinnamyl alcohols by
51 lic plant compounds, such as mustard oil and cinnamaldehyde, are TRPA1 agonists, it is unknown whethe
52 nylmethyl benzenesulfonamide and beta-chloro-cinnamaldehyde as an intermediate.
53 trophilic compounds allyl isothiocyanate and cinnamaldehyde as well as heat.
54                   One refill fluid contained cinnamaldehyde at ~34% (343 mg/ml), more than 100,000 ti
55 ilic reactivity of iminium ions derived from cinnamaldehyde by a factor of 14.
56 ral properties on the hydrogenation of trans-cinnamaldehyde by using a cobalt phosphide catalyst.
57                  Additionally, SJNP releases cinnamaldehyde (CA) upon CT linkage cleavage, elevating
58                  This study aimed to produce cinnamaldehyde (CA)-loaded nanostructured lipid carriers
59  sunflower oil (HOSO), tricaprylin (TC), and cinnamaldehyde (CA).
60 rations of proanthocyanidins (PAC) and trans-cinnamaldehyde (CA).
61 th most other common oral irritants, such as cinnamaldehyde, capsaicin, and alcohol, which irritate m
62 ti-component coating via layer deposition of cinnamaldehyde (CIN)-doped chitosan/poly(vinyl alcohol)/
63 f base of O-carboxymethyl chitosan (CMC) and cinnamaldehyde (CIN).
64 d cinnamic acids (hydroxycinnamoyl-SCoAs) to cinnamaldehydes; cinnamaldehydes are then reduced to cin
65 MS), highlighting the bioactive potential of cinnamaldehyde, cinnamic acid, benzoic acid, coumarin, l
66  such as allyl isothiocyanate (mustard oil), cinnamaldehyde (cinnamon), and allicin (garlic).
67 ed that 2,3-butanediol, hexanal, hexanol and cinnamaldehyde contributed the most to classification of
68                       However, no additional cinnamaldehyde coupling products could be detected in th
69 tives of two such compounds, mustard oil and cinnamaldehyde, covalently bind mouse TRPA1.
70 vestigated the impact of halogen radicals on cinnamaldehyde degradation rates.
71 nylmethyl benzenesulfonamide and beta-chloro-cinnamaldehyde, depending on whether one uses either NaI
72                    The Passerini coupling of cinnamaldehyde derivatives affords allylic esters that m
73 vation, this study presents the synthesis of cinnamaldehyde derivatives i.e., chalcones and pyrazoles
74 lation of 2-arylimidazo[1,2-a]pyridines with cinnamaldehyde derivatives to construct fused N-heterocy
75 Wadsworth-Emmons reaction, were treated with cinnamaldehyde derivatives, acetic acid, and borohydride
76  ratio when 20 mol % of the chiral imidazole-cinnamaldehyde-derived carbamate was utilized in the rea
77                      Higher release of trans-cinnamaldehyde enhanced bread crystallinity but gave low
78  Here, we investigated the toxicity of trans-cinnamaldehyde, eugenol, and carvacrol after intramuscul
79 ), antioxidant activity, and key bioactives (cinnamaldehyde, eugenol, and cinnamic acid) using two ex
80                                              Cinnamaldehyde, eugenol, caryophyllene, cinnamyl acetate
81 ivo vagal innervated mouse lung preparation, cinnamaldehyde evoked action potential discharge in mous
82                       In both studies, trans-cinnamaldehyde followed a second-order degradation kinet
83 imp preservation, where headspace release of cinnamaldehyde from emulsions at non-contact mode was mo
84                 We report here that peptidyl cinnamaldehydes function as reversible, slow-binding inh
85 ch-turnip peel extract (PS-TPE) and guar gum-cinnamaldehyde (GG-CA) for freshness monitoring and enha
86            Among the eight tested compounds, cinnamaldehyde had the greatest anti-neuroinflammatory c
87                                              Cinnamaldehyde halogenation proceeded most readily in bo
88                                In this work, cinnamaldehyde has been encapsulated in chitosan nanopar
89 ly are salicylic acid, tannic acid and trans-cinnamaldehyde have been identified.
90 anistic insight from kinetic mapping reveals cinnamaldehyde hydrogenation is structure-insensitive ov
91 at halogenated products of additives such as cinnamaldehyde (i.e., a-chlorocinnamaldehyde and a-bromo
92  to selectively orient the reactant molecule cinnamaldehyde in a configuration associated with hydrog
93 omprised key character aroma compounds, e.g. cinnamaldehyde in cinnamon.
94 he conjugate addition of nitromethane with a cinnamaldehyde in the presence of the Jorgensen-Hayashi
95 ns are capable of forming E,E,E-trienes from cinnamaldehydes in good yield.
96 in, sinapic acid, cinnamic acid, eugenol and cinnamaldehyde) in multilevel ratios.
97                                              Cinnamaldehyde inhalation in vivo mimicked capsaicin in
98 nnamaldehyde, with ozone having no effect on cinnamaldehyde-insensitive fibres.
99 ic analysis of an isolated Au(iii)-activated cinnamaldehyde intermediate.
100           For the catalytic hydrogenation of cinnamaldehyde, intermediate amounts of sulfur with inte
101 rocess evolves through a [3 + 2] 1,3-DC when cinnamaldehyde is used in the presence of an azomethine
102 ic acid were tentatively identified as trans-cinnamaldehyde metabolites.
103                         Interaction of trans-cinnamaldehyde modified CO functional groups of PLA and
104                     Saturating activation by cinnamaldehyde or mustard oil occluded potentiation but
105                                  They add to cinnamaldehyde or paraformaldehyde, for example, to prod
106         Treatment with allyl isothiocyanate, cinnamaldehyde, or GSK1016790A caused an increase in ATP
107 s did not result in selective degradation of cinnamaldehyde over other compounds (i.e., benzoate and
108            Products from radical coupling of cinnamaldehydes, particularly sinapaldehyde, which were
109 uinone and the electrophilic TRPA1 activator cinnamaldehyde produced antinociception that was lost in
110 innamaldehyde, and the controlled release of cinnamaldehyde promoted sustained antibacterial efficacy
111 alf-life values (DT(50) or t(1/2)) for trans-cinnamaldehyde ranged from 2.02 to 2.49 h, while for lim
112                                        Trans-cinnamaldehyde reduced bacterial and fungal growth in br
113 ty in enhancing C = O hydrogenation (through cinnamaldehyde reorientation), a general phenomenon exte
114 ipeptide Gly-Glu-Glu to the para position of cinnamaldehyde resulted in an inhibitor (Cinn-GEE) of su
115 urons that express TRPA1, a mustard oil- and cinnamaldehyde-sensitive channel, and that these respons
116 inate (CAS) and two natural aldehydes (trans-cinnamaldehyde (TC) and citral) were studied by evaluati
117 t-based oregano essential oil (OR) and trans-cinnamaldehyde (TCA) was studied.
118                                        Trans-cinnamaldehyde (TCA), carvacrol, and eugenol were assess
119 elivery of natural antimicrobial using trans-cinnamaldehyde (TCIN) as a model compound.
120 al Diabrotica to structural analogues of (E)-cinnamaldehyde, the major attractant for Diabrotica unde
121                                              Cinnamaldehyde, the most specific TRPA1 activator, excit
122 ng linoleic acid (LA) to SN38 and JQ-1 via a cinnamaldehyde thioacetal (CT) bond, facilitating co-del
123 d cyclization between beta-keto enamines and cinnamaldehydes to furnish the functionalized biphenyls.
124 were present in 50% (menthol, triacetin, and cinnamaldehyde) to 80% (ethyl maltol) of the samples.
125 T60/PLA40 (PBAT/PLA) with incorporated trans-cinnamaldehyde using cast-extrusion.
126 in essential oils i.e. carvacrol, thymol and cinnamaldehyde was developed following the Quality by De
127                                              Cinnamaldehyde was encapsulated in chitosan nanoparticle
128                                        Trans-cinnamaldehyde was more compatible in PLA which exhibite
129                           Vanillin and trans-cinnamaldehyde were bound to chitosan by Schiff base rea
130 yed to install a pyridyl to the alkene trans-cinnamaldehyde while Ag(I) ions are used in a second ste
131                              The reaction of cinnamaldehyde with iodonium ylide 1a catalyzed by (5S)-
132 eatment of the tosylhydrazone sodium salt of cinnamaldehyde with transition metal catalysts.
133 ansient receptor potential (TRP) A1 agonist, cinnamaldehyde, with ozone having no effect on cinnamald

 
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