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1 enzaldehyde, limonene, 2-nonanone, and ethyl octanoate).
2 lmitate) or/and M1 acetyl-CoA (e.g. [1-(13)C]octanoate).
3 ate, ethyl isovalerate, 1-pentanol and ethyl octanoate.
4 d ethyl butanoate, ethyl hexanoate and ethyl octanoate.
5 availability of one of their precursors, the octanoate.
6 oneogenesis from heptanoate are inhibited by octanoate.
7 lower than the rate of C(4) ketogenesis from octanoate.
8 flux were unchanged in the presence of added octanoate.
9  partial peroxisomal oxidation of oleate and octanoate.
10  or oxidation of the medium-chain fatty acid octanoate.
11 cose, sodium acetate (1,2-(13)C2) and sodium octanoate (1,2,3,4-(13)C4) suggested that these compound
12                     In contrast, with [3-13C]octanoate, [1-13C]hexanoate, [1-13C]butyrate, or [1,2-13
13 probenecid, 100%; 1 mM piroxicam, 100%; 1 mM octanoate, 100%.
14                                   Phorbol 12-octanoate-13-acetate derivatives translocate PKC-betaII
15           Under the catalysis of rhodium(II) octanoate, [3 + 2]-cyclization between enoldiazoacetamid
16 methyl phenyldiazoacetate catalyzed by Rh(2)(octanoate)(4) exhibits a substantial (13)C isotope effec
17 chondrial type II synthase for production of octanoate (a lipoic acid precursor) as well as longer fa
18 was developed for TFE and ammonium perfluoro-octanoate, a chemical used in the polymerization process
19 d and was found to be chain length specific: octanoate, a medium-chain fatty acid was transported in
20 ]oleate, a long-chain fatty acid, and [1-14C]octanoate, a medium-chain fatty acid, for 3 h in seven v
21 extracts of rats infused with [2,4,6,8-13C4]-octanoate, a source of [2-13C]acetyl-CoA.
22                                          The octanoate-activating enzyme is unknown, but we assume th
23 anoate metabolism and compared it to that of octanoate, an even-chain fatty acid which only provides
24                                        Bromo-octanoate, an inhibitor of beta-oxidation, and amino-oxy
25 s: 1-hexanol in meat aged for 15days, ethyl- octanoate and 2-pentylfuran in meat aged for 22days, and
26 athway; (ii). it functions with fatty acids (octanoate and decanoate) that cannot be used by wild-typ
27 te, ethyl isovalerate, ethyl caproate, ethyl octanoate and ethyl decanoate as the most abundant.
28                       Although the uptake of octanoate and heptanoate by the liver are similar, the r
29 vels of sulphur compounds, 2-nonanone, ethyl octanoate and lower contents of hexanol and heptanol tha
30                                              Octanoate and palmitate also exerted a dual effect on el
31 -ol, ethyl butanoate, ethyl hexanoate, ethyl octanoate and phenylethyl alcohol.
32               The organic anions probenecid, octanoate, and alpha-ketoglutarate reduced ochratoxin A
33 anol, octanal, nonanal, ethyl acetate, ethyl octanoate, and butane-2,3-dione) representative of the f
34                                     Acetate, octanoate, and palmitate inhibited the glucose-induced a
35 os) in combination with octanoic acid/sodium octanoate as a simple and effective surfactant system pr
36 the stressed heart postischemia and identify octanoate as an intervention by which myocardial metabol
37 cation of acetic acid, octen-3-ol, and ethyl octanoate as aroma contributors in Shiraz wine and deter
38                                       Methyl octanoate, beta-myrcene, trans-alpha-bergamotene, linalo
39 he OR52 family, in the ligand-free (apo) and octanoate-bound states.
40 ts are washed from the column using a sodium octanoate buffer before elution of bound antibodies.
41 eta-glucanase enhanced the increase of ethyl octanoate, but produced a decrease in the contents of de
42 f odour activity were ethyl hexanoate, ethyl octanoate, butyrolactone, isoamyl alcohols, acetaldehyde
43 [C2MIM][OAc] and 1-ethyl-3-methylimidazolium octanoate [C2MIM][OOct].
44                  The increasingly lipophilic octanoate (C8), decanoate (C10) and dodecanoate (C12) de
45                                        Thus, octanoate (C8), the precursor for lipoic acid synthesis,
46  response to 12.5 mM glucose was as follows: octanoate (C8:0), 3.4; linoleate (C18:2 cis/cis), 5.3; o
47 se (predominantly unlabeled) and 13C-labeled octanoate can account for the entire oxidative metabolis
48                                  Addition of octanoate caused a transient potentiation of glucose-ind
49                                              Octanoate caused an initial increase in VRAC activity fo
50 in apoptosis, and an ionic liquid of choline octanoate (COA) to treat early-stage melanoma.
51 pholipids of V. harveyi, particularly at low octanoate concentrations.
52 ing, we demonstrate that both heptanoate and octanoate contribute carbon to the TCA cycle in HEK293 T
53 ission under low-glucose conditions, whereas octanoate could not.
54  slightly increased by the addition of ethyl-octanoate, -decanoate and -dodecanoate, but decreased by
55 e and glutamine, we show that heptanoate and octanoate decrease the contribution of glucose-derived c
56 r concentration of ethyl decanoate and ethyl octanoate, diethyl succinate, hydroxylinalool, and 2-phe
57 ts permitted for organic production, sucrose octanoate ester (SOE) and soy lecithin that were mixed a
58     Ethyl propanoate, ethyl butanoate, ethyl octanoate, ethyl acetate, isoamyl acetate, isobutanol, 2
59 ng amounts of esters (terpenyl esters, ethyl octanoate, ethyl decanoate and hexyl acetate) and alcoho
60 ethylbutanoate, 3-methylbutyl acetate, ethyl octanoate, ethyl decanoate, 2-phenylethyl acetate, 2-phe
61        Six compounds (isoamyl acetate, ethyl octanoate, ethyl decanoate, 3-methylthio-1-propanol, car
62                   TFE and ammonium perfluoro-octanoate exposures were highly correlated, and therefor
63 ethylbutanal (wort), ethyl alcohol and ethyl octanoate (fermentation, maturation and filtration), or
64 er for anencephaly; the herbicide bromoxynil octanoate for spina bifida; and trifluralin and maneb fo
65               We demonstrate LipB can accept octanoate from its own ACP and noncognate ACPs, as well
66 ected in five samples with B-myrcene, methyl octanoate, geraniol and linalool being the predominant c
67 lated rat livers perfused with (13)C-labeled octanoate, heptanoate, or propionate.
68 ncentrations of labeled docosanoate, oleate, octanoate, hexanoate, butyrate, acetate, or dodecanedioa
69 l (HT, hydrophilic compound), hydroxytyrosol octanoate (HTC18, hydrophobic compound) and hydroxytyros
70  after the inhalation of Inavir (Laninamivir Octanoate Hydrate) to treat flu infection.
71                                Nevertheless, octanoate improved the rate of recovery of synaptic func
72 s presented with the medium-chain fatty acid octanoate in addition to hyperpolarized [1-(13)C(1)]pyru
73               We found that oxidation of 13C-octanoate in brain is avid and contributes approximately
74 tes indicated compartmentalized oxidation of octanoate in brain.
75 ys, propionate, valerate, caproate, and also octanoate increased Glc-6-Pase promoter activity by 6-16
76 tion of glycolate, glyoxylate, and 2-hydroxy octanoate indicate that the oxidation of glycolate to gl
77                 The lipoate analogue 8-bromo-octanoate inhibited LipL1 activity and arrested P. falci
78  reduced: BHB plasma levels were restored by octanoate injection; BHB production and palmitic acid ox
79  esters, such as methyl hexanoate and methyl octanoate, known to act as medfly pheromone and attracta
80 beta-damascenone, ethyl hexanoate, and ethyl octanoate levels.
81 ns, including acetic acid; octen-3-ol; ethyl octanoate; methyl-2-oxo-nonanoate; butanoic acid, 2-meth
82                     Ethyl butyrate and ethyl octanoate odour thresholds doubled or tripled in the pre
83 sting the effect of beta-hydroxybutyrate and octanoate on rat hippocampal synaptic transmission durin
84 LplA, a ligase that in presence of exogenous octanoate (or lipoate) can bypass loss of LipB.
85 ddition of either a medium-chain fatty acid (octanoate) or a long-chain fatty acid (palmitate).
86 acyltransferase, which attaches the required octanoate, or ghrelin itself.
87                                [2,4,6,8-13C4]octanoate oxidation in intact rats was determined by nuc
88                                 In contrast, octanoate oxidation remained unchanged.
89 eased, causing a decrease in oleate, but not octanoate, oxidation.
90                                    Perfluoro-octanoate-PAGE analysis of detergent-solubilized oligome
91 n by lithium dodecyl sulfate-PAGE, perfluoro-octanoate-PAGE, a membrane-based yeast two-hybrid system
92 hemical cross-linking experiments, perfluoro-octanoate-PAGE/Western blot, and affinity purification e
93 eaction), because it scavenges an endogenous octanoate pool to activate PDH.
94 he key odorants were ethyl propionate, ethyl octanoate, propanoic acid and 4-ethylphenol for JRE, dia
95  the production of the lipoic acid precursor octanoate, recent studies suggest an ability to produce
96                              Oleate, but not octanoate, requires carnitine binding to gain access to
97 dium-chain fatty acids such as palmitate and octanoate, respectively.
98                                              Octanoate significantly attenuated cell volume regulatio
99    These results are consistent with 8-bromo-octanoate specifically interfering with lipoate scavengi
100 he broad metabolic effects of heptanoate and octanoate supplementation, suggesting that therapeutic e
101                                Inhibition of octanoate-supported or octanoylcarnitine-supported respi
102                 With [1-13C]oleate or [1-13C]octanoate, the labeling ratio >1 indicates the partial p
103    Ghrelin O-acyltransferase (GOAT) attaches octanoate to proghrelin, which is processed to ghrelin,
104 olytopic membrane-bound enzyme that attaches octanoate to serine-3 of ghrelin.
105 sess the ability of beta-hydroxybutyrate and octanoate to support neuronal activity when glucose leve
106 mia was prevented by injection of lactate or octanoate, two sources of energy to support gluconeogene
107 trates including glucose, lactate, pyruvate, octanoate, [U-(13)C(3)]glycerol, and (2)H(2)O to probe v
108 s do not undergo peroxisomal oxidation, (ii) octanoate undergoes only one cycle of peroxisomal beta-o
109 ers (ethyl-, butyl-, isobutyl- and (iso)amyl octanoate) using lipase Palatase as the biocatalyst.
110  made up of octanoic acid/tetrabutylammonium octanoate vesicles for 10min.
111  analyses displayed a decrease only in ethyl octanoate volatility in presence of catechin, whereas no
112 d blood spectra revealed that label from 13C-octanoate was incorporated into glucose and ketones, whi
113  Under inhalation anaesthesia, [2,4,6,8-13C4]octanoate was infused into the jugular vein of the intac
114  ethyl isobutyrate, ethyl butyrate and ethyl octanoate was investigated in model solutions, by means
115 l-1-propanol, 3/2-methyl-1-butanol and ethyl octanoate were evaporated whereas the other volatile com
116 p, the infusions of [1-13C]oleate and [1-14C]octanoate were repeated.
117 es (chloromethyl propanoate, pentanoate, and octanoate) were identified as potential delayed acids (i
118 ymene, limonene, alpha-terpinolene and ethyl octanoate, were targeted.
119 toin, acetic acid, isobutyric acid and ethyl octanoate, were the main volatile compounds in dough; al
120  ethyl hexanoate, ethyl decanoate, and ethyl octanoate, whereas phenyl ethanol and 3-methyl-1-butanol
121 metabolized, and the medium-chain fatty acid octanoate, which is readily oxidized, did not affect ins
122 is acylated with an eight-carbon fatty acid, octanoate, which is required for its endocrine actions.
123 (ethyl isobutyrate, ethyl butyrate and ethyl octanoate) while gallic acid displayed no impact.

 
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