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1 hatidylcholine (POPC) bilayer interfaces and n-octanol.
2  12, 14, and 15 between perfluorodecalin and n-octanol.
3 obtained by cocrystallizing antiamoebin with n-octanol.
4 que because it is a simpler model to explain n-octanol actions on the GABAA receptor.
5 multiple sites to exert multiple actions, or n-octanol acts as a partial agonist to manifest these ac
6              Two models were used to explain n-octanol agonistic and potentiating actions on the alph
7                                 A mixture of n-octanol and dithizone was introduced as an effective a
8 on ratios for selected SVOCs between air and n-octanol as well as 8 other oligomers similar in chemic
9 ns on the alpha1beta2gamma2S GABAA receptor: n-octanol binds to multiple sites to exert multiple acti
10 ilicity of each tracer was determined by the n-octanol/buffer method.
11     The measured partition coefficient in an n-octanol/buffer system of AMPO was similar to those of
12 vatized analyte was extracted using a 1.0-uL n-octanol droplet hanging from the needle tip of a GC mi
13                                          The n-octanol effects on the gamma-aminobutyric acid type A
14 extraction in which a synergistic mixture of n-octanol enhanced with surfactant sodium dodecyl sulfat
15 ces of phosphatidylcholine bilayers and into n-octanol, have been determined by W. C. Wimley, S. H. W
16                            Coapplications of n-octanol increased peak currents evoked by 3 microM GAB
17       Conversely, the membrane intercalator, n-octanol, increased cholesterol oxidation, transfer, an
18                                 In addition, n-octanol modulated GABA-induced currents in a concentra
19 avior of sensitizer release in n-butanol and n-octanol occurs at an optimal temperature of 20 degrees
20 EFs) by severalfold compared with the use of n-octanol only as extractant solvent.
21 ilicity of the compounds (log P = 1.79-2.63, n-octanol/PBS).
22     One-minute preapplication of 1000 microM n-octanol slightly potentiated 3 microM GABA-induced cur
23 ne systems and finally the diisobutylamine + n-octanol system was selected to enhance the carbonation
24             Ethanol decreased the potency of n-octanol to inhibit ACh currents, possibly resulting fr
25 drophobic side-chains is larger than that of n-octanol to water transfer free energies.
26 ee energies of transferring side-chains from n-octanol to water, indicates that the magnitude of prot
27 ot observed when the peptide is dissolved in n-octanol, trifluoroethanol or sodium dodecyl sulfate mi
28                                              n-Octanol was also capable of evoking a small current wi
29 ations and no potentiation was observed when n-octanol was coapplied with 1000 microM GABA.
30 ctant sodium dodecyl sulfate (SDS) (0.10% in n-octanol) was applied as the extractant phase.
31                    When the logarithm of the n-octanol-water partition coefficient (log K(OW)) of POP
32 ting point, vapour pressure at 20 degrees C, n-octanol-water partition coefficient and solubility in
33 in tern eggs varied inversely with log10KOW (n-octanol-water partition coefficient), shifting egg con
34 yclic PAHs, namely, water solubility (S(w)), n-octanol-water partition coefficients (K(ow)), and orga
35  positively correlated with their respective n-octanol-water partition coefficients (R(2) = 0.65).
36 tential of the chalcogenopyrylium dye or the n-octanol/water partition coefficient, log P.
37 kyl and alkyl carboxylates between water and n-octanol were determined as a measure of their lipophil