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1 lyte trimethylamine N-oxide or the cosolvent 2,2,2-trifluoroethanol.
2 lvents acetonitrile, dimethyl sulfoxide, and 2,2,2-trifluoroethanol.
3 the corresponding imidazolium salts in basic 2,2,2-trifluoroethanol.
4 hanol, and a 1:1 (v/v) mixture of CH2Cl2 and 2,2,2-trifluoroethanol.
5 dichroic spectra obtained in the presence of 2,2,2-trifluoroethanol.
6 E = 1.8), 2-propanol (28 ps, KIE = 1.4), and 2,2,2-trifluoroethanol (4.4 ps, KIE = 3.2), which indica
7 8-65% in aqueous solutions containing 40-80% 2,2,2-trifluoroethanol, a lipomimetic solvent, and was m
8 ing folding, was dramatically accelerated by 2,2,2-trifluoroethanol, a solvent that stabilizes alpha-
10 re analyzed by circular dichroism in aqueous 2,2,2-trifluoroethanol and in buffered aqueous solutions
11 nthetic channel proteins were transferred to 2,2,2-trifluoroethanol and reconstituted into vesicle me
12 pha-helices in the lower dielectric solvents 2,2,2-trifluoroethanol, and a 1:1 (v/v) mixture of CH2Cl
13 ile and in acetonitrile solutions containing 2,2,2-trifluoroethanol, and several Arrhenius functions
14 ng ammonia as the amine component, employing 2,2,2-trifluoroethanol as a non-nucleophilic solvent in
16 ies of peptides from TFE/H2O mixtures (TFE = 2,2, 2-trifluoroethanol) back to water, the thermal unfo
17 f ImmE1 is approximately 80% in 1-butanol or 2,2,2-trifluoroethanol, consistent with a previous membr
18 oved by omission of the four data points for 2,2,2-trifluoroethanol-ethanol mixtures (F-test value fr
22 )3, prepared from readily available B2O3 and 2,2,2-trifluoroethanol, is as an effective reagent for t
23 detected by laser flash photolysis (LFP) in 2,2,2-trifluoroethanol (lambda = 580 nm, tau = 690 +/- 1
24 l chloride (2) in aqueous methanol, ethanol, 2,2,2-trifluoroethanol, n-propyl alcohol, isopropyl alco
25 anol-O-d (26 ps), 2-propanol-OD (40 ps), and 2,2,2-trifluoroethanol-O-d (14 ps) are longer than those
26 n donors (methanol, 2-methyl-2-propanol, and 2,2,2-trifluoroethanol) on SmI2-initiated 5-exo-trig ket
27 h NAD(+) and unreactive substrate analogues, 2,2,2-trifluoroethanol or 2,3,4,5,6-pentafluorobenzyl al
28 egions that promote aggregation in 25% (v/v) 2,2,2 trifluoroethanol (TFE) are different from those th
29 ubstrate, and this is facilitated by solvent 2,2,2-trifluoroethanol (TFE) acting as a proton shuttle.
30 1,1,1,3,3,3-hexafluoroisopropanol (HFIP) and 2,2,2-trifluoroethanol (TFE) as reaction media is descri
32 ed state of hen lysozyme formed in 60% (v/v) 2,2,2-trifluoroethanol (TFE) has been studied using hydr
33 ted proteins in aqueous solutions containing 2,2,2-trifluoroethanol (TFE) have shown that the formati
37 accomplished with Dowex 1 x 2 (CF3CH2O-) in 2,2,2-trifluoroethanol (TFE) or lithium trifluoroethoxid
38 )N-HSQC spectra of IA(3) in water and in 23% 2,2,2-trifluoroethanol (TFE) shows that the individual r
39 s been investigated in aqueous buffer and in 2,2,2-trifluoroethanol (TFE) using CD and NMR spectrosco
40 ts a helical conformation in the presence of 2,2,2-trifluoroethanol (TFE), a solvent known to stabili
41 s of helix-stabilizing cosolvents, including 2,2,2-trifluoroethanol (TFE), on the thermodynamics and
45 ies were recorded in the solvent system (40% 2,2,2-Trifluoroethanol (TFE)/water), which gave the larg
46 re reported for solvolyses in acetone/water, 2,2,2-trifluoroethanol(TFE)/water, and TFE/ethanol mixtu
47 as decreased markedly in the presence of 50% 2,2,2-trifluoroethanol, which causes loss of tertiary st
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