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1 elf-assembled monolayer of 2-(perfluorodecyl)ethanethiol.
2  than the other in competitive adsorption by ethanethiol.
3 tion of a phosphoprotein by beta-elimination/ethanethiol addition and conversion of phosphoserine and
4  previously reported, followed by sulfite or ethanethiol addition.
5  Bn, Et(2)N(CH(2))(2)] and N-(2-dialkylamino)ethanethiol [alkyl = X = Et, Bu, morpholinyl] using Sn(2
6 modified with sodium borohydride followed by ethanethiol, allowing the differentiation of the thioeth
7  PEG compounds decomposed in the presence of ethanethiol and hydroxide ion.
8 eagent 1 provides the dual readouts of odor (ethanethiol) and fluorescence (derivative of 7-hydroxyco
9 , diethyl phosphoramidate, and 2-(butylamino)ethanethiol) and one S-type vesicant simulant (2-chloroe
10 level of sulfur compounds (dimethyl sulfide, ethanethiol), and ester and alcohol compounds associated
11 d(-1)), consisting of a mix of methanethiol, ethanethiol, and propanethiol.
12 of the phosphopeptides in 0.52 N NaOH/1.36 M ethanethiol at 50 degrees C for 18 h or for even as shor
13            The results show that ethanol and ethanethiol both adsorb via Ch-H dissociation at 310 K,
14 horylated tryptic peptide in the presence of ethanethiol converted the phosphoserine residue to S-eth
15                              2-(Diethylamino)ethanethiol (DEAET) and 2-(dimethylamino)ethanethiol (DM
16 ylamino)ethanethiol (DMAET), 2-(diethylamino)ethanethiol (DEAET), and 2-mercaptoethanol (ME) with o-p
17 aining organic molecules, including ethanol, ethanethiol, diethyl ether, and diethyl sulfide, at the
18  derivatization reaction of 2-(dimethylamino)ethanethiol (DMAET), 2-(diethylamino)ethanethiol (DEAET)
19 ino)ethanethiol (DEAET) and 2-(dimethylamino)ethanethiol (DMAET), the thiol-containing hydrolysis pro
20 hydrogen sulfide (H2S), methanethiol (MeSH), ethanethiol (EtSH), and dimethyl sulfide (DMS) were asse
21 is designated WR-1065 [2-((aminopropyl)amino)ethanethiol] exerts its cytoprotective effects in part v
22             Phosphopeptide modification with ethanethiol, followed by LC QIT-MS/MS, identified four p
23 dition of exogenous imidazole, pyridine, and ethanethiol has no measurable effect on the functional p
24 ynthesis was about 20% for 40 mM S-glyceroyl-ethanethiol in 2,6-lutidine and imidazole buffers near n
25 n of aromatic methyl ethers, 2-(diethylamino)ethanethiol, is reported.
26  over the use of more common thiols, such as ethanethiol, is the easy extraction of both the deprotec
27 Siso)2(L1)] (PSiso = 2-(diisopropylphosphino)ethanethiol; L1 = pyrrolidine dithiocarbamate) was deter
28  treatment with dimethyl disulfide or thiol (ethanethiol or thiocresol) gives anomerically pure thiog
29 t best 0.6% of the CoM-dependent rate, while ethanethiol, propanethiol, glutathione, homocysteine, an
30 ished wines from these mutants, three VSCs - ethanethiol, S-ethyl thioacetate and diethyl disulfide -
31 nous ligands such as imidazole, pyridine, or ethanethiol, suggesting that the axial ligand to the spe
32 ividual binding of CoM, ethanesulfonate, and ethanethiol were determined and used to assess the contr
33 teine, cysteamine, and 2-[(aminopropyl)amino]ethanethiol (WR-1065) were synthesized by condensing the
34 ation of the glyceroyl thioester S-glyceroyl-ethanethiol yielded oligoglyceric acid.

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