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1 main, which was labeled by [(3)H]diisopropyl fluorophosphate.
2 rifluoromethyl ketone and methyl arachidonyl fluorophosphate.
3 bound the active-site inhibitor diisopropyl fluorophosphate.
4 ssical serine protease inhibitor diisopropyl fluorophosphate.
5 e-protease inhibitors, including diisopropyl fluorophosphate.
14 ncluding bromoenolactone, methyl arachidonyl fluorophosphate, AACOCF(3), 7,7-dimethyl-5,8-eicosadieno
15 rombin by hirudin and trypsin by diisopropyl fluorophosphate abolished the observed RhoA activation.
16 roup IV cPLA2 inhibitors (methyl arachidonyl fluorophosphate and methyl trifluoromethyl ketone), but
17 completely prevented by methyl-arachidonoyl-fluorophosphate and palmostatin B, and partially prevent
18 l ester (URB602) and MAFP (methylarachidonyl fluorophosphate)] and is unaffected by inhibitors of COX
19 could be affinity-labeled by [3H]diisopropyl fluorophosphate, but the proteolytically inactive 97-kDa
20 hyl)benzenesulfonyl fluoride and diisopropyl fluorophosphate completely inhibited Abeta degradation.
21 ide as fluorine sources, we prepared over 30 fluorophosphate-containing nucleotides, varying in nucle
22 cluding celecoxib, rofecoxib and diisopropyl fluorophosphate, demonstrate a distribution of compound
24 allenging leaving groups such as diisopropyl fluorophosphate (DFP) or venomous agent X, creating a ma
25 The irreversible AChE inhibitor diisopropyl fluorophosphate (DFP) usually caused a sustained increas
27 The addition of a CE inhibitor, diisopropyl fluorophosphate (DFP), to mouse serum in vitro significa
30 thrombin (reversed with inactive diisopropyl-fluorophosphate [DFP]-thrombin) and mediated via the pro
31 ylammonium fluoride, fluoromonophosphate, or fluorophosphate imidazolide as fluorine sources, we prep
33 h a serine proteinase inhibitor, diisopropyl fluorophosphate, indicated that they were active serine
34 ion of the properties of some of these metal fluorophosphates is reported, including reductive lithiu
36 s, as exemplified by studying interaction of fluorophosphate mRNA cap analogues with eukaryotic trans
38 developed a new method for the synthesis of fluorophosphate (oligo)nucleotide analogues containing a
39 inhibition of enzyme activity by diisopropyl fluorophosphate or phenylmethylsulfonyl fluoride imply t
40 hieve deactivation, 5 x 10(-7) M diisopropyl fluorophosphate, or the neutrophil immobilizing factor (
42 is technology using an activity-based probe (fluorophosphate) that is specific for serine hydrolases.
44 by the serine esterase inhibitor diisopropyl fluorophosphate, which specifically and stoichiometrical
45 mily of mid-late first row, transition metal fluorophosphates with 50 new compounds identified to dat
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