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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.
6      Purified PKA was blocked by diisopropyl fluorophosphate (1 mm), phenylmethylsulfonyl fluoride (3
7                           Methyl arachidonyl fluorophosphate (50 microm) also significantly inhibited
8  PD 98059, SB 203580, and methyl arachidonyl fluorophosphate (a specific cPLA(2) inhibitor).
9 y exposure to 100 mumol/l methyl arachidonyl fluorophosphate, a cPLA(2) inhibitor.
10                           Methyl arachidonyl fluorophosphate, a cPLA2 inhibitor, inhibited the effect
11      The enzyme was inhibited by diisopropyl fluorophosphate, a general serine class inhibitor, and m
12    All enzymes were inhibited by diisopropyl fluorophosphate, a general serine class inhibitor.
13                                  Diisopropyl fluorophosphate, a transition-state analog inhibitor of
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
23                                  Diisopropyl fluorophosphate (DFP) causes neurotoxicity related to an
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
26                                  Diisopropyl fluorophosphate (DFP) was used as a nerve gas mimic.
27  The addition of a CE inhibitor, diisopropyl fluorophosphate (DFP), to mouse serum in vitro significa
28 teins evoked by the OP compound, diisopropyl fluorophosphate (DFP).
29  agent organophosphate substrate diisopropyl fluorophosphate (DFP).
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
32                                        Using fluorophosphate imidazolide as fluorophosphorylating rea
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
35        The new and unusual features of these fluorophosphate materials include interlayer spaces or c
36 s, as exemplified by studying interaction of fluorophosphate mRNA cap analogues with eukaryotic trans
37                                We found that fluorophosphate nucleotide analogues can be used to moni
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 (
41                              14C-Diisopropyl fluorophosphate-radiolabeled CM from MP24.15-overexpress
42 is technology using an activity-based probe (fluorophosphate) that is specific for serine hydrolases.
43                                  Diisopropyl fluorophosphate, which inhibits NTE esterase activity, r
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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