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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 the sarin nerve agent surrogate, diisopropyl fluorophosphate.
7 monoesters or charged phosphate diesters and fluorophosphates.
8      Purified PKA was blocked by diisopropyl fluorophosphate (1 mm), phenylmethylsulfonyl fluoride (3
9                           Methyl arachidonyl fluorophosphate (50 microm) also significantly inhibited
10  PD 98059, SB 203580, and methyl arachidonyl fluorophosphate (a specific cPLA(2) inhibitor).
11 y exposure to 100 mumol/l methyl arachidonyl fluorophosphate, a cPLA(2) inhibitor.
12                           Methyl arachidonyl fluorophosphate, a cPLA2 inhibitor, inhibited the effect
13      The enzyme was inhibited by diisopropyl fluorophosphate, a general serine class inhibitor, and m
14    All enzymes were inhibited by diisopropyl fluorophosphate, a general serine class inhibitor.
15                                  Diisopropyl fluorophosphate, a transition-state analog inhibitor of
16 ncluding bromoenolactone, methyl arachidonyl fluorophosphate, AACOCF(3), 7,7-dimethyl-5,8-eicosadieno
17 rombin by hirudin and trypsin by diisopropyl fluorophosphate abolished the observed RhoA activation.
18 roup IV cPLA2 inhibitors (methyl arachidonyl fluorophosphate and methyl trifluoromethyl ketone), but
19  completely prevented by methyl-arachidonoyl-fluorophosphate and palmostatin B, and partially prevent
20 l ester (URB602) and MAFP (methylarachidonyl fluorophosphate)] and is unaffected by inhibitors of COX
21 could be affinity-labeled by [3H]diisopropyl fluorophosphate, but the proteolytically inactive 97-kDa
22 hyl)benzenesulfonyl fluoride and diisopropyl fluorophosphate completely inhibited Abeta degradation.
23 ide as fluorine sources, we prepared over 30 fluorophosphate-containing nucleotides, varying in nucle
24 cluding celecoxib, rofecoxib and diisopropyl fluorophosphate, demonstrate a distribution of compound
25                                  Diisopropyl fluorophosphate (DFP) causes neurotoxicity related to an
26 allenging leaving groups such as diisopropyl fluorophosphate (DFP) or venomous agent X, creating a ma
27  The irreversible AChE inhibitor diisopropyl fluorophosphate (DFP) usually caused a sustained increas
28                                  Diisopropyl fluorophosphate (DFP) was used as a nerve gas mimic.
29  The addition of a CE inhibitor, diisopropyl fluorophosphate (DFP), to mouse serum in vitro significa
30 teins evoked by the OP compound, diisopropyl fluorophosphate (DFP).
31  agent organophosphate substrate diisopropyl fluorophosphate (DFP).
32 thrombin (reversed with inactive diisopropyl-fluorophosphate [DFP]-thrombin) and mediated via the pro
33 ylammonium fluoride, fluoromonophosphate, or fluorophosphate imidazolide as fluorine sources, we prep
34                                        Using fluorophosphate imidazolide as fluorophosphorylating rea
35 h a serine proteinase inhibitor, diisopropyl fluorophosphate, indicated that they were active serine
36 ion of the properties of some of these metal fluorophosphates is reported, including reductive lithiu
37        The new and unusual features of these fluorophosphate materials include interlayer spaces or c
38 s, as exemplified by studying interaction of fluorophosphate mRNA cap analogues with eukaryotic trans
39                                We found that fluorophosphate nucleotide analogues can be used to moni
40  developed a new method for the synthesis of fluorophosphate (oligo)nucleotide analogues containing a
41 inhibition of enzyme activity by diisopropyl fluorophosphate or phenylmethylsulfonyl fluoride imply t
42 hieve deactivation, 5 x 10(-7) M diisopropyl fluorophosphate, or the neutrophil immobilizing factor (
43                              14C-Diisopropyl fluorophosphate-radiolabeled CM from MP24.15-overexpress
44 is technology using an activity-based probe (fluorophosphate) that is specific for serine hydrolases.
45                                  Diisopropyl fluorophosphate, which inhibits NTE esterase activity, r
46 by the serine esterase inhibitor diisopropyl fluorophosphate, which specifically and stoichiometrical
47 mily of mid-late first row, transition metal fluorophosphates with 50 new compounds identified to dat