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1  in the presence of only methyl arachidonoyl fluorophosphonate.
2 ion of the FAAH inhibitor methyl arachidonyl fluorophosphonate.
3 e blunted by the inhibitor methylarachidonyl fluorophosphonate.
4 ifluoromethyl ketone, and methyl arachidonyl fluorophosphonate.
5 ss to gamma-substituted derivatives of alpha-fluorophosphonates.
6                           Methyl arachidonyl fluorophosphonate (5 micromol/L), a dual inhibitor of i
7 on had been blocked using methyl arachidonyl fluorophosphonate, a nonselective inhibitor of 2-AG hydr
8 TCDD is clearly blocked by methylarachidonyl fluorophosphonate, a specific inhibitor of cPLA2, short
9         Its inhibition by methyl arachidonyl fluorophosphonate abrogates the AGE-enhanced activated n
10          In this study, we developed a novel fluorophosphonate activity-based protein profiling (ABPP
11  and PA were inhibited by methylarachidonoyl-fluorophosphonate, an inhibitor of Groups IV and VI PLA2
12 d the covalent inhibitor methyl arachidonoyl fluorophosphonate and located regions in the protein tha
13 hospholipase A inhibitor, methyl arachidonyl fluorophosphonate, and SDS-polyacrylamide gel electropho
14                           We have employed a fluorophosphonate-based affinity capture probe and mass
15         Competitive ABPP with broad-spectrum fluorophosphonate-based probes and specific beta-lactone
16 ntified a family of serine hydrolases termed fluorophosphonate binding hydrolases (Fphs) that play im
17  library to identify selective inhibitors of fluorophosphonate-binding serine hydrolases and lipases
18 commercially available ABPP probes including fluorophosphonate-biotin (FP-biotin) and FP-desthiobioti
19 ]CPO and the activity-based proteomic probes fluorophosphonate-biotin and fluorophosphonate-rhodamine
20 with 3,4-dichloroisocoumarin and diisopropyl fluorophosphonate, both mechanism-based inhibitors for t
21 ease is also inhibited by methyl arachidonyl fluorophosphonate but not by bromoenol lactone, indicati
22 eased substantially when methyl arachidonoyl fluorophosphonate, but not bromoenol lactone, was added,
23  group IV PLA(2) inhibitor methylarachidonyl fluorophosphonate, but not effectively by the group VI P
24 e Group IV PLA2 inhibitor methyl arachidonyl fluorophosphonate, confirming the important role for Gro
25 mpair inhibition of MAGL, especially that by fluorophosphonate derivatives (13- to 63-fold reduction
26 ensin II, bradykinin, anti-PRCP, diisopropyl-fluorophosphonate (DFP), phenylmethylsulfonyl fluoride (
27 ive structure and a complex with diisopropyl fluorophosphonate (DFP, a potent serine hydrolase inhibi
28 ivities in complex proteomes, a biotinylated fluorophosphonate (FP-biotin) was recently synthesized a
29  samples to enrich serine hydrolases using a fluorophosphonate (FP2) activity-based probe.
30 ucleophile reactive inhibitor, ethoxy oleoyl fluorophosphonate, identified S241 as the enzyme's catal
31                                            A fluorophosphonate inhibitor of FAAH containing a photoac
32 troduction of CF(2) and CFH in complex alpha-fluorophosphonates led to the synthesis of a fluorine-co
33            The cPLA(2) inhibitor arachidonyl fluorophosphonate (MAFP) and the COX-2 inhibitor NS-398
34                           Methyl arachidonyl fluorophosphonate (MAFP), a specific anandamide amidase
35 inding in the presence of methyl arachidonyl fluorophosphonate (MAFP), an irreversible active site in
36 alpha) inhibitors (10 muM methyl-arachidonyl fluorophosphonate [MAFP] or 20 muM arachidonyl trifluoro
37                            We used hexadecyl fluorophosphonate or palmostatin B to inhibit enzymes in
38 t, the substrate specificity for diisopropyl fluorophosphonate (P-F bond) was substantially decreased
39 d to a susceptible Anopheles gambiae strain, fluorophosphonate probe profiling with pirimiphos-methyl
40  proteomes by a single, active site-directed fluorophosphonate probe.
41 ide and larger protein substrates and bind a fluorophosphonate probe.
42 in asexual B. divergens using a biotinylated fluorophosphonate probe.
43 ate profiles, amide/ester selectivities, and fluorophosphonate reactivities of these mutants revealed
44 ehyde with sulfone-stabilized phosphonate or fluorophosphonate reagents followed by stannyldesulfonyl
45       By reacting this probe, a biotinylated fluorophosphonate referred to as FP-biotin, with crude t
46 roteomic probes fluorophosphonate-biotin and fluorophosphonate-rhodamine, mouse brain CPO-BP is ident
47 form and reacted with a structurally precise fluorophosphonate substrate mimic that identify the comp
48 id release, the data using methylarachidonyl fluorophosphonate suggest a key role for the cPLA2 in th
49 se by affinity labelling with a biotinylated fluorophosphonate suicide substrate.
50 s/metastasis in vivo, and methyl arachidonyl fluorophosphonate was highly effective in inhibiting EOC
51 2) irreversible inhibitor methyl-arachidonyl fluorophosphonate, we were able to isolate structural ch
52 covalent adduct between GlpG and diisopropyl fluorophosphonate, which mimics the oxyanion-containing
53 roup IV cPLA(2) inhibitor methyl arachidonyl fluorophosphonate, which we have previously found to blo