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1 ion of the FAAH inhibitor methyl arachidonyl fluorophosphonate.
2 e blunted by the inhibitor methylarachidonyl fluorophosphonate.
3 ifluoromethyl ketone, and methyl arachidonyl fluorophosphonate.
4 in the presence of only methyl arachidonoyl fluorophosphonate.
5 ss to gamma-substituted derivatives of alpha-fluorophosphonates.
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
10 and PA were inhibited by methylarachidonoyl-fluorophosphonate, an inhibitor of Groups IV and VI PLA2
11 d the covalent inhibitor methyl arachidonoyl fluorophosphonate and located regions in the protein tha
12 hospholipase A inhibitor, methyl arachidonyl fluorophosphonate, and SDS-polyacrylamide gel electropho
14 ]CPO and the activity-based proteomic probes fluorophosphonate-biotin and fluorophosphonate-rhodamine
15 with 3,4-dichloroisocoumarin and diisopropyl fluorophosphonate, both mechanism-based inhibitors for t
16 ease is also inhibited by methyl arachidonyl fluorophosphonate but not by bromoenol lactone, indicati
17 eased substantially when methyl arachidonoyl fluorophosphonate, but not bromoenol lactone, was added,
18 group IV PLA(2) inhibitor methylarachidonyl fluorophosphonate, but not effectively by the group VI P
19 e Group IV PLA2 inhibitor methyl arachidonyl fluorophosphonate, confirming the important role for Gro
20 mpair inhibition of MAGL, especially that by fluorophosphonate derivatives (13- to 63-fold reduction
21 ensin II, bradykinin, anti-PRCP, diisopropyl-fluorophosphonate (DFP), phenylmethylsulfonyl fluoride (
22 ive structure and a complex with diisopropyl fluorophosphonate (DFP, a potent serine hydrolase inhibi
23 ivities in complex proteomes, a biotinylated fluorophosphonate (FP-biotin) was recently synthesized a
25 ucleophile reactive inhibitor, ethoxy oleoyl fluorophosphonate, identified S241 as the enzyme's catal
27 troduction of CF(2) and CFH in complex alpha-fluorophosphonates led to the synthesis of a fluorine-co
30 inding in the presence of methyl arachidonyl fluorophosphonate (MAFP), an irreversible active site in
31 alpha) inhibitors (10 muM methyl-arachidonyl fluorophosphonate [MAFP] or 20 muM arachidonyl trifluoro
33 t, the substrate specificity for diisopropyl fluorophosphonate (P-F bond) was substantially decreased
37 ate profiles, amide/ester selectivities, and fluorophosphonate reactivities of these mutants revealed
38 ehyde with sulfone-stabilized phosphonate or fluorophosphonate reagents followed by stannyldesulfonyl
40 roteomic probes fluorophosphonate-biotin and fluorophosphonate-rhodamine, mouse brain CPO-BP is ident
41 id release, the data using methylarachidonyl fluorophosphonate suggest a key role for the cPLA2 in th
43 s/metastasis in vivo, and methyl arachidonyl fluorophosphonate was highly effective in inhibiting EOC
44 2) irreversible inhibitor methyl-arachidonyl fluorophosphonate, we were able to isolate structural ch
45 covalent adduct between GlpG and diisopropyl fluorophosphonate, which mimics the oxyanion-containing
46 roup IV cPLA(2) inhibitor methyl arachidonyl fluorophosphonate, which we have previously found to blo
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