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3 ompared against alpha-naphthyl acetate and 4-methylumbelliferyl acetate for their ability to detect h
4 tant enzyme was shown to rapidly hydrolyse 4-methylumbelliferyl acetate in paraoxon-treated cells, wh
5 r catalytic efficiencies for hydrolysis of 4-methylumbelliferyl acetate, heroin, and 6-monoacetylmorp
6 group of cocaine and the acetyl groups of 4-methylumbelliferyl acetate, heroin, and 6-monoacetylmorp
7 nd two of these, alpha-napthyl acetate and 4-methylumbelliferyl acetate, identified an esterase of ap
10 activity for a fluorogenic substrate, 2'-(4-methylumbelliferyl)-alpha-D-N-acetylneuraminic acid (4-M
11 ed with a fluorometric assay using the 2'-(4-methylumbelliferyl)-alpha-D-N-acetylneuraminic acid (MUN
12 uorometric enzyme assay (FA) 1 (FA-1), 2'-(4-methylumbelliferyl)-alpha-D-N-acetylneuraminic acid (MUN
13 yranoside 6-phosphate (pNP alphaGlc6P) and 4-methylumbelliferyl-alpha-D-glucopyranoside 6-phosphate (
14 yl-alpha-D-glucopyranoside 6-phosphate and 4-methylumbelliferyl-alpha-D-glucopyranoside 6-phosphate w
15 96-kD protein, but it was not active with 4-methylumbelliferyl-alpha-D-glucopyranoside as the substr
19 Oase, we have carried out the synthesis of 4-methylumbelliferyl-alpha-KDO (alpha-KDO-MU) by conjugati
21 against fluorogenic substrates, chitobiose-4-methylumbelliferyl and chitotriose-4-methylumbelliferyl,
22 biose-4-methylumbelliferyl and chitotriose-4-methylumbelliferyl, and enhances activity against chitoo
24 sensitive than the commonly used substrate 4-methylumbelliferyl beta-d-galactopyranoside (MUG), for t
28 opyranoside-6-phosphate (pNPbetaGlc6P) and 4-methylumbelliferyl-beta-D-glucopyranoside-6-phosphate (4
29 pyrrolidonyl-beta-naphthylamide (PYR), and 4-methylumbelliferyl-beta-D-glucuronide (MUG) was evaluate
30 -N,N'-diacetylchitobioside (MUF-diNAG) and 4-methylumbelliferyl-beta-D-N,N',N"-triacetylchitotrioside
31 drolyse the artificial lysozyme substrate, 4-methylumbelliferyl-beta-D-N,N',N''-triacetylchitotriosid
32 tern of activity toward the chitin analogs 4-methylumbelliferyl-beta-D-N,N'-diacetylchitobioside (MUF
33 to alanine or when cells were treated with 4-methylumbelliferyl-beta-d-xylopyranoside or chlorate to
34 face proteoglycans by a 72-h incubation in 4-methylumbelliferyl-beta-D-xyloside did not attenuate the
35 with inhibitors of proteoglycan synthesis (4-methylumbelliferyl-beta-D-xyloside) or sulfation (sodium
36 presence of a stimulator of CS synthesis, 4-methylumbelliferyl-beta-D-xyloside, reduced the amount o
37 s anticipated that similar thio-containing 4-methylumbelliferyl compounds will have applications in s
38 indicate that 7-diethylphospho-6,8-difluor-4-methylumbelliferyl (DEPFMU) is hydrolyzed specifically b
39 ees) describing the interaction of E2 with 4-methylumbelliferyl glycosides, determined by titrating t
42 GH18(C) releases methylumbelliferone from 4'-methylumbelliferyl-N,N',N"-triacetylchitotriose 2.7-fold
43 uorescently labelled inhibitor, MeU-diNAG (4-methylumbelliferyl-N,N'-diacetyl-beta-D-chitobioside).
44 H18(N)) releases methylumbelliferone from 4'-methylumbelliferyl-N,N'-diacetylchitobiose 13.6-fold fas
46 me : ligand dissociation constants for three methylumbelliferyl oligosaccharides and cellotriose show
48 we found that one substrate, 6,8-difluoro-4-methylumbelliferyl phosphate (DiFMUP), was much improved
49 is of a fluorogenic substrate-6,8-difluoro-4-methylumbelliferyl phosphate (DiFMUP)-with a microplate
51 activity when measured using 6,8-difluoro-4-methylumbelliferyl phosphate as a fluorogenic substrate.
52 d by the dephosphorylation of 6,8-difluoro-4-methylumbelliferyl/phosphate to a fluorescent 6,8-difluo
54 inophen sulfate (AS) and glucuronide (AG), 4-methylumbelliferyl sulfate (4MUS) and glucuronide (4MUG)
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