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1 bolism pathway, which led to accumulation of phenylacetate.
2 ammonia scavenger drugs sodium benzoate and phenylacetate.
3 monstrated in vivo by labeling with [1-(13)C]phenylacetate.
4 tivity to the pyruvate carboxylase inhibitor phenylacetate.
5 signals of the 13C-labeled anticancer agent phenylacetate.
6 recurrent malignant glioma were treated with phenylacetate.
7 rventional ( N -acetylcysteine and ornithine phenylacetate), 1 prognostic [ 13 C-methacetin breath te
9 leatoxin (0.5 microM) and 12-deoxyphorbol 13-phenylacetate 20-acetate (dPPA; 10 nM) potently induced
11 concept that L-ornithine and phenylbutyrate/phenylacetate act synergistically to produce sustained i
14 vatives, including the BN isostere of phenyl phenylacetate and BN1 triphenylmethane were prepared fro
15 metabolic pathways, including two pathways, phenylacetate and gamma-aminobutyric acid catabolism, wh
16 er study appears to be able to catalyze both phenylacetate and p-hydroxyphenylacetate decarboxylation
18 characterized by measuring the hydrolysis of phenylacetate and paraoxon in serum samples of 87 patien
20 ar, open-label, uncontrolled study of sodium phenylacetate and sodium benzoate therapy (Ammonul, Ucyc
21 ycle disorder and treatment with both sodium phenylacetate and sodium benzoate, in conjunction with o
23 nal/furfural for JPX, acetoin for MRE, ethyl phenylacetate and vanillin for MPX and acetaldehyde diet
24 nd branched ethyl esters, fatty acids, ethyl phenylacetate) and varietal compounds (4-mercapto-4-meth
25 ages displayed modifications in glutathione, phenylacetate, and 3-phenylpropionate metabolism, iron c
26 uctural optimization of valproate, butyrate, phenylacetate, and phenylbutyrate by coupling them with
27 r of phosphomevalonate decarboxylase, sodium phenylacetate, and the protein kinase inhibitor staurosp
29 rain degraded phenol, benzoate, biphenyl and phenylacetate as the sole sources of carbon at 2.5 M NaC
32 with an alternative route medication sodium phenylacetate/benzoate (Ucephan), or oral arginine suppl
34 ference in the mean plasma concentrations of phenylacetate between weeks 1 and 2 or between weeks 5 a
35 caceae, Lachnospiraceae, and Bacteroides and phenylacetate, butyrate, and acetate were the most influ
36 bol esters prostratin and 12-deoxyphorbol-13-phenylacetate can each induce HIV ex vivo from these lat
37 arboxylic acids by FeaB, and (in the case of phenylacetate) can be further degraded to enter central
38 alcohol, methyl 3-phenylpropionate, methyl 2-phenylacetate, cinnamaldehyde and methyl cinnamate were
40 re that quantitatively produces toluene from phenylacetate; complementary metagenomic and metaproteom
41 in vitro characterization studies of a novel phenylacetate decarboxylase from an anaerobic, sewage-de
45 13 dibutyrate (PDBu) and 12-deoxyphorbol 13-phenylacetate (dPPA) elicited a rapid, and sustained, in
46 ions of 1a with tert-butyl acetate and ethyl phenylacetate enolates resulted only in hydrodehalogenat
48 thesis, thereby detoxifying ammonia, and the phenylacetate excreting the ornithine-derived glutamine
49 te and prenylpyrophosphate pathways, indole, phenylacetate, flavonoid, cinnamoic ester govern aroma f
51 onase activity) or did not correlate at all (phenylacetate hydrolase and TBLase activities) with plas
53 acetate (I and II), isobutyrate (I and II), phenylacetate (II only), and indoleacetate (II only).
54 be fulfilled by the corresponding aryl acids phenylacetate, indoleacetate, and p-hydroxyphenylacetate
59 h its 5' and 3' ends to an alkylating agent (phenylacetate mustard) in an attempt to stabilize the tr
60 ine the antiproliferative activity of sodium phenylacetate (NaPa) against ovarian carcinoma cell line
62 nt study underlines the importance of sodium phenylacetate (NaPA), a drug approved for urea cycle dis
63 clohexen-1-yl)ethanone; terpinolene; ethyl 2-phenylacetate; naphthalene and 7 unknown compounds could
66 enzoate, alone or in combination with sodium phenylacetate or sodium phenylbutyrate, or sodium phenyl
67 -monoesters prostratin or 12-deoxyphorbol 13-phenylacetate, or for the macrocyclic lactone bryostatin
71 dy were to determine whether L-ornithine and phenylacetate/phenylbutyrate (administered as the pro-dr
73 ammonia with the ammonia scavenger ornithine phenylacetate prevented hepatocyte cell death and signif
75 n/dearomative ipso-annulation of N-(methyl-2-phenylacetate)propiolamides using arylsulfonyl radical,
76 nonresponders: 70.4 (57.0-95.5); P = 0.027], phenylacetate [responders: 0.175 (0.013-0.611) compared
77 The structural investigation of BN phenyl phenylacetate revealed the presence of a unique NH-carbo
78 between PON1 substrate specificity (paraoxon/phenylacetate substrate activity ratios) and -909g>c/Q19
79 by comparing the reactivity of benzoate and phenylacetate substrates in stoichiometric and catalytic
80 d dehalogenation of 4-bromobenzyl-2-chloro-2-phenylacetate to 4-bromobenzyl-2-phenylacetate with oran
81 ally, the regioselective addition of 2-oxo-2-phenylacetate to the least hindered side in a cis-select
82 nts were elicited by staurosporine or sodium phenylacetate treatment of LNCaP-Bcl-2 cells that overex
85 se of 400 mg/kg total body weight per day of phenylacetate was initially used and subsequently change
86 robic bacterial biosynthesis of toluene from phenylacetate was reported more than two decades ago, bu
87 ne anion 30, a synthetic equivalent of ethyl phenylacetate, was successfully employed in an alternati
88 Rate coefficients for triethyl phosphate and phenylacetate were determined using this method with k(1
89 ysophosphatidylcholines, sugar alcohols, and phenylacetates were inversely associated with LGA risk,
90 ibitor of tumor promotion 12-deoxyphorbol 13-phenylacetate, which differs only in its side chain, ind
91 nnich-type (imino-aldol) reactions of methyl phenylacetate with N-tert-butylsulfinyl imines as the ke
92 -2-chloro-2-phenylacetate to 4-bromobenzyl-2-phenylacetate with orange light in 7 h, whereas after 72
93 he increased levels of linalool oxide, ethyl phenylacetate, y-hexalactone and a-terpineol were observ