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1 en oxidation in both free acid and ibuprofen ester form.
2  and most of the Ubc2 was found in the thiol ester form.
3 ments either in its triacylglycerol or ethyl ester form.
4 ll as their acetyl, p-coumaroyl and caffeoyl ester forms.
5 cited state for the p-coumaroyl and caffeoyl ester forms.
6 itatively converts carboxylic acids to their ester forms.
7  that GB contains some polyprenols in acetic esters' form.
8 sed inhibitor, and the phosphate/phosphonate esters form adducts that mimic intermediates formed in r
9                                       3-MCPD esters form approximately 2-5 times faster from diacylgl
10  incubating the cells with the acetoxymethyl ester forms (benz2 AM or BAPTA AM).
11 ne-glutathione conjugate and suggest that an ester forms between the lactone and Ser-47.
12                                    Likewise, ester forms, but not carboxylic acid forms, of other mem
13 ss ratios of cholesterol ester to sitosterol ester formed by ACAT1 and ACAT2 were 1.6 and 7.2, respec
14 y unusual hydrolysis pathway from a putative ester, formed by the conjugation of raloxifene diquinone
15 fy conditions in which short-lived activated esters formed by the aqueous carbodiimide EDC promote is
16     The hydrosilyl-containing alkyl boronate esters formed by this method undergo transformations sel
17 ding an evolutionary link between amide- and ester-forming condensation enzymes.
18 on of alpha,beta-enals to racemic alpha-keto esters, forming gamma-butyrolactones with three contiguo
19 rein, we detail the development of a general ester-forming haloform coupling reaction using one equiv
20  Reductive conversion of the protected amino esters forms highly functionalized cyclopentyl beta-amin
21  rapidly taken up and converted to its inert ester form in peripheral tissues, such as lung, whereas
22 more than 90% of Ubc9 was found in the thiol ester form in the bFGF-treated explants.
23 ound that it is possible to assay ALA in the ester form in the concentration ranges: 5.10(-6)-1.10(-4
24 ion of a quinone structure, while the phenyl ester formed in bulk polymerization reactions was not de
25 nitroxide with the B-n-butylcatecholboronate ester formed in situ from urushiol and B-n-butylboronic
26 or confirmation of the identity of TAA fatty esters formed in BEAS-2B cells was obtained via selected
27 ions are reported of the heteroaryl boronate esters formed in situ, demonstrating the usefulness of t
28 ecificity by first analyzing the cholesteryl esters formed in the presence of symmetric PCs labeled a
29 dition, (1)H NMR data suggest that the ethyl esters form inclusion complexes with beta-cyclodextrin.
30                     The fact that amides and esters form less stable enolates than ketones might be s
31 report the synthesis of cyclophanes 18-20 by ester-forming macrocyclization reactions of diols 15 and
32            Hexyl-5-aminolevulinic acid is an ester form of 5-aminolevulinic acid with improved uptake
33 cyl chemistry, to study the behavior of this ester form of Abeta42 itself at neutral pH.
34 ng intracellular Ca2+ with the acetoxymethyl ester form of BAPTA (BAPTA AM).
35 naline, OAG, PDBu, CPA and the acetoxymethyl ester form of BAPTA (BAPTA-AM) was markedly inhibited by
36 ty evoked by either CPA or the acetoxymethyl ester form of BAPTA (BAPTA-AM).
37 ng intracellular Ca2+ with the acetyl methyl ester form of BAPTA, shortened the action potential and
38 e attributed to the use of the acetoxymethyl ester form of fura-2 to report [Ca2+]i, and that the ste
39 in which the membrane permeant acetoxymethyl ester form of fura-2 was used.
40 et or cat were loaded with the acetoxymethyl ester form of indo-1 (indo-1 AM) such that approximately
41           These were hydrolyzed to the ethyl ester form of the Taxol side chain enantiomers under aci
42 creased approximately twofold, and the thiol ester form of Ubc1 increased approximately threefold on
43 yltransferase activity sequesters retinol in ester form, preventing synthesis of retinoic acid, a cof
44         The mutant protein is trapped in the ester form, providing clear evidence for the structure o
45 monas lemoignei in organic media to catalyze ester-forming reactions was investigated.
46                        The quinoline boronic ester formed undergoes a range of important transformati
47  the proportions of Ubc3 and -7 in the thiol ester form were significantly higher in the bFGF-treated
48 and glycoside forms and syringic acid in the ester form were the major phenolic acids, and the major
49 ), seven hydroxylated metabolites, and three ester forms were separated in a single 8.0 min run using
50                      Both oils were in ethyl ester form, with the fish oil providing 0.88 g/d eicosap