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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
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
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
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.
31 report the synthesis of cyclophanes 18-20 by ester-forming macrocyclization reactions of diols 15 and
35 naline, OAG, PDBu, CPA and the acetoxymethyl ester form of BAPTA (BAPTA-AM) was markedly inhibited by
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
40 et or cat were loaded with the acetoxymethyl ester form of indo-1 (indo-1 AM) such that approximately
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
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