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1 m by which donor-acceptor norbornene systems epimerize.
2 ly dynamic stereocenters that can be readily epimerized.
3 e related 1-(4-nitrophenyl) cis diastereomer epimerized.
4 lyketide synthase (PKS) modules that produce epimerized (2S)-2-methyl-3-ketoacyl-ACP (acyl carrier pr
5  that are implicated in the generation of C2-epimerized (2S)-2-methyl-3-ketoacyl-ACP intermediates.
6  to give a carbapenam, which is subsequently epimerized and desaturated to give a carbapenem in a Car
7                     Erythrose 4-phosphate is epimerized and/or isomerized to threose 4-phosphate, whi
8                          Lewis acids rapidly epimerize aniline-substituted D-A cyclopropanes through
9 roposed alginate biosynthetic scaffold while epimerizing approximately every second d-mannuronate res
10 or example, 2-ketothiazoles 4 and 59 readily epimerize at pH 7.4, although they are fairly stable ste
11  the presence of weak acids, these complexes epimerize at the stereogenic carbon bonded to palladium.
12                    Monomeric Fapy-dA readily epimerized at 25 degrees C in phosphate buffer (pH 7.5).
13     The 1-(4-methoxyphenyl) cis diastereomer epimerized at a much faster rate into the corresponding
14               2-epi-5-epi-Valiolone is first epimerized at C-2 to give 5-epi-valiolone and then dehyd
15  In the presence of serum, rustmicin rapidly epimerizes at the C-2 position and is converted to a gam
16 strong C=N -> B(pin) coordination, would not epimerize before conversion to the derived ketone by hyd
17 Ala; and (iii) a small group of enzymes that epimerize cationic dipeptides.
18 nding macrolactones, while pentaketides with epimerized chiral centers were poorly processed by PikAI
19 panation, followed by ester hydrolysis under epimerizing conditions.
20 cluding one from Cytophaga hutchinsonii that epimerizes D-Ala-D-Ala; and (iii) a small group of enzym
21 the enolase superfamily that are involved in epimerizing dipeptides.
22 etase that synthesizes HC-toxin has only one epimerizing domain for conversion of L-Pro to D-Pro; the
23  from L-Phe but unimpaired from D-Phe; N975A epimerizes faster than Y976A from L-Phe.
24 g on a variety of animal-derived sulfated or epimerized GAGs.
25                                          The epimerized hexaketide failed to undergo cyclization and
26 m molecular dynamics simulations showing the epimerized hexaketide was accommodated within the Pik TE
27 gain-of-function processing of an unnatural, epimerized hexaketide.
28                        These lesions readily epimerize in water, an unusual property for nucleosides.
29 ydroxyl group, while the C2-methyl group was epimerized in a late stage of the synthesis.
30 stitution on the cyclohexanone ring was then epimerized into its thermodynamically stable cis counter
31 he holo-thiolation (holo-T) domain, and then epimerizing it (by epimerization domain) to the D-Phe-S-
32 n observed for parallel incubations using an epimerizing ketoreductase domain and the nonepimerizing
33 hydroxypentanoyl-SACP ([2-(2)H]-1a) with the epimerizing ketoreductase domain EryKR1 in the presence
34 -methyl-3-hydroxypentanoyl-SACP with the non-epimerizing ketoreductase domains EryKR6 and TylKR1, res
35 in (Pik) system, preventing the formation of epimerized macrolactones.
36 Synthesis of an analogous hexaketide with an epimerized nucleophilic hydroxyl group allowed for direc
37 by a conrotatory [6pai] photocyclization but epimerized on silica to cis-hexahydrocarbazol-4-ones (14
38 hile not required for recognition, cannot be epimerized or substituted.
39 nt-derived deuterium resides solely with the epimerized product (not substrate) in isomerizations car
40  fragments include more heavily sulfated and epimerized regions and, as with the endothelial HS chain
41 peptides that differ only by the presence of epimerized residues.
42 teins differ drastically in their ability to epimerize RS to RR and in their stereoselectivity when r
43 imerization although DdahC preferred the pre-epimerized substrate and identified T110 and H180 as imp
44 contraction step being performed on a double epimerized substrate.
45 acterize a line of knockout mice that cannot epimerize the 3beta-hydroxyl group of cholesterol and as
46 ility of the E domain in the TycB3 module to epimerize the aminoacyl thioester Phe-S-TycB3 and the di
47 ycle, and two RaS enzymes, which selectively epimerize the beta-carbon of threonine and desaturate hi
48 include kinetic protonation of an enolate to epimerize the C7 stereocenter and a stereoconvergent epo
49                    The PchE subunit does not epimerize the Cys-S-enzyme intermediate, but once amide
50          While the initiation module clearly epimerizes the aminoacyl thioester Phe1-S-TycA intermedi
51 f-life to longer than 24 hours and some EGCG epimerized to (+)-gallocatechin-3-gallate.
52 idine ring but in the pentose ring, which is epimerized to arabinose in the minor product.
53          The 19-epi-isomer is also partially epimerized to arborisidine upon preparative TLC purifica
54 ing-fused perhydroquinoline 15 that could be epimerized to its trans-fused counterpart 2 on sequentia
55 hanistic probe 5-fluorouridine that had been epimerized to the arabino isomer suggested that the Psi
56 driven process, the cis-piperidionone 16a is epimerized to the desired trans isomer 16b, which is dir
57 he mixture of the anti and syn diastereomers epimerized to the syn hydroxy ester during the oxido-red
58 ng the GalNAc salvage pathway, UDP-GalNGc is epimerized to UDP-GlcNGc, which might compete with the e
59 ylglucosamine (UDP-GlcNAc) precursor that is epimerized to UDP-N-acetylmannosamine (UDP-ManNAc) and t
60  biosynthetic enzymes to UDP-GalNAz and then epimerized to UDP-N-azidoacetylglucosamine (GlcNAz).
61 acturonate and UDP-D-glucuronate but did not epimerize UDP-D-Glc or UDP-D-Xyl.
62 t of Escherichia coli, and has been shown to epimerize UDP-galactose to UDP-glucose without the addit
63 a parallel demonstration of their ability to epimerize using the conventional amide synthesis alterna