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1 ity observed with the naturally occurring C5 ethyl group.
2 inyl substituents at the 2-position of the 5-ethyl group.
3 tion and reactivation or aging on loss of an ethyl group.
4 corresponding to the presence of a methyl or ethyl group.
5 being able to differentiate a methyl from an ethyl group.
6 dem oxidation and amidation of an unreactive ethyl group.
7 the heme vinyl substituents are replaced by ethyl groups.
8 inor when propyl groups were substituted for ethyl groups.
9 hosphonate)s containing a 2-phenyl (37) or 2-ethyl group (38), were prepared as metabolically stable
11 lacement of the 4-hydroxy group of 1 with an ethyl group abolishes activity (42), but again, incorpor
12 ethyl group of R-naproxen was replaced by an ethyl group) acts as a potent AKR1C3 inhibitor that disp
13 ement of the substrate's methoxy groups with ethyl groups affords a statistical 3:1 (anti,syn:syn,syn
14 yl adenosine revealed a binding site for the ethyl group against Trp-123, a residue that reaches acro
16 i system due to the steric impact of the two ethyl groups, an observation that explains the lack of e
18 red in 2.7% of the patients in the icosapent ethyl group and in 2.1% in the placebo group (P=0.06).
19 re increased steric interactions between the ethyl group and the carbonyl-LiN(TMS)(2) moiety destabil
20 eavage of the C-O bond of the N-[2-(vinyloxy)ethyl] group and removal of vinyloxide-anion leading to
21 es, a C-8 vinyl substituent is reduced to an ethyl group, and in the case of BChl c(F), the C-8(2) ca
22 ctions of ketones with an adjacent methyl or ethyl group are generally unselective, but that bulkier
24 butyl substituents and additional methyl and ethyl groups (as in sterically hindered phenalenyl radic
25 ed in 17.2% of the patients in the icosapent ethyl group, as compared with 22.0% of the patients in t
26 were observed for compounds that contain an ethyl group at C-9, with larger C-9 substituents tending
27 y synthesized compounds, compound 15 with an ethyl group at the 4-position showed the best activity a
29 dicated a possible binding mode in which the ethyl group at the 9-position of the molecule was orient
30 orm pyridinium salts with beta-(alkylammonio)ethyl group at the nitrogen atom in the presence of 2 eq
35 The configuration of the N-1-(1'-naphthyl)ethyl group dictates the conformation of the O-tert-buty
37 erivatives of the 2-[N-methyl-N-benzoylamino]ethyl group (E-G) demonstrated moderate stability, but t
38 erature (1)H NMR spectroscopy indicates fast ethyl group exchange between Ar(C2H5)SnSn(C2H5)Ar (Ar =
39 on of the indole N-1 position with methyl or ethyl groups gave a 10- to 30-fold decrease in affinity
40 ctural analog of DES that lacks hydroxyl and ethyl groups, had no effect on CRAC current and on store
41 -1H-imidazole-5-carboxylate), in which the 2-ethyl group has been replaced by photoactivable groups b
43 ther amine substituent, a 2-(cyclohexen-1-yl)ethyl group, induces a hydrophobic pocket in which it bi
44 case of BChl c(F), the C-8(2) carbon of this ethyl group is subsequently methylated once or twice by
46 ated in forming a complete set of deuterated ethyl groups, merging with the Diels-Alder reaction, a n
47 an antifungal polyketide that bristles with ethyl groups mounted onto a caged heterotricyclic core.
48 In outside-out patches, QA ions in which ethyl groups of TEA were replaced by methyl groups had a
52 clopropanated monoadduct exhibited symmetric ethyl groups on the malonate, consistent with regioselec
53 By deliberately incorporating inward-facing ethyl groups on the truxene faces, the resulting partial
55 osition showed preferential migration of the ethyl group over the methyl group to give 8-ketochlorins
56 gues of copro'gen-III were prepared where an ethyl group replaced one of the usual propionate residue
58 rger percentage of patients in the icosapent ethyl group than in the placebo group were hospitalized
59 a, were significantly lower in the icosapent ethyl group than in the placebo group, including the rat
60 n unusual strategy to install two additional ethyl groups that makes use of a thiocarbonyl ylide gene
62 studies revealed a small structural change (ethyl group to hydrogen) caused a functional shift from
63 inal products can be accounted for by facile ethyl group transfer from phosphorus to iridium followed
64 ly substituted stereocenters with methyl and ethyl groups underscores the enzyme's remarkable selecti
65 tride [(TIMMN(Mes))Fe(IV)(N)](+) (7) with an ethyl group using the triethyloxonium salt Et(3)OPF(6).
66 ces of the bis-(2-MeImH) complex to the four ethyl groups was possible through the use of 2D (1)H NMR