戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1  was established by synthesizing its optical antipode.
2 ites is higher for the template than for its antipode.
3 ve interactions of both the template and its antipode.
4 m epoxide hydrolase action on the natural JH antipode.
5 ntioselectivity (19 to 50%) for the opposite antipode.
6 he entire egg and converges uniformly on the antipode.
7 to 1.5 pmole as the calcium wave reaches the antipode.
8  diastereocontrol and allow access to either antipode.
9 h impactor material accumulates at the basin antipode.
10 could provide an easy access to both product antipodes.
11 h independent pathways leading to both amine antipodes.
12 rophenyl ester (Fmoc-L-Trp(OPfp)), and their antipodes.
13 in magnetization of the lunar crust at their antipodes.
14 ures injected simultaneously into the single antipodes.
15 concept provides access to both enantiomeric antipodes.
16 he (R)-compound is much more potent than its antipode against the four cancer cell lines examined.
17 nergy sites adsorb both the template and its antipode, although part of them may adsorb only the temp
18 sin-forming impacts accumulated at the basin antipode and recorded the ambient magnetic field.
19                  The natural product and its antipode are isolated with >95% ee.
20                            Instead, they are antipodes arising from separate enantiomeric biosynthese
21 h only slightly higher affinity than their S-antipodes at the 5-HT(2A) and 5-HT(2C) receptors.
22 , the relative amount of any pair of optical antipodes, constitutes a integral part of the work of an
23 -induced body pressure waves focusing at the antipode, could produce magnetization that can account f
24                                The unnatural antipode (-)-crispine A was similarly prepared in three
25 s(1,4,6)P(3), 4ab], together with the chiral antipodes D-Ins(1,4,6)P(3)(4a) and L-Ins(1,4,6)P(3)(4b),
26 tic evaluation of DPP-IV inhibition by the D-antipode, des-cyano, and amide analogues of NVP-DPP728,
27        Surprisingly, it was found that the D-antipode, despite being approximately 500-fold less pote
28 lly occurring (+)-fomannosin (1) and its (-)-antipode (ent-1) from alpha-D-glucose has been developed
29                                      The (+)-antipode exhibits interesting biological properties, but
30 ural (-)-garsubellin A and its unnatural (+)-antipode for biological evaluations.
31 sarpagine related indole alkaloids and their antipodes for biological screening.
32 ge opioid receptor ligands with both optical antipodes having high binding affinity.
33 0.93 microM) as the calcium wave reaches the antipode in the fertilized egg.
34 yeast reductases that delivered both alcohol antipodes in optically pure form.
35 dues in DPs affording either the (+)- or (-)-antipodes in the vicinity of the putative binding site a
36 lic NK-1 receptor (Substance-P) antagonist 1 antipode is described.
37      First, crustal disruption at the impact antipode is probably responsible for the observed antipo
38  similar inactivation parameters for the two antipodes, L-alpha-(1'-fluoro)vinyllysine (Ki = 630 +/-
39 onstitution to provide access to the natural antipode (+)-malbrancheamide.
40 hat the domain modeled by peptide III is one antipode of a conformational switch.
41 tiomer of peribysin E from the corresponding antipode of carvone led to a reassignment of the absolut
42 bsequent conjugate addition of the requisite antipode of lithium N-benzyl-N-(alpha-methylbenzyl)amide
43 scribed chemistry, in vitro screening of the antipode of natural dactylolide against the NCI's 60 can
44 ent enantioselectivity with access to either antipode of product.
45 strong anomaly regions, Gerasimovich crater, Antipode of Serenitatis basin, Hayford crater, Crisium b
46 synthesized via this method because only one antipode of sparteine is available in nature.
47            Acidic hydration of the unnatural antipode of the [10-(3)H]JHs gives the diol antipode wit
48 convergent, stereocontrolled route to either antipode of the cell adhesion inhibitor, peribysin E, ha
49                     Besides, in one step, an antipode of the cephalosol intermediate natural product
50 e synthesized by this enzyme is the isotopic antipode of the citrate synthesized by the (S)-citrate s
51                             To model another antipode of the switch, we introduced two strategic modi
52                                         Both antipodes of 2-azido-1-arylethanols were synthesized wit
53 heses of the natural (-) and non-natural (+) antipodes of batrachotoxin, as well both enantiomers of
54             This allows ready access to both antipodes of chiral beta-hydroxy nitriles and beta-hydro
55 enantiospecific oxidation peaks toward the R-antipodes of four beta-blocker representatives and addit
56 diastereoselective conjugate addition of the antipodes of lithium N-benzyl-N-(alpha-methylbenzyl)amid
57 ng differential expression of genes found at antipodes of rearrangements.
58 ochemical model accounting for the preferred antipodes of the alkanes is proposed and relies on the s
59                  Racemization of the optical antipodes of these compounds has been studied using dyna
60 materials and enables access to both optical antipodes of these increasingly useful nucleophilic cata
61 ss to the enantioselective syntheses of both antipodes of those alkaloids can be achieved by kinetic
62 erent enolates (R/S' mixtures), and the same antipodes of two different enolates (R/R' mixtures).
63 of a single enolate (R/S mixtures), opposite antipodes of two different enolates (R/S' mixtures), and
64 rprisingly, the mirror-image isomer (optical antipode) of cyclodal, c[-Arg-d-Phe-d-Lys-d-Dmt-] (2), a
65  negligible activities), whereas the optical antipode proved to be an H4R antagonist ([(35)S]GTPgamma
66       The method was also used to assess the antipode purity of EET standards, and to determine murin
67 ro activity in hemoglobin solutions than its antipode, racemate, and RSR13.
68   The crustal magnetic fields of the Imbrium antipode region are strong enough to deflect the solar w
69 s of conformationally rigid pseudorotational antipodes, revealed that in addition to their different
70 though unique, the synthetic routes to these antipodes share a number of key features, including nove
71        In a biochemical assay, their optical antipodes showed similar potencies, which could be ratio
72 y 20 degrees-wide band which vanishes at the antipode some minutes later.
73 iconal hemiacetal to cyclize the appropriate antipode to optically pure versicolorin B.
74 mplify a planetary dipole field at the basin antipode to ~43 microtesla.
75 ulation of susceptibility (S) genes that are antipodes to resistance (R) genes has been adopted as an
76 cyclo[3.1.0]hexane pseudosugar for the north antipode via an intramolecular olefin-ketocarbene cycloa
77 nerated a liganded structure whereby the (S)-antipode was found in the binding pocket.
78 des tested, a general preference for the (S)-antipode was observed, with high ee's for substrates cor
79 ids or their respective amino alcohols (both antipodes), we obtained a complete set of 24 protected c
80                                      The two antipodes were separated via chiral chromatography, and
81  antipode of the [10-(3)H]JHs gives the diol antipode with the same stereochemistry as that from epox