ライフサイエンスコーパス: reference compound

1 using relative peak areas with cannabinol as reference compound.

2 relative retention times with cannabinol as reference compound.

3 high-affinity GABAA antagonist was used as a reference compound.

4 that required for CA-4P, which was used as a reference compound.

5 in vivo in comparison to a (all amide bond) reference compound.

6 X, XII, and XIV using acetazolamide (AAZ) as reference compound.

7 -(AHX-DTPA-111In)NH2]exendin-4 was used as a reference compound.

8 mpound was confirmed by analysis of the pure reference compound.

9 to be at least 10-fold more potent than the reference compound.

10 comparable to that of letrozole chosen as a reference compound.

11 ty were calculated using alpha-tocopherol as reference compound.

12 he relative rate technique, with methanol as reference compound.

13 pared with butylated hydroxytoluene (BHT) as reference compound.

14 citrin (quercetin-3-O-rhamnoside), used as a reference compound.

15 l space sampled by ligands with respect to a reference compound.

16 th cyclopropane to produce a six-member ring reference compound.

17 the SE of the corresponding six-member ring reference compound.

18 -carboxamide) and the S = 0 [Fe(PaPy3)CO](+) reference compound.

19 ith cyclopropane to form a six-membered ring reference compound.

20 d linear combination analysis of known XANES reference compounds.

21 sed to monitor the concentrations of CPA and reference compounds.

22 ms, and delivered expected IC(50) values for reference compounds.

23 orders of magnitude lower than the relevant reference compounds.

24 ations and experimental data for appropriate reference compounds.

25 l shifts and by direct addition of authentic reference compounds.

26 polation of the loss kinetics of performance reference compounds.

27 using, e.g., the chlorinated derivatives as reference compounds.

28 mentally measured mass spectra from chemical reference compounds.

29 fects of ethanol extract of DP (EDP) and its reference compounds.

30 der spectrum of activity than numerous other reference compounds.

31 ng HRGC-O, in comparison with the respective reference compounds.

32 and IR analysis of the isolated cofactor and reference compounds.

33 alues of desirable low molecular weight (MW) reference compounds.

34 on cycloalkanes, cycloalkenes, and selected reference compounds.

35 ns the same characteristics as those the two reference compounds.

36 igh delta selectivity, H-Dmt-Tic--Lys(Z)-OH (reference compound 1) is a useful starting point for the

37 to the conformationally constrained 4-7 and reference compounds 1-3 catalyzed by alpha-2,6- and alph

38 exhibited comparable binding affinity to the reference compound, 1-(4-methoxybenzyl)-4-oxo-1,4-dihydr

39 re stable (DeltaE = -20.2 kcal/mol) isomeric reference compound 2,2-difluoropropane.

40 nformationally constrained 6 and 7 and their reference compounds 2 and 3 further supports the fact th

41 tion conditions have been optimized using as reference compounds 2-, 3-, 4-, or 6-monosubstituted man

42 sitivity of (68)Ga-OPS202, compared with the reference compound, (68)Ga-DOTATOC (an sst receptor agon

43 e mere addition of a key moiety found in the reference compound 7 (ABT-239) elevated the series to hi

44 porfiromycin C(8) cyclized imine (6) and its reference compound, 7-N-(1'-aminocyclohex-2'-yl)porfirom

45 ve are ca. 10 000 times more potent than the reference compound acyclovir and ca. 100 times more pote

46 ld enhancement in anti-VZV activity over the reference compound acyclovir, with no detectable in vitr

47 mutants analogous to those achieved with the reference compound ambroxol were attained with a more fa

48 comparable to what could be achieved by the reference compound and current clinical candidate TPCS(2

49 cterized in biological data sets to those of reference compounds and (ii) putative identification fro

50 by Pb L3-edge XANES measurements using solid reference compounds and also aqueous solutions of differ

51 tical comparison with chemically synthesized reference compounds and electrospray ionization-mass spe

52 Reference compounds and precursors were synthesized foll

53 equilibrium conditions and using performance reference compounds) and calculating.

54 switches between the analyte and a standard reference compound, and leads to gaps in the analyte dat

55 10 AR transactivation assays, 72 ER-binding reference compounds, and the in vivo uterotrophic assay.

56 57 strong activators (greater activity than reference compound apigenin), most of which were unrelat

57 spectroscopy, chemical shift assignments of reference compounds are required.

58 l ligands--one of the analyte and two of the reference compound) are collisionally activated, and the

59 these compounds and, by comparison with the reference compound BaMn2Bi2, we show that the Dirac carr

60 termined in vitro intrinsic clearance of six reference compounds (benzo[a]pyrene, 4-nonylphenol, di-t

61 re comparable to the ones determined for the reference compound butylhydroxytoluene.

62 been estimated relative to six-membered ring reference compounds by dimerization of dioxirane and or

63 l diffusivities of the two chemically stable reference compounds, caffeine and testosterone, were (1-

64 fragment ions and neutral losses to related reference compounds contained in METLIN, even if the pre

65 s analog may be chosen as NMR chemical shift reference compounds depending on the nature of the biomo

66 ectra of soil samples, along with a range of reference compounds differing in V-oxidation state and c

67 xidine, dinapsoline, and dinoxyline) and the reference compounds dopamine and quinpirole.

68 f the caffeinyl core and substituents of the reference compound (E)-8-(3-chlorostyryl)caffeine led to

69 Despite the lack of reference compounds, ECD of five oligomers ranging from

70 ing study was carried out on the analogs and reference compound (Erlotinib) into the ATP binding site

71 Since the emission from the reference compound Fluor-Et (the ethyl ester of fluoresc

72 The relative potency of C47 to the reference compound flutamide was over 5.2, whereas the d

73 Acetic acid (AA) was selected as a reference compound for complete oxidation and compared o

74 It is well studied as reference compound for H3R in rodent models for neurolog

75 Using the second emitter to introduce a reference compound for internal calibration, accurate ma

76 Spectral resolution allows the use of reference compounds for accurate quantification of conce

77 roteolytic fragments provide a useful set of reference compounds for analysis of the LPO(N) and LPO(C

78 (III) and Ru(III) analogues were prepared as reference compounds for assessing the effect of the 5d v

79 ing benzhydrylium ions, which can be used as reference compounds for characterizing a wide variety of

80 e developed as a new group of nonradioactive reference compounds for future radiotracers.

81 Even if reference compounds for the active drugs are readily obt

82 gonist activity in the T47D assay, while the reference compounds from other related nonsteroidal hPR

83 e (37) show improved potency compared to the reference compound FUT-175.

84 displaying a lower potency in vitro than the reference compound GS39783, the new compounds 6, 10, and

85 For comparison, the reference compound GYKI 52466 (2) had an IC50 of 6.9 mic

86 Competition kinetics with phenylalanine as a reference compound in pulse radiolysis experiments yield

87 ladders have been constructed of appropriate reference compounds in dichloromethane and in acetonitri

88 of five caged crown ethers and two polyether reference compounds in methanol solution.

89 A total of 560 reference compounds, including 8 odd n-alkanes, were ana

90 s-glutathione conjugate and a monofunctional reference compound indicates that the bivalent inhibitor

91 Infusion of a reference compound into one inlet provides a single-poin

92 The choice of the reference compound is especially important for geminal e

93 igands-2 mol of the analyte and 1 mol of the reference compound) is collisionally activated and under

94 simultaneously and separately in relation to reference compounds it is possible to make quantitative

95 On the basis of the availability of these reference compounds, it was shown that the metabolic hyd

96 ol, norepinephrine, propranolol) with chiral reference compounds (L-amino acids) are generated by ele

97 spectively, relative to a similar silicon pc reference compound lacking the TTF moieties.

98 parable or superior to the clinically tested reference compound [Lys40-(AHX-DTPA-111In)NH2]exendin-4

99 cting mu opioid receptor antagonist, and the reference compound methylnaltrexone, upon POI were inves

100 urements confirmed the results obtained from reference compounds, model samples, and real-world speci

101 of one or more of the three BisPEBs and the reference compound MPEP.

102 tion and identification by using enantiopure reference compounds of eleven racemic TAGs with C12-C22

103 The performance and reference compound (PRC) approach would be then applicab

104 The release of performance reference compounds (PRC) dosed to passive samplers prio

105 sed the dissipation rate of four performance reference compounds (PRCs) from passive samplers.

106 diffusive retardation factors as performance reference compounds (PRCs) that are diffusing out of the

107 strips that were preloaded with performance reference compounds (PRCs) were codeployed for 32 d alon

108 Performance reference compounds (PRCs) were used with PE and POM to

109 The nonradioactive reference compound PSMA-1007 and the precursor were prod

110 Methods: The nonradioactive reference compound PSMA-1007 and the precursor were prod

111 e in which a chiral analyte (A) and a chiral reference compound (ref*) are simultaneously coordinated

112 n branching ratios measured when pure chiral reference compounds (ref*D and ref*L) are employed in se

113 Such findings were absent with the added reference compound sitostanol.

114 an, rat, and mouse, which were "spiked" with reference compound solutions at known concentrations.

115 best-fit transformations between signals in reference compound spectra and the corresponding signals

116 nce is typically calibrated by addition of a reference compound such as 3-(trimethylsilyl)-propionic

117 minutes) was >7-fold slower than the slowest reference compound tested, AZD-1981.

118 This is made possible by the use of a reference compound that ionizes to a similar extent in b

119 demonstrated through direct comparison with reference compounds that the presence of a fluorine atom

120 Bromocriptine was used as a reference compound to compare the results obtained with

121 RIEs were normalized against one reference compound used across all methods to ensure com

122 The data clearly demonstrate that the reference compounds used to estimate the SE for highly s

123 rolyte compositions, comparable to a neutral reference compound, (v) the protonated weak base was str

124 cine and otonecine-type PAs by comparison to reference compounds via a spectral library.

125 For each series, a monofunctional reference compound was also prepared to determine the re

126 The precursor for radiolabeling and reference compounds was synthesized in up to five steps

127 LRI for all 552 reference compounds were also calculated based upon comp

128 polyethylene (LDPE) loaded with performance reference compounds were applied independently to measur

129 These reference compounds were randomly split into training (n

130 of pyrene and deuterated pyrene (performance reference compound) were within 0.1 log unit for all exp

131 known experimental log Ko/w values served as reference compounds, whereas the PCB compounds without k

132 taDeltalogR) were calculated relative to the reference compound WIN55,212-2 for Galphai/o, Galphas, G

133 antagonists was evaluated using a set of 39 reference compounds with known ERalpha activity.

134 he correlation of the log Kp/s values of the reference compounds with their log Ko/w values.

135 (R)-2 was more efficient than (R)-1 and the reference compounds, with some exceptions.

136 structures to be solved in complex with the reference compound ZM241385 and four related ligands at