ライフサイエンスコーパス: labeled compound

1 asurable metabolites derived from a specific labeled compound.

2 r) based on NMR coupling in the (15)N, (6)Li labeled compound.

3 PAR probes including biotin and fluorophore-labeled compounds.

4 nly by convenient synthetic accessibility to labeled compounds.

5 logue groups that correspond to isotopically labeled compounds.

6 ning the pharmacological properties of (18)F-labeled compounds.

7 ing the mass isotopomer distribution for all labeled compounds.

8 olute flux was quantified with fluorescently labeled compounds.

9 ile preparation of isotopically enriched 15N-labeled compounds.

10 e catalytic site in the presence of the spin-labeled compounds.

11 advantageously explored noninvasively using labeled compounds.

12 The F-18-labeled compounds, 16 and 18a-c, were prepared via a two

13 Seven F-18 labeled compounds [(18)F]18a-e, [(18)F]18g, and [(18)F]2

14 Spin-labeled compounds, 5-doxylstearic acid (5-DSA), 7-doxyls

15 diography of veins following uptake of (14)C-labeled compounds, analysis of leaf solute composition a

16 Idioblasts were supplied with various (14)C-labeled compounds and examined by micro-autoradiography

17 analysis and that assessment of purities of labeled compounds and metabolic labeling patterns requir

18 ond scalar coupling is investigated in (15)N labeled compounds and the stability of the IMHBs is corr

19 ively expensive and time-consuming, and many labeled compounds are not available in pure form.

20 Stable isotopically labeled compounds are regularly used as internal standar

21 Isotopically labeled compounds are utilized to confirm the assignment

22 magnitude and orientation information using labeled compounds, as well as the structure elucidation

23 The use of isotopically labeled compounds assisted in correcting analyte losses

24 Increased cell uptake of these two labeled compounds at stimulated iNOS levels, as well as

25 We prepared seven (99m)Tc/Re-labeled compounds by attaching known Tc/Re chelating age

26 es of Ir-catalyzed C-H borylations, uniquely labeled compounds can be prepared.

27 elf-supported on an aqueous solution of C2F5-labeled compounds causes the recruitment and immobilizat

28 Dual-labeled compounds containing nuclear and near-infrared f

29 Use of the labeled compound Cp(2)Ta((13)CH(2))(H) shows that the po

30 database for the analysis of uniformly (13)C-labeled compounds, currently contains 455 metabolites, a

31 specific activities, and the pattern of 13C-labeled compounds detected by NMR spectroscopy cumulativ

32 gradation tests with radio or stable isotope labeled compounds enable the detection of the formation

33 the MS/MS spectra of the native and U-(13)C-labeled compound enabled the assignment of the number of

34 the use of very low doses of a radionuclide-labeled compound for imaging studies or for assessing pl

35 The use of positron emitter-labeled compounds for somatostatin receptor imaging (SRI

36 tate the development and comparison of (90)Y-labeled compounds for targeted radiotherapy.

37 amylcysteinylglycine) and the stable-isotope labeled compound (GSX, gamma-glutamylcysteinylglycine-(1

38 tamyl-cystein-glycin] and the stable-isotope labeled compound [GSX, gamma-glutamyl-cystein-glycin-(13

39 r allografts demonstrated that all four F-18-labeled compounds had a high tumor uptake (2.5-3.7% ID/g

40 Studies of isotopically labeled compounds have been fundamental to understanding

41 PET and appropriately labeled compounds have the ability to provide informatio

42 erformance liquid chromatography analysis of labeled compounds in arterial plasma, had no significant

43 Biodistribution studies of the iodine-125-labeled compounds in MDA-MB-231 mouse xenografts exhibit

44 udies were done after the injection of 99mTc-labeled compounds in nude mice bearing tumors.

45 s requires careful analysis of recoveries of labeled compounds in the appropriate eluate fraction.

46 and output fluxes; only the fractions of the labeled compounds in the input and output fluxes are var

47 Other (13)C-labeled compounds included glutamate, aspartate, glutami

48 The incorporation of radioactivity from 14C-labeled compounds into metabolic intermediates and total

49 topomers in a labeled compound or mixture of labeled compounds is an example of this problem that is

50 tion studies in rats indicated that the F-18-labeled compounds localized in brain regions with high c

51 measure individual radiation doses of (90)Y-labeled compounds noninvasively.

52 ment of the distribution of isotopomers in a labeled compound or mixture of labeled compounds is an e

53 ul starting point for the synthesis of (18)F-labeled compounds prepared by the coupling of N-succinim

54 periments using (17)O and (18)O isotopically labeled compounds prove that this compound is a key inte

55 The analysis of the J(HN) couplings in (15)N-labeled compounds provides a simple and efficient method

56 absorbed dose to the renal cortex for (90)Y-labeled compounds retained within that subregion is appr

57 synthesis and evaluation of an indazole-spin-labeled compound that was designed as an effective chemi

58 the pathway was followed by using deuterium-labeled compounds that could be identified by using GCMS

59 rk describes the first application of (37)Cl-labeled compounds to isotope dilution mass spectrometry

60 on of beta-radiation associated with [(14)C]-labeled compounds to monitor the development of the conc

61 benzene and several easily synthesized (13)C-labeled compounds using (13)C-labeled iodomethane as the

62 Lung uptake of the (99m)Tc-labeled compound was markedly reduced in rats with pulmo

63 This labeled compound was taken up and metabolized by a cultu

64 Notably, <1 dpm (0.45 pCi) of (14)C-labeled compound was used in each assay, which is well b

65 A series of (13)C-labeled compounds was employed to investigate this biosy

66 In vivo localization of the respective (18)F-labeled compounds was evaluated by biodistribution studi

67 As a part of these studies, C(19)F3-labeled compounds were characterized and calibrated for

68 The (99m)Tc(CO)(3)-labeled compounds were injected into SCID mice bearing D

69 radiochromatograms simultaneously when (14)C-labeled compounds were injected into the gas chromatogra

70 d, and the corresponding tritiated and (11)C-labeled compounds were synthesized.

71 The corresponding 18F labeled compounds, which can be prepared readily, showed

72 of weanling rats to the stable isotopically labeled compound will be necessary to conclusively deter

73 as determined using a reference set of (14)C-labeled compounds with a range of potential environmenta

74 To this end, four (14)C-labeled compounds with different biodegradation and sorp