ライフサイエンスコーパス: nitroxide radical

1 l state and hence the electroactivity of the nitroxide radical.

2 al motion of the water proton spins past the nitroxide radical.

3 ds to its corresponding catalytically active nitroxide-radical.

4 ganic solvents in the presence of paramagnet nitroxide radicals.

5 e-coupled clusters of copper(II) with stable nitroxide radicals.

6 A stable nitroxide radical, 1-oxyl-4-bromo-2,2,5,5-tetramethylpyr

7 eling of these plasma activities by a stable nitroxide radical, 2,2,6, 6-tetramethyl-1-piperidinyloxy

8 trapping studies show the intermediacy of a nitroxide radical and a C-nitroso species during this re

9 nthesized two series of compounds in which a nitroxide radical and a fullerene C(60) moiety were kept

10 mechanistic model that includes the observed nitroxide radical and C-nitroso compound intermediates h

11 The ORCA is based on spirocyclohexyl nitroxide radicals and poly(ethylene glycol) chains conj

12 Nitroxide radicals are introduced into the reverse micel

13 Nitroxide radicals are paramagnetic contrast agents, use

14 Stable nitroxide radicals are potent antioxidants and are among

15 d their one-electron oxidation products, the nitroxide radicals, as intermediates in this pathway.

16 ements larger than 10 were obtained with bis-nitroxide radical at 14.1 T and low temperature ( approx

17 space coupling is found between the diagonal nitroxide radicals at the conformationally constrained N

18 tic resonance (EPR) spectroscopy of a stable nitroxide radical attached site-specifically to a macrom

19 These nitroxide radical-based nanostructures have longitudinal

20 arization of solvent molecules that approach nitroxide radical-based spin labels within <5-10 A.

21 ound, which is transformed into a persistent nitroxide radical by further photolysis.

22 recent reports that the coupling factor for nitroxide radicals cannot be quantified due to the diffi

23 Nitroxide radicals could be converted to their correspon

24 With one model 2,2,6,6-TMPi nitroxide radical, evidence for an alternate pathway, wh

25 e examine a family of polythiophenes bearing nitroxide radical groups, showing that while both specie

26 TEMPO oxoammonium salts and three homologous nitroxide radicals have been prepared and characterized.

27 We attach nitroxide radicals (i.e., spin labels) to multiple phosp

28 ument, a technique was developed for imaging nitroxide radicals in the whole stomach.

29 tation of PTH1R[168-198] was determined from nitroxide-radical induced relaxation of NMR signals util

30 On the basis of nitroxide radical-induced relaxation studies, the centra

31 Through-bond coupling between the adjacent nitroxide radicals is mediated by the nitroxide-m-phenyl

32 Nitroxide radicals possess important antioxidant activit

33 ylpiperidine (PP-H), which produces a stable nitroxide radical (PP(*)) product upon reaction with O(2

34 tetramethylrhodamine (5-TAMRA) and the small nitroxide radical TEMPO were synthesized and tested to i

35 ected spin labeling (SDSL) utilizes a stable nitroxide radical to obtain structural and dynamic infor

36 tilizes site-specific attachment of a stable nitroxide radical to probe the structure and dynamics of

37 rand 6 (Val-95), due to the proximity of the nitroxide radical to the backbone 15N and NH nuclei of t

38 The ability of stable nitroxide radicals to detoxify hypervalent heme proteins

39 The conversion of nitroxide radicals to the 2,2-DMPy products by CYP3A4 or

40 Use of the nitroxide radical trap TEMPO affords phosphonate 10, pre

41 cleotide-independent labeling scheme, stable nitroxide radicals were attached to eight specific pRNA

42 pening metathesis polymerization (ROMP), and nitroxide radicals were incorporated at three different

43 Nitroxide radicals were introduced at selected positions

44 ad portion of XJB-5-131 consists of a stable nitroxide radical, which has been extensively investigat

45 lutathionyl radical (GS(*)), interactions of nitroxide radicals with GS(*) and thiols have not been s

46 ys, a mechanism involving interaction of the nitroxide radicals with heme iron (Fe(III)), followed by

47 determined whether this novel interaction of nitroxide radicals with heme iron has any relevance in r