ライフサイエンスコーパス: diphenylamine

1 chiometry was 4:1 between manganese(III) and diphenylamine.

2 he epsilon(C)-value was identical to that of diphenylamine.

3 old greater than those of typical commercial diphenylamines.

4 enoxyl radical of the incarcerated 4-hydroxy-diphenylamine (1-OH).

5 l antagonists, niflumic acid (NFA), dichloro-diphenylamine 2-carboxylic acid (DCDPC) and diisothiocya

6 Diphenylamine-2-carboxylate (a chloride channel blocker)

7 tiinflammatory drugs that are derivatives of diphenylamine-2-carboxylate (DPC).

8 are blocked in a voltage-dependent manner by diphenylamine-2-carboxylate (DPC); the affinity of S1118

9 nductance regulator (CFTR) channel inhibitor diphenylamine-2-carboxylate (DPC; 100 microM).

10 regulator (CFTR) blockers glybenclamide and diphenylamine-2-carboxylate did not affect ATP release f

11 pendent inhibition of CFTR by venom, whereas diphenylamine-2-carboxylate showed no state-dependence o

12 Application of either venom or diphenylamine-2-carboxylate to channels that were either

13 significantly by the Cl- channel (50 mumol/L diphenylamine-2-carboxylate) and the Na(+)-K(+)- 2Cl- co

14 ited by arylaminobenzoates (flufenamic acid, diphenylamine-2-carboxylate).

15 nication, sensitivity of channel activity to diphenylamine-2-carboxylate, a chloride channel blocker,

16 annels by anthacene-9-carboxylic acid (A9C), diphenylamine-2-carboxylic acid (DPC), 4,4'-diisothiocya

17 (3-phenylpropylamino)benzoic acid (NPPB), or diphenylamine-2-carboxylic acid (DPC), and the effects o

18 presence of the apical Cl- channel blockers diphenylamine-2-carboxylic acid (DPC, 1 mM), DIDS (300 m

19 d in the presence of the Cl- channel blocker diphenylamine-2-carboxylic acid on the apical side and a

20 hCFTR activation, and it was blocked by DPC (diphenylamine-2-carboxylic acid) and was DIDS (4, 4'-dii

21 diisothiocyanostilbene-2,2'-disulfonic acid, diphenylamine-2-carboxylic acid, and glybenclamide.

22 hat the incorporation of ring nitrogens into diphenylamines affords compounds that display a compromi

23 hat the incorporation of ring nitrogens into diphenylamines affords compounds which display a comprom

24 , phenoxazine, phenothiazine, carbazole, and diphenylamine analogues were synthesized from 2, 4-diami

25 adelta(13)C-trends for the identification of diphenylamine and aniline oxidation in contaminated subs

26 parable oxidative stability to commonly used diphenylamine and phenothiazine RTAs had significantly g

27 stable to one-electron oxidation relative to diphenylamines and phenothiazines (E degrees ranging fro

28 tron-rich arenes (e.g., N,N-dimethylaniline, diphenylamine, and carbazole) through an initial one-ele

29 Substituted diphenylamine antioxidants (SDPAs) and benzotriazole UV

30 en atoms into the aryl rings of conventional diphenylamine antioxidants enables the preparation of re

31 Aniline and diphenylamine are converted by 11a-c at 180 degrees C to

32 Diphenylamines are widely used to protect petroleum-deri

33 methylbenzyl)-diphenylamine (diAMS), dioctyl-diphenylamine (C8C8), and dinonyl-diphenylamine (C9C9) w

34 ), dioctyl-diphenylamine (C8C8), and dinonyl-diphenylamine (C9C9) were the most dominant congeners of

35 the finding that inhibition of the CFTR with diphenylamine carboxylate in C127/wt cells conferred sim

36 secretion into the cyst lumen was blocked by diphenylamine carboxylic acid (DPC) and glibenclamide in

37 s(imidazolinylamino)- and 4,4'-bis(guanidino)diphenylamine compounds, CD27 and CD25, respectively.

38 antitrypanosomal activity of these symmetric diphenylamine compounds.

39 amines derived from saturated substrates and diphenylamines decompose by N-O homolysis followed by di

40 r N-phenylanthranilic acid methyl ester or a diphenylamine derivative and are similarly shown to be r

41 diment, 4,4'-bis(alpha,alpha-dimethylbenzyl)-diphenylamine (diAMS), dioctyl-diphenylamine (C8C8), and

42 rent kinetic isotope effects for aniline and diphenylamine dioxygenation with those from abiotic oxid

43 ue to an efficient charge migration from the diphenylamine donor to the pyrene pi-acceptor.

44 phenazine via unimolecular rearrangements of diphenylamine (DPA) and its nitro substituents (NDPA).

45 Diphenylamine (DPA) and methoxyacrylate (MOA)-stilbene a

46 Aniline (AN) and diphenylamine (DPA) are examples of toxic nonvolatile co

47 Diphenylamine (DPA), a known inhibitor of polyene and is

48 molecules including methyl centralite (MC), diphenylamine (DPA), N-nitrosodiphenylamine (N-NO-DPA),

49 2,4-dinitrotoluene (2,4-DNT) and 11-74 ng of diphenylamine (DPA).

50 catalyzed the reaction of bromobenzene with diphenylamine in the presence of base to produce 94% of

51 on both the fate and behavior of substituted diphenylamines in the environment as well as their relev

52 ol, prochloraz, flutriafol, myclobutanil and diphenylamine) in fruit-based baby food.

53 nd 2-chloroaniline derivatives yields stable diphenylamine intermediates, which are selectively conve

54 ole ring was replaced with a freely rotating diphenylamine moiety were also prepared.

55 g reduction of unreacted manganese(III) with diphenylamine or barium diphenylamine sulphonate forming

56 hose derived from unsaturated substrates and diphenylamines, or saturated substrates and N-phenyl-bet

57 focused on modifications of the hydrophobic diphenylamine portion positioned in S1 and extending tow

58 kyl-, alkoxyl-, and dialkylamino-substituted diphenylamines raises their oxidation potentials systema

59 conditions representative of those at which diphenylamine RTAs are used industrially.

60 lteration levels (>25.0%, w/w) reaction with diphenylamine-sulfuric acid was found adequate to indica

61 manganese(III) with diphenylamine or barium diphenylamine sulphonate forming a product lambda(max) 5

62 (9,9-di-n-octylfluorene-alt-N-(4-butylphenyl)diphenylamine) (TFB [f8-tfb]) (electron-donor) and poly(

63 poly(9,9-dioctylfluorene-co-N-(4-butylphenyl)diphenylamine) (TFB) with F8BT.

64 9,9-dioctylfluorene-co-N-(4-(3-methylpropyl))diphenylamine), TFB) on ITO; (3) TPDSi(2) + TFB blends o

65 For diphenylamine, the C and N isotope enrichment was normal

66 all increases of 0.3-0.5 V on going from the diphenylamines to the dipyrimidylamines.

67 End-capping with a diphenylamine unit further red-shifted the absorption an

68 iated with the biodegradation of aniline and diphenylamine using pure cultures of Burkholderia sp. st

69 Analysis of headspace concentrations of diphenylamine using solid phase micro-extraction (SPME)

70 i.e., ability to accept charge transfer from diphenylamine was: 2-pyran-4-ylidene malononitrile (pyra

71 Substituted diphenylamines were, unexpectedly, found to be the prima

72 othiazine, iminodibenzyl, iminostilbene, and diphenylamine-were examined.

73 This protocol allows the coupling of diphenylamines with a sterically hindered but electronic