ライフサイエンスコーパス: phenylhydrazine

1 ctive groups that covalently bind amines and phenylhydrazine.

2 phenylacetylene, styrene, ethylbenzene, and phenylhydrazine.

3 II with either t-[(14)C]butylamine or [(14)C]phenylhydrazine.

4 The structure of the phenylhydrazine adduct of 1(ox) (2) is reported, and 2D

5 UV-vis spectroscopic pH titration of phenylhydrazine adducts of 1(ox) and 4, 2, and 11, respe

6 ed BLO reacts in an irreversible manner with phenylhydrazine, an amine substrate analog, and catalyze

7 eration and were lethal after treatment with phenylhydrazine, an inducer of hemolysis.

8 Py17XNL, phenylhydrazine and hemin caused premature mobilization

9 tion catalysed by HRP-C during turnover with phenylhydrazine and its vulnerability towards inactivati

10 hesized using a variety of benzaldehydes and phenylhydrazines and characterized.

11 and glyoxylate, reaction of glyoxylate with phenylhydrazine, and oxidative conversion of phenylhydra

12 ing of CP47, D2, and D1 with methylamine and phenylhydrazine approached a one-to-one stoichiometry, a

13 Phenylhydrazine binding significantly perturbs the orien

14 aining intact LTQ in the apoBLO reacted with phenylhydrazine, both in the presence and absence of the

15 )-4,5,6-trihydroxyhexane-1,2-diylidene)bis(N-phenylhydrazine carbothioamide), was used to make a comp

16 der with respect to substrate and inhibitor (phenylhydrazine) concentration.

17 alphaF55A MADH has also been determined with phenylhydrazine covalently bound to TTQ in the active si

18 ring vinamidinium moiety at position 9, with phenylhydrazine derivatives as the key step.

19 After phenylhydrazine derivatization and trypsin digestion, we

20 ation of the cells with hydrogen peroxide or phenylhydrazine did not affect A23187-induced uptake of

21 from classical spot tests using aniline and phenylhydrazine dyes that enable molecular recognition o

22 new reagent, 4-(9-fluorenylmethyloxycarbonyl)phenylhydrazine (FmPH).

23 reatment of a sulfidodiiron(II) complex with phenylhydrazine gave an isolable mixed-valence FeII-Fe(I

24 as the result of oxidative stress induced by phenylhydrazine, hydrogen peroxide, tert-butyl hydropero

25 interaction with nine fSWNTs, n-propylamine, phenylhydrazine, hydroxyl, phenydicarboxy, phenyl, sulfo

26 Phenylhydrazine inactivation of the C30A mutant gave at

27 In addition, when challenged with phenylhydrazine-induced anemia, EpoR-HM mice failed to r

28 h a reduced serum PA are anemic and prone to phenylhydrazine-induced anemia.

29 high bacterial load, features reproduced by phenylhydrazine-induced hemolysis or hemin administratio

30 were analyzed under basal conditions, after phenylhydrazine-induced hemolysis, and after induction o

31 eficient mice, we show that lack of ROCK1 in phenylhydrazine-induced oxidative stress model results i

32 Phenylhydrazine-induced stress caused higher mortality i

33 The response of bone marrow to phenylhydrazine-induced stress was, unlike that of splee

34 ted and analysed by reverse-phase HPLC after phenylhydrazine-induced suicide inactivation.

35 Inspection of the crystal structure of phenylhydrazine-inhibited QHNDH suggests that Asp33(gamm

36 Hemolytic anemia was stimulated by phenylhydrazine injection.

37 l of beta-conditionally deficient mice after phenylhydrazine is severely compromised because of their

38 Experiments with phenylhydrazine, KCl, quinine, merocyanine 540, the calp

39 resonance Raman spectra of this adduct and a phenylhydrazine-labeled model compound of lysine tyrosyl

40 by electronic and NMR spectroscopies, and by phenylhydrazine-modification experiments.

41 n inactivators of monoamine oxidase, namely, phenylhydrazine, N-cyclopropyl-alpha-methylbenzylamine,

42 Mice were treated with phenylhydrazine on day 0 and day 1 to induce hemolytic a

43 mic iron availability (e.g., iron dextran or phenylhydrazine) on the induction, kinetics, and size of

44 layed during stress hematopoiesis induced by phenylhydrazine or by 5-fluorouracil, suggesting impairm

45 The 400 nm species does not react with phenylhydrazine or ethylamine and is stable toward pH bu

46 me by [1-14C]beta-aminopropionitrile, [U-14C]phenylhydrazine, or [35S]homocysteine thiolactone was ob

47 lone (PMP) derivatization in comparison with phenylhydrazine (PHN) derivatization.

48 rence from wild-type mice in both normal and phenylhydrazine (PHZ)-induced stress erythropoiesis, PPA

49 w cells obtained from mice that had received phenylhydrazine plus ACK2.

50 w cells obtained from mice that had received phenylhydrazine plus control IgG or with marrow cells ob

51 ge and an accompanying spreading lesion with phenylhydrazine pretreatment (e.g., increases in circula

52 Induction of hemolytic anemia with phenylhydrazine resulted in a drop in the Hct from appro

53 s study, stress induced by 5-fluorouracil or phenylhydrazine revealed a delay in the recovery of eryt

54 e and comparison to the oxidants diamide and phenylhydrazine revealed that oxidation does not partici

55 is in the adult, we compared the response to phenylhydrazine stress in 3 genetically deficient models

56 r, under extreme demand for porphyrins (e.g. phenylhydrazine stress), these adaptations appear inadeq

57 Addition of phenylhydrazine to the copper-loaded protein produced a

58 ve reagents (diamide, hydrogen peroxide, and phenylhydrazine) to cross-link sulfhydryl groups and wit

59 We suggest reasons why phenylhydrazine-treated C. cinereus peroxidase was more

60 U-GM content to less than half that found in phenylhydrazine-treated control mice and nearly totally

61 In phenylhydrazine-treated Lyn-/- mice, extramedullary sple

62 throblasts were isolated from the spleens of phenylhydrazine-treated mice, and Epo stimulation result

63 revious studies using bone marrow cells from phenylhydrazine-treated, anemic mice, we find that both

64 o 20-fold over that observed with 1-acetyl-2-phenylhydrazine treatment alone.

65 o monitor thiol redox status during in vitro phenylhydrazine treatment and over the course of in vivo

66 Results from phenylhydrazine treatment of HRP-C wild-type and mutant

67 mally seen following induction of anaemia by phenylhydrazine treatment.

68 wild-type and C30A mutant enzymes, although phenylhydrazine was 10 times more potent than N-cyclopro

69 labeling reactions, t-[(14)C]butylamine and phenylhydrazine were employed as probes.

70 Reaction of hydrazine or phenylhydrazine with ((tbs)L)Fe3(thf) yields triiron mu(

71 ion of ferric APX with the suicide substrate phenylhydrazine yields predominantly (60%) a covalent ha