ライフサイエンスコーパス: phenylethylamine

1 etaldehyde, 4-hydroxyphenylacetaldehyde, and phenylethylamine.

2 and identified it to be a biogenic amine, 2-phenylethylamine.

3 ive sensory neurons that also responded to 2-phenylethylamine.

4 s the anti-Markovnikov addition product beta-phenylethylamine.

5 monoamines such as serotonin, tyramine, and phenylethylamine.

6 of serotonin, norepinephrine, dopamine, and phenylethylamine.

7 ffects for para-substituted benzylamines and phenylethylamines.

8 (*) from three chiral benzylic substrates (1-phenylethylamine, 1-phenylethanol, and alpha-vinylbenzyl

9 t study, this is exemplified by subjecting 1-phenylethylamine (1a) and analogous benzylic amines to D

10 The simplest phenylethylamine, 2-phenylethylamine itself, is without

11 6 receptors a series of compounds, including phenylethylamines 6, pyrroloethylamine 7, and phenylpipe

12 In our study, alpha-phenylethylamine (alpha-PEA) allowed an efficient 1-3 st

13 nd rTAAR1, respectively) insensitive to beta-phenylethylamine, amphetamine (AMPH), and methamphetamin

14 N-methyl-4-phenylpyridinium, phenylethylamine, amphetamine, and methylenedioxymethamp

15 methyl N-Boc-phosphoramidates derived from 1-phenylethylamine and 1,2,3,4-tetrahydronaphthalen-1-ylam

16 nt amine, followed by putrescine, histamine, phenylethylamine and cadaverine.

17 Tryptamine, phenylethylamine and histamine (with the single exceptio

18 The formation of 2-phenylethylamine and phenylacetaldehyde in mixtures of p

19 hanism because the Ea of formation of both 2-phenylethylamine and phenylacetaldehyde remained unchang

20 e that the benzenesulfonamide portion of the phenylethylamine and phenylpiperazine analogues can be "

21 revalence of tyramine followed by histamine, phenylethylamine and putrescine; and total amine levels

22 lative affinity for indoleethylamines versus phenylethylamines and temperature-activity relationships

23 indole, the neurotransmitter precursor beta-phenylethylamine, and a variety of peroxidase and laccas

24 mitters including serotonin, norepinephrine, phenylethylamine, and dopamine.

25 adienyl)ethanol, and the aromatized product, phenylethylamine, and that the two pathways do not cross

26 ytryptamine, a decreased preference for beta-phenylethylamine, and, similar to MAO A, was more sensit

27 do not exhibit aggression and only levels of phenylethylamine are increased.

28 get compounds using Shi epoxidation or (R)-1-phenylethylamine as a source of chirality.

29 not a requirement for the binding of certain phenylethylamines at 5-HT(2A) receptors, the presence of

30 The discovery of novel uracil phenylethylamines bearing a butyric acid as potent human

31 ation of biogenic and dietary amines such as phenylethylamine, benzylamine, dopamine, and tyramine.

32 lycine and agmatine and neuromodulators beta-phenylethylamine (beta-PEA) and taurine are important bi

33 beta-Phenylethylamine (betaPEA) is a trace amine present in t

34 -aryl[or (1S,2S)-1-alkyl]-2-(phenylseleno)-2-phenylethylamines by reaction with t-BuLi and subsequent

35 spermidine, putrescine, histamine, tyramine, phenylethylamine, cadaverine and serotonin) were determi

36 Thus, phenylethylamine can be used as a carbon and nitrogen so

37 reactions of QHNDH with chiral deuterated 2-phenylethylamines demonstrated that the enzyme abstracts

38 During phenylethylamine-dependent growth, aromatic amine dehydr

39 The binding of dopamine, a hydroxylated phenylethylamine derivative, displays the same pH depend

40 Measurements indicated that phenylethylamine-fed cells generate H2O2 at 30 times the

41 n studies involving enzymatic depletion of 2-phenylethylamine from a carnivore odor indicate it to be

42 ptamine), norepinephrine, dopamine, and beta-phenylethylamine; in humans and mice, these neurochemica

43 of serotonin, norepinephrine, dopamine, and phenylethylamine increased, and serotonin metabolite 5-h

44 One such cue, carnivore-derived 2-phenylethylamine, is a key component of a predator odor

45 The simplest phenylethylamine, 2-phenylethylamine itself, is without significant central

46 The phenylalkylamine, particularly the phenylethylamine, moiety is a common structural feature

47 Two prey species, rat and mouse, avoid a 2-phenylethylamine odor source, and loss-of-function studi

48 without significant changes of the K(m) for phenylethylamine or dopamine or the IC(50) for deprenyl

49 0-fold slower in catalyzing the oxidation of phenylethylamine or of serotonin.

50 are synthesized in one step from allenes and phenylethylamines or benzylamines, respectively.

51 , spermine, spermidine), aromatic (tyramine, phenylethylamine) or heterocyclic (histamine, tryptamine

52 ependent biosynthesis of the TPQ cofactor in phenylethylamine oxidase (PEAO) and histamine oxidase fr

53 ling of the C2, C4, and C5 oxygens of TPQ in phenylethylamine oxidase (PEAO) from Arthrobacter globif

54 y of the topa quinone biogenesis reaction in phenylethylamine oxidase from Arthrobacter globiformis (

55 Second, phenylethylamine oxidase is an unusual catabolic enzyme

56 ect, the periplasmic compartmentalization of phenylethylamine oxidase serves the same purpose as the

57 atic that E. coli can synthesize a catabolic phenylethylamine oxidase that stoichiometrically generat

58 thway that is required for the catabolism of phenylethylamine (PEA) and its hydroxylated derivatives

59 ntinuous intravenous infusion over 30 min of phenylethylamine (PEA), an endogenous substrate of MAOB,

60 ), whereas MAOB preferentially oxidizes beta-phenylethylamine (PEA).

61 inatorial library of 10 structurally related phenylethylamines (PEAs) is investigated for chiral sepa

62 ss 38 mammalian species indicates enriched 2-phenylethylamine production by numerous carnivores, with

63 ncluding serotonin, histamine, tryptamine, 2-phenylethylamine, putrescine, and agmatine.

64 The quantity of biogenic amines (tryptamine, phenylethylamine, putrescine, cadaverine, histamine, ser

65 ight biogenic amines (cadaverine, histamine, phenylethylamine, putrescine, spermine, spermidine, tyra

66 apparent affinities for a preferred ligand, phenylethylamine, rivaling those seen with mammalian phe

67 amine dehydrogenase-catalyzed reaction with phenylethylamine shows complex pressure and temperature

68 AMDA does contain a phenylethylamine skeleton within a tricyclic ring system

69 Putrescine, cadaverine, tryptamine, beta-phenylethylamine spermidine, spermine were analysed by U

70 xtent, also by degradation of phenylalanine, phenylethylamine, styrene, and creatinine.

71 of the achiral parent ligand with a chiral 1-phenylethylamine substituent on the open face of the com

72 to perpendicular to the aromatic ring of the phenylethylamine substrate or cyclohexadiene ring of CHD

73 Certain phenylethylamines, such as 1-(4-bromo-2,5-dimethoxypheny

74 which exhibits a higher preference for beta-phenylethylamine than for the MAO A preferred substrate

75 roles in the neurotoxicity produced by this phenylethylamine, the primary source of DA responsible f

76 This suggests that for 2-phenylethylamine, the rate-limiting step in the single-t

77 s was prepared from N-(o-nitrophenylsulfenyl)phenylethylamines through BINOL-phosphoric acid [(R)-TRI

78 tivity (from 0.02mgkg(-1) for spermidine and phenylethylamine to 0.2mgkg(-1) for spermine) when compa

79 imethyl N-Boc-phosphoramidate derived from 1-phenylethylamine to the N-Boc alpha-aminophosphonate pre

80 , in enclosed laboratory cultures, growth on phenylethylamine triggered induction of the OxyR H2O2 st

81 Tyramine, beta-phenylethylamine, tryptamine, and octopamine are biogeni

82 of six biogenic amines (histamine, tyramine, phenylethylamine, tryptamine, putrescine, and cadaverine

83 cted during substrate (either benzylamine or phenylethylamine) turnover, by anaerobic incubation with

84 Phenylethylamine, tyramine, and dopamine are oxidized by

85 Neither tryptamine nor phenylethylamine was detected in the monitored samples;

86 model compound, first (S)- and/or (RS)-alpha-phenylethylamine was used, and their diastereomeric salt

87 Tryptamine and phenylethylamine were not detected in pressure-treated s

88 Methylamine and phenylethylamine were not determined in any vinegar.

89 permine, histamine, tyramine, tryptamine and phenylethylamine) were determined.

90 permine, histamine, tyramine, tryptamine and phenylethylamine) were determined.

91 es, tyramine, histamine, tryptamine and beta-phenylethylamine, were detected in practically all ferme

92 ion of histamine, tyramine, tryptamine and 2-phenylethylamine, which eliminates the purification step

93 In contrast, the reaction of 2-phenylethylamine with QHNDH does not exhibit a significa