ライフサイエンスコーパス: 5-hydroxytryptophan

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1 ted by biogenic amine precursors (L-DOPA and 5-hydroxytryptophan).

2 ke up and metabolize the serotonin precursor 5-hydroxytryptophan.

3 ith further improvement with the addition of 5-hydroxytryptophan.

4 rin-dependent hydroxylation of tryptophan to 5-hydroxytryptophan.

5 e precursor levodopa and serotonin precursor 5-hydroxytryptophan.

6 of molecular oxygen into tryptophan to form 5-hydroxytryptophan.

7 o produce 5-HT from its immediate precursor, 5-hydroxytryptophan.

8 tron emission tomography (PET) marker [(11)C]5-hydroxytryptophan ([(11)C]5-HTP) for this purpose.

9 s, adjunct treatment with the 5-HT precursor 5-hydroxytryptophan (5-HTP) elevates 5-HTExt beyond the

10 (1) determination ex vivo of accumulation of 5-hydroxytryptophan (5-HTP) in tissue from the dorsal an

11 Accumulation of 5-hydroxytryptophan (5-HTP) in vivo, in the presence of

12 cted, treatment with the serotonin precursor 5-hydroxytryptophan (5-HTP) increased the intensity of s

13 ribution of the immediate precursor of 5-HT, 5-hydroxytryptophan (5-HTP), in two model opisthobranch

14 ated during lactation and after injection of 5-hydroxytryptophan (5-HTP).

15 Following oxidation of 5-hydroxytryptophan (5-HTPP) at a pyrolytic graphite ele

16 Central serotonin (5-hydroxytryptophan, 5-HT) modulates somatosensory trans

17 ive by itself, was then combined either with 5-hydroxytryptophan (5HTP), a serotonin precursor, or wi

18 The concentrations of 5HT and 5-hydroxytryptophan (5HTP, an index of 5HT synthesis) we

19 further show that 7-azatryptophan (7AW) and 5-hydroxytryptophan (5HW) can also serve as a FRET accep

20 tryptophan analogues, 7-azatryptophan (7AW), 5-hydroxytryptophan (5HW), and 4-, 5-, and 6-fluorotrypt

21 The set of tryptophan analogues includes 5-hydroxytryptophan, 7-azatryptophan, 4-fluorotryptophan

22 The tryptophan analogues, 5-hydroxytryptophan, 7-azatryptophan, 4-fluorotryptophan

23 Tyrosine and the serotonin-precursor 5-hydroxytryptophan also activate AHR signaling in combi

24 1P) antagonist, N-acetyl-5-hydroxytryptophyl-5-hydroxytryptophan amide, and by 1.0 microM tropisetron

25 5-Hydroxytryptophan and 7-azatryptophan have red-shifted

26 els of 5-HT, its precursors L-tryptophan and 5-hydroxytryptophan and the metabolite 5-hydroxyindole a

27 roxyindoles serotonin (5-hydroxytryptamine), 5-hydroxytryptophan, and 5-hydroxyindole acetic acid are

28 ired for the synthesis of physostigmine from 5-hydroxytryptophan, as shown by in vitro total reconsti

29 lectively monitors the fluorescence yield of 5-hydroxytryptophan by exciting the reaction mix at 300

30 rs, such as l-(11)C-methionine and l-1-(11)C-5-hydroxytryptophan, demonstrated promising results, inc

31 The unfolding data show that 5-hydroxytryptophan does not perturb the stability of wi

32 rm-Raman spectroscopy proves the presence of 5-hydroxytryptophan, epidermal TPH activity is completel

33 Chemical-quench analyses show that 5-hydroxytryptophan forms with a rate constant of 1.3 s(

34 etically encoded the noncanonical amino acid 5-hydroxytryptophan in both E. coli and eukaryotes, enab

35 t spectral characteristics of tryptophan and 5-hydroxytryptophan is presented.

36 er an initial increase in the 5-HT precursor 5-hydroxytryptophan it too decreased with increasing amm

37 of the purified fusion enzyme is 80 nmol of 5-hydroxytryptophan/min/mg.

38 The 5-hydroxytryptophan residue was shown to allow rapid, ch

39 alanine and tryptophan, forming tyrosine and 5-hydroxytryptophan, respectively.

40 precursor of dopamine), and tryptophan into 5-hydroxytryptophan (the precursor of serotonin), respec

41 yindole acetic acid, but not L-tryptophan or 5-hydroxytryptophan, were reduced in the medulla by 45 a

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