assay
≥98% (HPLC)
form
solid
storage condition
protect from light
color
off-white to tan
solubility
H2O: ≥10 mg/mL
SMILES string
Cl[H].NCCc1cccc(O)c1
InChI
1S/C8H11NO.ClH/c9-5-4-7-2-1-3-8(10)6-7;/h1-3,6,10H,4-5,9H2;1H
InChI key
GTIWCKXKQGMMQZ-UHFFFAOYSA-N
Biochem/physiol Actions
Dopamine receptor agonist; biological precursor to dopamine.
Disclaimer
Photosensitive
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
D L Murphy et al.
Journal of neural transmission. Supplementum, 52, 39-48 (1998-06-13)
Marked, dose-dependent elevations in the urinary excretion of phenylethylamine, para-tyramine, and meta-tyramine were observed in depressed patients treated for three or more weeks with 10, 30, or 60 mg/day of the partially-selective inhibitor of MAO-B, selegiline (l-deprenyl). In comparative studies
H Wayment et al.
Journal of neurochemistry, 70(5), 1941-1949 (1998-05-08)
Experiments were conducted to determine how (-)-cocaine and S(+)-amphetamine binding sites relate to each other and to the catechol substrate site on the striatal dopamine transporter (sDAT). In controls, m-tyramine and S(+)-amphetamine caused release of dopamine from intracellular stores at
S C Yeung et al.
General pharmacology, 16(5), 517-519 (1985-01-01)
The concentration of homovanillic acid and p-tyramine in the female corpus striatum were increased after ovariectomy. The increases were reversed by chronic administration of estradiol benzoate and potentiated by progesterone. It is proposed that these changes are the consequence of
D A Durden et al.
Neurochemical research, 18(9), 995-1002 (1993-09-01)
Using a new ultrasensitive method the trace biogenic amines, phenylethylamine, meta-tyramine and para-tyramine have been quantitated in brain regions obtained from a single rat. Phenylethylamine concentrations in ng/g wet tissue (mean +/- std. error) were as follows: caudate 2.71 +/-
P L Walker et al.
Annals of clinical biochemistry, 25 ( Pt 3), 304-309 (1988-05-01)
A simple, reliable method for the analysis of urinary meta- and para-tyramine has been developed. Sample purification was achieved by a weak anion-exchange column, followed by extraction into ethyl acetate at pH 10.2. The heptafluorobutyryl derivative was measured by packed
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