69577
α-Methyl-DL-tyrosine
≥95% (NT)
Synonym(s):
DL-2-Methyl-3-(4-hydroxyphenyl)alanine, AMPT
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
4-(HO)C6H4CH2C(CH3)(NH2)CO2H
CAS Number:
Molecular Weight:
195.22
EC Number:
211-523-0
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
2938704
MDL number:
assay
≥95% (NT)
form
powder
ign. residue
≤0.05%
mp
>300 °C (lit.)
application(s)
peptide synthesis
SMILES string
CC(N)(Cc1ccc(O)cc1)C(O)=O
InChI
1S/C10H13NO3/c1-10(11,9(13)14)6-7-2-4-8(12)5-3-7/h2-5,12H,6,11H2,1H3,(H,13,14)
InChI key
NHTGHBARYWONDQ-UHFFFAOYSA-N
Other Notes
Inhibitor (Ki 5 uM) of tyrosine hydroxylase
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Tyrosine hydroxylase inhibitors.
K E Moore et al.
Federation proceedings, 30(3), 859-870 (1971-05-01)
Kinuyo Iwata et al.
The Journal of reproduction and development, 57(3), 379-384 (2011-03-02)
Ketosis is found in various pathophysiological conditions, including diabetes and starvation, that are accompanied by suppression of gonadal activity. The aim of the present study was to determine the role of ketone body in the brain in regulating pulsatile luteinizing
Ewa Bromek et al.
Journal of neurochemistry, 118(5), 806-815 (2011-06-10)
The cytochrome P450-mediated synthesis of dopamine from tyramine has been shown in vitro. The aim of the present study was to demonstrate the ability of rat cytochrome P450 (CYP) 2D to synthesize dopamine from tyramine in the brain in vivo.