| Weight | 137.182 g/mol |
|---|---|
| Formula | C8H11NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
m-Tyramine (588-05-6)
Score:
#903 in Neuroscience
,
#1828 in Biochemistry
,
#3969 in Biology
,
#4997 in Chemistry
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- Sigma-Aldrich - m-Tyramine386.25 USD
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- Identification and Distribution of m-Tyramine in the Rat (Biochemistry and Cell Biology, 1974)
- Evidence for the presence of m-tyramine, p-tyramine, tryptamine, and phenylethylamine in the rat brain and several areas of the human brain. (Biological Psychiatry, 1978)
- MASS FRAGMENTOGRAPHY OF PHENYLETHYLAMINE, m AND pTYRAMINE AND RELATED AMINES IN PLASMA, CEREBROSPINAL FLUID, URINE, AND BRAIN (Journal of Neurochemistry, 1979)
- Interactions between p-tyramine, m-tyramine, or -phenylethylamine and dopamine on single neurones in the cortex and caudate nucleus of the rat (Canadian Journal of Physiology and Pharmacology, 1980)
- The biosynthesis of p-tyramine, m-tyramine, and -phenylethylamine by rat striatal slices (Journal of Neuroscience Research, 1983)
- Therapeutic Implications in Parkinsonism of m-Tyramine Formation from L-Dopa in Man (Nature, 1971)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CC(=C1)O)CCN
-
InChIKeyGHFGJTVYMNRGBY-UHFFFAOYSA-N
- Pubchem - m-Tyramine
- Wikipedia - m-tyramine
meta-Tyramine, also known as m-tyramine and 3-tyramine, is an endogenous trace amine neuromodulator and a structural analog of phenethylamine. It is a positional isomer of para-tyramine, and similarly to it, has effects on the adrenergic and dopaminergic systems. meta-Tyramine is produced in humans via aromatic amino acid decarboxylase-mediated metabolism of meta-tyrosine.
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m-Tyramine
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