| Identification | Back Directory | [Name]
4-(2-METHYLAMINO-ETHYL)-PHENOL | [CAS]
370-98-9 | [Synonyms]
n-methyl-tyramin
methyl-4-tyramine
N-METHYL-P-TYRAMINE
p-(2-methylaminoethyl)-pheno
p-(2-methylaminoethyl)phenol
4-(2-METHYLAMINO-ETHYL)-PHENOL
N-Methyltyramine hydrochloride
4-HYDROXY-N-METHYLPHENETHYLAMINE
Phenol,4-[2-(methylamino)ethyl]-
METHYLTYRAMINE, N-(P)(PLEASE CALL)
2-(4-hydroxyphenyl)ethyl-methylammonium
4-[2-(Methylamino)ethyl]phenol
N-Methyl-p-tyramine | [EINECS(EC#)]
206-731-3 | [Molecular Formula]
C9H13NO | [MDL Number]
MFCD00870493 | [MOL File]
370-98-9.mol | [Molecular Weight]
151.21 |
| Chemical Properties | Back Directory | [Melting point ]
130～131℃ | [Boiling point ]
270.9±15.0 °C(Predicted) | [density ]
1.035±0.06 g/cm3(Predicted) | [storage temp. ]
Refrigerator | [solubility ]
DMSO (Slightly), Methanol (Slightly) | [form ]
Solid | [pka]
9.86±0.15(Predicted) | [color ]
Pale Beige to Light Beige | [InChI]
InChI=1S/C9H13NO/c1-10-7-6-8-2-4-9(11)5-3-8/h2-5,10-11H,6-7H2,1H3 | [InChIKey]
AXVZFRBSCNEKPQ-UHFFFAOYSA-N | [SMILES]
C1(O)=CC=C(CCNC)C=C1 |
| Hazard Information | Back Directory | [Uses]
N-Methyltyramine is a protoalkaloid that can be isolated from various plant species. N-Methyltyramine is an α2-adrenoreceptor antagonist. N-Methyltyramine enhances appetite and digestion of foods by stimulating gastrin and pancreatic secretions. N-Methyltyramine can relax mouse small intestinal smooth muscle and inhibits small intestinal propulsion[1][2]. | [Definition]
ChEBI: N-methyltyramine is a member of tyramines. It has a role as a mouse metabolite. It is a conjugate base of a N-methyltyraminium. | [References]
[1] Stohs SJ, et al. A review of the receptor binding and pharmacological effects of N-methyltyramine. Phytother Res. 2015 Jan;29(1):14-6. DOI:10.1002/ptr.5231
[2] Ni J, et al. Effect of N-methyltyramine on the regulation of adrenergic receptors via enzymatic epinephrine synthesis for the treatment of gastrointestinal disorders. Biomed Pharmacother. 2019 Mar;111:1393-1398. DOI:10.1016/j.biopha.2018.12.145 |
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