N-Methyltyramine Powder

N-Methyltyramine can be found in nature from plants such as barley and Citrus aurantium, the latter being commonly used for Synephrine content (N-Methyltyramine is converted to Synephrine by Dopamine β -hydroxylase). Unlike Synephrine, N-Methyltyramine has not been observed to display any lipolytic activity, due to the lack of a beta-hydroxyl or a beta-ketone. It's mechanisms of action imply that it acts as a peripheral sympathomimetic compound. NMT is similar to Synephrine and Hordenine, with the addition of a hydroxyl group at β distinguishing Synephrine from NMT, and substitution of a dimethyl group at the N terminal resulting in Hordenine.

This product has to increase coronary blood flow and renal blood flow, reducing myocardial oxygen consumption and a significant diuretic effect; especially powerful boost from the intensity and adrenaline-induced cardiac rhythm quite than dopamine and hydroxyl Flynn (Synephrine). Is an excellent anti-shock drugs. Is also important to drug synthesis intermediates.

N-Methyltyramine (NMT), also known as 4-hydroxy-N-methylphenethylamine, is a natural phenethylamine alkaloid found in a variety of plants. As the name implies, it is the N-methyl analog or derivative of the well-known biogenic amine, tyramine, with which it shares many pharmacological properties (see below). Biosynthetically, NMT is produced by the N-methylation of tyramine via the action of the enzyme tyramine N-methyltransferase.