3D-FF104462 - 1r-1-4-fluorophenylethanamine | 374898-01-8

3-Fluorophenylamine Hydrochloride

N-Benzyl-α,α-dimethyl-4-fluorophenethylamine

N-Benzylidene-α,α-dimethyl-4-fluorophenethylamine

α,α-Dimethyl-4-fluorophenethylamine hydrochloride

3-Fluorophenethylamine is a fluorinated analog of phenethylamine that binds to the same receptors and has a similar effect on neurotransmitters as the parent compound. 3-Fluorophenethylamine inhibits the production of tumor necrosis factor-α (TNF-α) in vitro, which may be due to its ability to inhibit prostaglandin synthesis by binding to cyclooxygenase. This drug has also been shown to have anti-inflammatory effects that are mediated by inhibition of TNF-α production and activation of nuclear factor kappa B (NFκB) pathways in hippocampal neurons.

4-Fluorophenethylamine is a fluorinated amine with the chemical formula C8H11FO. It is a 5-HT agonist and has been shown to have affinity constants for the CB2 receptor. 4-Fluorophenethylamine has been shown to be an uptake inhibitor of amines, as well as being a hydrogen bond donor.

2-Fluorophenethylamine is a molecule that can switch between two forms, one hydrophobic and one hydrophilic. When it is in the hydrophobic form, 2-fluorophenethylamine can bind to water molecules to form potential use products. When 2-fluorophenethylamine is in the hydrophilic form, it can desorb from the surface of water. 2-Fluorophenethylamine has been shown to be a neurotransmitter and may have potential use as an anti-depressant or anti-anxiety medication. It has also been suggested that 2-fluorophenethylamine may be used for the treatment of Parkinson's disease, because of its ability to inhibit dopamine degradation. An experiment conducted with spectra found that 2-fluorophenethylamine reacts with hydrogen bonds and other weak interactions to form dimers and monomers. The vibrational spectrum of this molecule shows that there are no strong

4-Fluorophenethylamine hydrochloride is a membrane-active agent that can be used to study the effects of substances on lipid bilayers. The drug has been shown to disrupt bilayers and multilayers with increasing concentrations, and it can also be used to measure the degree of resistance to osmotic disruption. 4-Fluorophenethylamine hydrochloride is moderately toxic, but it is not known how the drug affects membrane surface proteins or how it interacts with other drugs. This product may be used as an intermediate in organic chemistry reactions involving electron transfer.