Op het Web is voldoende informatie around dosering en werkingsduur te vinden maar omdat het toch een handvol verschillende...
It inhibits a reuptake of dopamine, but is a Considerably much better serotonin reuptake inhibitor. This has guide to various results in animal research.
One characteristic of the drug is the fact that since it differs molecularly than professional benzos, it does not display up on most screening drug checks.
The physiological and toxicological Homes of this compound will not be recognised. This products is intended for forensic and study purposes.
four-Fluoroamphetamine is really a substituted amphetamine which offers results somewhere between People of amphetamine and MDMA. ItÂ’s been a member of the research chemical market place Considering that the late 2000s.
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This has led the online community to speculate that the milder not comfortable cognitive and/or physical Unwanted side effects and better efficacy being a nootropic related to this substance are at the very least partially on account of lowered activity in the alpha-one adrenergic receptors causing noticeably much less norepinephrine reuptake inhibition.
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four-Fluoroamphetamine functions as a releasing agent and reuptake inhibitor of dopamine, serotonin, and norepinephrine, developing stimulating amphetamine-like results at decrease doses and euphoric, entactogenic outcomes just like MDMA at dosages higher than 100mg. The system of action of 4-FA efficiently boosts the amounts of the norepinephrine, dopamine, and serotonin neurotransmitters in bigger doses within the website brain by binding to and partially blocking the transporter proteins that Typically take away These monoamines from the synaptic cleft.
Experiments reveal that four-flourine amphetamine substitutions Restrict action on the compound on the alpha-1 adrenergic receptor with the above 200-fold increased check here selectivity for A2 receptors over A1 receptors. It's got also been shown that four-substitution of a hydrogen with fluorine within more info the aromatic ring of norepinephrine creates a beta-adrenergic agonist with little alpha exercise.
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Scientific tests demonstrate that 4-flourine amphetamine substitutions limit activity in the compound with the alpha-one adrenergic receptor with an over 200-fold elevated selectivity for A2 receptors above A1 receptors. It's also been demonstrated that 4-substitution of a hydrogen with fluorine to the aromatic ring of norepinephrine provides a beta-adrenergic agonist with little alpha activity.