Amphetamine hydrochloride

Biochem/physiol Actions Sympathomimetic with more potent central effects than amphetamine. It is transported into terminals via the monoamine transporters and induces release of dopamine, norepinephrine, epinephrine, and serotonin.

Biochem/physiol Actions Sympathomimetic with more potent central effects than amphetamine. It is transported into terminals via the monoamine transporters and induces release of dopamine, norepinephrine, epinephrine, and serotonin.

Biochem/physiol Actions Sympathomimetic with more potent central effects than amphetamine. It is transported into terminals via the monoamine transporters and induces release of dopamine, norepinephrine, epinephrine, and serotonin.

General description Octopamine is a biogenic amine, which functions as a neurotransmitter, neuromodulator and neurohormone. It is used to regulate various behaviors, such as learning, memory&nbsp:and aggression.

General description Octopamine is a biogenic amine, which functions as a neurotransmitter, neuromodulator and neurohormone. It is used to regulate various behaviors, such as learning, memory&nbsp:and aggression.

Amphetamine, 100mL, 1/bx (US Only) (Not Available For Sale into Canada) (Must be Refrigerated). AMPHETAMINE 100ML 1/BX (DROP)

Application Cocaine hydrochloride has been used: in saline control to study the effects of cocaine self-administration in mouse brain as adopamine (DA), noradrenaline (NA), and serotonin (5-HT) reuptake inhibitor to evoke neurotransmitter release

Application Cocaine hydrochloride has been used: in saline control to study the effects of cocaine self-administration in mouse brain as adopamine (DA), noradrenaline (NA), and serotonin (5-HT) reuptake inhibitor to evoke neurotransmitter release

Application Cocaine hydrochloride has been used: in saline control to study the effects of cocaine self-administration in mouse brain as adopamine (DA), noradrenaline (NA), and serotonin (5-HT) reuptake inhibitor to evoke neurotransmitter release

CYSTEAMINE HYDROCHLORIDE

Eliprodil is a non-competitive NMDA receptor antagonist which acts at the polyamine modulatory site. Eliprodil is selective for NMDA epsilon 2 (NR2B-containing receptors) over NR2A- and NR2C-containing receptors (IC50 values are 1, &gt: 100 and &gt:

Eliprodil is a non-competitive NMDA receptor antagonist which acts at the polyamine modulatory site. Eliprodil is selective for NMDA epsilon 2 (NR2B-containing receptors) over NR2A- and NR2C-containing receptors (IC50 values are 1, &gt: 100 and &gt: