Nomifensine – 50 mg

Brand:
Cayman
CAS:
24526-64-5
Storage:
-20
UN-No:
Non-Hazardous - /

Nomifensine is an inhibitor of norepinephrine (NE) and dopamine (DA) reuptake.{25265} It inhibits uptake of NE, DA, and serotonin (5-HT) in rat brain synaptosomes with IC50 values of 6.6, 48, and 830 nM, respectively. It is selective for DA, NE, and 5-HT uptake inhibition over binding to dopamine D2, α1- adrenergic-, 5-HT2, and muscarinic receptors (IC50s = 43,000, 1,200, 3,800, and >13,000 nM, respectively, in rat brain membranes). Nomifensine is selective for inhibition of NE over DA uptake in vivo with minimal inhibitory doses of 28 and less than 57 µmol/kg, respectively. It decreases the time Wistar Kyoto, but not Sprague-Dawley, rats spend immobile in the forced swim test but also increases locomotor activity in the open field test in Wistar Kyoto and Sprague-Dawley rats when administered at a chronic dose of 10 mg/kg.{48733}  

 

Available on backorder

SKU: 29330 - 50 mg Category:

Description

An inhibitor of norepinephrine and dopamine reuptake; inhibits uptake of NE, DA, and 5-HT in rat brain synaptosomes (IC50s = 6.6, 48, and 830 nM, respectively); selective for DA, NE, and 5-HT uptake inhibition over binding to dopamine D2, α1- adrenergic-, 5-HT2, and muscarinic receptors (IC50s = 43,000, 1,200, 3,800, and >13,000 nM, respectively, in rat brain membranes); is selective for inhibition of NE over DA uptake in vivo with minimal inhibitory doses of 28 and < 57 µmol/kg, respectively; decreases the time Wistar Kyoto, but not Sprague-Dawley, rats spend immobile in the forced swim test but also increases locomotor activity in the open field test in Wistar Kyoto and Sprague-Dawley rats at 10 mg/kg


Formal name: 1,2,3,4-tetrahydro-2-methyl-4-phenyl-8-isoquinolinamine

Synonyms:  (±)-Nomifensine

Molecular weight: 238.3

CAS: 24526-64-5

Purity: ≥95%

Formulation: A crystalline solid