Flunamine
Flunamine is a broad-spectrum monoamine transporter inhibitor that inhibits the uptake of dopamine (DA), 5-hydroxytryptamine (5-HT), and noradrenaline (NA) in rat brain synaptosomes. The IC50 values of Flunamine for DA and 5-HT uptake in rat striatal synaptosomes are 0.26 μM and 0.17 μM, respectively, and the IC50 values for 5-HT and NA uptake in hypothalamic synaptosomes are 0.24 μM and 0.092 μM, respectively. Flunamine acts through broad-spectrum inhibition of dopaminergic, serotonergic, and noradrenergic monoamine reuptake and is used in research related to depression and Parkinson's disease.
Nos produits utilisent uniquement pour la recherche. Nous ne vendons pas aux patients.
- CAS No.: 50366-32-0
- Formule: C15H15F2NO
- Masse moléculaire:263.29
-
Stockage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Activité biologique
Description
IC50 & Target
[2]|
DAT 0.26 μM (IC50) |
SERT 0.17 μM (IC50) |
SERT 0.24 μM (IC50) |
NET 0.092 μM (IC50) |
In Vitro
Flunamine (preincubation for 10 min; uptake incubation for 5 min) inhibits the uptake of 5-HT and NA in rat hypothalamic synaptosomes, with IC50 values of 0.24 μM and 0.092 μM, respectively[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
-
CAS No. 50366-32-0
-
Masse moléculaire 263.29
-
Formule C15H15F2NO
-
SMILES
FC1=CC=C(C=C1)C(OCCN)C2=CC=C(F)C=C2
-
Livraison
Room temperature in continental US; may vary elsewhere.
-
Stockage
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureté et documentation
Références
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)