92629-87-3

Dexnafenodone Chemical Structure
92629-87-3

Chemical Structure

Dexnafenodone

Synonym(s): (S)-Nafenodone free base; LU-43706 free base

  • No. CAS: 92629-87-3
  • Formula:C20H23NO
  • Molecular Weight:293.41

IUPAC Name: (S)-2-(2-(dimethylamino)ethyl)-2-phenyl-3,4-dihydronaphthalen-1(2H)-one

InChIKey: IOKKIRANVRFSAH-FQEVSTJZSA-N

SMILES: C(CN(C)C)[C@]1(C(=O)C=2C(CC1)=CC=CC2)C3=CC=CC=C3

Biological Activity: Dexnafenodone ((S)-Nafenodone free base; LU-43706 free base) is a novel antidepressant candidate molecule that selectively inhibits the norepinephrine synaptosomal uptake transporter. Dexnafenodone inhibits the fast inward Na+ current and slow inward Ca2+ current in cardiomyocytes. Dexnafenodone inhibits voltage-gated and receptor-activated Ca2+ influx in vascular smooth muscle, depletes norepinephrine-sensitive intracellular Ca2+ stores, suppresses agonist-stimulated Ca2+ influx, relaxes precontracted vascular smooth muscle, inhibits spontaneous myogenic activity, and modulates cardiac electrophysiology, exerting negative chronotropic and negative inotropic effects. Dexnafenodone can be used in the research of depression[1][2].

Referencia número Nombre del producto Pureza Descripciòn Pricing
HY-105521
Dexnafenodone Dexnafenodone ((S)-Nafenodone free base; LU-43706 free base) is a novel antidepressant candidate molecule that selectively inhibits the norepinephrine synaptosomal uptake transporter. Dexnafenodone inhibits the fast inward Na+ current and slow inward Ca2+ current in cardiomyocytes. Dexnafenodone inhibits voltage-gated and receptor-activated Ca2+ influx in vascular smooth muscle, depletes norepinephrine-sensitive intracellular Ca2+ stores, suppresses agonist-stimulated Ca2+ influx, relaxes precontracted vascular smooth muscle, inhibits spontaneous myogenic activity, and modulates cardiac electrophysiology, exerting negative chronotropic and negative inotropic effects. Dexnafenodone can be used in the research of depression.
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