Dexnafenodone hydrochloride
Dexnafenodone hydrochloride ((S)-Nafenodone; LU-43706) is a novel antidepressant candidate molecule that selectively inhibits the norepinephrine synaptosomal uptake transporter. Dexnafenodone hydrochloride inhibits the fast inward Na+ current and slow inward Ca2+ current in cardiomyocytes. Dexnafenodone hydrochloride 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 hydrochloride can be used in the research of depression.
연구목적의 판매만을 진행합니다. 환자를 대상으로 한 판매는 하지 않습니다.
- CAS No.: 94096-42-1
- 화학식: C20H24ClNO
- 분자량:329.86
-
보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
All Calcium Channel Isoforms
More
Biological Activity
Dexnafenodone hydrochloride ((S)-Nafenodone) inhibits potassium chloride- and norepinephrine-induced contractions of isolated rat aortic strips with equal potency; it possesses voltage-sensitive Ca2+ channel blocking activity, with an IC50 of 2.5×10‑6 M for inhibiting Ca2+-induced contractions of potassium-depolarized aortas. It also inhibits norepinephrine-induced phasic contractions mediated by intracellular calcium stores in a calcium-free environment, and suppresses spontaneous myogenic activity of rat portal veins with an IC50 of 1.4×10‑6 M[1].
Dexnafenodone hydrochloride inhibits 45Ca2+ influx in isolated rat aortic strips stimulated by potassium chloride and norepinephrine, but does not alter 45Ca2+ influx under resting conditions. The I50 value of this compound for inhibiting potassium chloride-induced calcium influx is 2.1×10‑5 M[1].
Dexnafenodone hydrochloride exerts concentration-dependent negative chronotropic and negative inotropic effects in isolated spontaneously beating guinea pig right atria, and prolongs the sinus node recovery time. Its IC50 value for chronotropic inhibition is 1×10-5 M, and the IC50 value for inotropic inhibition is 5×10-6 M[2].
Dexnafenodone hydrochloride exerts a concentration-dependent inhibitory effect on isolated guinea pig myocardium, producing negative chronotropic and negative inotropic effects with corresponding IC50 values of 1×10‑5 M and 5×10‑6 M, respectively, and shifts the calcium concentration-response curve to the right[1].
Dexnafenodone hydrochloride ((S)-Nafenodone) reduces the action potential amplitude and Vmax of atrial and ventricular myocytes, does not alter the resting membrane potential, and increases the ERP/APD90 ratio[2].
Dexnafenodone hydrochloride inhibits slow calcium-mediated contraction of potassium-depolarized cardiomyocytes, and suppresses isoproterenol-induced slow action potentials at high concentrations[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
-
CAS No. 94096-42-1
-
분자량 329.86
-
화학식 C20H24ClNO
-
SMILES
O=C1[C@](C2=CC=CC=C2)(CCN(C)C)CCC3=C1C=CC=C3.[H]Cl
-
Synonyms
(S)-Nafenodone; LU-43706
-
선적
Room temperature in continental US; may vary elsewhere.
-
보관
Please store the product under the recommended conditions in the Certificate of Analysis.
순도&문서
References
[1]. Pérez-Vizcaíno F, et al. Effects of (S)-nafenodone on 45Ca2+ fluxes and contractions in rat isolated vascular smooth muscle. European journal of pharmacology. 1993 Feb 23;232(1):105-11. [Content Brief]
[2]. Pérez-Vizcaino F, et al. Effects of (S)-nafenodone, a new antidepressant, in isolated guinea-pig atrial and ventricular muscle fibres. European journal of pharmacology. 1991 Jun 18;199(1):43-50. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
- Dexnafenodone
- 94096-42-1
- (S)-Nafenodone
- LU-43706
- LU43706
- LU 43706
- LU-43706
- Calcium Channel
- Sodium Channel
- dopamine receptors
- 5-HT2 receptors
- protein kinase C
- voltage-sensitive L-type Ca2+ channel
- muscarinic M1 receptors
- α-adrenoceptors
- rat aortic strips
- noradrenaline synaptosomal uptake transporter
- fast inward Na+ channel
- histamine H1 receptors
- Inhibitor
- inhibitor
- inhibit