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.
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- CAS 番号: 94096-42-1
- 分子式: C20H24ClNO
- 分子量:329.86
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
Calcium Channel アイソフォーム固有の製品をすべて表示
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生物活性
製品説明
体外実験
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.
化学情報
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CAS 番号 94096-42-1
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分子量 329.86
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分子式 C20H24ClNO
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SMILES
O=C1[C@](C2=CC=CC=C2)(CCN(C)C)CCC3=C1C=CC=C3.[H]Cl
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別名
(S)-Nafenodone; LU-43706
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
[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
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
Keywords
- 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