Eclanamine
Eclanamine is an orally effective non-tricyclic antidepressant and an adrenergic receptor modulator. Eclanamine blocks biogenic amine uptake and enhances α2-receptor sensitivity, and long-term administration induces downregulation and desensitization of cortical β-receptors. Eclanamine is used in the study of depression.
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研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- CAS 番号: 67450-44-6
- 分子式: C16H22Cl2N2O
- 分子量:329.26
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
Adrenergic Receptor 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
IC50 & Target
[1]|
α2-adrenergic receptor |
β adrenergic receptor |
体外実験
Eclanamine weakly inhibits the binding of (3H)-dihydroalpranolol (DHA) in rat brain cortex tissue homogenates (inhibition rate below 50%)[3].
Eclanamine induces gene mutations in CHO/HPRT and AS52 cells[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. .
体内実験
Eclanamine (1-30 mg/kg/day; i.v.; continuous infusion; treatment duration of 8 to 168 h) dose-dependently downregulates cerebral cortical β-adrenergic receptor (beta-AR) density in female Sprague-Dawley rats[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Sprague-Dawley rats (female, 280-320 g)[3]
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Dosage:1, 3, 10, and 30 mg/kg/day
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Administration:i.v.; continuous infusion; 24 h
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Result:Dose-dependently reduced the density of beta-adrenergic receptors (Bmax) in the cerebral cortex with a significant dose-response relationship.
The minimum effective dose that significantly down-regulated beta-AR at 24 hours was 3.0 mg/kg/day.
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Animal Model:Sprague-Dawley rats (female)[3]
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Dosage:10 mg/kg/day
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Administration:i.v.; continuous infusion; 8, 16, 24, 48, 72, and 168 hours
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Result:Resulted in a significant reduction in the number of beta-AR at 16 and 24 hours.
The peak effect was observed at 72 hours, at which time it produced a similar degree of down-regulation to imipramine.
化学情報
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CAS 番号 67450-44-6
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分子量 329.26
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分子式 C16H22Cl2N2O
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SMILES
CCC(N(C1=CC(Cl)=C(C=C1)Cl)[C@H]2[C@@H](CCC2)N(C)C)=O
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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
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)