Benzquinamide
Benzquinamide (P2647; BZQ; Benzoquinamide) is an orally active binder of dopamine receptors and adrenergic receptors. Benzquinamide specifically targets dopamine D2, D3, D4 receptors and α-2A, α-2B, α-2C adrenergic receptors. Benzquinamide regulates blood pressure and heart rate, attenuates the pressor effect of adrenaline, and exhibits activities such as antiemesis, anxiolysis, and reduction of histamine-induced bronchoconstriction. Benzquinamide has good safety and does not deplete serotonin or norepinephrine in the brain. Benzquinamide can be used in studies related to nausea/vomiting, mental disorders, anxiety states, neurosis, and psychosis.
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- CAS 番号: 63-12-7
- 分子式: C22H32N2O5
- 分子量:404.50
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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生物活性
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化学情報
- 純度とドキュメンテーション
- 参考文献
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Help & FAQs
生物活性
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α adrenergic receptor |
D2 Receptor |
D3 Receptor |
D4 Receptor |
Benzquinamide binds to human dopamine D2, D3, and D4 receptors, with the highest affinity for the D4 subtype (Ki=574 nM)[1].
Benzquinamide (10 μM) binds to human α2A, α2B, and α2C adrenergic receptors, with the highest affinity for the α2C subtype (Ki=545 nM), and does not produce meaningful binding to histamine H1 receptors or muscarinic M1-M5 receptors[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Benzquinamide (5-20 mg/kg; i.p.) inhibits isolation-induced fighting behavior in male mice starting at 5 mg/kg (i.p.) without causing muscle relaxation or impaired coordination[2].
Benzquinamide (0.4-1.6 mg/kg; i.v.; 4.0-6.0 mg/kg; p.o.) blocks apomorphine-induced emesis in dogs with an intravenous ED50 of approximately 0.9 mg/kg, and fully blocks emesis at 6.0 mg/kg (p.o.)[2].
Benzquinamide (10-25 mg/kg; i.v.) does not deplete brain serotonin or norepinephrine concentrations in dogs at doses up to 25 mg/kg (i.v.)[2].
Benzquinamide (10 mg/kg; i.v.) does not exhibit neuromuscular activity in Felis catus at 10 mg/kg (i.v.)[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Rat with anxiety-related behavior[2]
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Dosage:16.5 mg/kg (disrupting avoidance behavior); 60.5 mg/kg (disrupting escape behavior)
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Administration:i.p.
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Result:Disrupted conditioned avoidance behavior with an ED50 of 16.5 mg/kg (i.p.).
Disrupted escape behavior with an ED50 of 60.5 mg/kg (i.p.).
Achieved a specificity score (escape ED50 to avoidance ED50 ratio) of 3.7.
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Animal Model:Mature aggressio nmale mice[2]
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Dosage:5 mg/kg; 10 mg/kg; 20 mg/kg
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Administration:i.p.
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Result:Inhibited isolation-induced fighting behavior starting at 5 mg/kg (i.p.).
Caused no muscle relaxation or interference with muscular coordination at doses that reduced or prevented fighting.
化学情報
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CAS 番号 63-12-7
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分子量 404.50
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分子式 C22H32N2O5
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SMILES
O=C(C1CN2CCC3=CC(OC)=C(OC)C=C3C2CC1OC(C)=O)N(CC)CC
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別名
P2647; BZQ; Benzoquinamide
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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)
Benzquinamide 関連分類
HY-U00244 関連分類
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