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 No.: 63-12-7
- 화학식: C22H32N2O5
- 분자량:404.50
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보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
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Biological Activity
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Chemical Information
- 순도&문서
- References
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Help & FAQs
Biological Activity
제품 설명
IC50 & Target
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α adrenergic receptor |
D2 Receptor |
D3 Receptor |
D4 Receptor |
In Vitro
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.
In Vivo
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.
Chemical Information
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CAS No. 63-12-7
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분자량 404.50
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화학식 C22H32N2O5
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SMILES
O=C(C1CN2CCC3=CC(OC)=C(OC)C=C3C2CC1OC(C)=O)N(CC)CC
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Synonyms
P2647; BZQ; Benzoquinamide
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선적
Room temperature in continental US; may vary elsewhere.
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보관
Please store the product under the recommended conditions in the Certificate of Analysis.
순도&문서
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Benzquinamide Related Classifications
HY-U00244 Related Classifications
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