A6CDQ
A6CDQ is a human organic cation transporter (hOCT) inhibitor with antidepressant-like activity that can cross the blood-brain barrier. A6CDQ potently inhibits the transport activities mediated by hOCT1, hOCT2 and hOCT3. A6CDQ exhibits significant antidepressant-like effects in the mouse tail suspension test. A6CDQ can be used in studies related to depression.
For research use only. We do not sell to patients.
- CAS No.: 1005550-46-8
- Formula: C8H8ClN3
- Molecular Weight:181.62
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
A6CDQ (10-8-10-3 M; 1 min) inhibits hOCT1, hOCT2, and hOCT3-mediated MPP+ transport in stably transfected HEK293 cells, with IC50 values of 3.0 μM (hOCT1), 16.4 μM (hOCT2), and 3.9 μM (hOCT3)[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:ICR mice with Depression (male, 20−24 g)[1]
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Dosage:0.1 mg/kg; 0.3 mg/kg; 1.0 mg/kg; 3.0 mg/kg; 10 mg/kg; 30 mg/kg
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Administration:i.p.; single dose
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Result:Significantly reduced immobility time compared to saline at 1.0 mg/kg.
Reached an ED50 of 0.23 mg/kg.
Chemical Information
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CAS No. 1005550-46-8
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Molecular Weight 181.62
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Formula C8H8ClN3
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SMILES
NC1=NC2=C(CN1)C=C(Cl)C=C2
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)