PSN09
PSN09 is a blood-brain barrier-permeable agonist of PSAM4-GlyR and PSAM4-5-HT3 receptors with high affinity. 18F-labeled PSN09 serves as a radiotracer for PET imaging in non-human primates.
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- 화학식: C20H18FN3O
- 분자량:335.37
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보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
All 5-HT Receptor Isoforms
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Biological Activity
제품 설명
IC50 & Target
[1]|
5-HT3 Receptor |
In Vitro
PSN09 potently binds to PSAM4-GlyR in transfected HEK-293 cells, with a Ki of 1.86 nM[1].
PSN09 potently binds to PSAM4-5-HT3 in transfected HEK-293 cells, with a Ki value of 5.67 nM[1].
PSN09 (0.1-100 μM) potently activates PSAM4-GlyR in transfected HEK-293 cells, with an EC50 of 8.3 nM[1].
PSN09 (0.1-100 μM) potently activates PSAM4-5-HT3 in transduced HEK-293 cells, with an EC50 of 16.8 nM[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Monkey transduced with PSAM4-GlyR (11-year-old male, Lenti-hSyn-PSAM4-GlyR injected into left amygdala)[1]
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Dosage:1 mg/kg
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Administration:i.v.; single dose; administered 10 minutes before [18F]FDG injection
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Result:Did not significantly alter [18F]FDG arterial input functions.
Reduced MRGlu in the target transduced left amygdala by 19%, and decreased the target-to-mirror MRGlu ratio by 3%.
Chemical Information
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분자량 335.37
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화학식 C20H18FN3O
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SMILES
FC1=CC=C(C=C1)COC2=NC3=CC4=C(C5CNCC4C5)C=C3N=C2
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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)