SEN 78702
SEN 78702 is an orally active, selective, full α7 nAChR agonist, with a pEC50 of 6.13. SEN 78702 has an acceptable hERG inhibition (IC50: 15.8 μM). SEN 78702 induces memory enhancement.
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- CAS. Nr.: 1205530-63-7
- Formel: C17H22FN5O
- Molecular Weight:331.39
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Speicherung:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biologische Aktivität
Beschreibung
IC50 & Target
pEC50: 6.13 (α7 nAChR); IC50: 15.8 μM (hERG)[1]
Cellular Effect
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| CHO | IC50 |
15.8 μM
Compound: 12, SEN78702, WYE-308775
|
Inhibition of human ERG expressed in CHO cells
Inhibition of human ERG expressed in CHO cells
|
[PMID: 23083093] |
| GH4-C1 | EC50 |
0.74 μM
Compound: 12, SEN78702, WYE-308775
|
Agonist activity at rat alpha7 nAchR expressed in rat GH4C1 cells assessed as stimulation of calcium flux by FLIPR
Agonist activity at rat alpha7 nAchR expressed in rat GH4C1 cells assessed as stimulation of calcium flux by FLIPR
|
[PMID: 23083093] |
| GH4-C1 | EC50 |
10.7 μM
Compound: 12, SEN78702, WYE-308775
|
Agonist activity at rat alpha7 nAchR expressed in rat GH4C1 cells by patch clamp assay
Agonist activity at rat alpha7 nAchR expressed in rat GH4C1 cells by patch clamp assay
|
[PMID: 23083093] |
Chemical Information
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CAS. Nr. 1205530-63-7
-
Molecular Weight 331.39
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Formel C17H22FN5O
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SMILES
O=C(NC1=CC(C2=CC(F)=CN=C2)=NN1)CCCN3CCCCC3
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Versand
Room temperature in continental US; may vary elsewhere.
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Speicherung
Please store the product under the recommended conditions in the Certificate of Analysis.
Reinheit & Dokumentation
Verweise
Calculators
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)