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 No.: 1205530-63-7
- Formule: C17H22FN5O
- Masse moléculaire:331.39
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Stockage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Activité biologique
Description
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 No. 1205530-63-7
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Masse moléculaire 331.39
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Formule C17H22FN5O
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SMILES
O=C(NC1=CC(C2=CC(F)=CN=C2)=NN1)CCCN3CCCCC3
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureté et documentation
Références
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)