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.
For research use only. We do not sell to patients.
- CAS No.: 1205530-63-7
- Formula: C17H22FN5O
- Molecular Weight:331.39
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
pEC50: 6.13 (α7 nAChR); IC50: 15.8 μM (hERG)[1]
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Cell Line
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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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Molecular Weight 331.39
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Formula C17H22FN5O
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SMILES
O=C(NC1=CC(C2=CC(F)=CN=C2)=NN1)CCCN3CCCCC3
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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)