Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H13N3O2 |
| Molecular Weight | 231.2505 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C(N1CCCCC1)C2=CC3=NON=C3C=C2
InChI
InChIKey=XFVRBYKKGGDPAJ-UHFFFAOYSA-N
InChI=1S/C12H13N3O2/c16-12(15-6-2-1-3-7-15)9-4-5-10-11(8-9)14-17-13-10/h4-5,8H,1-3,6-7H2
| Molecular Formula | C12H13N3O2 |
| Molecular Weight | 231.2505 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
CNS Activity
Originator
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Glutamatergic targets for enhancing extinction learning in drug addiction. | 2010-12 |
|
| Evaluation of the pro-cognitive effects of the AMPA receptor positive modulator, 5-(1-piperidinylcarbonyl)-2,1,3-benzoxadiazole (CX691), in the rat. | 2009-01 |
|
| Current management of the cognitive dysfunction in Parkinson's disease: how far have we come? | 2008-08 |
|
| Acute effects of the ampakine farampator on memory and information processing in healthy elderly volunteers. | 2007-06 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:32:20 GMT 2025
by
admin
on
Mon Mar 31 18:32:20 GMT 2025
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| Record UNII |
7X6P5N8K2L
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| Record Status |
Validated (UNII)
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29710
Created by
admin on Mon Mar 31 18:32:20 GMT 2025 , Edited by admin on Mon Mar 31 18:32:20 GMT 2025
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| Code System | Code | Type | Description | ||
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FARAMPATOR
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DB15012
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211735-76-1
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CHEMBL1276138
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7X6P5N8K2L
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100000174953
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4118151
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8534
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DTXSID90175413
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C65620
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QQ-90
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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TARGET->POSITIVE ALLOSTERIC MODULATOR (PAM) |
Low-impact AMPAR PAMs decrease AMPAR deactivation (channel closing) alone to augment synaptic currents
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
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