Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C10H12FNO2 |
| Molecular Weight | 197.2062 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NCC(CC(O)=O)C1=CC=C(F)C=C1
InChI
InChIKey=QWHXHLDNSXLAPX-UHFFFAOYSA-N
InChI=1S/C10H12FNO2/c11-9-3-1-7(2-4-9)8(6-12)5-10(13)14/h1-4,8H,5-6,12H2,(H,13,14)
| Molecular Formula | C10H12FNO2 |
| Molecular Weight | 197.2062 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 16:59:15 UTC 2023
by
admin
on
Sat Dec 16 16:59:15 UTC 2023
|
| Record UNII |
6DAU7M5P3D
|
| Record Status |
Validated (UNII)
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| Record Version |
|
-
Download
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Common Name | English | ||
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Code | English |
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WIKIPEDIA |
Designer-drugs-4-Fluorophenibut
Created by
admin on Sat Dec 16 16:59:15 UTC 2023 , Edited by admin on Sat Dec 16 16:59:15 UTC 2023
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| Code System | Code | Type | Description | ||
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6DAU7M5P3D
Created by
admin on Sat Dec 16 16:59:15 UTC 2023 , Edited by admin on Sat Dec 16 16:59:15 UTC 2023
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DTXSID00966612
Created by
admin on Sat Dec 16 16:59:15 UTC 2023 , Edited by admin on Sat Dec 16 16:59:15 UTC 2023
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103611
Created by
admin on Sat Dec 16 16:59:15 UTC 2023 , Edited by admin on Sat Dec 16 16:59:15 UTC 2023
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52237-19-1
Created by
admin on Sat Dec 16 16:59:15 UTC 2023 , Edited by admin on Sat Dec 16 16:59:15 UTC 2023
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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TARGET -> AGONIST |
It is less potent as a GABAB receptor agonist than baclofen but more potent than phenibut.
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TARGET -> AGONIST |
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |
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