Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C20H23FN4O2 |
| Molecular Weight | 370.4206 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCN(CC)CCN1C(CC2=CC=C(F)C=C2)=NC3=C1C=CC(=C3)[N+]([O-])=O
InChI
InChIKey=ZTWHIDCAGRMKTC-UHFFFAOYSA-N
InChI=1S/C20H23FN4O2/c1-3-23(4-2)11-12-24-19-10-9-17(25(26)27)14-18(19)22-20(24)13-15-5-7-16(21)8-6-15/h5-10,14H,3-4,11-13H2,1-2H3
| Molecular Formula | C20H23FN4O2 |
| Molecular Weight | 370.4206 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 10:14:47 GMT 2025
by
admin
on
Wed Apr 02 10:14:47 GMT 2025
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| Record UNII |
LQS4YF6P6L
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| Record Status |
Validated (UNII)
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| Record Version |
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-
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Common Name | English | ||
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Preferred Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English |
| Classification Tree | Code System | Code | ||
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WIKIPEDIA |
Designer-drugs-Flunitazene
Created by
admin on Wed Apr 02 10:14:47 GMT 2025 , Edited by admin on Wed Apr 02 10:14:47 GMT 2025
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DEA NO. |
9756
Created by
admin on Wed Apr 02 10:14:47 GMT 2025 , Edited by admin on Wed Apr 02 10:14:47 GMT 2025
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| Code System | Code | Type | Description | ||
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2249-36-7
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admin on Wed Apr 02 10:14:47 GMT 2025 , Edited by admin on Wed Apr 02 10:14:47 GMT 2025
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DTXSID401342106
Created by
admin on Wed Apr 02 10:14:47 GMT 2025 , Edited by admin on Wed Apr 02 10:14:47 GMT 2025
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PRIMARY | |||
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156588967
Created by
admin on Wed Apr 02 10:14:47 GMT 2025 , Edited by admin on Wed Apr 02 10:14:47 GMT 2025
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PRIMARY | |||
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LQS4YF6P6L
Created by
admin on Wed Apr 02 10:14:47 GMT 2025 , Edited by admin on Wed Apr 02 10:14:47 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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SALT/SOLVATE -> PARENT |
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TARGET -> AGONIST |
In vitro data suggest that flunitazene is much less potent than fentanyl. Emax=118% of Fentanyl
EC50
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
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