Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C22H28N2O2 |
| Molecular Weight | 352.4699 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(=O)N(C1CCN(CC(O)C2=CC=CC=C2)CC1)C3=CC=CC=C3
InChI
InChIKey=JEFVHLMGRUJLET-UHFFFAOYSA-N
InChI=1S/C22H28N2O2/c1-2-22(26)24(19-11-7-4-8-12-19)20-13-15-23(16-14-20)17-21(25)18-9-5-3-6-10-18/h3-12,20-21,25H,2,13-17H2,1H3
| Molecular Formula | C22H28N2O2 |
| Molecular Weight | 352.4699 |
| 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
Mon Mar 31 22:28:14 GMT 2025
by
admin
on
Mon Mar 31 22:28:14 GMT 2025
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| Record UNII |
6Q4XAW26T4
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| Record Status |
Validated (UNII)
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| Record Version |
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Code | English | ||
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WIKIPEDIA |
List_of_fentanyl_analogues
Created by
admin on Mon Mar 31 22:28:14 GMT 2025 , Edited by admin on Mon Mar 31 22:28:14 GMT 2025
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CDC |
?-hydroxy Fentanyl
Created by
admin on Mon Mar 31 22:28:14 GMT 2025 , Edited by admin on Mon Mar 31 22:28:14 GMT 2025
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DEA NO. |
9830
Created by
admin on Mon Mar 31 22:28:14 GMT 2025 , Edited by admin on Mon Mar 31 22:28:14 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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BETAHYDROXYFENTANYL
Created by
admin on Mon Mar 31 22:28:14 GMT 2025 , Edited by admin on Mon Mar 31 22:28:14 GMT 2025
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PRIMARY | |||
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DB01453
Created by
admin on Mon Mar 31 22:28:14 GMT 2025 , Edited by admin on Mon Mar 31 22:28:14 GMT 2025
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PRIMARY | |||
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NB 009
Created by
admin on Mon Mar 31 22:28:14 GMT 2025 , Edited by admin on Mon Mar 31 22:28:14 GMT 2025
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PRIMARY | |||
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Betahydroxyfentanyl
Created by
admin on Mon Mar 31 22:28:14 GMT 2025 , Edited by admin on Mon Mar 31 22:28:14 GMT 2025
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PRIMARY | .BETA.-hydroxyfentanyl has similar effects to fentanyl. Side effects of fentanyl analogs are similar to those of fentanyl itself, which include itching, nausea and potentially serious respiratory depression, which can be life-threatening. Fentanyl analogs have killed hundreds of people throughout Europe and the former Soviet republics since the most recent resurgence in use began in Estonia in the early 2000s, and novel derivatives continue to appear. | ||
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DTXSID40859650
Created by
admin on Mon Mar 31 22:28:14 GMT 2025 , Edited by admin on Mon Mar 31 22:28:14 GMT 2025
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PRIMARY | |||
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78995-10-5
Created by
admin on Mon Mar 31 22:28:14 GMT 2025 , Edited by admin on Mon Mar 31 22:28:14 GMT 2025
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PRIMARY | |||
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6Q4XAW26T4
Created by
admin on Mon Mar 31 22:28:14 GMT 2025 , Edited by admin on Mon Mar 31 22:28:14 GMT 2025
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PRIMARY | |||
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62278
Created by
admin on Mon Mar 31 22:28:14 GMT 2025 , Edited by admin on Mon Mar 31 22:28:14 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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TARGET -> AGONIST |
EC50
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SALT/SOLVATE -> PARENT |
APPROXIMATE PURE ANHYDROUS DRUG CONTENT (IN PERCENT)
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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PARENT -> METABOLITE ACTIVE |
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |
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