Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C28H32N2O |
| Molecular Weight | 412.5665 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(=O)N(C1=CC=CC=C1)C2(CCN(CCC3=CC=CC=C3)CC2)C4=CC=CC=C4
InChI
InChIKey=BXCJXJLHYMWMQU-UHFFFAOYSA-N
InChI=1S/C28H32N2O/c1-2-27(31)30(26-16-10-5-11-17-26)28(25-14-8-4-9-15-25)19-22-29(23-20-28)21-18-24-12-6-3-7-13-24/h3-17H,2,18-23H2,1H3
| Molecular Formula | C28H32N2O |
| Molecular Weight | 412.5665 |
| 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
Mon Mar 31 23:12:58 GMT 2025
by
admin
on
Mon Mar 31 23:12:58 GMT 2025
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| Record UNII |
L9P31JAO37
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| Record Status |
Validated (UNII)
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| Record Version |
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| Name | Type | Language | ||
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Preferred Name | English | ||
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Common 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 |
List_of_fentanyl_analogues
Created by
admin on Mon Mar 31 23:12:58 GMT 2025 , Edited by admin on Mon Mar 31 23:12:58 GMT 2025
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CDC |
4-Phenyl fentanyl
Created by
admin on Mon Mar 31 23:12:58 GMT 2025 , Edited by admin on Mon Mar 31 23:12:58 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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4-PHENYLFENTANYL
Created by
admin on Mon Mar 31 23:12:58 GMT 2025 , Edited by admin on Mon Mar 31 23:12:58 GMT 2025
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PRIMARY | |||
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4-PHENYLFENTANYL
Created by
admin on Mon Mar 31 23:12:58 GMT 2025 , Edited by admin on Mon Mar 31 23:12:58 GMT 2025
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PRIMARY | 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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DB09168
Created by
admin on Mon Mar 31 23:12:58 GMT 2025 , Edited by admin on Mon Mar 31 23:12:58 GMT 2025
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PRIMARY | |||
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10319503
Created by
admin on Mon Mar 31 23:12:58 GMT 2025 , Edited by admin on Mon Mar 31 23:12:58 GMT 2025
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PRIMARY | |||
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DTXSID001018402
Created by
admin on Mon Mar 31 23:12:58 GMT 2025 , Edited by admin on Mon Mar 31 23:12:58 GMT 2025
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PRIMARY | |||
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L9P31JAO37
Created by
admin on Mon Mar 31 23:12:58 GMT 2025 , Edited by admin on Mon Mar 31 23:12:58 GMT 2025
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PRIMARY | |||
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120448-97-7
Created by
admin on Mon Mar 31 23:12:58 GMT 2025 , Edited by admin on Mon Mar 31 23:12:58 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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SALT/SOLVATE -> PARENT |
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SALT/SOLVATE -> PARENT |
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TARGET -> AGONIST |
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
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