Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C22H26F2N2O |
| Molecular Weight | 372.4514 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(=O)N(C1CCN(CC(F)C2=C(F)C=CC=C2)CC1)C3=CC=CC=C3
InChI
InChIKey=HVODMMOXSRCMCA-UHFFFAOYSA-N
InChI=1S/C22H26F2N2O/c1-2-22(27)26(17-8-4-3-5-9-17)18-12-14-25(15-13-18)16-21(24)19-10-6-7-11-20(19)23/h3-11,18,21H,2,12-16H2,1H3
| Molecular Formula | C22H26F2N2O |
| Molecular Weight | 372.4514 |
| 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 19:04:41 UTC 2023
by
admin
on
Sat Dec 16 19:04:41 UTC 2023
|
| Record UNII |
G9884GP5UD
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
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WIKIPEDIA |
List_of_fentanyl_analogues
Created by
admin on Sat Dec 16 19:04:41 UTC 2023 , Edited by admin on Sat Dec 16 19:04:41 UTC 2023
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
G9884GP5UD
Created by
admin on Sat Dec 16 19:04:41 UTC 2023 , Edited by admin on Sat Dec 16 19:04:41 UTC 2023
|
PRIMARY | |||
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146167150
Created by
admin on Sat Dec 16 19:04:41 UTC 2023 , Edited by admin on Sat Dec 16 19:04:41 UTC 2023
|
PRIMARY | |||
|
2376328-79-7
Created by
admin on Sat Dec 16 19:04:41 UTC 2023 , Edited by admin on Sat Dec 16 19:04:41 UTC 2023
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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TARGET -> AGONIST |
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
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