Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C24H32N2O2 |
| Molecular Weight | 380.5231 |
| 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(COC)CCN(CCC3=CC=CC=C3)CC2
InChI
InChIKey=GARXJOUQUSNOGK-UHFFFAOYSA-N
InChI=1S/C24H32N2O2/c1-3-23(27)26(22-12-8-5-9-13-22)24(20-28-2)15-18-25(19-16-24)17-14-21-10-6-4-7-11-21/h4-13H,3,14-20H2,1-2H3
| Molecular Formula | C24H32N2O2 |
| Molecular Weight | 380.5231 |
| 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
Tue Apr 01 16:55:29 GMT 2025
by
admin
on
Tue Apr 01 16:55:29 GMT 2025
|
| Record UNII |
03DNV05OD4
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
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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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Common Name | English |
| Classification Tree | Code System | Code | ||
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WIKIPEDIA |
List_of_fentanyl_analogues
Created by
admin on Tue Apr 01 16:55:29 GMT 2025 , Edited by admin on Tue Apr 01 16:55:29 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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DB09179
Created by
admin on Tue Apr 01 16:55:29 GMT 2025 , Edited by admin on Tue Apr 01 16:55:29 GMT 2025
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PRIMARY | |||
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124716
Created by
admin on Tue Apr 01 16:55:29 GMT 2025 , Edited by admin on Tue Apr 01 16:55:29 GMT 2025
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PRIMARY | |||
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R-30490
Created by
admin on Tue Apr 01 16:55:29 GMT 2025 , Edited by admin on Tue Apr 01 16:55:29 GMT 2025
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PRIMARY | |||
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03DNV05OD4
Created by
admin on Tue Apr 01 16:55:29 GMT 2025 , Edited by admin on Tue Apr 01 16:55:29 GMT 2025
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PRIMARY | |||
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60618-49-7
Created by
admin on Tue Apr 01 16:55:29 GMT 2025 , Edited by admin on Tue Apr 01 16:55:29 GMT 2025
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PRIMARY | |||
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DTXSID30209423
Created by
admin on Tue Apr 01 16:55:29 GMT 2025 , Edited by admin on Tue Apr 01 16:55:29 GMT 2025
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PRIMARY | |||
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R-30490
Created by
admin on Tue Apr 01 16:55:29 GMT 2025 , Edited by admin on Tue Apr 01 16:55:29 GMT 2025
|
PRIMARY | R-30490 was first synthesised by a team of chemists at Janssen Pharmaceutica led by Paul Janssen, who were investigating the structure-activity relationships of the fentanyl family of drugs. R-30490 was found to be the most selective agonist for the .MU.-opioid receptor out of all the fentanyl analogues tested, but it has never been introduced for medical use in humans, although the closely related drug sufentanil is widely used for analgesia and anesthesia during major surgery. |
| Related Record | Type | Details | ||
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TARGET -> AGONIST |
| Related Record | Type | Details | ||
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ACTIVE MOIETY |
