Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C22H26N2O |
| Molecular Weight | 334.4546 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C=CC(=O)N(C1CCN(CCC2=CC=CC=C2)CC1)C3=CC=CC=C3
InChI
InChIKey=RFQNLMWUIJJEQF-UHFFFAOYSA-N
InChI=1S/C22H26N2O/c1-2-22(25)24(20-11-7-4-8-12-20)21-14-17-23(18-15-21)16-13-19-9-5-3-6-10-19/h2-12,21H,1,13-18H2
| Molecular Formula | C22H26N2O |
| Molecular Weight | 334.4546 |
| 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
Sat Dec 16 10:19:34 GMT 2023
by
admin
on
Sat Dec 16 10:19:34 GMT 2023
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| Record UNII |
T64K7YD33B
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| Record Status |
Validated (UNII)
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| Record Version |
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WIKIPEDIA |
Designer-drugs-Acrylfentanyl
Created by
admin on Sat Dec 16 10:19:34 GMT 2023 , Edited by admin on Sat Dec 16 10:19:34 GMT 2023
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DEA NO. |
9811
Created by
admin on Sat Dec 16 10:19:34 GMT 2023 , Edited by admin on Sat Dec 16 10:19:34 GMT 2023
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WIKIPEDIA |
List_of_fentanyl_analogues
Created by
admin on Sat Dec 16 10:19:34 GMT 2023 , Edited by admin on Sat Dec 16 10:19:34 GMT 2023
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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100000176035
Created by
admin on Sat Dec 16 10:19:34 GMT 2023 , Edited by admin on Sat Dec 16 10:19:34 GMT 2023
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PRIMARY | |||
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10314851
Created by
admin on Sat Dec 16 10:19:34 GMT 2023 , Edited by admin on Sat Dec 16 10:19:34 GMT 2023
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PRIMARY | |||
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ACRYLFENTANYL
Created by
admin on Sat Dec 16 10:19:34 GMT 2023 , Edited by admin on Sat Dec 16 10:19:34 GMT 2023
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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. Acrylamide is generally avoided in drug discovery due to its probable neurotoxicity and carcinogenicity. | ||
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ACRYLFENTANYL
Created by
admin on Sat Dec 16 10:19:34 GMT 2023 , Edited by admin on Sat Dec 16 10:19:34 GMT 2023
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PRIMARY | |||
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82003-75-6
Created by
admin on Sat Dec 16 10:19:34 GMT 2023 , Edited by admin on Sat Dec 16 10:19:34 GMT 2023
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PRIMARY | |||
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T64K7YD33B
Created by
admin on Sat Dec 16 10:19:34 GMT 2023 , Edited by admin on Sat Dec 16 10:19:34 GMT 2023
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PRIMARY | |||
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ACRYLFENTANYL
Created by
admin on Sat Dec 16 10:19:34 GMT 2023 , Edited by admin on Sat Dec 16 10:19:34 GMT 2023
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PRIMARY | |||
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DTXSID701036742
Created by
admin on Sat Dec 16 10:19:34 GMT 2023 , Edited by admin on Sat Dec 16 10:19:34 GMT 2023
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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TARGET -> AGONIST |
BINDING
Ki
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SALT/SOLVATE -> PARENT | |||
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TARGET -> AGONIST |
EC50
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |
