Details
Stereochemistry | ACHIRAL |
Molecular Formula | C21H26N2O |
Molecular Weight | 322.4439 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(=O)N(C1CCN(CC2=CC=CC=C2)CC1)C3=CC=CC=C3
InChI
InChIKey=POQDXIFVWVZVML-UHFFFAOYSA-N
InChI=1S/C21H26N2O/c1-2-21(24)23(19-11-7-4-8-12-19)20-13-15-22(16-14-20)17-18-9-5-3-6-10-18/h3-12,20H,2,13-17H2,1H3
Molecular Formula | C21H26N2O |
Molecular Weight | 322.4439 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: P35372|||G8XRH8|||Q5TDA1|||Q9UN57 Gene ID: 4988.0 Gene Symbol: OPRM1 Target Organism: Homo sapiens (Human) Sources: https://www.drugbank.ca/drugs/DB09182 |
213.0 nM [Ki] |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:03:09 GMT 2023
by
admin
on
Fri Dec 15 18:03:09 GMT 2023
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Record UNII |
9BV2D1A57H
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Record Status |
Validated (UNII)
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Record Version |
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-
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WIKIPEDIA |
List_of_fentanyl_analogues
Created by
admin on Fri Dec 15 18:03:09 GMT 2023 , Edited by admin on Fri Dec 15 18:03:09 GMT 2023
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DEA NO. |
8334
Created by
admin on Fri Dec 15 18:03:09 GMT 2023 , Edited by admin on Fri Dec 15 18:03:09 GMT 2023
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Code System | Code | Type | Description | ||
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BENZYLFENTANYL
Created by
admin on Fri Dec 15 18:03:09 GMT 2023 , Edited by admin on Fri Dec 15 18:03:09 GMT 2023
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PRIMARY | |||
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1474-02-8
Created by
admin on Fri Dec 15 18:03:09 GMT 2023 , Edited by admin on Fri Dec 15 18:03:09 GMT 2023
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PRIMARY | |||
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9BV2D1A57H
Created by
admin on Fri Dec 15 18:03:09 GMT 2023 , Edited by admin on Fri Dec 15 18:03:09 GMT 2023
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PRIMARY | |||
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DTXSID00163705
Created by
admin on Fri Dec 15 18:03:09 GMT 2023 , Edited by admin on Fri Dec 15 18:03:09 GMT 2023
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PRIMARY | |||
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BENZYLFENTANYL
Created by
admin on Fri Dec 15 18:03:09 GMT 2023 , Edited by admin on Fri Dec 15 18:03:09 GMT 2023
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PRIMARY | Benzylfentanyl has a Ki of 213nM at the mu opioid receptor, binding around 200x less strongly than fentanyl itself. 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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DB09182
Created by
admin on Fri Dec 15 18:03:09 GMT 2023 , Edited by admin on Fri Dec 15 18:03:09 GMT 2023
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PRIMARY | |||
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252141
Created by
admin on Fri Dec 15 18:03:09 GMT 2023 , Edited by admin on Fri Dec 15 18:03:09 GMT 2023
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PRIMARY | |||
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73402
Created by
admin on Fri Dec 15 18:03:09 GMT 2023 , Edited by admin on Fri Dec 15 18:03:09 GMT 2023
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PRIMARY | |||
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216-014-7
Created by
admin on Fri Dec 15 18:03:09 GMT 2023 , Edited by admin on Fri Dec 15 18:03:09 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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TARGET -> AGONIST |
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SALT/SOLVATE -> PARENT |
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Related Record | Type | Details | ||
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PARENT -> IMPURITY |
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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Related Record | Type | Details | ||
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ACTIVE MOIETY |
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