U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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
Structure of 4-PHENYLFENTANYL

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

HIDE SMILES / InChI

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 Thu Jul 06 15:55:38 UTC 2023
Edited
by admin
on Thu Jul 06 15:55:38 UTC 2023
Record UNII
L9P31JAO37
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-PHENYLFENTANYL
Common Name English
N-(1-PHENETHYL-4-PHENYL-4-PIPERIDYL)-N-PHENYL-PROPANAMIDE
Systematic Name English
PROPANAMIDE, N-PHENYL-N-(4-PHENYL-1-(2-PHENYLETHYL)-4-PIPERIDINYL)-
Systematic Name English
Classification Tree Code System Code
WIKIPEDIA List_of_fentanyl_analogues
Created by admin on Thu Jul 06 15:55:38 UTC 2023 , Edited by admin on Thu Jul 06 15:55:38 UTC 2023
Code System Code Type Description
WEB RESOURCE
4-PHENYLFENTANYL
Created by admin on Thu Jul 06 15:55:38 UTC 2023 , Edited by admin on Thu Jul 06 15:55:38 UTC 2023
PRIMARY
WIKIPEDIA
4-PHENYLFENTANYL
Created by admin on Thu Jul 06 15:55:38 UTC 2023 , Edited by admin on Thu Jul 06 15:55:38 UTC 2023
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.
DRUG BANK
DB09168
Created by admin on Thu Jul 06 15:55:38 UTC 2023 , Edited by admin on Thu Jul 06 15:55:38 UTC 2023
PRIMARY
PUBCHEM
10319503
Created by admin on Thu Jul 06 15:55:38 UTC 2023 , Edited by admin on Thu Jul 06 15:55:38 UTC 2023
PRIMARY
EPA CompTox
DTXSID001018402
Created by admin on Thu Jul 06 15:55:38 UTC 2023 , Edited by admin on Thu Jul 06 15:55:38 UTC 2023
PRIMARY
FDA UNII
L9P31JAO37
Created by admin on Thu Jul 06 15:55:38 UTC 2023 , Edited by admin on Thu Jul 06 15:55:38 UTC 2023
PRIMARY
CAS
120448-97-7
Created by admin on Thu Jul 06 15:55:38 UTC 2023 , Edited by admin on Thu Jul 06 15:55:38 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
TARGET -> AGONIST
Related Record Type Details
ACTIVE MOIETY