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

Details

Stereochemistry ACHIRAL
Molecular Formula C23H24N2O2
Molecular Weight 360.4489
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-Benzylfuranylfentanyl

SMILES

O=C(N(C1CCN(CC2=CC=CC=C2)CC1)C3=CC=CC=C3)C4=CC=CO4

InChI

InChIKey=GDPJXHFICUEJBT-UHFFFAOYSA-N
InChI=1S/C23H24N2O2/c26-23(22-12-7-17-27-22)25(20-10-5-2-6-11-20)21-13-15-24(16-14-21)18-19-8-3-1-4-9-19/h1-12,17,21H,13-16,18H2

HIDE SMILES / InChI

Molecular Formula C23H24N2O2
Molecular Weight 360.4489
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 21:07:41 UTC 2023
Edited
by admin
on Thu Jul 06 21:07:41 UTC 2023
Record UNII
57C1B6YU31
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-Benzylfuranylfentanyl
Common Name English
N-BENZYL FURANYL NORFENTANYL
Common Name English
BENZYL FURANYL FENTANYL [NFLIS-DRUG]
Common Name English
FURANYL BENZYL FENTANYL
Common Name English
BENZYL FU-F
Common Name English
2-FURANCARBOXAMIDE, N-PHENYL-N-(1-(PHENYLMETHYL)-4-PIPERIDINYL)-
Systematic Name English
BENZYL FURANYL FENTANYL
Common Name English
N-(1-BENZYLPIPERIDIN-4-YL)-N-PHENYLFURAN-2-CARBOXAMIDE
Systematic Name English
N-PHENYL-N-(1-(PHENYLMETHYL)-4-PIPERIDINYL)-2-FURANCARBOXAMIDE
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID801036769
Created by admin on Thu Jul 06 21:07:42 UTC 2023 , Edited by admin on Thu Jul 06 21:07:42 UTC 2023
PRIMARY
CAS
497240-21-8
Created by admin on Thu Jul 06 21:07:42 UTC 2023 , Edited by admin on Thu Jul 06 21:07:42 UTC 2023
PRIMARY
PUBCHEM
42853213
Created by admin on Thu Jul 06 21:07:42 UTC 2023 , Edited by admin on Thu Jul 06 21:07:42 UTC 2023
PRIMARY
FDA UNII
57C1B6YU31
Created by admin on Thu Jul 06 21:07:42 UTC 2023 , Edited by admin on Thu Jul 06 21:07:42 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Assumed an agonist
Related Record Type Details
ACTIVE MOIETY