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

Details

Stereochemistry ACHIRAL
Molecular Formula C23H30N2O
Molecular Weight 350.4971
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-PHENYLPROPYLNORFENTANYL

SMILES

CCC(=O)N(C1CCN(CCCC2=CC=CC=C2)CC1)C3=CC=CC=C3

InChI

InChIKey=CKBFKWWOUYBCRH-UHFFFAOYSA-N
InChI=1S/C23H30N2O/c1-2-23(26)25(21-13-7-4-8-14-21)22-15-18-24(19-16-22)17-9-12-20-10-5-3-6-11-20/h3-8,10-11,13-14,22H,2,9,12,15-19H2,1H3

HIDE SMILES / InChI

Molecular Formula C23H30N2O
Molecular Weight 350.4971
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 21:18:46 UTC 2023
Edited
by admin
on Thu Jul 06 21:18:46 UTC 2023
Record UNII
GBD33DI2IP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-PHENYLPROPYLNORFENTANYL
Common Name English
PROPANAMIDE, N-PHENYL-N-(1-(3-PHENYLPROPYL)-4-PIPERIDINYL)-
Systematic Name English
N-PHENYL-N-(1-(3-PHENYLPROPYL)-4-PIPERIDINYL)PROPANAMIDE
Systematic Name English
HOMOFENTANYL
Common Name English
R-5029
Code English
N-PHENYL-N-(1-(3-PHENYLPROPYL)PIPERIDIN-4-YL)PROPANAMIDE
Systematic Name English
Classification Tree Code System Code
WIKIPEDIA List_of_fentanyl_analogues
Created by admin on Thu Jul 06 21:18:47 UTC 2023 , Edited by admin on Thu Jul 06 21:18:47 UTC 2023
Code System Code Type Description
CAS
59708-54-2
Created by admin on Thu Jul 06 21:18:47 UTC 2023 , Edited by admin on Thu Jul 06 21:18:47 UTC 2023
PRIMARY
EPA CompTox
DTXSID701034384
Created by admin on Thu Jul 06 21:18:47 UTC 2023 , Edited by admin on Thu Jul 06 21:18:47 UTC 2023
PRIMARY
FDA UNII
GBD33DI2IP
Created by admin on Thu Jul 06 21:18:47 UTC 2023 , Edited by admin on Thu Jul 06 21:18:47 UTC 2023
PRIMARY
PUBCHEM
618626
Created by admin on Thu Jul 06 21:18:47 UTC 2023 , Edited by admin on Thu Jul 06 21:18:47 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Related Record Type Details
ACTIVE MOIETY