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

Details

Stereochemistry ACHIRAL
Molecular Formula C23H21FN2O2
Molecular Weight 376.4234
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 5-FLUORO-PB-22

SMILES

FCCCCCN1C=C(C(=O)OC2=C3N=CC=CC3=CC=C2)C4=C1C=CC=C4

InChI

InChIKey=MBOCMBFDYVSGLJ-UHFFFAOYSA-N
InChI=1S/C23H21FN2O2/c24-13-4-1-5-15-26-16-19(18-10-2-3-11-20(18)26)23(27)28-21-12-6-8-17-9-7-14-25-22(17)21/h2-3,6-12,14,16H,1,4-5,13,15H2

HIDE SMILES / InChI

Molecular Formula C23H21FN2O2
Molecular Weight 376.4234
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 Sat Dec 16 02:17:36 UTC 2023
Edited
by admin
on Sat Dec 16 02:17:36 UTC 2023
Record UNII
QCB63R9792
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
5-FLUORO-PB-22
Common Name English
5F-QUPIC
Common Name English
J3.226.299F
Code English
5F-PB-22
Code English
1H-INDOLE-3-CARBOXYLIC ACID, 1-(5-FLUOROPENTYL)-, 8-QUINOLINYL ESTER
Systematic Name English
QUPIC N-5-(FLUOROPENTYL) ANALOG
Common Name English
5F-PB22
Code English
Classification Tree Code System Code
WIKIPEDIA Designer-drugs-5F-PB-22
Created by admin on Sat Dec 16 02:17:36 UTC 2023 , Edited by admin on Sat Dec 16 02:17:36 UTC 2023
DEA NO. 7225
Created by admin on Sat Dec 16 02:17:36 UTC 2023 , Edited by admin on Sat Dec 16 02:17:36 UTC 2023
Code System Code Type Description
CAS
1400742-41-7
Created by admin on Sat Dec 16 02:17:36 UTC 2023 , Edited by admin on Sat Dec 16 02:17:36 UTC 2023
PRIMARY
WIKIPEDIA
5F-PB-22
Created by admin on Sat Dec 16 02:17:36 UTC 2023 , Edited by admin on Sat Dec 16 02:17:36 UTC 2023
PRIMARY
EVMPD
SUB189888
Created by admin on Sat Dec 16 02:17:36 UTC 2023 , Edited by admin on Sat Dec 16 02:17:36 UTC 2023
PRIMARY
PUBCHEM
72710774
Created by admin on Sat Dec 16 02:17:36 UTC 2023 , Edited by admin on Sat Dec 16 02:17:36 UTC 2023
PRIMARY
EPA CompTox
DTXSID60857138
Created by admin on Sat Dec 16 02:17:36 UTC 2023 , Edited by admin on Sat Dec 16 02:17:36 UTC 2023
PRIMARY
SMS_ID
100000175527
Created by admin on Sat Dec 16 02:17:36 UTC 2023 , Edited by admin on Sat Dec 16 02:17:36 UTC 2023
PRIMARY
FDA UNII
QCB63R9792
Created by admin on Sat Dec 16 02:17:36 UTC 2023 , Edited by admin on Sat Dec 16 02:17:36 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Mouse AtT-20 neuroblastoma cells stably transfected with human CB2
EC50
TARGET -> AGONIST
Mouse AtT-20 neuroblastoma cells stably transfected with human CB1
EC50
Related Record Type Details
ACTIVE MOIETY