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Details

Stereochemistry ACHIRAL
Molecular Formula C26H18FNO2
Molecular Weight 395.425
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FDU-PB-22

SMILES

FC1=CC=C(CN2C=C(C(=O)OC3=CC=CC4=C3C=CC=C4)C5=C2C=CC=C5)C=C1

InChI

InChIKey=RCEKSVIFQKKFLS-UHFFFAOYSA-N
InChI=1S/C26H18FNO2/c27-20-14-12-18(13-15-20)16-28-17-23(22-9-3-4-10-24(22)28)26(29)30-25-11-5-7-19-6-1-2-8-21(19)25/h1-15,17H,16H2

HIDE SMILES / InChI

Molecular Formula C26H18FNO2
Molecular Weight 395.425
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P21554|||Q5UB37
Gene ID: 1268.0
Gene Symbol: CNR1
Target Organism: Homo sapiens (Human)
1.19 nM [Ki]
Target ID: P34972
Gene ID: 1269.0
Gene Symbol: CNR2
Target Organism: Homo sapiens (Human)
2.43 nM [Ki]
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:40:03 UTC 2023
Edited
by admin
on Sat Dec 16 10:40:03 UTC 2023
Record UNII
85E88884ZQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FDU-PB-22
Common Name English
1H-INDOLE-3-CARBOXYLIC ACID, 1-((4-FLUOROPHENYL)METHYL)-, 1-NAPHTHALENYL ESTER
Systematic Name English
NAPHTHALEN-1-YL 1-((4-FLUOROPHENYL)METHYL)-1H-INDOLE-3-CARBOXYLATE
Systematic Name English
1-((4-FLUOROPHENYL)METHYL)-1H-INDOLE-3-CARBOXYLIC ACID, 1-NAPHTHALENYL ESTER
Systematic Name English
Classification Tree Code System Code
WIKIPEDIA Designer-drugs-FDU-PB-22
Created by admin on Sat Dec 16 10:40:03 UTC 2023 , Edited by admin on Sat Dec 16 10:40:03 UTC 2023
Code System Code Type Description
EPA CompTox
DTXSID90101691
Created by admin on Sat Dec 16 10:40:03 UTC 2023 , Edited by admin on Sat Dec 16 10:40:03 UTC 2023
PRIMARY
MANUFACTURER PRODUCT INFORMATION
FDU-PB-22
Created by admin on Sat Dec 16 10:40:03 UTC 2023 , Edited by admin on Sat Dec 16 10:40:03 UTC 2023
PRIMARY Several cannabimimetic quinolinyl carboxylates (PB-22, Item No. 14096 and BB-22, Item No. 14099) and cannabimimetic carboxamide derivatives (ADB-FUBINACA, Item No. 14292 and ADBICA, Item No. 14293) have been identified as designer drugs in illegal products.1 FDU-PB-22 is a derivative of PB-22 in which the pentyl side chain is replaced by a 4-fluorobenzyl group, a functional group also found in indazole-based synthetic cannabinoids such as ADB-FUBINACA. Additionally, the 8-quinolinol is replaced by a naphthalene group, similar to the structure of AM2201 (Item No. 10707).2,3,1 The physiological and toxicological properties of this compound are not known.
CAS
1883284-94-3
Created by admin on Sat Dec 16 10:40:03 UTC 2023 , Edited by admin on Sat Dec 16 10:40:03 UTC 2023
PRIMARY
WIKIPEDIA
FDU-PB-22
Created by admin on Sat Dec 16 10:40:03 UTC 2023 , Edited by admin on Sat Dec 16 10:40:03 UTC 2023
PRIMARY FDU-PB-22 is an derivative of JWH-018 that is presumed to be a potent agonist of the CB1 receptor and has been sold online as a "legal high". FDU-PB-22 is a controlled substance in Germany and is banned in Japan and Sweden.
PUBCHEM
119025888
Created by admin on Sat Dec 16 10:40:03 UTC 2023 , Edited by admin on Sat Dec 16 10:40:03 UTC 2023
PRIMARY
FDA UNII
85E88884ZQ
Created by admin on Sat Dec 16 10:40:03 UTC 2023 , Edited by admin on Sat Dec 16 10:40:03 UTC 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY