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Details

Stereochemistry ACHIRAL
Molecular Formula C21H23FN2O
Molecular Weight 338.4185
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 5F-SDB-006

SMILES

FCCCCCN1C=C(C(=O)NCC2=CC=CC=C2)C3=C1C=CC=C3

InChI

InChIKey=VFLXAWVAWXHMFB-UHFFFAOYSA-N
InChI=1S/C21H23FN2O/c22-13-7-2-8-14-24-16-19(18-11-5-6-12-20(18)24)21(25)23-15-17-9-3-1-4-10-17/h1,3-6,9-12,16H,2,7-8,13-15H2,(H,23,25)

HIDE SMILES / InChI
5F-SDB-006 is a synthetic cannabinoid. It is considered to be a constituent of illicit smoking mixtures "spice".

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Pharmacological evaluation of synthetic cannabinoids identified as constituents of spice.
2016
The synthesis and pharmacological evaluation of adamantane-derived indoles: cannabimimetic drugs of abuse.
2013-07-17

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Name Type Language
1H-INDOLE-3-CARBOXAMIDE, 1-(5-FLUOROPENTYL)-N-(PHENYLMETHYL)-
Preferred Name English
5F-SDB-006
Common Name English
N-BENZYL-1-(5-FLUOROPENTYL)-1H-INDOLE-3-CARBOXAMIDE
Systematic Name English
Classification Tree Code System Code
WIKIPEDIA Designer-drugs-5F-SDB-006
Created by admin on Mon Mar 31 22:49:49 GMT 2025 , Edited by admin on Mon Mar 31 22:49:49 GMT 2025
Code System Code Type Description
PUBCHEM
91936847
Created by admin on Mon Mar 31 22:49:49 GMT 2025 , Edited by admin on Mon Mar 31 22:49:49 GMT 2025
PRIMARY
CAS
1776086-02-2
Created by admin on Mon Mar 31 22:49:49 GMT 2025 , Edited by admin on Mon Mar 31 22:49:49 GMT 2025
PRIMARY
FDA UNII
4UP4SXX8BW
Created by admin on Mon Mar 31 22:49:49 GMT 2025 , Edited by admin on Mon Mar 31 22:49:49 GMT 2025
PRIMARY
WIKIPEDIA
5F-SDB-006
Created by admin on Mon Mar 31 22:49:49 GMT 2025 , Edited by admin on Mon Mar 31 22:49:49 GMT 2025
PRIMARY
EPA CompTox
DTXSID601032523
Created by admin on Mon Mar 31 22:49:49 GMT 2025 , Edited by admin on Mon Mar 31 22:49:49 GMT 2025
PRIMARY