5F-SDB-006 (also known as 5-fluoro-SDB-006) acts as a potent agonist for the cannabinoid receptors, with an EC50 of 50 nM for human CB1 receptors, and 123 nM for human CB2 receptors.
5F-SDB-006 is the terminally fluorinated analog of SDB-006, just as STS-135 is the terminally fluorinated analog of APICA. Given the known metabolic liberation of amantadine in the related compound APINACA, it is suspected that metabolic hydrolysis of the amide group of 5F-SDB-006 may release benzylamine.
5F-SDB-006 has formal name: N-Benzyl-1-(5-fluoropentyl)-1H-indole-3-carboxamide. The chemical formula for 5F-SDB-006 is C21H23FN2O with a molecular weight of 338.43
Effect and dosage of 5F-SDB-006:
5F-SDB- 006 similar effect to SDB-006.
Toxicology of 5F-SDB-006:
The toxicity and long-term health effects of recreational 5F-SDB-006 use do not seem to have been studied in any scientific context and the exact toxic dosage is unknown.
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Purity: 99,7% min
Molecular weight: 338.43
5F-SDB-006 is intended for research and forensic purposes in a controlled laboratory for study only and is NOT intended for human consumption.
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