5F-AKB48: Difference between revisions

>David Hedlund
===Dangerous interactions=== {{DangerousInteractions/Intro}} {{DangerousInteractions/Cannabis}}
>Tracer
m Grammatics
Line 9: Line 9:
Unlike [[cannabis]], the chronic abuse of [[synthetic cannabinoids]] has been [[Synthetic_cannabinoid#Deaths|associated with multiple serious injuries deaths]] and [[Synthetic cannabinoid#Harm potential|more dangerous side effects and toxicity]] in general. Therefore, it is strongly discouraged to take this substance for extended periods of time or in excessive doses.
Unlike [[cannabis]], the chronic abuse of [[synthetic cannabinoids]] has been [[Synthetic_cannabinoid#Deaths|associated with multiple serious injuries deaths]] and [[Synthetic cannabinoid#Harm potential|more dangerous side effects and toxicity]] in general. Therefore, it is strongly discouraged to take this substance for extended periods of time or in excessive doses.
==Chemistry==
==Chemistry==
5F-AKB48, or N-(adamantan-1-yl)-1-(5-fluoropentyl)-1H-indazole-3-carboxamide, is a synthetic [[Chemical class::indazole cannabinoid]] as it contains a substituted indazole group. This indazole moeity is substituted at R<sub>1</sub> with a fluoropentyl chain, a substitution shared with [[5F-PB-22]]. Additionally, the indazole is substituted at R<sub>3</sub> with a carboxamide group.  This carboxamide group is N-substituted at its terminal amine group with an adamantane group. This group consists of four fused cyclohexane rings in a unique structure called a diamondoid. 5F-AKB48 is an analog of [[STS-135]] in which the core indole structure is substituted with an indazole base.
5F-AKB48, or N-(adamantan-1-yl)-1-(5-fluoropentyl)-1H-indazole-3-carboxamide, is a synthetic [[Chemical class::indazole cannabinoid]] as it contains a substituted indazole group. This indazole moeity is substituted at R<sub>1</sub> with a fluoropentyl chain, a substitution shared with [[5F-PB-22]]. Additionally, the indazole is substituted at R<sub>3</sub> with a carboxamide group.  This carboxamide group is N-substituted at its terminal amine group with an [[adamantane]] group. This group consists of four fused cyclohexane rings in a unique structure called a diamondoid. 5F-AKB48 is an analog of [[STS-135]] in which the core indole structure is substituted with an indazole base.


==Pharmacology==
==Pharmacology==