FUBIMINA: Difference between revisions

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[[Category:CB1 receptor agonists]]
[[Category:CB1 receptor agonists]]
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File:FUBIMINA structure.png|FUBIMINA
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Latest revision as of 21:02, 16 March 2025

FUBIMINA (also known as BIM-2201) is a synthetic cannabinoid that is an indazole-based synthetic cannabinoid. It is a potent agonist of the CB1 receptor, which is the primary binding site of the endocannabinoid Anandamide. It is closely related to other synthetic cannabinoids like 5F-ADB, AMB-FUBINACA, and MDMB-FUBINACA.

Chemistry[edit]

FUBIMINA is an indazole-based synthetic cannabinoid. It is part of the Indazole family of cannabinoids which are known for their strong agonist activity at the CB1 receptor. The chemical structure of FUBIMINA is similar to that of other synthetic cannabinoids like 5F-ADB, AMB-FUBINACA, and MDMB-FUBINACA, which all contain a fluorobenzyl group.

Pharmacology[edit]

FUBIMINA is a potent agonist of the CB1 receptor, which is the primary binding site of the endocannabinoid Anandamide. The CB1 receptor is primarily located in the brain and is responsible for the psychoactive effects of THC. FUBIMINA's strong agonist activity at the CB1 receptor is believed to be responsible for its psychoactive effects.

Effects[edit]

The effects of FUBIMINA are similar to those of other synthetic cannabinoids and include feelings of euphoria, altered perception, and adverse effects such as anxiety and paranoia. Due to its potency and the lack of research on its effects, FUBIMINA is considered to be a potentially dangerous substance.

Legal Status[edit]

The legal status of FUBIMINA varies by country. In some countries, it is classified as a controlled substance due to its potential for abuse and the health risks associated with its use.

See Also[edit]

References[edit]

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