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5F-AB-PINACA

A fluorinated indazole-3-carboxamide, full agonist at CB1 and CB2, convulsant in mice; a narcotic in France.

Level of detail

Harm-reduction warning

No characterised human dose: animal / in vitro data only. Effect profile, safety margin and acute toxicity are not documented in human clinical practice. Extremely potent compound: severe effects, seizures and deaths reported in the literature.

C₁₈H₂₅FN₄O₂

CAS 1800101-60-3

Family
Synthetic CB receptor agonistNew psychoactive substance
Molar mass
348.42 g/mol

Updated on

In plain terms

5F-AB-PINACA has nothing to do with hemp: it is a molecule made in the laboratory. It acts on the same receptors as THC. In mice it causes convulsions; in Japan, road accidents with impaired consciousness were reported with five synthetic cannabinoids including this one. In France it is classed as a narcotic.

Receptors and activity

Target network

CB1Agonistno measured value
  • Activates

The lower the cited value, the closer the target sits to 5F-AB-PINACA: one ring per factor of 100. A target with no measured value stays on the edge.

Where these targets live

Where each target has been found in humans, according to the cited studies. The map shows the target, not an effect of 5F-AB-PINACA.

Brain, side view
Body, front view
Blood

CB1CB1 found in 7 regions of the body

  1. Basal gangliadenseMost dense in basal ganglia outflow nuclei1
  2. CerebellumdenseVery dense in the cerebellum1
  3. HippocampusdenseVery high concentrations in the hippocampus2
  4. AmygdaladenseHigh concentrations in the amygdala2
  5. CortexpresentPresent throughout the neocortex2
  6. Adipose tissuepresentExpressed in adipose tissue3
  7. GutpresentColonic epithelium, smooth muscle and plexus4

Cited values

  1. CB1Agonistno measured value cited
  2. CB2Agonistno measured value cited
Bar length follows the measured value (Ki, Kd, EC50 or IC50), on one scale shared by every entry, from 100 µM to 0.1 nM. A target with no cited value has no bar.

Pharmacology

5F-AB-PINACA is a synthetic cannabinoid agonist of the indazole-3-carboxamide family, the 5-fluorinated analogue of AB-PINACA. Banister et al. (2015) synthesised and tested it with other compounds (AB-FUBINACA, ADB-FUBINACA, AB-PINACA, ADB-PINACA, 5F-ADB-PINACA…): all act as high-potency agonists at CB1 (EC50 of 0.24 to 21 nM) and CB2 (EC50 of 0.88 to 15 nM) receptors. Whereas Δ9-THC is a partial agonist, 5F-AB-PINACA behaves as a full agonist with high intrinsic efficacy: in mice, Wilson et al. (2019) observe convulsions attenuated by a CB1 antagonist but not by diazepam, which suggests that benzodiazepines may not be enough to control them. Kaneko (2017) links road accidents in Japan to five synthetic cannabinoids, including 5F-AB-PINACA, with impaired consciousness, anterograde amnesia, catalepsy, tachycardia and vomiting. No published human pharmacokinetics were found in the sources consulted.

History

Source
Clandestine synthesis, outside any pharmaceutical channel. No natural occurrence: the molecule is absent from cannabis and from any other plant. It has been found in smoking products in Japan (Kaneko 2017).

Origin

Laboratory synthesis

No biosynthetic pathway: an entirely synthetic molecule, with no plant precursor. The skeleton combines an indazole-3-carboxamide nucleus, an N1-(5-fluoropentyl) chain and a primary L-valinamide head.

Classification

Family, origin and source verification

Family

Synthetic CB receptor agonist › New psychoactive substance

Class

indazole-3-carboxamide

Verification

Classification, sources and binding values checked on 20 October 2026; text read against its sources and Wikipedia.

Wikipedia (English)

5F-AB-PINACA (new tab)

Article paired by the molecule's structure (InChIKey), revision read on 19 October 2026. Read as a second opinion, never cited as a source.

References

Identifiers

Names

IUPAC name
N-[(2S)-1-amino-3-methyl-1-oxobutan-2-yl]-1-(5-fluoropentyl)indazole-3-carboxamide
Other names
5-fluoro-AB-PINACA

Identifiers

Formula
C₁₈H₂₅FN₄O₂
CAS
1800101-60-3
InChIKey
WCBYXIBEPFZUBG-HNNXBMFYSA-N
SMILES
CC(C)[C@@H](C(=O)N)NC(=O)C1=NN(C2=CC=CC=C21)CCCCCF

Machine-readable entry (JSON)

LLM ingestion format: a structured superset of the entry (identifiers, binding, versioned legal status). Full corpus.