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AB-005

A synthetic cannabinoid with a CB2 preference, classified as a narcotic in France; human data are lacking.

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.

C₂₃H₃₂N₂O

CAS 895155-25-6

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

Updated on

In plain terms

AB-005 is a laboratory molecule with no connection to hemp: a pharmaceutical laboratory described it in 2010, after which clandestine manufacturers took it up to spray it onto plant material sold as smoking blends. It binds to the same receptors as THC, with a marked preference for the CB2 receptor. What it does in human beings remains unknown, no clinical study or published medical case concerns it, and it is classified as a narcotic in France.

Receptors and activity

Target network

CB2Partial agonistKi = 1 nM · human[3H]CP55,940 displacement, recombinant human CB2 (CHO cells); cAMP efficacy lower than that of Δ9-THC
  • Activates

The lower the cited value, the closer the target sits to AB-005: 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 AB-005.

Brain, side view
Body, front view
Blood

CB2CB2 found in 5 regions of the body

  1. SpleendenseHighly abundant in the spleen1
  2. Immune cellspresentMainly B cells and natural killer cells1
  3. SkinpresentKeratinocytes, mast cells and nerve fibres2
  4. GutpresentImmune cells of the colonic mucosa3
  5. BonepresentPresent on osteoclasts4

Cited values

  1. CB2Partial agonistKi = 1 nM · human83 out of 100

    Hess et al. 2016, Forensic Toxicol (new tab) · [3H]CP55,940 displacement, recombinant human CB2 (CHO cells); cAMP efficacy lower than that of Δ9-THC

  2. CB1Partial agonistKi = 59.4 nM · human54 out of 100

    Hess et al. 2016, Forensic Toxicol (new tab) · [3H]CP55,940 displacement, recombinant human CB1 (CHO cells); cAMP efficacy lower than that of Δ9-THC

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

AB-005 is an indol-3-yl ketone: the indole nucleus carries a 2,2,3,3-tetramethylcyclopropyl group at position 3 and, on its nitrogen, a (1-methylpiperidin-2-yl)methyl chain. It is a chimeric compound, assembled from fragments of UR-144 and AM-1248, arising from a pharmaceutical programme in search of selective CB2 agonists (Frost and colleagues, 2010). The two available sets of measurements agree on a strong affinity for CB2 and a weaker one for CB1: 0.48 nM and 5.5 nM in Frost's work, 1.04 nM and 59.4 nM in the independent re-evaluation by Hess and colleagues (2016). The decisive point is functional: in that same study, most of the synthetic cannabinoids tested behaved as full agonists at the CB receptors, whereas AB-005 activated them with an efficacy lower than that of THC, itself a partial agonist in this system. Full agonism at the CB1 receptor, which accounts for the clinical severity of many compounds in this family, is therefore not established for AB-005. Its azepane isomer, also found on the illicit market, showed no CB1 affinity up to 10 µM and behaves as a moderate CB2 antagonist: two powders bearing the same name may have opposite pharmacologies. No human data, pharmacokinetic or clinical, have been published.

History

Source
A molecule from a pharmaceutical laboratory: it comes from the selective CB2 receptor agonist programme at Abbott Laboratories, described by Frost and colleagues in the Journal of Medicinal Chemistry in 2010. No natural occurrence, either in hemp or in any other plant. Derivatives of this series subsequently reached the illicit market; AB-005 appeared there in turn, accompanied by an azepane isomer, and the UNODC lists it among the synthetic cannabinoid receptor agonists of its early warning system.

Origin

Laboratory synthesis

No biological pathway: the molecule is entirely synthetic. Its framework combines two motifs already known from synthetic cannabinoids, the tetramethylcyclopropyl ketone of UR-144 and XLR-11 on the one hand, and the (1-methylpiperidin-2-yl)methyl chain of AM-1220 and AM-1248 on the other, grafted onto an indole nucleus.

Classification

Family, origin and source verification

Family

Synthetic CB receptor agonist › New psychoactive substance

Class

tetramethylcyclopropylketone

Verification

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

Wikipedia (English)

AB-005 (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
[1-[(1-methylpiperidin-2-yl)methyl]indol-3-yl]-(2,2,3,3-tetramethylcyclopropyl)methanone
Other names
AB005 · [1-[(1-methyl-2-piperidinyl)methyl]-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)-methanone

Identifiers

Formula
C₂₃H₃₂N₂O
CAS
895155-25-6
InChIKey
MOBWRRIAIHYXLB-UHFFFAOYSA-N
SMILES
CN1CCCCC1Cn1cc(C(=O)C2C(C)(C)C2(C)C)c2ccccc21

Machine-readable entry (JSON)

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