CUMYL-NBMINACA
Synthetic cannabinoid with an indazole core, full CB1 agonist, French status not settled.
C₂₅H₂₉N₃O
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.
Data sheet
Names
- IUPAC name
- 1-(2-bicyclo[2.2.1]heptanylmethyl)-N-(2-phenylpropan-2-yl)indazole-3-carboxamide
- Other names
- SGT-152 · Cumyl-BC[2.2.1]HpMINACA
Identifiers
- Formula
- C₂₅H₂₉N₃O
- Molar mass
- 387.50 g/mol
- CAS
- 1631074-60-6
- PubChem CID
- 117650372(new tab)
- InChIKey
- MLRLLZWQYJJPEX-UHFFFAOYSA-N
Class
- Family
- Synthetic cannabinoid (SCRA)
Updated on
Receptors and activity
- CB1Agonist95 out of 100
Ki de 0,25 à 1,87 nM pour la série norbornylméthyle, l'indazole étant le plus affin ; EC50 de 1,78 à 169 nM, l'indazole tendant à être le plus puissant (Pulver et coll., 2023)
Subjective signature
- Calm
- 10 out of 100
- Relaxation of body and mind; reduced mental noise without marked drowsiness.
- Clarity
- 4 out of 100
- Sustained attention and clear thinking; functional lucidity, not euphoria.
- High
- 15 out of 100
- Euphoria and sensory intensity; altered perception of time and space.
- Appetite
- 12 out of 100
- Stimulation of hunger and of taste appreciation (the “munchies” effect).
- Sleep
- 10 out of 100
- Sedative effect: aids sleep onset and the continuity of deep sleep.
Pharmacology
Cumyl-NBMINACA is a synthetic cannabinoid of the indazole-3-carboxamide family, a full agonist at the CB1 cannabinoid receptor. Pulver et al. (2023) report, for the norbornylmethyl series, an affinity constant Ki between 0.25 and 1.87 nM, the indazole being the most affine derivative, with an EC50 from 1.78 to 169 nM for the same series. Giorgetti et al. (2025) described its phase I metabolism from two authentic urine samples, in which 13 phase I metabolites were identified, and proposed urinary biomarkers based on the norbornylmethyl chain. Its legal status in France remains to be settled: it is not named on the ANSM list, and whether it meets the generic definition of indazole-3-carboxamides depends on how the cycloalkylmethyl substituent is interpreted. No clinical study and no controlled human toxicology data are published in the sources consulted.
Key sources.
- Giorgetti et coll., métabolisme de phase I humain de trois cannabinoïdes de synthèse à noyau cumyle dont le Cumyl-NBMINACA, Drug Test Anal, 2025 (new tab)PMID 39218806
- Pulver et coll., pharmacologie, prévalence en Allemagne et données analytiques des cannabinoïdes de synthèse à chaînes cyclobutylméthyle et norbornylméthyle, Drug Test Anal, 2023 (new tab)PMID 36541839
- ANSM, Liste consolidée des substances classées comme stupéfiants, mise à jour du 16 février 2026 (annexe IV, définition des dérivés du 3-carboxamide indazole) (new tab)
- OICS, Liste verte des substances psychotropes sous contrôle international, édition 2026 (new tab)
- PubChem, CUMYL-NBMINACA, CID 117650372 (new tab)
History
- Source
- Synthetic molecule: the sources consulted class it among synthetic cannabinoids, with no plant origin reported in those sources. Purified standards of Cumyl-NBMINACA were isolated from herbal blend material within the European ADEBAR plus project (Giorgetti et al., 2025). Pulver et al. (2023) report that the cyclobutylmethyl and norbornylmethyl side chains allowed these substances to circumvent German legislation, and that the market life cycle of these substances was less than one year.
Origin (pharmaceutical research → illicit market)
No biosynthetic pathway: Cumyl-NBMINACA is a synthetic molecule, chemically classed among the indazole-3-carboxamides, with no known link to a plant or a living organism.
Legal framework
- European Union
At European Union level, no harmonised control measure is documented in the sources consulted: control falls under national legislation.
- France
Cumyl-NBMINACA is not named on the ANSM consolidated list of narcotics (updated 16 February 2026). The relevant framework is the generic definition of indazole-3-carboxamide derivatives, listed in annex IV of that consolidated list. The amide condition is met: the cumyl group is among the listed substituents. The condition on the N1 nitrogen requires a cycloalkylmethyl-type substituent, and the norbornylmethyl chain is a bicyclic ring: the text does not say whether this case falls within that category. As this cannot be decided with certainty, the French status is classed as evolving. The international status is separate: the compound is not listed on the INCB Green List 2026.
Sources: EUR-Lex, UNODC, CND, ANSM, IUPHAR/BPS, ChEBI, EUDA. Our method.
References
- Giorgetti et coll., métabolisme de phase I humain de trois cannabinoïdes de synthèse à noyau cumyle dont le Cumyl-NBMINACA, Drug Test Anal, 2025 (new tab)PMID 39218806
- Pulver et coll., pharmacologie, prévalence en Allemagne et données analytiques des cannabinoïdes de synthèse à chaînes cyclobutylméthyle et norbornylméthyle, Drug Test Anal, 2023 (new tab)PMID 36541839
- ANSM, Liste consolidée des substances classées comme stupéfiants, mise à jour du 16 février 2026 (annexe IV, définition des dérivés du 3-carboxamide indazole) (new tab)
- OICS, Liste verte des substances psychotropes sous contrôle international, édition 2026 (new tab)
- PubChem, CUMYL-NBMINACA, CID 117650372 (new tab)
Structured data
- SMILES
- CC(C)(C1=CC=CC=C1)NC(=O)C2=NN(C3=CC=CC=C32)CC4CC5CCC4C5
- InChIKey
- MLRLLZWQYJJPEX-UHFFFAOYSA-N
LLM ingestion format: a structured superset of the entry (identifiers, binding, versioned legal status). Full corpus.