AB-CHMINACA is an indazole-based synthetic cannabinoid (CB) with 10-fold higher affinity relating to the main CB1 receptor (Ki = 0.9 nM) in contrast to JWH 018 .
AB-CHMINACA was initially synthesized by Pfizer, Inc. as an effective powerful CB1 receptor modulator for possible therapeutic usage, however not too long ago had been discovered together with AB-PINACA in prohibited herbal products.
AB-CHMINACA is structurally relevant to AB-FUBINACA which includes a cyclohexyl group replaced for the 4-fluorophenyl group. The physical and toxicological attributes associated with the substance haven’t been identified. The product was created for research and forensic purposes.
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This research chemical is not intended for human consumption. This cannabinoid ship direct from our lab to any country in the world.
Presumes no tolerance
Threshold < 1 mg Light 1 – 2 mg
Common 1 – 3 mg
Strong 4 – 5 mg
Heavy > 5 mg
Total 1 – 2 hours
Onset 0 – 20 minutes
Peak 30 – 60 minutes
Offset 10 – 20 minutes
Afterglow 15 – 30 minutes
AB-CHMINACA is an indazole-based synthetic cannabinoid. It is a potent agonist of the CB₁ receptor and CB₂ receptor and fully substitutes for Δ⁹-THC in rat discrimination studies, while being 16x more potent
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