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5-cl-adb-a (MDMB-4en-P) is a synthetic cannabinoid with an indazole core and a terminal alkene on the side chain. It is structurally similar to 5F-MDMB-PINACA (5F-ADB). It has chiral properties. Although the enantiomers were not separated in the laboratory, the S-enantiomer was found in samples. The chemical cannot be easily converted into other restricted substances, and it has never been evaluated by the WHO Expert Committee on Drug Dependence. Contact Legit Cannabinoids today to Buy 5-cl-adb-a online!

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Chemshopa sells 5-CL-ADB-A (MDMB-4en-P).

5-cl-adb-a (MDMB-4en-P) is a synthetic cannabinoid with an indazole core and a terminal alkene on the side chain. It is structurally similar to 5F-MDMB-PINACA (5F-ADB). It has chiral properties. Although the enantiomers were not separated in the laboratory, the S-enantiomer was found in samples. The chemical cannot be easily converted into other restricted substances, and it has never been evaluated by the WHO Expert Committee on Drug Dependence. Contact Legit Cannabinoids today to Buy 5-cl-adb-a online!

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What are the Administration Routes for 5-cl-adb-a (MDMB-4en-P)?

The most likely mode of administration for 5-cl-adb-a (MDMB-4en-P) in humans appears to be smoking the chemical after it has been sprayed onto plant material or vaping it after preparation in liquid. It was discovered in confiscated smoking-related materials. However, it is unknown what dosage is needed to produce pharmacological effects in humans. We have 5-cl-adb-a (MDMB-4en-P) for sale at Legit Cannabinoids. Order yours today! 5-CL-ADB-A for Sale

What Characteristics Does 5-cl-adb-a (MDMB-4en-P) Have?

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5-cl-adb-a (MDMB-4en-P) is extensively metabolized, as are many other synthetic cannabinoids. Unlike some other synthetic cannabinoids, the parent product was discovered in genuine urine samples. The most abundant metabolite in human liver microsomes, hepatocytes, and real urine samples was 5-cl-adb-a (MDMB-4en-P). The Ki of 5-cl-adb-a (MDMB-4en-P) for human cannabinoid type 1 (hCB1) receptors is 3.26 nM. It’s also a complete and potent agonist, reducing forskolin-stimulated cyclic adenosine monophosphate (cAMP) accumulation (EC50 = 0.33 nM).

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