SGT-67 Buy

SGT-67 Buy

260,00 3.000,00 

SGT-67

Sgt - 263b powder is a very strong substance. They are slightly less anesthetic and are very good painkillers, sedatives and a strong sleep aid. based on research conducted by our laboratory in 2019,
SGT - 263 (also known as CUMYL - 5F - P7AICA or 5F - CUMYL - P7AICA) is a synthetic cannabinoid based on pyrrolo[2,3 - b]pyridine - 3 - carboxamide.

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SGT-67 Buy, SGT-67 belongs to a type of designer drug called synthetic cannabinoids.
The 5F-APICA equivalent SGT-67 (5F-CUMYL-PICA) has an N-cumyl group instead of an N-adamantyl group. It is hypothesized that 5F-CUMYL-PICA functions as a cannabinoid receptor agonist. This article is intended for use in forensic and research settings.

Within the synthetic cannabinoid family, Sgt-67 is a recently discovered research compound. The IUPAC name of the compound is 1-(5-fluoropentyl)-n-(2-phenylpropan-2-yl)-1h-indole-3-carboxamide.

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In a study on SGT-67, urine collection and in vivo rat plasma were compared to the metabolism and clearance of the research chemical using rat and human liver microsomes and hepatocytes.

In addition, hypothermia was investigated and microsome therapy was used.

Hypothermia studies also showed that while treatment with microsomes resulted in rapid metabolic clearance, in vivo metabolism took longer and allowed detection in rat plasma. In the identification of 28 metabolites, the research chemical showed hypothermic properties.

Special features of SGT-67 (5F-CUMYL-PICA)

Formula for a molecule: C23H27FN2O

Weight in molecules: 366,471

N-(2-phenylpropan-2-yl)-1-(5-fluoropentyl)-1H-indole-3-carboxamide is the chemical name.

CAS number: 1400742-18-8

Appearance: Powder white

Purity: (GCMS confirmation required)

Pharmacology Until now, little attention has been paid to its pharmaceutical properties. However, at its core it is a synthetic member of the indazole family of cannabinoids. Its closest relative differs only in that the formula now provides for an N-cumyl group instead of the N-adamantyl group. It should target the CB2 receptor and exhibit 5F-CUMYL selectivity for the CBI receptor.

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