Sprout
Bluelight Crew
Will update thread as and when I can.
The first generation of synthetics were the brainchild of Dr Huffman brginning in 1984. Many of the compounds he synthesised eventually found their way into the posterchildren of the synthetics in mainstream society: K2 and Spice blends.
The most commonly encountered example of the JWH-x series (those are his initials, not nomenclature...) was JWH-018.
JWH-018 Megathread
It seems ChinaChem is still thoroughly creating novel Cannabinoids at a ridiculous rate, even in the face of the legislature and precursor controls.
Four SCRA's were recently seized from a clandestine laboratory and identified as:
N-(1-Amino-3,3-dimethyl-1-oxobutan-2-yl)-1-benzyl-1H-indazole-3-carboxamide (ADB-BINACA);
N-(1-Amino-3-methyl-1-oxobutan-2-yl)-1-(4-fluorobenzyl)-1H-indole-3-carboxamide (AB-FUBICA);
N-(1-Amino-3,3-dimethyl-1-oxobutan-2-yl)-1-(4-fluorobenzyl)-1H-indole-3-carboxamide (ADB-FUBICA);
N-(1-Amino-3-methyl-1-oxobutan-2-yl)-1-benzyl-1H-indole-3-carboxamide (AB-BICA)
Identification and Analysis Paper
Of note is that AB-BICA was not even known to exist until this point. There is absolutely zero information from a chemical, biological, pharmacological or toxicological perspective.
These products were not being manufactured for the borderline licit RC trade, rather for the black market illicit drug trade.
The first generation of synthetics were the brainchild of Dr Huffman brginning in 1984. Many of the compounds he synthesised eventually found their way into the posterchildren of the synthetics in mainstream society: K2 and Spice blends.
The most commonly encountered example of the JWH-x series (those are his initials, not nomenclature...) was JWH-018.
JWH-018 Megathread
From this paperpaper said:The in vitro microsomal metabolism of JWH-015, a ligand that exhibits a high binding affinity at the peripheral cannabinoid receptor CB2, has been studied. A total of 22 metabolites were identified and structurally characterized. The metabolites are products of: 1) monohydroxylation on the naphthalene ring (m/z 344, M20 and M21), indole ring (m/z 344, M17 and M18 ), or the N-alkyl group (m/z 344, M14); 2) arene oxidation leading to dihydrodiols (m/z 362, M12 and M15); 3) dihydroxylation on the naphthalene ring (m/z 360, M7) or indole ring (m/z 360, M13), resulting from a combination of monohydroxylations on both the naphthalene and indole rings (m/z 360, M16), or a combination of monohydroxylations on the naphthalene ring and on the N-propyl group (m/z 360, M9); 4) trihydroxylation (m/z 378, M1, M3, M4, M6, and M10); 5) N-dealkylation (m/z 286, M19); 6) N-dealkylation and monohydroxylation on the naphthalene ring (m/z 302, M11); 7) N-dealkylation and dihydrodiol formation from arene oxidation (m/z 320, M2 and M5); 8 ) dehydrogenation after monohydroxylation on the N-alkyl group (m/z 326, M22); 9) dehydrogenation and monohydroxylation on the indole ring (m/z 342, M8 ).
It seems ChinaChem is still thoroughly creating novel Cannabinoids at a ridiculous rate, even in the face of the legislature and precursor controls.
Four SCRA's were recently seized from a clandestine laboratory and identified as:
N-(1-Amino-3,3-dimethyl-1-oxobutan-2-yl)-1-benzyl-1H-indazole-3-carboxamide (ADB-BINACA);
N-(1-Amino-3-methyl-1-oxobutan-2-yl)-1-(4-fluorobenzyl)-1H-indole-3-carboxamide (AB-FUBICA);
N-(1-Amino-3,3-dimethyl-1-oxobutan-2-yl)-1-(4-fluorobenzyl)-1H-indole-3-carboxamide (ADB-FUBICA);
N-(1-Amino-3-methyl-1-oxobutan-2-yl)-1-benzyl-1H-indole-3-carboxamide (AB-BICA)
Identification and Analysis Paper
Of note is that AB-BICA was not even known to exist until this point. There is absolutely zero information from a chemical, biological, pharmacological or toxicological perspective.
These products were not being manufactured for the borderline licit RC trade, rather for the black market illicit drug trade.
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