1'-<wbr/>Naphthoyl-<wbr/>2-<wbr/>methylindole

1′-Naphthoyl-2-methylindole

CAT N°: 14801

A large number of synthetic cannabinoids (CBs) have been detected in herbal blends sold for recreational use.{19508} 1’-Naphthoyl indole represents the simplest form of this group of cannabimimetics. While the addition of an N-alkyl chain of four or more carbons generates compounds which potently activate CB receptors, short chain lengths are inactive at both central CB1 and peripheral CB2.{16797} This suggests that 1’-naphthoyl indole should have no appreciable affinity for either receptor. 1’-Naphthoyl-2-methylindole differs structurally from 1’-naphthoyl indole by having a methyl group attached at the two position of the indole ring. The biological activities of this compound have not been characterized. This product is intended for forensic and research applications.

Territorial Availability: Available through Bertin Technologies only in France

Technical Warning: Bertin Technologies restricts the sale of this product to licensed controlled substance laboratories and qualified academic research institutions. Please contact us for further details.

Special Advice: Please check regulation status before ordering; additionel fees can apply.

  • Synonyms
    • (2-methyl-1H-indol-3-yl)-1-naphthalenyl-methanone
  • Correlated keywords
    • CBs cannabinoids forensics sciences cannabimimetics CB1 CB2 receptors agonists spices synthetic analytical references standards herbal blends N-alkyl alkyl chains carbons central peripheral naphthoyls methylindoles recreational use 1’-naphthoyl indoles 1s 1’ additions 4s activates shorts inactives affinity 1’-naphthoyl-2-methylindole 2s methyls groups positions rings research applications
  • Product Overview:
    A large number of synthetic cannabinoids (CBs) have been detected in herbal blends sold for recreational use.{19508} 1’-Naphthoyl indole represents the simplest form of this group of cannabimimetics. While the addition of an N-alkyl chain of four or more carbons generates compounds which potently activate CB receptors, short chain lengths are inactive at both central CB1 and peripheral CB2.{16797} This suggests that 1’-naphthoyl indole should have no appreciable affinity for either receptor. 1’-Naphthoyl-2-methylindole differs structurally from 1’-naphthoyl indole by having a methyl group attached at the two position of the indole ring. The biological activities of this compound have not been characterized. This product is intended for forensic and research applications.

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