JWH 200-d5

JWH 200-d5 Chemische Eigenschaften,Einsatz,Produktion Methoden

• Beschreibung

  JWH 200-d₅ contains five deuterium atoms at the 2', 4' ,5', 6', and 7' positions. It is intended for use as an internal standard for the quantification of JWH 200 by GC- or LC-mass spectrometry. JWH 200 is an aminoalkylindole that acts as a cannabinoid (CB) receptor ligand. It binds to the CB₁ receptor with high-affinity (IC₅₀ = 7.8-42 nM).^1,2 The effects of JWH 200 in locomotor activity, tail-flick latency, hypothermia, and ring-immobility tests are comparable or superior to Δ⁹-THC or WIN 55,212.³ It potently inhibits the contraction of electrically-stimulated mouse vas deferens (IC₅₀ = 3.7-6.0 nM).^4,5

• Einzelnachweise

  1. Eissenstat, M.A., Bell, M.R., D'Ambra, T.E., et al. Aminoalkylindoles: Structure-activity relationships of novel cannabinoid mimetics J. Med. Chem. 38,3094-3105(1995).
  2. Huffman, J.W., Mabon, R., Wu, M.J., et al. 3-indolyl-1-naphthylmethanes: New cannabimimetic indoles provide evidence for aromatic stacking interactions with the CB₁ cannabinoid receptor Bioorgan. Med. Chem. 11(4),539-549(2003).
  3. Compton, D.R., Gold, L.H., Ward, S.J., et al. Aminoalkylindole analogs: Cannabimimetic activity of a class of compounds structurally distinct from D 9-tetrahydrocannabinol J. Pharmacol. Exp. Ther. 263(3),1118-1126(1992).
  4. Pacheco, M., Childers, S.R., Arnold, R., et al. Aminoalkylindoles: Actions on specific G-protein-linked receptors J. Pharmacol. Exp. Ther. 257(1),170-183(1991).
  5. Bell, M.R., D'Ambra, T.E., Kumar, V., et al. Antinociceptive (aminoalkyl) indoles J. Med. Chem. 34,1099-1110(1991).

JWH 200-d5 Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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