JWH 200-<wbr/>d<sub>5</sub> (exempt preparation)

JWH 200-d5 (exempt preparation)

CAT N°: 10682

JWH 200-d5 (exempt preparation) 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 (exempt preparation) 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).{16961,16684} The effects of JWH 200 in locomotor activity, tail-flick latency, hypothermia, and ring-immobility tests are comparable or superior to ?9-THC or WIN 55,212.{16963} It potently inhibits the contraction of electrically-stimulated murine vas deferens (IC50 = 3.7-6.0 nM).{16960,16962}

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
    • [1-[2-(4-morpholinyl)ethyl]-1H-indol-3-yl-2′,4′,5′,6′,7′-d5]-1-naphthalenyl-methanone
  • Correlated keywords
    • cannabinoids receptors agonists CB1 pain antinociception deuterateds deuterium GC/MS GC-MS LC/MS LC-MS mass spectrometry MS cannabinoids cbs synthetic JWH-200-d5 JWH200-d5 10903 analytical references standards
  • Product Overview:
    JWH 200-d5 (exempt preparation) 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 (exempt preparation) 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).{16961,16684} The effects of JWH 200 in locomotor activity, tail-flick latency, hypothermia, and ring-immobility tests are comparable or superior to ?9-THC or WIN 55,212.{16963} It potently inhibits the contraction of electrically-stimulated murine vas deferens (IC50 = 3.7-6.0 nM).{16960,16962}

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