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JWH 018 adamantyl analog

Item No. 9000799

Synonyms
Synonyms
  • AB-001
Technical Information
Formal Name
(1-pentyl-1H-indol-3-yl)tricyclo[3.3.1.13,7]dec-1-yl-methanone
CAS Number
1345973-49-0
Molecular Formula
C24H31NO
Formula Weight
Purity
≥97%
Formulation
A crystalline solid
DMF: 30 mg/mlDMSO: 30 mg/mlEthanol: 1 mg/ml
λmax
214, 247, 305 nm
SMILES
CCCCCN1C2=CC=CC=C2C(C([C@@]3(C4)CC5CC4CC(C5)C3)=O)=C1
InChi Code
InChI=1S/C24H31NO/c1-2-3-6-9-25-16-21(20-7-4-5-8-22(20)25)23(26)24-13-17-10-18(14-24)12-19(11-17)15-24/h4-5,7-8,16-19H,2-3,6,9-15H2,1H3/t17-,18?,19?,24?
InChi Key
SHWDYCMMUPPWQM-AECLTTBISA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    JWH 018 adamantyl analog is a mildly selective agonist of the peripheral cannabinoid receptor, where the naphthalene ring is substituted with an adamantyl group.1 Adamantyl substitutions provide structural rigidity and bulk. Though no biological activity has been reported for JWH 018 adamantyl analog, Δ8-THC analogs with adamantyl substituted for the carbon side chain demonstrate improved affinity and selectivity of central cannabinoid and peripheral cannabinoid receptor binding.2 This synthetic cannabinoid has been identified in a herbal product.3 This product is intended for research and forensic applications.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Sobolevsky, T., Prasolov, I., and Rodchenkov, G. Detection of JWH-018 metabolites in smoking mixture post-administration urine. Forensic Sci. Int. 200(1-3), 141-147 (2010).

    2. Lu, D., Meng, Z., Thakur, G.A., et alAdamantyl cannabinoids: A novel class of cannabinergic ligands. J. Med. Chem. 48(14), 4576-4585 (2005).

    3. Kneisel, S., Westphal, F., Bisel, P., et alIdentification and structural characterization of the synthetic cannabinoid 3-(1-adamantoyl)-1-pentylindole as an additive in 'herbal incense'. J. Mass. Spectrom. 47(2), 195-200 (2012).