Cannabinoïdes

Applications JWH 018 is the 18th compound synthesized in a series of more than 470 analogs and metabolites of ∆9-Tetrahydrocannabinol (THC) (T293200), the active component of marijuana. JWH 018 acts as cannabinoid receptor.Controlled substance.Synthetic Cannabinoids References Matsuda, L., et al.: Nature, 346, 561 (1990), Gerard, C., et al.: Biochem. J., 279, 129 (1991), Parkkari, T., et al.: Bioorg. Med. Chem., 14, 5252 (2006), Salo, O., et al.: J. Med. Chem., 49, 554 (2006),

OMDM-1 ((Z)-N-[(2S)-1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl]octadec-9-enamide) is a selective and metabolically stable anandamide cellular uptake (ACU)

GP 1a: potent CB2 receptor agonist (EC50=7.1), 30x CB2 over CB1 preference, boosts P-ERK1/2, aids skin healing, anti-inflammatory.

Applications Labelled analogue of a cannabimimetic indole derivative that acts as a CB2 receptor agonist with weak CB2 activity. It has been shown to possess immunomodulatory effects and may be useful in the treatment of pain and inflammation. Synthetic cannabinoids References Aung, M.M. et al.: Drug Alc. Depend., 60, 133 (2000); Ghosh, S. et al.: Mol. Immunol., 43, 2169 (2006); Ehrhart, J. et al.: J. Neuroinflam., 2, 29 (2005); Romero-Sandoval, A. et al.: Anethesiol., 106, 787 (2007);

Applications A synthetic cannabimimetic indole derivative which acts as a potent and selective agonist for the cannabinoid receptor CB1. Synthetic cannabinoids References Willis P.G. et al.: J. Lab. Cpd. Radiopharmac., 46, 799 (2003);

PSNCBAM-1 (PSNCBAM 1) is a CB1 receptor negative allosteric modulator (EC50 = 0.1 μM) with hypophagic effects in vivo.

Applications 4′-Chloroacetanilide is an impurity of Acetaminophen (A161220), an analgesic and antipyretic agent used as a pain reliever to treat headache, muscle aches, and arthritis (1,2,3,4). References (1) Călinescu, O., et al.: J. Chromatogr. Sci. 50(4), 335-42, (2012)(2) McGill, M. R. and Jaeschke, H. Pharm Res. 30, 2174 (2013)(3) Fairbrother, J.E., et al.: Anal. Profiles Drug Subs., 3, 1 (1974) (4) Hinson, J.A., et al.: Rev. Biochem. Toxicol., 2, 103 (1980)

Stability Temperature, Moisture, Light, and Oxygen Sensitive Applications N-Acetyl-4-benzoquinone imine-D3 is deuterium labeled N-Acetyl-4-benzoquinone Imine (A170000). N-Acetyl-4-benzoquinone Imine (NAPQI) is a toxic metabolite of Acetaminophen (A161220), an analgesic and antipyretic agent used as a pain reliever to treat headache, muscle aches, and arthritis (1,2,3). N-Acetyl-4-benzoquinone Imine can react with cysteine residues of hepatic proteins to yield Acetaminophen-cysteine (A161255) (4). References (1) Jaeschke, H., et al.: Toxicol. Sci., 89, 31 (2006) (2) O’Malley G. F., et al.: J Med Toxicol. 11, 317 (2015)(3) McGill, M. R. and Jaeschke, H. Pharm Res. 30, 2174 (2013)(4) Frey, S. M., et al.: J Med Toxicol. 11, 218 (2015)

Applications Rimonabant Hydrochloride is a potent and selective CB1 cannabinoid antagonist used to investigate CB receptor properties (1). Rimonabant Hydrochloride is also an anti-obesity agent (2). Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References (1) Carai, M.A.M., et al.: Life Sci., 77, 2339 (2005) (2) Janiak, P., et al.: Kidney Int. 72, 1345 (2007)