Cannabinoids

Applications Used in the preparation of CB1 cannabinoid receptor agonists and brain imaging agents.
References Deng, H. et al; J. Med. Chem. 48, 6386 (2005)

Applications 1-Pentyl-3-(4-methoxynaphthoyl)indole is an analgesic chemical which acts as cannabinoid agonist at the CB1 and CB2 receptors. Synthetic Cannabinoids
References Huffman, J., et al.: Bioorg. Med. Chem., 11, 539 (2003); De Freitas, G., et al.: Eur. J. Med. Chem., 44, 2482 (2009);

Applications cis-2-Decen-1-ol is an intermediate in the synthesis of Falcarinol which is a covalent cannabinoid CB1 receptor antagonist and induces pro-allergic effects in skin. A natural pesticide produced by carrots and red ginseng, protecting hosts roots from various fungal diseases. It has been shown to have nutritional benefits, reducing the risk of developing specific forms of cancer.
References Czepa, A., et al.: J. Agric. Food Chem., 52, 4508 (2004), Radulovic, N., et al.: Chem. Nat. Compds., 44, 390 (2008),

Applications Nitrosobenzene (cas# 586-96-9) is a useful research chemical.

Applications KML-29 is an extremely specific monoacylglycerol lipase (MAGL) inhibitor. KML-2 should be useful to distinguish between actions of 2-arachidonoyl glycerol (an endogenous ligand of cannabinoid receptors that is deactivated by MAGL) and anandamide, another endocannabinoid.
References Ueda, N. et al.: Chem. Biol., 19, 545 (2012);

Applications JWH-007 is a novel cannabinoid receptor agonist at both the CB1 and CB2 receptors. Synthetic cannabinoids
References Pertwee, R.G., et al.: Euro. J. Pharmacol., 284, 241 (1995); Wiley, J.L., et al.: J. Pharmacol. Experiment. Therap., 285, 995 (1998);

Applications A labelled synthetic cannabinoid with antiemetic, antiglaucoma, and CNS activity. Antiemetic. Controlled substance (hallucinogen).
References Rubin, A., et al.: Clin. Pharmacol. Ther., 22, 85 (1977), Stark, P., et al.: J. Pharmacol. Exp. Ther., 214, 124 (1980), Souter, R.W., et al.: Anal. Profiles Drug Subs., 10, 499 (1981), Ward, A., Drugs, 30, 127 (1985),

Applications (5Z,​8Z,​11Z,​14Z)​-5,​8,​11,​14-​Eicosatetraenoic Acid 2-​[[(1,​1-​Dimethylethoxy)​carbonyl]​amino]​ethyl Ester is an intermediate used in synthesizing O-Arachidonoyl ethanolamine hydrochloride (A765130), a partial agonist at CB1 receptor and a full agonist at CB2 receptor. O-Arachidonoyl ethanolamine hydrochloride can be isolated from constituent of human and rat brain. It can be used to prepare antimicrobial arachidonic acid derivative.
References Kvasenkov, O. I. RU 2171610 C2 20010810 (2001); Sharir, H., et al.: J Neuroimmune Pharmacol. 7, 856 (2012)

Applications 1-Pentyl-1H-indazole-3-carboxylic Acid is a useful synthetic intermediate in the synthesis of N-(1-Methyl-1-phenylethyl)-1-pentyl-1H-indazole-3-carboxamide (M327300); a cannabinoid indazole compound that can potentially be used for treating pain and nausea, for stimulating appetite, and for inducing a positive mood change.
References Bowden, M.J., et al.: PCT Int. Appl. WO 2014167530 A1 20141016. Oct 16, 2014

Applications (1-Pentyl-1H-indol-3-yl)(2,2,3,3-tetramethylcyclopropyl)methanone is an Indol-3-ylcycloalkyl Ketone with high affinity for the CB2 cannabinoid receptor. Tetramethylcyclopropyl group was found to lead to high affinity CB2 agonists. Synthetic Cannabinoids
References Malan, T., et al.: Curr. Opin. Pharmacol., 3, 62 (2003), Cabral, G., et al.: J. Leukocyte Biol., 78, 1192 (2005), Beltramo, M., et al.: Eur. J. Neurosci., 23, 1530 (2006), Dziadulewicz, E., et al.: J. Med. Chem., 50, 3851 (2007),

Applications 5-(4-Chlorophenyl)-1-(2,4-dichlorophenyl)-4-methylpyrazole-3-carboxylic Acid is used in the preparation of biarylpyrazole based derivatives as cannabinoid CB1 receptor antagonists. It is metabolite M9 of Rimonabant (R517800), an antiobesity agent.
References Kang, S.Y. et al.: Bioorg. Med. Chem. Lett., 18, 2385 (2008); Fulp, A. et al.: Bioorg. Med. Chem. Lett., 21, 5711 (2011); Bergstrom, M.A. et al.: Drug Metab. and Dispos., 39, 1823 (2011);

Applications RCS-4 is a synthetic JWH 018 cannabinoid analog that has been identified as a component of several different ‘herbal incense’ products. Synthetic Cannabinoids
References Gandhi, A., et al.: Bioanalysis, 6, 1471 (2014);

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)

Applications Labelled JWH 081 (P283600). An analgesic chemical which acts as a cannabinoid agonist at the CB1 and CB2 receptors.
References Huffman, J., et al.: Bioorg. Med. Chem., 11, 539 (2003), De Freitas, G., et al.: Eur. J. Med. Chem., 44, 2482 (2009),

Applications Labelled JWH 19 (H296800). An N-1 alkyl indole cannabinoid receptor agonist. The N-1 alkyl chain length of cannabimimetic indoles influences CB1 and CB2 receptor binding.
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 D'Ambra, T., et al.: J. Med. Chem., 35, 124 (1992), Cheng, Y., et al.: Biochem. Pharmacol., 22, 3099 (1973), Pertwee, R., et al.: Eur. J. Pharmacol., 284, 241 (1995),

Applications An N-1 alkyl indole cannabinoid receptor agonist. The N-1 alkyl chain length of cannabimimetic indoles influences CB1 and CB2 receptor binding.
References D'Ambra, T., et al.: J. Med. Chem., 35, 124 (1992), Cheng, Y., et al.: Biochem. Pharmacol., 22, 3099 (1973), Pertwee, R., et al.: Eur. J. Pharmacol., 284, 241 (1995),

Applications Labelled JWH-200 (M723765). An analgesic compound which acts as a partial agonist at both the CB1 and CB2 cannabinoid receptors.
References Compton, D., et al.: J. Pharmacol. Exper. Ther., 263, 1118 (1992), Tetko, I., et al.: J. Med. Chem., 44, 2411 (2001), Huffman, J., et al.: Bioorg. Med. Chem., 11, 539 (2003),