This is an audio version of the: 00:00:39 1 00:01:44 2 Pharmacology 00:02:34 Pharmacokinetics 00:03:39 3 Usage 00:05:53 4 Detection in biological fluids 00:07:03 5 00:07:12 6 is a more natural way of learning, when compared to reading. Only began at around, but spoken language has existed long ago. By listening is a great way to: - increases imagination and understanding - improves your listening skills - improves your own spoken accent - learn while on the move - reduce eye strain Now learn the vast amount of general knowledge available on Wikipedia through audio (audio article).

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JWH-018indole) or is an analgesic chemical from the naphthoylindole family that acts as a full agonist at both the and cannabinoid receptors, with some selectivity for CB2. It produces effects in animals similar to those of, a cannabinoid naturally present in cannabis, leading to its use in synthetic cannabis products such as 'legal cannabis herbal incense blends' which in some countries are sold legally as 'incense', labeled 'not for human consumption'. This video is targeted to blind users. Attribution: text available under image source in video • published: 09 Oct 2015 • views: 7642.

JWH-176 JWH-176 is an drug which acts as a. Its at the CB 1 receptor is only 26.0nM, making it more potent than itself, however JWH-176 is particularly notable in that it is a containing no. This demonstrates that reasonably high-affinity binding and agonist effects can be produced by compounds with no capacity at all, relying merely on interactions to bind to the receptor. It was discovered by, and named after, Dr. See also• References• Huffman JW, Padgett LW. Recent Developments in the Medicinal Chemistry of Cannabimimetic Indoles, Pyrroles and Indenes.

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Current Medicinal Chemistry, 2005; 12: 1395-1411. • Roger Pertwee. Handbook of Experimental Pharmacology Volume 168, p 269. ISBN 3-540-22565-X. JWH-147 JWH-147 is an drug used in scientific research, which acts as a agonist at both the. It is somewhat selective for the CB 2 subtype, with a of 11.0nM at CB 1 vs 7.1nM at CB 2.