JWH-007

JWH-007

(2-Methyl-1-pentyl-1H-indol-3-yl)(naphthalen-1-
yl)methanone (JWH–007)

Allied Chemicals GmbH (AL-GMBH) is a leading Specialty Chemicals & Science Based Company in Germany. We deliver an extensive range of high quality Specialty Chemicals & Allied Products to several sectors.

The chemical preparation of all our products are synthesized. These substances possesses sterile effect, so you must be fully aware of what you are purchasing hence there’s no prejudice involved in the offer and acceptance.

Available for sale here is JWH-007:

JWH-007 is an analgesic chemical from the naphthoylindole family, which acts as a cannabinoid agonist at both the CB1 and CB2 receptors. It was first reported in 1994 by a group including the noted cannabinoid chemist John W. Huffman.

It was the most active of the first group of N-alkyl naphoylindoles discovered by the team led by John W Huffman, several years after the family was initially described with the discovery of the N-morpholinylethyl compounds pravadoline (WIN 48,098), JWH-200 (WIN 55,225) and WIN 55,212-2 by the Sterling Winthrop group.

Several other N-alkyl substituents were found to be active by Huffman’s team including the n-butyl, n-hexyl, 2-heptyl, and cyclohexylethyl groups, but it was subsequently determined that the 2-methyl group on the indole ring is not required for CB1 binding, and tends to increase affinity for CB2 instead.

Consequently, the 2-desmethyl derivative of JWH-007, JWH-018, has slightly higher binding affinity for CB1, with an optimum binding of 9.00 nM at CB1 and 2.94 nM at CB2, and JWH-007 displayed optimum binding of 9.50 nM at CB1 and 2.94 nM at CB2.

You can buy JWH-007 with a purity of 98%>! Buy JWH-007 in our store without any problems. The product is intended for research purposes only and is not sold for consumption purposes.

By ordering / purchasing JWH-007, you automatically agree with our general terms and conditions that you only purchase the product for research purposes and that you do not use the product for other purposes.

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