Variation of the alkyl side chain in 铻?sup>8-THC was written by Huffman, John W.;Lainton, Julia A. H.;Dai, Dong;Jordan, Robert D.;Duncan, Sammy G. Jr.. And the article was included in Life Sciences in 1995.Category: bromides-buliding-blocks This article mentions the following:
The synthesis of (2’RS)-2′-methyl-, (3’RS)-, (3’S)-3′-methyl-, and 4′-methyl-铻?sup>8-THC has been carried out, and the pharmacol. of all four compounds has been investigated. All four compounds showed typical cannabinoid activity both in vitro and in vivo. The 2′-Me compound is somewhat more active than 铻?sup>8-THC, while the 4′-Me isomer is less active. The 3′-methyl-铻?sup>8-THC has approx. the same activity as the parent cannabinoid. In the experiment, the researchers used many compounds, for example, Isopentyltriphenylphosphonium bromide (cas: 28322-40-9Category: bromides-buliding-blocks).
Isopentyltriphenylphosphonium bromide (cas: 28322-40-9) belongs to organobromine compounds. Most of the natural organobromine compounds are produced by marine organisms, and several brominated metabolites with antibacterial, antitumor, antiviral, and antifungal activity have been isolated from seaweed, sponges, corals, molluscs, and others. Commercially available organobromine pharmaceuticals include the vasodilator nicergoline, the sedative brotizolam, the anticancer agent pipobroman, and the antiseptic merbromin. Category: bromides-buliding-blocks
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary