(zonk)
Bluelighter
- Joined
- May 24, 2008
- Messages
- 687
I was hoping someone could briefly clear this up for me. Magnolol and honokiol both have agonist actions at cb1 receptors. Honokiol more so but Magnolol's metabolite tetrahydromagnolol is way more potent but here's where what I'm reading throws me off. Most reports say it 17x more potent at cb2 receptors and greatly selective to cb2 over cb1 however other reports I've read say if i remember right it is 120x more potent at cb1 than magnolol. I can't seem to locate it's ki values for cb1? Also can't find much references to other magnolia compounds like tetrahydrohonokiol etc...