I am sort of interested in analogs. I say sort of because I’m less interested in their shared properties with a drug, and more with their different
properties. I am basically interested in synthesis/design of new compounds based of tryptamines/phenethylamines that have potential uses in medicine,
rather than recreationally. I have been running docking simulations of proteins with a couple different molecules, and I don’t currently want to
synthesize these compounds, but I do have a question about a specific grouping of compounds. It seems that when Substituted phenethylamines have a
benzyl group added onto their nitrogen, they become more active, but they also become more toxic. Why is this? Is the added toxicity due to metabolism
products, is the compound itself more toxic, or is it something completely different? |