User talk:108.162.112.136

I believe that the lower structure in the top frame on the right is incorrect. It is not the racemic isomer but is a different isomer that would have a different conformation and presumably different activity. The structure shown for Cesamet (nabilone) at the FDA website (https://www.accessdata.fda.gov/drugsatfda_docs/label/2006/018677s011lbl.pdf) shows only the one isomer and makes reference only to a (+/-) racemate. The lower molecule as drawn is a diasteriomer. Jbossart (talk) 00:49, 28 March 2018 (UTC)