Hey there,

does anyone know anything re binding efficiency to 5HT-2A receptors for different salts of DMT and DMT allies?

e.g. from memory -

DMT phosphate(?) [i.e. DMT with phosphoric acid] is stronger binding than other DMT salts.

or does it all become DMT past the blood/brain barrier?

basically so e.g. a table could be made up of different strengths of DMT types.

and e.g. bufotenine (Bufo citrate is lower binding apparently)

even anecdotal reports may be handy?