Yeah, affinity about the same, but MDA is far more efficacious. At least when it comes to IP3 production.
But it doesn't matter cause the affinity is so small incomparison to SERT that I doubt there is much going on there... well maybe, Well when rats are given NEUROTOXIC doses of MDMA, big doses around the 10mg/kg range, they get brain concentrations of MDMA around 10µM. Recreationally, we get more like 1mg/kg so we could geuss our brain concentration is more like 1µM, (probably less, maybe half, because we're talking oral vs IP) which is right around dopamine/serotonin release EC50s, but about 10 times lower than the 5-HT2A Kd, so you've be getting like 5% binding or something.
I'm just gonna make a table here for my own ammusement
Species..............Dose.........[Plasma]....[Brain]
Normal Human...1mg/kg.....1µM...........(1µM)
Overdose...........unknown..1.6µM........3.6µM
Rat.....................10mg/kg...6.2µM........5µM
hmm... those concentrations aren't at the same time, for the human and the rat, the plasma is peak, and the rat brain is peak as well, which happens at about 1 hour, vs 20minutes for plasma. The overdose is just when the found him, probably around T+12, poor fucker. Probably had some metabolism of plasma MDMA.
STILL- Why is MDA more hallucinogenic? I don't have a fucking clue, but it certainly isn't because of innate agonism at 5-HT2A
Those numbers came from-
Normal human: De La Torre et al., (2000) Ann N Y Acad Sci. 914:225-37
Overdose: De Letter et al., (2004) Forensic Sci Int. 141(2-3):85-90
Rat plasma: Colado et al., (1995) Brit J Pharmacol 115:1281-1289
Rat Brain: Esteban et al., (2001)Psychopharmacol 154:251–260